GE

Technical Publication
LOGIQ e
Basic Service Manual
Direction Number: 5561650-100 English
Rev. 3

All Material Copyright © 2015 by General Electric Company Inc.

All Rights Reserved.
Product Information

This Manual covers the software version of R8.x.x, R9.x.x for LOGIQ e ultrasound
system.

GE

Copyright © 2015, General Electric Company.

GE Medical Systems, a General Electric Company, going to
market as GE
Manufacturer:
GE Medical Systems (China) Co., Ltd.
No. 19, Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu, P.R. China 214028
TEL: +86 510 85225888; FAX: +86 510 85226688
www.gehealthcare.com
Revision history
Revision History

DATE
REV (YYYY/MM/DD) REASON FOR CHANGE

Rev.1 2015/03/10 Initial Release

Rev.2 2015/06/05 Add software wiping information

Rev.3 2015/08/28 Update spare part list

List of Effected Pages (LOEP)

Chapter Number Revision Chapter Number Revision

Front Rev. 3 Chapter 7 Rev. 3

Front matter Rev. 3 Chapter 8 Rev. 3

TOC Rev. 3 Chapter 9 Rev. 3

Chapter 1 Rev. 3 Chapter 10 Rev. 3

Chapter 2 Rev. 3 Chapter 11 Rev. 3

Chapter 3 Rev. 3 Chapter 12 Rev. 3

Chapter 4 Rev. 3 Index Rev. 3

Chapter 5 Rev. 3 Rear Cover Rev. 3

Chapter 6 Rev. 3

Please verify that you are using the latest revision of this document. Information
pertaining to this document is maintained on MyWorkshop/ePDM (GE electronic Product
Data Management). If you need to know the latest revision, contact your distributor, local
GE Sales Representative or in the USA call the GE Ultrasound Clinical Answer Center at
1 800 682 5327 or 1 262 524 5698.

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Important precautions

Translation policy

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Damage in transportation
All packages should be closely examined at time of delivery. If
damage is apparent, write “Damage In Shipment” on ALL copies
of the freight or express bill BEFORE delivery is accepted or
“signed for” by a GE representative or hospital receiving agent.
Whether noted or concealed, damage MUST be reported to the
carrier immediately upon discovery, or in any event, within 14
days after receipt, and the contents and containers held for
inspection by the carrier. A transportation company will not pay a
claim for damage if an inspection is not requested within this 14
day period.

Certified electrical contractor statement - For USA Only

All electrical Installations that are preliminary to positioning of
the equipment at the site prepared for the equipment shall be
performed by licensed electrical contractors. Other connections
between pieces of electrical equipment, calibrations and testing
shall be performed by qualified GE personnel. In performing all
electrical work on these products, GE will use its own specially
trained field engineers. All of GE’s electrical work on these
products will comply with the requirements of the applicable
electrical codes.
The purchaser of GE equipment shall only utilize qualified
personnel (i.e., GE’s field engineers, personnel of third-party
service companies with equivalent training, or licensed
electricians) to perform electrical servicing on the equipment.

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Omission and errors
If there are any omissions, errors or suggestions for improving
this documentation, contact the GE Global Documentation
Group with specific information listing the system type, manual
title, part number, revision number, page number and
suggestion details.
Mail the GE Medical Systems (China) Co., Ltd.
information to: No. 19 Changjiang Road
Wuxi National Hi-Tech Dev. Zone
Jiangsu
P.R.China 214028

GE employees should use TrackWise to report service

documentation issues.
These issues will then be in the internal problem reporting tool
and communicated to the writer.

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Service Safety Considerations

DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH,

ARE PRESENT IN THIS EQUIPMENT. USE EXTREME
CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

WARNING Use all Personal Protection Equipment (PPE) such as gloves,

safety shoes, safety glasses, and kneeling pad, to reduce the
risk of injury.

For a complete review of all safety requirements, refer to

Chapter 1 in the Service Manual.

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Legal notes
The contents of this publication may not be copied or duplicated
in any form, in whole or in part, without prior written permission
of GE.
GE may revise this publication from time to time without written
notice.

Proprietary to GE
Permission to use this Advanced Service Software and related
documentation (herein called the material) by persons other
than GE employees is provided only under an Advanced
Service Package License relating specifically to this Proprietary
Material. This is a different agreement from the one under which
operating and basic service software is licensed. A license to
use operating or basic service software does not extend to or
cover this software or related documentation.
If you are a GE employee or a customer who has entered into
such a license agreement with GE to use this proprietary
software, you are authorized to use this Material according to
the conditions stated in your license agreement.
However, you do not have the permission of GE to alter,
decompose or reverse-assemble the software, and unless you
are a GE employee, you may not copy the Material. The
Material is protected by Copyright and Trade Secret laws; the
violation of which can result in civil damages and criminal
prosecution.
If you are not party to such a license agreement or a GE
Employee, you must exit this Material now.

Trademarks
All products and their name brands are trademarks of their
respective holders.

Copyrights
All Material Copyright © 2015 by General Electric Company Inc.
All Rights Reserved.

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 Table of Contents

Translation policy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-2

Damage in transportation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-11
Certified electrical contractor statement - For USA Only - - - - - - - - - - - - i-11
Omission and errors - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-12
Service Safety Considerations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-13
Legal notes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14
Proprietary to GE - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14
Trademarks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14
Copyrights - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14
Table of Contents
Chapter 1 — Introduction
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-2
Manual Overview
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3
Contents in this service manual - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3
Typical users of the Basic Service Manual - - - - - - - - - - - - - - - - - - - - - 1-4
LOGIQ e models covered by this manual - - - - - - - - - - - - - - - - - - - - - - 1-5
General Caution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-6
Important conventions
Conventions used in book - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-7
Standard hazard icons - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-9
Product icons
Label Icon Description- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-11
Safety considerations
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-19
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-19
Human Safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-19
Mechanical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-22
Electrical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-24
Battery Safety- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-26
Dangerous procedure warnings
Lockout/Tagout (LOTO) requirements
Returning probes and repair parts
EMC, EMI and ESD
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-32
What is EMC? - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-32
CE Compliance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-32
Electrostatic discharge (ESD) prevention - - - - - - - - - - - - - - - - - - - - - 1-33

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 Customer assistance
Contact information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-34
Phone numbers for Customer Assistance - - - - - - - - - - - - - - - - - - - - - 1-35
System manufacturer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-35
Factory Site - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-35
Chapter 2 — Site Preparations
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-2
General requirements
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-3
Ultrasound system environmental requirements- - - - - - - - - - - - - - - - - - 2-3
Electrical requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-6
EMI limitations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-9
Probes environmental requirements - - - - - - - - - - - - - - - - - - - - - - - - - 2-11
Facility needs
Purchaser responsibilities - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-12
Required facility needs - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-13
Desirable features- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-14
Suggested and Alternate Ultrasound Room Layout - - - - - - - - - - - - - - 2-15
Networking setup requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-16
Environmental Dangers
Patient Environment IEC60601-1and ANSI AAMI ES60601-1 - - - - - - - 2-19
Chapter 3 — System Setup
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-2
Setup reminders
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3
Average setup time - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3
Setup warnings- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3
Receiving and unpacking the equipment
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6
Receiving the LOGIQ e - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6
Unpacking the LOGIQ e - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-7
Packing the Equipment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-11
Preparing for setup
Verify customer order - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-12
Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-12
EMI protection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-12
Completing the setup
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-13
System specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-13
Electrical specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-14
Power On / Boot Up - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-15
Power Off/Shutdown - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17
Connecting probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-18
System Configuration
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-20

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 LOGIQ e configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-21
Connecting Cables - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-24
Peripheral/Accessories Connector Panel - - - - - - - - - - - - - - - - - - - - - 3-25
Available probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-30
Software Options configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-31
Connectivity setup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-31
Paperwork after setup
User’s Manual(s) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-33
Product Locator Installation Card - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-33
Peripherals Installation
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-34
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-35
Furnished materials - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-36
Peripherals Installation Instructions - - - - - - - - - - - - - - - - - - - - - - - - - 3-38
Chapter 4 — General Procedures and Functional Checks
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2
Special Equipment required - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2
General procedures
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-3
Caution and Warning - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-4
Power ON/Boot Up - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-5
Power shut down - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-11
Removable media - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13
Archiving and loading presets - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13
Where are the User Manuals and the Service Manual? - - - - - - - - - - - 4-15
How to display or print the PDF files from the Manual CD-ROM? - - - - 4-15
Lockout/Tagout (LOTO) requirements- - - - - - - - - - - - - - - - - - - - - - - - 4-16
Functional checks
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-17
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-18
Operator Panel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-18
Soft Menu Key Tour - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-19
Monitor Display- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-20
Performance Tests - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-21
Software Configuration Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-52
Peripheral Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-52
Chapter 5 — Components and Functions (Theory)
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-2
Block Diagram and Theory
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3
Block Diagram - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3
General Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4
Top Console- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4
Power Diagram
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5

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 Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5
AC Power - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5
Battery Charging- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-6
Air Flow Distribution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-6
Common Service Platform
Contents in this Chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-7
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-7
The usage for security cable - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-8
Global Service User Interface (GSUI) - - - - - - - - - - - - - - - - - - - - - - - - - 5-9
Service Login - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-9
Access/Security - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-10
Customer Service Home Page - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-13
Chapter 6 — Service Adjustments
LCD Monitor adjustments
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2
Monitor Adjustments - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2
Chapter 7 — Diagnostics/Troubleshooting
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-2
Gathering Trouble Data
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3
Collect Vital System Information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3
Collect a Trouble Image with Logs - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-5
USB Quick Save
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-7
Check and Record the P3 Key Function - - - - - - - - - - - - - - - - - - - - - - - 7-7
Setting the P3 Key to USB Quick Save - - - - - - - - - - - - - - - - - - - - - - - - 7-8
Screen Capture
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-9
Check and Record the P1 Key Function - - - - - - - - - - - - - - - - - - - - - - 7-10
Setting the P1 Key to Screen Capture- - - - - - - - - - - - - - - - - - - - - - - - 7-10
Capturing a Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-11
Reset the P1 Key to Customer’s Functionality - - - - - - - - - - - - - - - - - - 7-12
Global Service User Interface (GSUI)
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-13
Common Diagnostics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-13
Network Configuration
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-17
Network Configuration- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-17
Chapter 8 — Replacement Procedures
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-2
Warnings and important information
Warnings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-3
Returning/shipping probes and repair parts - - - - - - - - - - - - - - - - - - - - - 8-4

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 Disassembly/Re-assembly
Warning and Caution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-5
Handle Assy (Part No. 5483188) - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-6
Advanced Isolation Cart Components Replacement- - - - - - - - - - - - - - - 8-7
Loading the software
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-13
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-13
Customer provided prerequisite - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-13
Data Management - moving all images - - - - - - - - - - - - - - - - - - - - - - - 8-14
Backing up the Patient Archive and System Configurations - - - - - - - - 8-14
Recording important settings and parameters - - - - - - - - - - - - - - - - - - 8-15
Loading the System Software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-16
Chapter 9 — Renewal Parts
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-2
List of Abbreviations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-2
Renewal Parts Lists
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-3
Power Cable - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-4
Operator Console Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-5
LCD Assy- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-6
Keyboard Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-7
Bottom Assy- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-9
E-Isolation Cart and Advanced Isolation Cart - - - - - - - - - - - - - - - - - - 9-14
Accessories and Kits- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-17
Probe - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-20
Manuals- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-22
Chapter 10 — Care and Maintenance
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-2
Protecting Health Information
Hide Patient Data - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-3
Protecting Health Information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-4
Software Wiping to Erase Patient Data (For R9.x.x only) - - - - - - - - - - 10-5
Users- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-9
Logon - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-11
Warnings
Why do maintenance
Periodic maintenance inspections - - - - - - - - - - - - - - - - - - - - - - - - - 10-13
Keeping records - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-13
Quality assurance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-14
Maintenance task schedule
How often should maintenance tasks be performed? - - - - - - - - - - - - 10-15
Tools required
Standard GE tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-17
GE-2 tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-19
Special tools, supplies and equipment used for maintenance - - - - - - 10-20

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 System maintenance
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-21
Preliminary checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-21
Functional checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-23
Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-25
Optional Diagnostic Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-26
Probe maintenance- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-27
Battery Performance Maintenance - - - - - - - - - - - - - - - - - - - - - - - - - 10-29
Electrical safety tests
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-30
Safety test overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-30
Leakage current limits - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-33
Outlet test - wiring arrangement - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-35
Grounding continuity - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-36
Chassis leakage current test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-37
Probe leakage current test- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-39
When there's too much leakage current …
AC/DC Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-42
Chassis Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-42
Probe Fails- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-43
Peripheral Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-43
Still Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-43
New Unit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-43
ECG Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-43
Inspection Paperwork
Ultrasound Inspection Forms - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-44
Electrical Safety Tests Log
Chapter 11 — Docking Cart Setup
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-2
Set Up Docking Cart
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-4
Setup Reminders - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-5
Receiving and Unpacking the Equipment - - - - - - - - - - - - - - - - - - - - - 11-8
Preparing for Installation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-12
Peripheral Installation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-14
Options Installation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-24
Paperwork - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-38
Cart Using
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-39
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-39
Height Adjustment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-39
Locking the Wheels- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-40
Mounting the System to Cart - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-40
Release the System from Docking Cart- - - - - - - - - - - - - - - - - - - - - - 11-41
Switch the Three Probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-42
System Operation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-42

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 Docking Cart Functions (Theory)
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-43
Block Diagram - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-43
Information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-44
Supported External Interface/Port- - - - - - - - - - - - - - - - - - - - - - - - - - 11-44
Diagnostics/Troubleshooting
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-45
Troubleshooting - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-45
Gathering Trouble Data - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-45
Troubleshooting Trees - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-46
Chapter 12 — Docking Cart Servicing
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-2
List of Abbreviations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-2
Replacement Procedure
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-3
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-3
Disassembly/Re-assembly- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-3
Renewal Parts
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-12
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-12
Power Cable - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-13
Operator Console Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-14
Docking Station - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-15
Probe Holder - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-17
Shelf Service - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-19
Bottom and Wheels- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-20
Panel and Cabinet - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-21
Gas Spring and Gas Spring Lever - - - - - - - - - - - - - - - - - - - - - - - - - 12-21
Power Box and Extended Life Battery- - - - - - - - - - - - - - - - - - - - - - - 12-21
Care & Maintenance
Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-23
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-23
Why do Maintenance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-25
Maintenance Task Schedule - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-26
Tools Required - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-28
Cleaning Dusk Screen- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-29
Safety Test- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-30
Safety Test (continued) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-33
When There’s Too Much Leakage Current... - - - - - - - - - - - - - - - - - - 12-34
Inspection Paper Work - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-35
Index

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i-22 LOGIQ e – Basic Service Manual
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 Chapter 1

Introduction

This chapter describes important issues related to

safely servicing the Ultrasound system and Docking
Cart. The service provider must read and understand all
the information presented here before installing or
servicing the units.

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Introduction

Overview

Contents in this chapter

• ‘Overview’ on page 1-2
• ‘Manual Overview’ on page 1-3
• ‘Important conventions’ on page 1-7
• ‘Product icons’ on page 1-11
• ‘Safety considerations’ on page 1-19
• ‘Dangerous procedure warnings’ on page 1-29
• ‘Lockout/Tagout (LOTO) requirements’ on page 1-30
• ‘Returning probes and repair parts’ on page 1-31
• ‘EMC, EMI and ESD’ on page 1-32
• ‘Customer assistance’ on page 1-34

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 Manual Overview

Manual Overview

This manual provides installation and service information for the

LOGIQ e Ultrasound system and docking cart. It is divided in
twelve chapters as shown below.

Contents in This Section

• ‘Contents in this service manual’ on page 1-3
• ‘Typical users of the Basic Service Manual’ on page 1-4
• ‘LOGIQ e models covered by this manual’ on page 1-5
• ‘General Caution’ on page 1-6

Contents in this service manual

The manual is divided into twelve chapters.
In the beginning of the manual, before chapter 1, you will find
the Revision overview, the Important precautions including
Translation policy, Damage in transportation, Certified electrical
contractor statement, Omission & errors, Service safety
considerations and Legal notes, and the Table of Contents
(TOC).

Table 1-1: Contents in this manual

Chapter Chapter title Description

number
1. ‘Introduction’ Contains a content summary and warnings.
2. ‘Site Contains pre-setup requirements for the
Preparations’ LOGIQ e and Docking Cart.
3. ‘System Setup’ Contains setup procedure with procedure
checklist for the system.
4. ‘General Contains functional checks for the system that
Procedures and must be performed as part of the installation, or
Functional as required during servicing and periodic
Checks’ maintenance.

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Introduction

Table 1-1: Contents in this manual (Continued)

Chapter Chapter title Description

number
5. ‘Components Contains block diagrams and functional
and Functions explanations of the electronics for the system.
(Theory)’
6. ‘Service Contains instructions on how to make any
Adjustments’ available adjustments to the LOGIQ e system.
7. ‘Diagnostics/ Provides procedures for running diagnostic or
Troubleshooting’ related routines for the LOGIQ e system.
8. ‘Replacement Provides disassembly procedures and
Procedures’ reassembly procedures for all changeable FRU
on the system.
9. ‘Renewal Parts’ Contains a complete list of replacement parts for
LOGIQ e system.
10. ‘Care and Provides periodic maintenance procedures for
Maintenance’ LOGIQ e system.
11. ‘Docking Cart Provides setup information for Docking Cart,
Setup’ including use, test and trouble shooting of
Docking Cart.
12. Provides service information for Docking Cart,
including replacement, spare parts and
‘Docking Cart
Maintenance.
Servicing’
N/A Index A quick way to the topic you’re looking for.

Typical users of the Basic Service Manual

• Service personnel (installation, maintenance, etc.)
• Hospital’s service personnel
• Contractors (some parts of Chapter 2 - Pre-Installation)
NOTE: Not all features, products, probes or peripherals described in
this document may ba available or cleared for sale in all
markets. Please refer to the user manual or contact your local
sale representative to get the latest information.

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 Manual Overview

LOGIQ e models covered by this manual

Table 1-2: LOGIQ e Model Designations (For R8.x.x)

Model Number Description

5483518 LOGIQ e Console for USA

5483522 LOGIQ e Console Generic version

5498957 LOGIQ e Console for CKD

5499582 LOGIQ e Console for Canada

5483520 LOGIQ e Console for Korea

5483521 LOGIQ e Console for China

Table 1-3: LOGIQ e Model Designations (For R9.x.x)

Model Number Description

5604173 LOGIQ e Console Generic version

NOTE: When not otherwise specified, the contents of this manual

applies to all LOGIQ e models.

Purpose of the operator manual(s)

The operator manuals should be fully read and understood

before operating the LOGIQ e and also kept near the unit for
quick reference.
The online versions of the operator manuals are available via
the Help function on LOGIQ e’s operator panel.

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Introduction

General Caution

CAUTION Standard maintenance must be performed by authorized

service personnel for the lifetime of the product (7 years).

CAUTION Proceed cautiously when crossing door or elevator thresholds

with the Docking Cart or Isolation Cart. Use the handle to push/
pull the system, e.g., do not use the Docking Cart external
LCD. Failure to do so may cause serious injury or system
damage.

CAUTION Capacity load of the Docking Cart: The maximum capacity load
of the Storage rack (1) is 2kg, DVD-RW Shelf (2) is 2kg, B/W
Printer Shelf (3) is 4kg, Color Printer Shelf (4) is 7kg, refer to
the following figure.

Figure 1-1. Capacity load of the Docking Cart

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 Important conventions

Important conventions

Conventions used in book

Important conventions, used in this document, are described
next.

Model designations

This manual covers the LOGIQ e Ultrasound systems listed in:

‘LOGIQ e models covered by this manual’ on page 1-5.

Icons

Pictures, or icons, are used wherever they will reinforce the

printed message. The icons, labels, and conventions used on
the product and in the service information are described in this
chapter.

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Introduction

Safety precaution messages

Various levels of safety precaution messages may be found on

the equipment and in the service information. The different
levels of concern are identified by a flag word that precedes the
precautionary message. Known or potential hazards to
personnel are labeled in one of three ways:
• DANGER
• WARNING
• CAUTION

DANGER Danger is used to indicate the presence of a hazard that will

cause severe personal injury or death if the instructions are
ignored.

WARNING Warning is used to indicate the presence of a hazard that can

cause severe personal injury and property damage if
instructions are ignored.

CAUTION Caution is used to indicate the presence of a hazard that will or

can cause minor personal injury and property damage if
instructions are ignored. Equipment damage possible.

NOTE: Notes are used to provide important information about an item

or a procedure.
NOTE: Be sure to read the notes; the information contained in a note
can often save you time or effort.

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 Important conventions

Standard hazard icons

Important information will always be preceded by either the
exclamation point (!) contained within a triangle, or the symbols
for “Danger”, “Warning” or “Caution”, as seen throughout this
chapter. In addition to text, several different graphical icons
(symbols) may be used to make you aware of specific types of
hazards that could possibly cause harm. Even if a symbol isn’t
used in this manual, it may be included for your reference.

Table 1-4: Standard hazard icons

ELECTRICAL

MECHANICAL

RADIATION

LASER

HEAT

PINCH

NOTE: Even if a symbol isn’t used on the product or in this manual, it

may be included for your reference.

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Introduction

Standard Icons that indicate that a special procedure is to be used

Some others icons make you aware of specific procedures that

should be followed.

Table 1-5: Standard Icons that indicates that a special procedure is to be used

Avoid Static Electricity Tag and Lock Out Wear Eye Protection

Hand Protection Foot Protection Wear Eye Protection

Be sure to read the notes; the information contained in a note

can often save you time or effort.

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 Product icons

Product icons

The following table describes the purpose and location of safety

labels and other important information provided on the
equipment.

Label Icon Description

The following table describes the purpose and location of safety
labels and other important information provided on the
equipment.

Table 1-6: Product Icons

Label/Icon Purpose/Meaning Location

Identification and Rating Plate • Manufacture’s name and Rating plate

address
• Date of manufacture
• Model and serial numbers
• Electrical ratings (Volts, Amps,
phase, and frequency)

Date of manufacture: The date Bottom

could be a year, year and
month, or year, month and day,
as appropriate. See ISO 8601
for date formats.

Catalog or model number Bottom

ＲＥＦ
Serial number Bottom

ＳＮ
Direct Current: For products to Bottom
be powered from a DC supply

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Introduction

Table 1-6: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

Input Bottom

For use with adapter GE part Bottom

number 5460229-x

Description Bottom

Model Rear of Docking Cart

Only for use with LOGIQ e Rear of Docking Cart

series (Software version should
be R8.x.x or higher)

Made in China Rear of Docking Cart

Type/Class Label Used to indicate the degree of

safety or protection.

IP Code (IPX8) Indicates the degree of Bottom of Footswitch

IPX8: MKF 2-MED GP26 protection provided by the
enclosure per IEC60 529.
IPX8 can be used in an
operating room environment.

Authorized European Bottom panel

Representative address.

United States only Bottom panel

Prescription Requirement label.

Type BF Applied Part (man in Beside the probe

the box) symbol is in connector
accordance with IEC 878-02-03.

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 Product icons

Table 1-6: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

General Warning. Various

“CAUTION” - Dangerous Various

voltage” (the lightning flash with
arrowhead) is used to indicate
electric shock hazards.

“ON” indicates the power on See the Console

position of the power switch. Overview section for
CAUTION: This Power Switch location information.
DOES NOT ISOLATE Mains
Supply.

“Protective Earth” indicates the Inside of AC adapter

protective earth (grounding)
terminal.

NRTL Listing and Certification Bottom

Mark is used to designate
conformance to nationally
recognized product safety
standards. The Mark bears the
name and/or logo of the testing
laboratory, product category,
safety standard to which
conformity is assessed and a
control number.

Type CF Defib-Proof Applied ECG Module

Part (heart in the box with
paddle) symbol is in accordance
with IEC 60878-02-06.

“Consult accompanying Various

documents“ is intended to alert
the user to refer to the operator
manual or other instructions
when complete information
cannot be provided on the label.

Do not push the system. Rear of Docking Cart/

Isolation Cart

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Introduction

Table 1-6: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

This symbol indicates that Bottom

waste electrical and electronic
equipment must not be
disposed of as unsorted
municipal waste and must be
collected separately. Please
contact an authorized
representative of the
manufacturer for information
concerning the
decommissioning of your
equipment.

The separate collection symbol Battery Pack if contains

is affixed to a battery, or its Pb/Cd/Hg
packaging, to advise you that
the battery must be recycled or
disposed of in accordance with
local or country laws. The letters
below the separate collection
symbol indicate whether certain
elements
(Pb=Lead,Cd=Cadmium,
Hg=Mercury) are contained in
the battery. To minimize
potential effects on the
environment and human health,
it is important that all marked
batteries that you remove from
the product are properly
recycled or disposed. For
information on how the battery
may be safely removed from the
device, please consult the
service manual or equipment
instructions. Information on the
potential effects on the
environment and human health
of the substances used in
batteries is available at this url:
http://www.gehealthcare.com/
euen/weee-recycling/index.html

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 Product icons

Table 1-6: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

No hazardous substance, above

the maximum concentration
value, is present. Maximum
concentration values for
electronic information products,
as set by the People’s Republic
of China Electronic Industry
Standard SJ/T11364-2006,
include the hazardous
substances of lead, mercury,
hexavalent chromium,
cadmium, polybrominated
biphenyl (PBB), and
polybrominated diphenyl ether
(PBDE).

Indicates the presence of Probe and Rear Panel,

hazardous substance(s) above China Rating Plate
the maximum concentration
value. Maximum concentration
values for electronic information
products, as set by the People’s
Republic of China Electronic
Industry Standard SJ/
T11364-2006, include the
hazardous substances of lead,
mercury, hexavalent chromium,
cadmium, polybrominated
biphenyl (PBB), and
polybrominated diphenyl ether
(PBDE). “10” indicates the
number of years during which
the hazardous substance(s) will
not leak or mutate so that the
use of this product will not result
in any severe environmental
pollution, bodily injury, or
damage to any assets.

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Introduction

Table 1-6: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

Indicates the presence of Rating Plate

hazardous substance(s) above
the maximum concentration
value. Maximum concentration
values for electronic information
products, as set by the People’s
Republic of China Electronic
Industry Standard SJ/
T11364-2006, include the
hazardous substances of lead,
mercury, hexavalent chromium,
cadmium, polybrominated
biphenyl (PBB), and
polybrominated diphenyl ether
(PBDE). “20” indicates the
number of years during which
the hazardous substance(s) will
not leak or mutate so that the
use of this product will not result
in any severe environmental
pollution, bodily injury, or
damage to any assets.

When closing the LCD cover, Bottom

use caution to avoid injuring
hands or fingers as there is a
closing mechanism which
allows the LCD cover to
automatically close.

Do not connect the DVD-RW to DVD-RW

the system while scanning.
The DVD-RW can be used
when connecting to the Docking
Cart.

GOST symbol: Russia Bottom Note: Only after

Regulatory Country Clearance. Russian regulatory
registration is complete,
this label will be located
on the console rating
plate.

This product consists of devices Bottom

that may contain mercury, which
must be recycled or disposed of
in accordance with local, state,
or country laws. (Within this
system, the backlight lamps in
the monitor display, contain
mercury.)

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 Product icons

Table 1-6: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

INMETRO Certification: TUV Rating plate Note: Only

Rheinland Brazil after Brazilian regulatory
registration is complete,
this label will be located
on the console rating
plate.

Disconnect the probe connector Docking Cart Top Cover

of Three-Probe Port before
remove the system from
Docking Cart Platform,
otherwise the probe cable will
be damaged.

Guidance on how to connect the Docking Cart Top Cover

system to the docking cart and
how to release it.
When put the system on
docking cart top cover, avoid
injuring the fingers and hands.
Make sure the system’s handle
is locked well after mounting the
system to docking cart top
cover. When connecting the
probe connector to the system,
press the probe connector
locking lever up. When
releasing the system from the
docking cart, disconnect the
probe connector of Three-Probe
Port from the system before
lifting up the system.

Do not disconnect the probe Probe Connector of

connector of Three-probe Port Three-Probe Port
from the system when the
system is in use.

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Introduction

Table 1-6: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

Do not let the 3-Probe Port drop 3-Probe Port

down when mounting it to the
docking cart. The 3-Probe Port
will be damaged if it drops on
hard surface.

When pushing the Extended Power Box

Life Battery in to the power box,
use caution to avoid injuring
fingers and hands.

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 Safety considerations

Safety considerations

Introduction
The following safety precautions must be observed during all
phases of operation, service and repair of this equipment.
Failure to comply with these precautions or with specific
warnings elsewhere in this manual, violates safety standards of
design, manufacture and intended use of the equipment.

Contents in this Section

• ‘Human Safety’ on page 1-19
• ‘Mechanical safety’ on page 1-22
• ‘Electrical safety’ on page 1-24
• ‘Battery Safety’ on page 1-26

Human Safety
• Operating personnel must not remove the system covers.
• Servicing should be performed by authorized personnel
only.
Only personnel who have participated in a LOGIQ e Training
Seminar are authorized to service the equipment.

DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING

DEATH, ARE PRESENT IN THIS EQUIPMENT. USE
EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.

WARNING If the covers are removed from an operating LOGIQ e, some

metal surfaces may be warm enough to pose a potential heat
hazard if touched, even while in shutdown mode.

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Introduction

Human Safety (continued)

WARNING Explosion Warning

DO NOT operate the equipment in an explosive atmosphere.
Operation of any electrical equipment in such an environment
constitutes a definite safety hazard.

WARNING DO NOT substitute parts or modify equipment

Because of the danger of introducing additional hazards, ONLY
install GE approved parts. DO NOT perform any unauthorized
modification of the equipment.

WARNING Ensure that the Ultrasound system is turned off and unplugged
Wait for at least 20 seconds for capacitors to discharge as
there are no test points to verify isolation. The amber light on
the OP panel ON/OFF button will turn off.
Ultrasound system components may be energized. Always
refer to the Ultrasound system's Proprietary Service Manual for
LOTO warnings and cautions

WARNING Risk of electrical shock, Ultrasound system must be turned off

and disconnected from power source. Cord must be controlled
at all times.
Wait for at least 20 seconds for capacitors to discharge as
there are no test points to verify isolation. The amber light on
the OP panel on/off button will turn off.
Ultrasound System components may be energized. Always
refer to the Ultrasound system's Proprietary Service Manual for
LOTO warnings and cautions

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 Safety considerations

Human Safety (continued)

WARNING Use all Personal Protection Equipment (PPE) such as gloves,

safety shoes, safety glasses, and kneeling pad, to reduce the
risk of injury.

WARNING Beware of possible sharp edges on all mechanical parts. If

sharp edges are encountered, the appropriate PPE should be
used to reduce the risk of injury.

WARNING Wear all PPE including gloves as indicated in the chemical

MSDS.

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Introduction

Mechanical safety

WARNING While the software install procedure is designed to preserve

data, you should save any patient data, images, system setups
to removable media or hardcopy before doing a software
upgrade.

WARNING Ultrasound probes are highly sensitive medical instruments

that can easily be damaged by improper handling. Use care
when handling and protect from damage when not in use. do
not use a damaged or defective probe. Failure to follow these
precautions can result in serious injury and equipment
damage.

WARNING Never use a probe that has fallen to the floor. Even if it looks
OK, it may be damaged.

CAUTION LOGIQ e system weighs 5.2 kg or more, depending on

installed peripherals, when ready for use. Care must be used
when moving it or replacing its parts.
ALWAYS:
• Use the handle to move the Ultrasound system.
• Do not let the Ultrasound system strike walls or door frame.

NOTE: Special care should be taken when transporting the Ultrasound

system in a vehicle:
• Before transporting, place the system in its special storage
case.
• Ensure that the system is firmly secured while inside the
vehicle.
• Secure system with straps or as directed otherwise to
prevent motion during transport.
• Prevent vibration damage by driving cautiously. Avoid
unpaved roads, excessive speeds, and erratic stops or
starts.

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 Safety considerations

Mechanical safety (continued)

CAUTION The Docking Cart weighs 53 kg (117 lb.) or more, depending on

installed peripherals, when ready for use. Care must be used
when moving it or replacing its parts.
Failure to follow the precautions listed below could result in
injury, uncontrolled motion and costly damage.
ALWAYS:
• be sure the pathway is clear
• use slow, careful motions
• Limit movement to a slow careful walk.
• use two people when moving on inclines or lifting more
than 16 kg (35 lbs)

WARNING When the docking cart is raised for a repair or moved along any
incline, use external caution since it may become unstable and
tip over.

CAUTION Make sure the console be fixed well to avoid the console falling
down when moving Docking Cart.

CAUTION Do not move Docking Cart with big incline angle.

Do

CAUTION The Docking Cart is not water proof. Do not expose the
Docking Cart to water or any kind of liquid.
Never set liquids on the Docking Cart to ensure that liquid does
not drip into the unit

CAUTION Put peripherals in correct position to avoid Docking Cart

overload.

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Introduction

Mechanical safety (continued)

NOTE: Special care should be taken when transporting the Docking
Cart in a vehicle.
• Secure the unit in an upright position.
• Lock the wheels (brake)

Electrical safety

Safe practices

Follow these guidelines to minimize shock hazards whenever

you are using the Ultrasound system:
• To minimize shock hazard, the equipment chassis must be
connected to an electrical ground.
• The Ultrasound system is equipped with a three-conductor
AC power cable. This must be plugged into an approved
electrical outlet with safety ground.
• The power outlet used for this equipment should not be
shared with other types of equipment.
• Both the system power cable and the power connector must
meet international electrical standards

WARNING Connecting a LOGIQ e to the wrong voltage level will most

likely destroy it.

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 Safety considerations

Probes

Follow these guidelines before connecting a probe to the

Ultrasound system:
• Inspect the probe prior to each use for damage or
degradation to the:
• housing
• cable strain relief
• lens
• seal
• connector pins
• locking mechanism
• Do not use a damaged or defective probe.
• Never immerse the probe connector or adapter into any
liquid.

Peripherals

Refer to the Patient Safety Environment section of the User’s

Manual for peripheral isolation information.

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Introduction

Battery Safety
To avoid the risk of injury, follow the warning and cautions to
make sure that the battery does not burst, ignite, or generate
heat of fumes.

WARNING • The battery has a safety device. Do not disassemble or

alter the battery.
• Do not short-circuit the battery by directly connecting the
negative terminals with metal objects.
• Do not heat the battery or discard it in a fire.
• Do not charge the battery near a heat source, such as a
fire or heater.
• Do not leave the battery in direct sunlight.
• Do not drop packs from height to prevent them from
possible malfunction damage.
• Do not drop packs from height to prevent them from
possible malfunction damage.
• Do not pierce the battery with a sharp object, hit it, or step
on it.
• Do not use a damaged battery.
• Do not solder a battery.
• Do not connect the battery to an electrical power outlet.
• Do not contact PCM (Power Control and Monitor, it’s a
small board in the battery) directly to prevent packs from
ESD damage.
• In case of longer non-use of the LOGIQ e, please make
sure the battery is removed.

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 Safety considerations

Battery Safety (continued)

Temperature Requirements

The battery should be charged, discharged and stored within the

parameters outlined below:
• Operating temperature:
• Charge: 10 - 30°C (50 - 86°F).
• Discharge: 10 - 40°C (50 - 104°F)

CAUTION To ensure the power supplied to the system during system use,
DO NOT disconnect the system power cord from the AC outlet
when the environmental temperature is below 10°C(50°F) or
above 30°C(86°F). The battery will possibly not be charged
properly in the environment temperature of below 10°C (50°F)
or above 30°C(86°F) and can not supply power to the system.

• Storage temperature:
• Storage time < 3 months: -20 - 40°C (-4 - 104°F)
• Storage time >= 3 months: -20 - 20°C (-4 - 68°F)

WARNING Do not expose the battery to temperature over 60°C (140°F).

Keep it away from fire and other heat sources.

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Introduction

Battery Safety (continued)

CAUTION To avoid the battery bursting, igniting, or fumes from the

battery causing equipment damage, observe the following
precautions:
• Do not immerse the battery in water or allow it to get wet.
• Do not put the battery into a microwave oven or
pressurized container.
• If the battery leaks or emits an odor, remove it from all
possible flammable sources.
• If the battery emits an odor or heat, is deformed or
discolored, or in a way appears abnormal during use,
recharging or storage, immediately remove it and stop
using it. If you have any questions about the battery,
consult GE or your local representative.
• Use only GE recognized batteries.
• When the system isn't powered on continuously more than
6 months, in order to prevent leakage and deterioration in
performance of CMOS battery, power on the system at
least once per 6 months for more than 10 hours to have
CMOS battery fully charged. Time and date need to be
re-setup.

NOTE: The battery shall be shipped in about 30% charged state. Those
packs have to be fully charged and discharged up to 3 times to
utilize Li-lon smart packs before use.

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 Dangerous procedure warnings

Dangerous procedure warnings

Warnings, such as the example below, precede potentially

dangerous procedures throughout this manual. Instructions
contained in the warnings must be followed.

DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING

DEATH, ARE PRESENT IN THIS EQUIPMENT. USE
EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.

WARNING If the covers are removed from an operating LOGIQ e, some

metal surfaces may be warm enough to pose a potential heat
hazard if touched, even while in shutdown mode.

WARNING Explosion Warning

DO NOT operate the equipment in an explosive atmosphere.
Operation of any electrical equipment in such an environment
constitutes a definite safety hazard.

WARNING DO NOT substitute parts or modify equipment

Because of the danger of introducing additional hazards, ONLY
install GE approved parts. DO NOT perform any unauthorized
modification of the equipment.

WARNING SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC

INVALID MAY CAUSE THE DAMAGE OF SYSTEM
FILES.

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Introduction

Lockout/Tagout (LOTO)
requirements

Follow Lockout/Tagout requirements by ensuring you are in total

control of the AC power plug at all times during the service
process.
To apply Lockout/Tagout (LOTO):
1. Plan and prepare for shutdown.
2. Shutdown the equipment.
3. Isolate the equipment.
4. Remove/disconnect the battery, if present.
5. Apply Lockout/Tagout Devices.
6. Control all stored and residual energy.
7. Verify isolation.
All potentially hazardous stored or residual energy is relieved.

WARNING Energy Control and Power Lockout for LOGIQ e.

When servicing parts of the Ultrasound system where there is
exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as
there are no test points to verify isolation.
6. Remove/disconnect the battery, if present.
Ultrasound System components may be energized.

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 Returning probes and repair parts

Returning probes and repair parts

Equipment being returned must be clean and free of blood and

other infectious substances. GE policy states that body fluids
must be properly removed from any part or equipment prior to
shipment. GE employees, as well as customers, are responsible
for ensuring that parts/equipment have been properly
decontaminated prior to shipment. Under no circumstance
should a part or equipment with visible body fluids be taken or
shipped from a clinic or site (for example, body coils or an
ultrasound probe).
The purpose of the regulation is to protect employees in the
transportation industry, as well as the people who will receive or
open this package.
NOTE: The US Department of Transportation (DOT) has ruled that
“items that were saturated and/or dripping with human blood
that are now caked with dried blood; or which were used or
intended for use in patient care” are “regulated medical waste”
for transportation purposes and must be transported as a
hazardous material.
NOTE: The USER/SERVICE staff should dispose of all the waste
properly, per federal, state, and local waste disposal regulations.
The Ultrasound system is not meant to be used for long-term
storage of patient data or images. The user is responsible for the
data on the system and a regular backup is highly
recommended.
If the system is sent for repair, please ensure that any patient
information is backed up and erased from the system before
shipping. It is always possible during system failure and repair to
lose patient data. GE is not responsible for the loss of this data.
If PHI (Patient Healthcare Information) data needs to be sent to
GE employees for service purposes, GE will ascertain
agreement from the customer. Patient information shall only be
transferred by approved service processes, tools and devices
restricting access, protecting or encrypting data where required,
and providing traceability in the form of paper or electronic
documents at each stage of the procedure while maintaining
compliance with cross-border restrictions of patient information
transfers.

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Introduction

EMC, EMI and ESD

Contents in this Section

• ‘What is EMC?’ on page 1-32
• ‘CE Compliance’ on page 1-32
• ‘Electrostatic discharge (ESD) prevention’ on page 1-33

What is EMC?
Electromagnetic compatibility describes a level of performance
of a device within its electromagnetic environment. This
environment consists of the device itself and its surroundings
including other equipment, power sources and persons with
which the device must interface. Inadequate compatibility results
when a susceptible device fails to perform as intended due
interference from its environment or when the device produces
unacceptable levels of emission to its environment. This
interference is often referred to as radio–frequency or
electromagnetic interference (RFI/EMI) and can be radiated
through space or conducted over interconnecting power of
signal cables. In addition to electromagnetic energy, EMC also
includes possible effects from electrical fields, magnetic fields,
electrostatic discharge and disturbances in the electrical power
supply.

CE Compliance
LOGIQ e conforms to all applicable conducted and radiated
emission limits and to immunity from electrostatic discharge,
radiated and conducted RF fields, magnetic fields and power
line transient requirements.
For applicable standards, refer to the Safety Chapter of the
Ultrasound system’s User’s Manual.
NOTE: For CE Compliance, it is critical that all covers, screws,
shielding, gaskets, mesh, clamps, are in good condition,
installed tightly without skew or stress. Proper installation
following all comments noted in this service manual is required
in order to achieve full EMC performance.

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 EMC, EMI and ESD

Electrostatic discharge (ESD) prevention

WARNING DO NOT touch any boards with integrated circuits prior to

taking the necessary ESD precautions.
Always connect yourself, via an arm-wrist strap, to the advised
ESD connection point located on the rear of the Ultrasound
system (near the power connector).
Follow general guidelines for handling of electrostatic sensitive
equipment.

WARNING Risk of electrical shock, Ultrasound system must be turned off.

Avoid all contact with electrical contacts, conductors and
components. Always use non-conductive handles designed for
the removal and replacement of ESD sensitive parts. All parts
that have the potential for storing energy must be discharged or
isolated before making contact.

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Introduction

Customer assistance

Contact information
If this equipment does not work as indicated in this service
manual or in the user manual, or if you require additional
assistance, please contact the local distributor or appropriate
support resource, as listed below.
Before you call, identify the following information, and acquire
image (Alt+D) to send to the Customer Care team:
1. System ID serial number.
2. Software version.
3. Date and time of occurrence.
4. Sequence of events leading to issue.
5. Is the issue repeatable?
6. Imaging mode, probe, preset/application.
7. Media brand, speed, capacity, type.
8. Save secondary image capture, cine loop, 4D multi-volume
loop.
NOTE: Restart the application before resuming clinical scanning.

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 Customer assistance

Phone numbers for Customer Assistance

Table 1-7: Phone numbers for Customer Assistance

LOCATION PHONE NUMBER

USA Service: On-site 1-800-437-1171

GE Healthcare - GE Medical Systems
Ultrasound & Primary Care Diagnostics, LLC Service Parts 1-800-558-2040
9900 Innovation Drive
Application Support 1-800-682-5327 or
Wauwatosa, WI 53226
1-262-524-5698

Canada 1-800-668-0732

Latin America Service 1-262-524-5300

Application Support 1-262-524-5698

Europe Phone: +33 (0) 130-831-300

GE Ultraschall Deutschland Gmbh & Co. KG (General Imaging and Cardiac)
Beethovenstrasse 239 +49 (0) 212-2802-652
Postfach 11 05 60, D-42655 Solingen
Germany Fax: +49 (0) 2122-8024-31

Asia (Singapore)
GE Ultrasound Asia Tel: +65 6291-8528
Service Department - Ultrasound
298 Tiong Bahru Road #15-01/06
Central Placa
Singapore 168730 Fax: +65-6291-7006

Japan Support Center Phone: 81-426-48-2940

Fax: 81-426-48-2905

System manufacturer
Refer to Basic User Manual/User Guide for the information.
Please use the latest revision of the document.

Factory Site
Refer to Basic User Manual/User Guide for the information.
Please use the latest revision of the document.

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Introduction

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 Chapter 2

Site Preparations

This chapter provides the information required to plan

and prepare for the setup of an Ultrasound system and
Docking Cart. Included are descriptions of the facility
and electrical needs to be met by the purchaser of the
units.

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Site Preparations

Overview

Contents in this chapter

• ‘Overview’ on page 2-2
• ‘General requirements’ on page 2-3
• ‘Facility needs’ on page 2-12
• ‘Environmental Dangers’ on page 2-19

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 General requirements

General requirements

Contents in this Section

• ‘Ultrasound system environmental requirements’ on
page 2-3
• ‘Electrical requirements’ on page 2-6
• ‘Electrical requirements for Docking Cart’ on page 2-8
• ‘EMI limitations’ on page 2-9
• ‘EMI prevention/abatement’ on page 2-10
• ‘Probes environmental requirements’ on page 2-11

Ultrasound system environmental requirements

If the Ultrasound system is very cold or hot

When unpacking the Ultrasound system, allow the temperature

of the Ultrasound system to stabilize before powering up. The
following table describes guidelines for reaching operational
temperatures from storage or transport temperatures.

CAUTION If the Ultrasound system is very cold or hot, do not turn on its
power until it has had a chance to acclimate to its operating
environment.

Table 2-1: System Acclimation Time Chart

Degree C 50 45 40 35 30 25 20 15 10 5 0 -5

Degree F 122 113 104 95 86 77 68 59 50 41 32 23

hours 4 2 0 0 0 0 0 0 0 2 4 6

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Site Preparations

Environmental specifications

The system and Docking Cart should be operated, stored, or

transported within the parameters outlined below. Either its
operational environment must be constantly maintained or the
unit must be turned off.
Table 2-2: System Environmental Requirements

Operational Storage Transport

(with probe) LOGIQ e LOGIQ e

Temperature 10 - 40°C -5 - 50°C -5 - 50°C

50 - 104°F 23 - 122°F 23 - 122°F

Humidity 30 - 75% 10 - 90% 10 - 90%

non-condensing non-condensing non-condensing

Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa

Table 2-3: Environmental Requirements for Docking Cart

Operation Storage Transport

Temperature 10 - 40°C -5 - 50°C -5 - 50°C

50 - 104°F 23 - 122°F 23 - 122°F

Humidity 30 - 75% 10 - 90% 10 - 90%

non-condensing non-condensing non-condensing

Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa

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 General requirements

Environmental specifications (continued)

Table 2-4: Environmental Requirements for an Ultrasound Room for Docking Cart

Item Values

Power Source Refer to Table 2-6 on page 2-8.

Power Rating 500VA (100V-120V); 500VA (220-240V)

Radiation Shielding NONE REQUIRED for ULTRASOUND ENERGY

Floor Landing Approximately 680 - 800 kg/m2 without Accessories

Floor Condition Gradient: WITHIN 5 degrees

Weight 53 kg without Accessories

NOTE: Temperature in degrees Celsius (ºC) conversion to

degrees F (ºF): (ºF) = (ºC * 9/5) + 32

CAUTION Ensure that the probe face temperature does not exceed the
normal operation temperature range.

CAUTION The LOGIQ e system and probe connector is not waterproof.

Do not expose the device to water or any kind of liquid.

Lighting

Bright light is needed for Ultrasound system installation, updates

and repairs. However, operator and patient comfort may be
optimized if the room light is subdued and indirect. Therefore a
combination lighting system (dim/bright) is recommended. Keep
in mind that lighting controls and dimmers can be a source of
EMI which could degrade image quality. These controls should
be selected to minimize possible interference.

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Site Preparations

Electrical requirements

General requirements

NOTE: GE requires a dedicated power and ground for the proper

operation of its Ultrasound equipment. This dedicated power
shall originate at the last distribution panel before the Ultrasound
system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not
shared with any other circuit), and a full size ground wire from
the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not
shared with any other circuit, and a full size ground wire from the
distribution panel to the Ultrasound outlet.
NOTE: Please note that image artifacts can occur, if at any time within
the facility, the ground from the main facility's incoming power
source to the Ultrasound system is only a conduit.

Electrical requirements for Adapter

Table 2-5: Electrical Specifications for Adapter

Adapter Model AHM150PS19-XA1048

Input Voltage 100-240VAC

Input Current 1.5A at 115VAC

0.75A at 230VAC

Output Power 150W

Output Voltage 19.0VDC

Output Current 7.89A

Frequency 50/60Hz

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 General requirements

Site circuit breaker

CAUTION Power outage may occur. The LOGIQ e requires a dedicated

single branch circuit. To avoid circuit overload and possible loss
of critical care equipment, make sure you do not have any
other equipment operating on the same circuit.

It is recommended that the branch circuit breaker for the

Ultrasound system be readily accessible.

CAUTION POWER OUTAGE MAY OCCURE.

The LOGIQ e requires a dedicated single branch circuit. To
avoid circuit overload and possible loss of critical care
equipment, make sure you DO NOT have any other equipment
operating on the same circuit.

Site power outlets

A dedicated AC power outlet must be within reach of the

Ultrasound system without extension cords. Other outlets
adequate for the external peripherals, medical and test
equipment needed to support this Ultrasound system must also
be present within 1 m (3.2 ft.) of the Ultrasound system.
Electrical installation must meet all current local, state, and
national electrical codes.

Unit power plug

If the Ultrasound system arrives without a power plug, or with

the wrong plug, you must contact your GE dealer or the
installation engineer must supply what is locally required.

Power stability requirements

Voltage drop-out:
Max 10 ms.
Power transients:
Less than 25% of nominal peak voltage for less than 1
millisecond for any type of transient, including line frequency,
synchronous, asynchronous, or aperiodic transients.

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Electrical requirements for Docking Cart

Table 2-6: Electrical requirements for Docking Cart

PARAMETER AREA LIMITS

Voltage Range 100-240V~ 350VA

Power All applications More than or equal to 750 VA

Line Frequency All applications 50/60Hz (±2Hz)

Power Transients All applications Less than 25% of nominal peak voltage for less
than 1 millisecond for any type of transient,
including line frequency, synchronous,
asynchronous, or aperiodic transients.

Decaying Oscillation All applications Less than 15% of peak voltage for less than 1
millisecond.

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 General requirements

EMI limitations
Ultrasound systems are susceptible to Electromagnetic
Interference (EMI) from radio frequencies, magnetic fields, and
transients in the air or wiring. They also generate EMI. The
Ultrasound system complies with limits as stated on the EMC
label. However there is no guarantee that interference will not
occur in a particular installation.
Possible EMI sources should be identified before the Ultrasound
system is installed.
Electrical and electronic equipment may produce EMI
unintentionally as the result of a defect. Some of these sources
include:
• medical lasers
• scanners
• cauterizing guns
• computers
• monitors
• fans
• gel warmers
• microwave ovens
• light dimmers
• mobile phones
• in-house wireless phones (DECT phones)
• wireless computer keyboard and mouse
• air conditioning system
• High Frequency (HF) surgery equipment
• general AC/DC adapters
The presence of a broadcast station or broadcast van may also
cause interference.
See: ‘EMI prevention/abatement’ on page 2-10 for EMI
prevention tips.

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EMI prevention/abatement

Table 2-7: EMI prevention/abatement

EMI RULE DETAILS

Be aware of Radio • Keep the Ultrasound system at least 5 meters (15 feet) away from other EMI
Frequency sources sources.
• Special shielding may be required to eliminate interference problems caused by
high frequency, high powered radio or video broadcast signals.

Ground the Poor grounding is the most likely reason an Ultrasound system will have noisy
Ultrasound system images. Check grounding of the power cord and power outlet.

Replace all screws, • After you finish repairing or updating the Ultrasound system, replace all covers
Radio Frequency and tighten all screws.
gaskets, covers, • Any cable with an external connection requires a magnet wrap at each end.
cores • Install all covers. Loose or missing covers or Radio Frequency gaskets allow
radio frequencies to interfere with the ultrasound signals.

Replace broken If more than 20% or a pair of the fingers on an Radio Frequency gasket are
Radio Frequency broken, replace the gasket. Do not turn on the Ultrasound system until any loose
gaskets metallic part is removed.

Do not place labels Where applicable, never place a label where Radio Frequency gaskets meet the
where Radio Ultrasound system. Otherwise, the gap created will permit Radio Frequency
Frequency gaskets leakage. Or, if a label has been found in such a position, move the label.
touch metal

Use GE specified The interconnect cables are grounded and require ferrite beads and other
harnesses and shielding. Also, cable length, material, and routing are all important; do not change
peripherals from what is specified.

Take care with Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.
cellular phones

Properly route Where applicable, do not allow cables to lie across the top of the Card Rack or
peripheral cables hang out of the peripheral bays. Loop the excess length for peripheral cables
inside the peripheral bays. Attach the monitor cables to the frame.

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 General requirements

Probes environmental requirements

Operation and storage temperatures for probes

Table 2-8: Operation and storage temperatures for probes

Conditions Temperature

Operation: 10 to 40 ºC (50 to 104 ºF)

Storage: -5 to 50 ºC (23 to 122 ºF)

Temperature in degrees Celsius (ºC) conversion to degrees F (ºF):

(ºF) = (ºC * 9/5) + 32

NOTE: SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED

FOR STORAGE TEMPERATURES OF -5 TO + 50 degrees C.
WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS,
THE PRODUCT SHOULD BE KEPT IN ROOM
TEMPERATURE FOR 10 HOURS BEFORE USE.

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Facility needs

Purchaser responsibilities
The work and materials needed to prepare the site is the
responsibility of the purchaser. Delay, confusion, and waste of
manpower can be avoided by completing pre-installation work
before delivery. Purchaser responsibility includes:
• Procuring the materials required
• Completing the preparations before delivery of the
Ultrasound system
• Paying the costs for any alterations and modifications not
specifically provided in the sales contract
NOTE: All electrical installations that are preliminary to the positioning
of the equipment at the site prepared for the equipment must be
performed by licensed electrical contractors. Other connections
between pieces of electrical equipment, calibrations, and testing
must also be performed by qualified personnel. The products
involved (and the accompanying electrical installations) are
highly sophisticated and special engineering competence is
required. All electrical work on these products must comply with
the requirements of applicable electrical codes. The purchaser
of GE equipment must only utilize qualified personnel to perform
electrical servicing on the equipment.
The desire to use a non–listed or customer provided product or
to place an approved product further from the Ultrasound
system than the interface kit allows, presents challenges to the
installation team. To avoid delays during installation, such
variances should be made known to the individuals or group
performing the installation at the earliest possible date
(preferably prior to the purchase).
The ultrasound suite must be clean prior to delivery of the
Ultrasound system. Carpet is not recommended because it
collects dust and creates static. Potential sources of EMI
(electromagnetic interference) should also be investigated
before delivery. Dirt, static, and EMI can negatively impact
Ultrasound system reliability.

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 Facility needs

Required facility needs

NOTE: GE requires a dedicated power and ground for the proper
operation of its Ultrasound equipment. This dedicated power
shall originate at the last distribution panel before the Ultrasound
system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not
shared with any other circuit), and a full size ground wire from
the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not
shared with any other circuit, and a full size ground wire from the
distribution panel to the Ultrasound outlet.
NOTE: Please note that image artifacts can occur, if at any time within
the facility, the ground from the main facility's incoming power
source to the Ultrasound unit is only a conduit.
• Dedicated single branch power outlet of adequate
amperage meeting all local and national codes which is
located less than 2.5 m (8 ft.) from the unit’s proposed
location
• Door opening is at least 76 cm (30 in) wide
• Proposed location for unit is at least 0.2m (0.67 ft.) from the
wall for cooling
• Power outlet and place for any external peripheral are within
2 m (6.5 ft.) of each other with peripheral within 1 m of the
unit to connect cables.
• Power outlets for other medical equipment and gel warmer
• Power outlets for test equipment and modem within 1 m (3.2
ft.) of unit
• Clean and protected space to store transducers (in their
cases or on a rack)
• Material to safely clean probes (done with a plastic
container, never metal)
For the amperage requirements, see: ‘Electrical requirements’
on page 2-6.

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Site Preparations

Desirable features
• Door is at least 92 cm (3 ft.) wide
• Circuit breaker for dedicated power outlet is easily
accessible
• Sink with hot and cold water
• Receptacle for bio–hazardous waste, like used probe
sheaths
• Emergency oxygen supply
• Storage for linens and equipment
• Nearby waiting room, lavatory, and dressing room
• Dual level lighting (bright and dim)
• Lockable cabinet ordered by GE for its software and
proprietary manuals

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 Facility needs

Suggested and Alternate Ultrasound Room Layout

Recommended standard floor plan and a minimal floor plan for
ultrasound equipment:

18 IN .
(46 C M) LINEN SUPPLY

P R O C ESSIN G
DE DIC AT E D
P O WE R
R E C EP TA C LE

R OOM ,
C O NS O LE
F IL M

E XAM IN AT IO N
C O UN T E R
C AB INE T

F IL M VIE WE R F OOT
SW
F ILE

TAB LE
TO P
C O UN T E R TO P S TOO L

SIN K
76 IN .
(193 C M)

SU C T IO N LINE
24 IN .
E ME R G E C Y (61 C M)
OX Y G EN
SE CR E TA R YS O R
DO C TO R ' S DES K

O VE R HE A D P AT IEN T
LI G HT S DIMME R TO ILE T
F A C ILI T Y

DOO R
42 IN .
(107 C M)
A 14 by 17 foot R ecommended F loor P lan
S cale : E ach square equals one square foot

F IL M VIE WE R LINEN SUPPLY

SIN K
F IL M SUPPLIES P R OB ES /SUPPLIES

E XT E R NA L
PE R IP HE R A LS
DE DIC AT E D P O WE R
O UT LE T S
F OOT L O G IQ B oo k X P
SW

S TOO L C ONS OLE

E XAM IN A R IO N G E C AB INE T
24 IN . TAB LE F OT S O F T WA R E
(61 C M) 76 IN .
(193 C M)
A ND MA NU A LS
DOO R
30 IN .
(76 C M)
A n 8 by 10 foot Minimal F loor P lan

Figure 2-1. Suggested Ultrasound Room Layout

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Site Preparations

Networking setup requirements

Stand alone Ultrasound system (without network connection)

None.

Scanner connected to hospital’s network

Supported networks:
Wireless LAN

Purpose of the DICOM network function

DICOM services provide the operator with clinically useful

features for moving images and patient information over a
hospital network.
Examples of DICOM services include the transfer of images to
workstations for viewing or transferring images to remote
printers.
As an added benefit, transferring images in this manner frees up
the on-board monitor and peripherals, enabling viewing to be
done while scanning continues.
With DICOM, images can be archived, stored, and retrieved
faster, easier, and at a lower cost.

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 Facility needs

DICOM option setup requirements

To configure the Ultrasound system to work with other network

connections, the site’s network administrator must provide
information to complete the form “Worksheet for DICOM
Network Information in ”Figure 2-2 on page 2-18. Ensure that
there are no spaces in any field of the form.
Entries must include:
• A host name, local port number, AE Title, IP address and
Net Mask for the Ultrasound system.
• The IP addresses for the default gateway and other routers
at the site for ROUTING INFORMATION.
• The host name, IP address, port and AE Title for each
device the site wants connected to the Ultrasound system
for DICOM APPLICATION INFORMATION. A field for the
make (manufacturer) and the revision of the device, is also
included. This information may be useful for error solving.

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Site Preparations

DICOM option setup requirements (continued)

Figure 2-2. Worksheet for DICOM Network Information

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 Environmental Dangers

Environmental Dangers

Commercial devices such as laser cameras, printers, VCRs and external monitors,
usually exceed allowable leakage current limits and, when plugged into separate AC
outlets, are in violation of patient safety standards. Suitable electrical isolation of such
external AC outlets, or providing the device with extra protective earth, will be required
in order to meet IEC60601-1 standards for electrical leakage.

Patient Environment IEC60601-1and ANSI AAMI ES60601-1

Sub Clause 3.79 and figure A.9 (IEC60601-1:2005 and ANSI AAMI
ES60601-1:2005)
Such an area is an environment in which medical diagnosis, monitoring or treatment is
carried out. It is very difficult to attach unique dimensions to the PATIENT
ENVIROMENT.
In practice a distance of 2,5 m (8.2 ft.) above the floor on which the medical personnel
stand and a horizontal distance of 1,5 m (4.9 ft.) have justified themselves as
indicative of the dimensions of the Patient Environment.
The patient environment/vicinity will be depicted as a dashed line in this procedure.
See example below.

1. Patient environment

Figure 2-3. Patient environment

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 Chapter 3

System Setup

This chapter contains information needed to install

LOGIQ e system.

Included is a procedure that describes how to receive

and unpack the equipment and how to file a damage or
loss claim.

How to prepare the facility and unit of the actual

installation, and how to check and test the unit, probes,
and external peripherals for electrical safety are also
included in this procedure.

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System Setup

Overview

Contents in this chapter

• ‘Overview’ on page 3-2
• ‘Setup reminders’ on page 3-3
• ‘Receiving and unpacking the equipment’ on page 3-6
• ‘Preparing for setup’ on page 3-12
• ‘Completing the setup’ on page 3-13
• ‘System Configuration’ on page 3-20
• ‘Connectivity setup’ on page 3-31
• ‘Paperwork after setup’ on page 3-33
• ‘Peripherals Installation Instructions’ on page 3-38

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 Setup reminders

Setup reminders

Contents in this Section

• ‘Average setup time’ on page 3-3
• ‘Setup warnings’ on page 3-3

Average setup time

• Unpacking the LOGIQ e: 20 minutes
• Set up LOGIQ e wo/options: 30 minutes
• DICOM Network Configuration: 30 minutes
The LOGIQ e installation and functional checkout will take
approximately one hour. LOGIQ e consoles with optional
equipment may take slightly longer.

Setup warnings

DANGER WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE

OF OPENING THE AC GROUND LINE (I.E., METER’S
GROUND SWITCH IS OPEN), DON’T TOUCH THE
ULTRASOUND SYSTEM!

CAUTION To prevent electrical shock, connect the unit to a properly

grounded power outlet. Do not use a three to two prong
adapter. This defeats safety grounding.

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System Setup

Setup warnings (continued)

CAUTION Do not wear the ESD wrist strap when you work on live circuits
and more than 30 V peak is present.

CAUTION Do not operate this unit unless all board covers and frame
panels are securely in place. System performance and cooling
require this.

1. There are no operator serviceable components. To prevent

shock, do not remove any covers or panels. Should
problems or malfunctions occur, unplug the power cord.
Only qualified service personnel should carry out servicing.
NOTE: For information regarding packing labels, refer to LABELS
ON PACKAGE.
2. After being transported, the unit may be very cold or hot. If
this is the case, allow the unit to acclimate before you turn it
on. It requires one hour for each 2.5×C increment it's
temperature is below 10×C or above 40×C.

DANGER Equipment damage possibility. Turning the system on without

acclimation after arriving at site may cause the system to be
damaged.

CAUTION If the Ultrasound system is very cold or hot, do not turn on its
power until it has had a chance to acclimate to its operating
environment.

The following table describes guidelines for reaching operational

temperatures from storage or transport temperatures.

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 Setup reminders

Setup warnings (continued)

DANGER WHEN USING ANY TEST INSTRUMENT THAT IS

CAPABLE OF OPENING THE AC GROUND LINE
(I.E., METER’S GROUND SWITCH IS OPEN),
DON’T TOUCH THE UNIT!

DANGER To prevent electrical shock, connect the unit to a properly

grounded power outlet. Do not use a three to two prong
adapter. This defeats safety grounding.

DANGER Do not operate this unit unless all board covers are securely in
place.

CAUTION Operator Manual(s)

The User Manual(s) should be fully read and understood
before operating the LOGIQ e and kept near the Ultrasound
system for quick reference.

CAUTION Acoustic Output Hazard

Although the ultrasound energy transmitted from the LOGIQ e
probe is within AIUM/NEMA standards, avoid unnecessary
exposure. ultrasound energy can produce heat and mechanical
damage.

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System Setup

Receiving and unpacking the

equipment

Contents in this Section

• ‘Receiving the LOGIQ e’ on page 3-6
• ‘Unpacking the LOGIQ e’ on page 3-7
• ‘Moving into Position’ on page 3-10

Receiving the LOGIQ e

Overview

Improper handling during transportation may harm the

equipment inside the package even if the package itself is
undamaged.

Examine all packages

Examine package closely at time of delivery, as described in the

procedure below.

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 Receiving and unpacking the equipment

Unpacking the LOGIQ e

When a new system arrives, check that any components are not
damaged and are not in short supply. If shipping damage or
shortage occurs, contact the address shown in Chapter 1
1. Cut the four PLASTIC BANDs
2. Cut the adhesive tape and open top covers of paper carton.

Adhesive tape

Plastic Bands

Figure 3-1. Open Top Covers of Paper Carton

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System Setup

Unpacking the LOGIQ e (continued)

3. Take out the Paper pad.
4. Take out console together with 2 interleavers from console
package.
5. Take out the interleavers beside Accessories Package
6. Take out Accessories Package.

Paper Pad

Console and interleavers

Console Package

Accessories Package

Figure 3-2. Unpacking the equipment

CAUTION Do not lift the unit by the rubber band. Equipment damage
may result.

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 Receiving and unpacking the equipment

Unpacking the LOGIQ e (continued)

7. Remove 2 interleavers.
8. Remove plastic bag.

Interleaver

Console

Interleaver

Figure 3-3. Removing interleavers and plastic bag

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System Setup

Unpacking the LOGIQ e (continued)

NOTE: Check the shipping container for special instructions. Verify that
the container is intact. In some cases a secondary container
may be used. If so, ask the carrier for unpacking instructions.

Figure 3-4. Labels on Package

CAUTION Please carefully unpack the system, and do not dispose the
package of LOGIQ e, so that it can be reused for service.

Moving into Position

CAUTION Do not lift the unit by the rubber band. Use handle to move
system.

CAUTION Equipment Damage Possibility. Lifting the console by holding

covers may damage the covers. Do not lift the console by
holding any covers.

In general, a single adult can move the LOGIQ e. Before

moving, store all loose parts in original accessory box or in back
pack. Return probes to original box.

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 Receiving and unpacking the equipment

Packing the Equipment

Please pack LOGIQ e in the reverse order of unpacking.

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System Setup

Preparing for setup

Verify customer order

Compare items received by the customer to that which is listed
on the delivery order. Report any items that are missing, back
ordered, or damaged.

Physical inspection

System Voltage Settings

Verify that the system arrived intact (visual inspection).

If the system has been damaged, please refer to ‘Damage in
transportation’ on page i-11 in the beginning of this manual.
• Verify that the scanner is set to the correct voltage. The
Voltage settings for the LOGIQ e Scanner is found on a
label located on the AC adapter.
• 220-240VAC(China); 100-120VAC(USA/Japan);
220-240VAC(Europe, Latin America).

WARNING Connecting a LOGIQ e system to the wrong voltage level

will most likely destroy the scanner.

EMI protection
The LOGIQ e has been designed to minimize the effects of
Electro-Magnetic Interference (EMI). Many of the covers,
shields, and screws are provided primarily to protect the system
from image artifacts caused by this interference. For this reason,
it is imperative that all covers and hardware are installed and
secured before the unit is put into operation.
See ‘EMI limitations’ on page 2-9 for more information about
EMI protection.

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 Completing the setup

Completing the setup

Contents in this Section

• ‘System specifications’ on page 3-13
• ‘Electrical specifications’ on page 3-14
• ‘Power On / Boot Up’ on page 3-15
• ‘Power Off/Shutdown’ on page 3-17
• ‘Connecting probes’ on page 3-18

System specifications

System requirements verification

• Verify that the site meets the requirements listed in

Chapter 2.
(See: ‘Facility needs’ on page 2-12.)
• Verify that the specifications below don’t conflict with any
on-site conditions.

Physical dimensions

The physical dimensions vary from product to product. You may

copy and use the table below in your local manuals or local core
content.
• Height: 70 mm (2.75 in) console only; 100 mm (3.94 in) with
handle
• Length: 346 mm (13.62 in) console only; 375 mm (14.76 in)
with handle
• Width: 295 mm (11.61 in) console only; 343 mm (13.50 in)
with handle

Console Weight

• Weight (with battery): approx. 5.2 kg (11.5 lbs)

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System Setup

Electrical specifications

WARNING Connecting a LOGIQ e to the wrong voltage level will most

likely destroy it.

Verification of the system’s voltage setting

Verify that the mains voltage specified for the LOGIQ e is

available on-site.

Electrical specifications for LOGIQ e

Figure 3-5. AC Adapter label

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 Completing the setup

Power On / Boot Up
NOTE: After turning off a system, wait at least ten seconds before
turning it on again. The system may not be able to boot if power
is recycled too quickly.

System Power On

Lower the handle. Plug the AC adapter output connector into the
system DC input port (located on the system’s rear panel) with
the arrow side upward. Plug the AC adapter power cord into a
grounded, protective earth outlet

ＵＰ

Figure 3-6. Connect AC adapter

When power is applied to the system, power is distributed to the

Cooling Unit, Control Panel, LCD, Peripherals and the Back-end
Processor.

CAUTION The system should rest on the handle to allow an air gap to
prevent overheating.

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System Setup

Power on the system

Press the Power On/Off switch at the front of the system once.

Figure 3-7. Power On/Off Switch

When the Power On/Off switch on the Control Panel is pressed

once, the Back-end Processor starts and the software code is
distributed to initiate the scanner.
No status messages are displayed during this process.

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 Completing the setup

Power Off/Shutdown
NOTE: After turning off a system, wait at least ten seconds before
turning it on again. The system may not be able to boot if power
is recycled too quickly.

Back-end Processor Power off

To power off the system:

1. Press the Power On/Off switch at the front of the system
once.
2. The system-Exit window is displayed.

Figure 3-8. System Exit Window

3. Using the Trackball or Select key, select Shutdown.

4. The shutdown process takes a few seconds and is complete
when the power status LED is turned off.
5. Disconnect the probes.Clean or disinfect all probes as
necessary. Store them in their shipping cases to avoid
damage.
6. Close LCD cover.

System Shutdown

Disconnect the Mains Power Cable if necessary. For example:

Relocating the system.

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System Setup

Connecting probes

Connect a probe

NOTE: It is not necessary to turn OFF power to connect or disconnect a

probe.

CAUTION Do not allow the probe head to hang freely. Excessive impact
to the probe will result in irreparable damage.

CAUTION To prevent probe connector pins damage, or PCB board

damage, do not use excessive force when connecting the
probes.

CAUTION Keep the probe cables away from the wheels.

Do not bend the probe cables.
Do not cross cables between probes.

Follow these steps to connect a probe:

Probes can be connected at any time, whether the unit is On or
Off.
Carefully open the system LCD display, plug the probe
connector into the probe port, then lock the probe latch upward.
NOTE: Please ensure that the probe latch is in an unlocked position
before you connect the probe to the system.
1. Before connecting the probe:
a. Do a visual check of the probe pins and system sockets.
b. Remove any dust or foam rests from the probe pins.
c. Verify the probe and the probe cable for any visual
damage.

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 Completing the setup

Connect a probe (continued)

2. Position the probe cable so that it is not resting on the floor.

Probe Latch

Figure 3-9. Probe connectors

Disconnect a probe

Follow these steps to disconnect a probe:

1. Remove the connector from the port.
2. Ensure that the probe head is clean before placing the
probe in its storage case.

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System Setup

System Configuration

Contents in this Section

• ‘LOGIQ e configuration’ on page 3-21
• ‘Electrical requirements for Adapter’ on page 3-22
• ‘Approved peripherals’ on page 3-22
• ‘Connecting Cables’ on page 3-24
• ‘Peripheral/Accessories Connector Panel’ on page 3-25
• ‘Pin Assignment’ on page 3-26
• ‘Available probes’ on page 3-30
• ‘Software Options configuration’ on page 3-31

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 System Configuration

LOGIQ e configuration

System Specification

The physical dimensions of the LOGIQ e console with old LCD

are summarized as below:

Table 3-1: Physical Dimensions of LOGIQ e

Height Width Depth Unit

Console Console Console

Console with Console with Console with
Only Handle Only Handle Only Handle Unit

70 100 295 343 346 375 mm

2.75 3.94 11.61 13.50 13.62 14.76 inches

Figure 3-10. Overall Dimensions and Weight

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System Setup

Electrical requirements for Adapter

Table 3-2: Electrical Specifications for Adapter

Adapter Model AHM150PS19-XA1048

Input Voltage 100-240VAC

Input Current 1.5A at 115VAC

0.75A at 230VAC

Output Power 150W

Output Voltage 19.0VDC

Output Current 7.89A

Frequency 50/60Hz

Approved peripherals

Table 3-3: Approved peripherals

Device Manufacturer Model Interface Remark

B/W Printer SONY UP-D897 B/W USB1.1 Port

Printer

SONY UP-D898MD B/W USB1.1 Port

Printer

Mitsubishi P95DW USB1.1 Port For R8.x.x only

Color Printer SONY UP-D25MD Color USB1.1 Port

Printer

DVD RW LITEON LITEON eUAU108 USB Port

LITEON LITEON eBAU108 USB Port

3-pedal footswitch Steute MKF 2-MED GP26 USB Port

USB Wireless Card NetGear NetGear USB Port

WNA1000M
Wireless USB
Micro Adapter

NetGear I-O DATA USB Port For R8.x.x only

WN-G300U

NetGear NetGear USB Port

WNA3100M
Wireless USB
Micro Adapter

EDIMAX AC1200 Wireless USB Port For R9.x.x only

Dual-Band USB
Adapter

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 System Configuration

Table 3-3: Approved peripherals

Device Manufacturer Model Interface Remark

ECG-USB NORAV ECGUSB1D-EX USB Port

Barcode Scanner Honeywell XENON 1900 USB Port

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System Setup

Connecting Cables

WARNING Equipment damage possibility. Be sure to use the following

recommended connecting cables to connect recording devices
and a network with LOGIQ e console.

Table 3-4: List of Connecting Cables

Name Part No. Figure NOTE

USB Cable For USB Printer &

USB DVD-RW

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 System Configuration

Peripheral/Accessories Connector Panel

LOGIQ e peripherals and accessories can be properly
connected using the side connector panel.

Figure 3-11. Left Side and Rear Connector Panel

1. 3 USB Ports for Printers (B/W, Color and USB), Memory

Stick, Footswitch, DVD-RW, Wireless LAN Adapter, USB
Hub, USB HDD, ECG
2. SD card port
3. Security lock
4. Port for DC In (AC Adapter)
5. Docking Port
6. HDMI Port
7. Network Port
NOTE: Each outer (case) ground line of peripheral/accessory
connectors are protectively grounded. Signal ground lines are
not isolated.

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System Setup

Pin Assignment

Pin Assignment of DC in put

Connector: 4 Pin, Female

Table 3-5: Pin Assignment of DC input

Pin No. Signal Pin No. Signal

1 +20V 3 GND

2 +20V 4 GND

Pin Assignment of USB1

Table 3-6: Pin Assignment of USB1

Pin No. Signal Pin No. Signal

1 +5VDC 3 DATA+

2 DATA- 4 GND

Pin Assignment of USB2

Table 3-7: Pin Assignment of USB2

Pin No. Signal Pin No. Signal

1 +5VDC 3 DATA+

2 DATA- 4 GND

Pin Assignment of USB3

Table 3-8: Pin Assignment of USB3

Pin No. Signal Pin No. Signal

1 +5VDC 3 DATA+

2 DATA- 4 GND

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 System Configuration

Pin Assignment of External HDMI

Table 3-9: Pin Assignment of HDMI

Pin No. Signal Pin No. Signal

1 TMDS Data2+ 11 TMDS Clock Shield

2 TMDS Data2 Shield 12 TMDS Clock-

3 TMDS Data2- 13 CEC

4 TMDS Data1+ 14 Reserved (N.C. on

device)

5 TMDS Data1 Shield 15 SCL

6 TMDS Data1- 16 SDA

7 TMDS Data0+ 17 DDC/CEC Ground

8 TMDS Data0 Shield 18 +5V Power

9 TMDS Data0- 19 Hot Plug Detect

10 TMDS Clock+

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System Setup

Peripheral Connection

NOTE: Please refer to the operation manual of each peripheral for

information needed by the user to operate the system safely.
To install the peripherals, See ‘Peripherals Installation’ on
page 3-34 for more information.

Table 3-10: Peripheral Connection

No. Steps Corresponding Graphic

1. Connect DVD-RW.
Connect the DVD-RW to the system.
The DVD-RW can be properly
connected using either of the 3 USB
ports.
NOTE: Do not connect the DVD-RW to
the system while scanning.

2. Connect Footswitch.
Connect the footswitch to the system.
The footswitch can be properly
connected using either of the 3 USB
ports.

3. Connect SD Card.
Connect SD Card to the system. Insert
the SD Card into the SD Card port.

4. Connect Wireless LAN Adapter.

Connect the Wireless LAN Adapter to
the system. The wireless LAN adapter
can be properly connected using either
of the 3 USB ports.

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 System Configuration

Table 3-10: Peripheral Connection

No. Steps Corresponding Graphic

5. Connect Color Printer.

Connect the Color Printer to the system.
The Color Printer can be properly
connected using either of the 3 USB
ports.

6. Connect ECG.
Connect the ECG to the system. The
ECG can be properly connected using
either of the 3 USB ports.

7. Connect Barcode Reader.

Connect the Barcode Reader to the
system. The Barcode Reader can be
properly connected using either of the 3
USB ports.

8. Connect HDMI.
Connect the external monitor to the
system. The monitor can be properly
connected using the HDMI port.

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System Setup

Available probes
See in specification in the LOGIQ e User Reference Manual for
Probes and intended use.
The LOGIQ e system (Software R8.x.x) supports C1-5-RS,
8C-RS, 9L-RS, 12L-RS, L4-12t-RS, L8-18i-RS, L10-22-RS,
E8C-RS, 3Sc-RS and 6S-RS probes.
The LOGIQ e system (Software R9.x.x) supports C1-5-RS,
8C-RS, 4C-RS, 9L-RS, 12L-RS, L4-12t-RS, L8-18i-RS,
L10-22-RS, LK760-RS, E8C-RS, 3Sc-RS, 6S-RS and 6Tc-RS
probes.

Table 3-11: List of Probes for LOGIQ e

Material of Catalog Part

Probe Name Headshell TYPE Number Number

C1-5-RS NORYL CONVEX H40462LA 5384875

E8C-RS VALOX MICRO-CONVEX H40402LN 5434195

8C-RS VALOX MICRO-CONVEX H40402LS 5434194

12L-RS NORYL LINEAR H40402LY 5409291

3SC-RS VALOX Phased Array H45041DL 47237516

9L-RS VALOX LINEAR H40442LL 5213143

6S-RS VALOX SECTOR H45021RP 5394465

L4-12t-RS VALOX LINEAR H48062AB 5435010

L8-18i-RS VALOX LINEAR H40462LF 5397810

L10-22-RS VALOX LINEAR H48312AH 5441887

4C-RS VALOX CONVEX H4000SR 5488477

LK760-RS VALOX LINEAR H44901AF KN100106

6Tc-RS VALOX SECTOR H45551ZE 5548914

NOTE: Please refer to User Manual for the applications of the probes.

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 System Configuration

Software Options configuration

Software Option installation introduction

Refer to the LOGIQ e Basic User Manual, Chapter 16,

Customizing Your System for information on configuring items
like Hospital, Department, Language, Units (of measure), Date,
Time and Date Format.
For information on configuring Software Options, Refer to the
LOGIQ e Basic User Manual, Chapter 16, Customizing Your
System.
For information on configuring DICOM Connectivity, Refer to the
LOGIQ e Basic User Manual, Chapter 16, Customizing Your
System.

Connectivity setup
To be able to use the network functions when connected to a
hospital network, the scanner must have a proper network
address.
• Before you can set up the scanner, you need to collect some
information.
• The Worksheet can be used for gathering this information.
• Typical source for this information is the network
administrator.

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System Setup

Connectivity setup (continued)

Site System Information

Floor: Comments:
Site:

Dept: Room:

LOGIQ SN: Type: REV:

CONTACT INFORMATION

Name Title Phone E-Mail Address

TCP/IP Settings

Name - AE Title:

IP Settings Remote Archive Setup

IP Address: Remote Archive IP:

Subnet Mask: Remote Archive Name:
Default Gateway:

Services (Destination Devices)

Device Type Manufacturer Name IP Address Port AE Title
1
2
3
4
5
6
7
8
9
10
11
12

Figure 3-12. Connectivity Installation Worksheet

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 Paperwork after setup

Paperwork after setup

NOTE: During and after setup, the documentation (i.e. CDs with
documentation, User Manuals, Installation Manuals, etc.) for the
LOGIQ e and the peripherals must be kept as part of the original
Ultrasound system documentation. This ensures that all relevant
safety and user information is available during the operation and
service of the complete Ultrasound system.

User’s Manual(s)
User Check that the correct User Manual(s) for the system and
software revision, is included with the installation. Specific
language versions of the User Manual may also be available.
Check with your GE Sales Representative for availability.

Product Locator Installation Card

NOTE: The Product Locator Installation Card shown may not be the
same as the provided Product Locator card.

Figure 3-13. Product Locator Installation Card (Example)

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System Setup

Peripherals Installation

Contents in this Section

• ‘Overview’ on page 3-35
• ‘Furnished materials’ on page 3-36
• ‘Peripherals Installation Instructions’ on page 3-38
• ‘Color USB Printer Installation’ on page 3-38
• ‘DVD-RW Installation’ on page 3-41
• ‘Wireless Lan Adapter Installation’ on page 3-43
• ‘Footswitch Installation’ on page 3-61
• ‘Barcode Scanner Installation’ on page 3-63
• ‘ECG Installation’ on page 3-66
• ‘ECG Intended Use’ on page 3-67
• ‘Technical Specification of ECG’ on page 3-68

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 Peripherals Installation

Overview
This section describes how to install and configure the
peripherals validated for the LOGIQ e.
About the operation check-out of peripherals, See ‘Peripheral
Checks’ on page 4-52 for more information.

Table 3-12: LOGIQ e Peripherals

Description Power Control Model

B/W USB Printer 100-120VAC/240VAC USB port UP-D897

50/60Hz 1.5a/0.8A

100-120VAC/240VAC USB port UP-D898MD

50/60Hz
1.3A/0.6A

100-120VAC/240VAC USB port P95DW (For R8.x.x only)

50/60Hz
1.5-0.8A

Color USB Printer 100-240VAC USB port UP-D25MD

50/60hZ
1.7/1.0A

DVD-RW 100-240VAC USB port eUAU108

1.5A

100-240VAC USB port eBAU108

1.5A

3-Pedal 5V USB port MKF 2-MED GP26

Footswitch

USB Wireless USB port NetGear WNA1000M Wireless

Adapter USB Micro Adapter

USB port I-O DATA WN-G300U (For R8.x.x

only)

USB port NetGear WNA3100M Wireless

USB Micro Adapter

USB port AC1200 Wireless Dual-Band USB

Adapter (For R9.x.x only)

Barcode Scanner USB port XENON1900

ECG USB 5V 80mA USB port ECGUSB1D-EX

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System Setup

Furnished materials
This section describes the materials furnished with the
Peripherals and with the system.
Retain the original carton and packing materials in case
transport is needed in the future.
• UP-D898MD B/W Printer

Table 3-13: Materials furnished with B/W Printer

Item Description Quantity Note

1 UP-D898MD B/W Printer 1

2 Paper Roll 1

3 USB cable 1

4 AC Power Cord 1

• Color USB Printer

Table 3-14: Materials furnished with Color USB Printer

Item Description Quantity Note

1 UP-D25MD Color USB Printer 1

2 Paper Roll 1

3 AC Power Cord 1

4 USB cable 1

• DVD-RW (LITEON DVD-RW)

Table 3-15: Materials furnished with DVD-RW

Item Description Quantity Note

1 DVD-RW 1

2 USB cable 1

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 Peripherals Installation

Furnished materials (continued)

• USB Wireless Adapter

Table 3-16: Materials furnished with the Wireless LAN

Item Description Quantity Note

1 Wireless Adapter 1

• 3 Pedal Footswitch

Table 3-17: Materials furnished with the Footswitch

Item Description Quantity Note

1 Footswitch 1

• Barcode Scanner

Table 3-18: Materials furnished with the Barcode Scanner

Item Description Quantity Note

1 Barcode Scanner 1

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System Setup

Peripherals Installation Instructions

Color USB Printer Installation

Tools
No special tools needed.

Manpower
One person 5 minutes.

Preparations
1. Unpack the Color USB Printer.

Installation Procedure
1. Place the device in a suitable place.
2. Connect power cord and USB Cable on the Printer.

Figure 3-14. Color Printer USB cable and Power Cord connect

3. Connect the power cord to the outlet on the wall, then turn
on the printer.

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 Peripherals Installation

Color USB Printer Installation (continued)

4. Connect USB cable to LOGIQ e USB port.

Figure 3-15. Color Printer connection

Setting up Color printer for Printing Report

1. Connect the color printer to the USB port of the system.
2. Power on the printer and the system.
3. After the system completes booting up, enter Utility ->
System -> Peripherals, select UP-D25MD for Standard
Printer.

Figure 3-16. Peripheral Page

4. Select Save.

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System Setup

Assigning Printer Key to the Printer

Example below assign P2 on the control panel to Color Printer
UP-D25MD.
1. Select Connectivity -> Service, select Standard Print in the
Service list.

Figure 3-17. Service Page

2. Select Connectivity -> Button, select Print2 in Print Button

list, then select the original setting in Printflow View field and
select “<<“.

Figure 3-18. Button Page

3. Select Standard Print, then press “>>“ to add the standard

printer to the Printflow View.

Figure 3-19. Standard Print setting

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 Peripherals Installation

DVD-RW Installation

Tools
No special tools needed.

Manpower
One person 5 minutes.

Preparations
1. Unpack the DVD-RW.
2. Ensure no physical damage.

Installation Procedure
1. Place the device in a suitable place.
2. Connect the USB Cable on the DVD-RW.

Figure 3-20. Connect USB cable on DVD-RW

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System Setup

DVD-RW Installation (continued)

3. Connect USB cable to LOGIQ e USB port.

Figure 3-21. DVD-RW connection

WARNING Do Not connect DVD-RW with the system while scanning.

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 Peripherals Installation

Wireless Lan Adapter Installation

Tools
No special tools needed.

Manpower
One person 5 minutes.

Preparations
1. Unpack the Wireless LAN Adapter.
2. Ensure no physical damage.

Installation Procedure
1. Connect the Wireless LAN Adapter to the USB port on the
LOGIQ e system.

Figure 3-22. Connect Wireless LAN Adapter to the system

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System Setup

Wireless Lan Adapter Installation (continued)

2. Enter Utility -> Connectivity -> TCP/IP and select
Configuration to configure wireless network.

Figure 3-23. Wireless configuration

3. Config the wireless Lan setting with local IT person.

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 Peripherals Installation

Configuring the Wireless Network (Option)

A Wireless Network (WLAN) is available on the LOGIQ e. When

the WLAN is active, an icon appears in the status bar to indicate
whether the WLAN is installed or disconnected.

Wireless LAN (WLAN) Specifications

The Wireless LAN (WLAN) supports the following network
protocols

Wireless LAN (WLAN) Specifications for Software R8.x.x

Security (Encryption)
• WPA2-PSK [AES], WPA-PSK [AES/TKIP], and 40bit (also
called 64-bit) and 128-bit WEP data encryption
Radio Data Rate
• Up to 150 Mbps----NETGEAR WNA1000M
• Up to 300 Mbps---I-O DATA WN-G300U
Frequency
• 2.4 GHz, 5 GHz
WPA-Enterprise
• Not Supported

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System Setup

Wireless LAN (WLAN) Specifications for Software R9.x.x

Security (Encryption)
• None/Open
• Shared
• WPA-Personal
• WPA2-Personal
• WPA-Enterprise
• WPA2-Enterprise
Encryption
• None
• WEP
• TKIP
• AES
Authentication
• None
• Microsoft PEAP using MSCHAP v2
• Cisco EAP/LEAP/PEAP
• Username/password
• Limited support for server certificate verification using
pre-installed trusted root CAS
• Client certificates not supported
• User authentication/confirmation prompts not supported

I-O DATA WN-G300U / Netgear WNA1000M

This wireless adapter supports the following network protocols:
Standards
• IEEE 802.11n, 802.11g, 802.11b
Supported Standards
NETGEAR WNA1000M
• FCC Part 15 Class B
• R&TTE Directive
• Canada Requirements
I-O DATA WN-G300U
• Japan’s Radio Law
WPA-ENTERPRISE
NOTE: I-O DATA WN-G300U is only supported on Software R8.x.x.

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 Peripherals Installation

Wireless Adapter AC1200 (For R9.x.x only)

This wireless adapter supports the following network protocols:
Standards
• IEEE 802.11n, 802.11g, 802.11a, 802.11b
Radio Data Rate
• 2.4GHz Up to 300 Mbps
• 5GHz up to 867 Mbps
Frequency
• 2.4000 - 2.4835GHz (subject to local regulations)
• 5.150 - 5.825GHz (subject to local regulations)
Supported Standards
• CE
• FCC

NetGear Wireless Adapter WNA3100

This wireless adapter supports the following network protocols:
Standards
• IEEE 802.11n, 802.11g, 802.11b
Radio Data Rate
• 300 Mbps
Frequency
• 2.4 GHz
WPA-Enterprise
• Not Supported

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System Setup

Connecting to the WLAN

To connect the LOGIQ e to the WLAN,
1. Press Utility --> Connectivity --> TCP/IP --> Wireless
Network --> Configuration.

Figure 3-24. WLAN settings on TCPIP

The Wireless Network Configuration tool appears. Available

Wireless Networks appear.
2. Check “Enable Wireless Connection”.
3. Highlight the wireless network you want to use.
4. Press Connect from the bottom of the Configuration tool.
The Active Wireless LAN indicator appears on the display.

Figure 3-25. Active Wireless LAN Indicator

NOTE: If the WLAN fails to connect, review and/or recreate the

Wireless connection on the Security Tab.

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 Peripherals Installation

Adding a Wireless Network (For R8.x.x)

To add a WLAN profile (even for a network which is not yet
available),
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Security. The Wireless Network Configuration
tool appears. Available Wireless Networks appear.
2. Select the Security tab.
3. Select Add...
4. Add the following information to the Wireless Network
Properties page:
• Network Name (SSID)
• Network Authentication (Open, Shared Key, WPA, WPA
PSK, WPA2, or WPA2 PSK).
• Data Encryption
• Network Key
• Key Index
5. After you have filled in all the required information, press
OK. To cancel adding this profile, press Cancel.

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System Setup

Adding a Wireless Network (For R9.x.x)

To add a WLAN profile (even for a network which is not yet
available),
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Configuration -> Security. The Wireless Network
Configuration tool appears. Available Wireless Networks
appear.
2. Select the Security tab.
3. Select Add...
4. Obtain and enter the correct information for each wireless
network setting.
a. Enter a Network Name (SSID), then press OK.
A new window appears so you can enter the settings for
this network.
b. On the connection page, check the appropriate box
based on how you want the LOGIQ e to connect to this
network.

Figure 3-26. WLAN Properties Connection Page

The LOGIQ e attempts to connect to available wireless

networks based on the options you enable. If multiple
networks are available, connection attempts begin with
the network appearing topmost on the list.

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 Peripherals Installation

Adding a Wireless Network (For R9.x.x) (continued)

c. Select the Security tab.

Figure 3-27. WLAN Properties Security Page

d. Select the Security Type from the available options.

Figure 3-28. WLAN Security Types

NOTE: Dialog boxes vary, depending on the Security Type

selected.

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System Setup

Adding a Wireless Network (For R9.x.x) (continued)

e. Select the Encryption Type from the available options.

Figure 3-29. WLAN Encryption Types

f. For Personal networks, enter the Network key.

g. For Enterprise network, choose the network
authentication method and press Settings.

Figure 3-30. WLAN Network Authentication Method

Detailed settings for Enterprise networks are complex

and must be correct for the connection to succeed.
Ensure you have all the required information/settings
and work with your site’s IT Network Administrator as
needed.
NOTE: Creditials must be entered at this time. The LOGIQ e
does not support automatic prompting for user
credentials.
• For Microsoft PEAP networks, press Advanced and
enter User authentication credentials (username and
password).
• For Cisco networks, enter user credentials in the PEAP
Properties dialog after pressing the Settings button.

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Adding a Wireless Network (For R9.x.x) (continued)

NOTE: IMPORTANT: User credentials are not validated until
you attempt to connect to the network.
h. When you have correctly entered all required settings,
press OK in the Wireless Network Properties dialog.
Your settings will be validated and you may be
prompted about certain settings which are not
recommended or supported.
Examples: “Automatic connection to unencrypted
networks is not recommended. Reminder to enter user
credentials for Enterprise networks.”
i. If changes are necessary, press Customize. Make
corrections, then press OK. Settings will be validated
again.
5. After you have filled in all the required information, press
OK. To cancel adding this profile, press Cancel.

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System Setup

Removing a WLAN
To remove a WLAN profile (even for a network which is not
available),
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Security. The Wireless Network Configuration
tool appears. Available Wireless Networks appear.
2. Select the Security tab.
3. Select Remove.

Customizing Wireless Network Settings

To customize an existing WLAN profile,
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Configuration. The Wireless Network
Configuration tool appears. Available Wireless Networks
appear.
2. Select the Security tab.
3. Select Customize...
4. Add the following information:
a. Network Name (SSID)
b. Network Authentication (Open, Shared Key, WPA PSK,
or WPA2 PSK).
c. Data Encryption
d. Network Key
e. Key Index
5. After you have filled in all the required information, press
OK. To cancel adding this profile, press Cancel.

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 Peripherals Installation

Refreshing a WLAN
Refreshes the list of available Wireless Networks. To refresh the
Wireless Network,
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Configuration. The Wireless Network
Configuration tool appears. Available Wireless Networks
appear.
2. Highlight the wireless network you want to refresh.
3. Press Refresh from the bottom of the Configuration tool.

Setting a WLAN as Non-Preferable

When you make a WLAN non-preferable, you disconnect the
network from the system and delete all connection settings from
the system. Afterwards, the system WILL NOT try to reconnect
to this WLAN automatically. And if you want to reconnect, you
will need to re-add this WLAN.
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Configuration. The Wireless Network
Configuration tool appears. Available Wireless Networks
appear.
2. Highlight the wireless network you want to set as
non-preferred.
3. Press Make Non-Preferable from the bottom of the
Configuration tool. You wil receive the following message to
confirm this decision: “Are you sure you wish to make
network _______ non-preferable? Network will be
disconnected and system will not reconnect to this network
automatically. Network connection settings will be deleted
from the system.”

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System Setup

Monitoring the WLAN

If there are wireless network communication problems, you can
monitor the wireless network events.
To monitor Wireless Networking events,
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Configuration. The Wireless Network
Configuration tool appears. Available Wireless Networks
appear.
2. Select the Monitor Tab.

Figure 3-31. Monitor Tab

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 Peripherals Installation

WLAN Diagnostics
Running diagnostics is good if you think the adapter might be
bad. Diagnostics also tell you if the connection is behaving
properly. Sometimes the scanner connects by accident to
another internal device which uses the TCP/IP protocol. The
diagnostics would show if there are errors when performing the
full two-way communication. For example, if the IP address
starts with 197 or 169 (loopback addresses), then something is
wrong.
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Configuration. The Wireless Network
Configuration tool appears. Available Wireless Networks
appear.
2. Select the Diagnostics Tab.

Figure 3-32. WLAN Diagnostics Tab

3. Select Run Diagnostics.

Figure 3-33. Diagnostic Results

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Repairing the WLAN

Occasionally you may need to repair a WLAN that has lost its
connection to the LOGIQ e. To repair the Wireless Network,
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Configuration. The Wireless Network
Configuration tool appears. Available Wireless Networks
appear.
2. Select the Diagnostics Tab.
3. Select Repair.
NOTE: DO NOT cancel the Repair operation after you have
selected to repair the Wireless LAN connection.
If the WLAN is functioning properly, the following message
appears. Confirm your decision to repair (Yes), or cancel (No).

Figure 3-34. Repair Message

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 Peripherals Installation

Available WLAN Channels

The available WLAN channels show availability of wireless
connect points that the scanner can talk to. Each channel
supports a finite number of users and has limited signal
strength. This may effect the ability to connect, the throughput
and the connection dropping out.
To check the available WLAN channels,
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Configuration. The Wireless Network
Configuration tool appears. Available Wireless Networks
appear.
2. Select the Properties Tab.

Figure 3-35. Properties Tab

3. Select Available Channels....

Figure 3-36. Available Channels

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System Setup

Disconnecting from the WLAN

To disconnect from the Wireless Network,
1. Press Utility--> Connectivity--> TCP/IP--> Wireless
Network--> Configuration. The Wireless Network
Configuration tool appears.
2. Select the WLAN you are connected to.
3. Select Disconnect.

Viewing WLAN Online Help

To view the WLAN Online Help, press Help.

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 Peripherals Installation

Footswitch Installation

Tools
No special tools needed.

Manpower
One person 5 minutes.

Preparations
1. Unpack the Footswitch.
2. Ensure no physical damage.

Installation Procedure
1. Connect the Footswitch to the USB port on the LOGIQ e
system.

Figure 3-37. Connect Footswitch to the system

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Footswitch Installation (continued)

Configuring Footswitch
Footswitch supports these configurations: No Function, Rec/
Pause, Freeze, Next Heartcycle, Prev Heartcycle, Print 1, Print
2, Print 3, Print 4, Update, Next Step (Scan Assistant), Previous
Step (Scan Assistant), Scan Assistant Pause/Resume or Mark
Cine. The default setting is No Function.
Enter Utility -> Application -> Settings to configure the
Footswitch functions.

Figure 3-38. Configuring Footswitch Functions

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Barcode Scanner Installation

Tools
No special tools needed.

Manpower
One person 1 minute.

Preparations
1. Unpack the Barcode Scanner.
2. Ensure no physical damage.

Installation Procedure
1. Connect the Barcode Scanner to the USB port on the
LOGIQ e system.

Figure 3-39. Connect Barcode Scanner to the system

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Barcode Scanner Installation (continued)

NOTE: After the Barcode Scanner is connected to the Docking
Cart, the cable of the Barcode Scanner can be hung in the
cable hook.

Figure 3-40. Barcode Scanner cable

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Barcode Scanner Installation (continued)

Set Up Barcode Scanner

The barcode scanner needs to be set up before the first use.
To set up the barcode scanner, follow the steps below:
1. Power on the system. Connect barcode scanner to the
system.
2. Scan the three barcodes.
First scan the Remove Custom Defaults barcode (1), then
scan the Activate Defaults barcode (2). This is to reset the
scanner to the factory default settings. Finally, scan the USB
Serial barcode (3). The Barcode scanner is ready for use.

Figure 3-41. Barcode

NOTE: Only the printed barcodes on the paper can be scanned. If

you do not have the printed version, be sure to print them to
the paper first and scan them on the paper.

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ECG Installation

Tools
• No special tools needed.

Manpower
• 1 person 1 minute.

Preparation
1. Unpack the ECG.
2. Ensure no physical damage.

Figure 3-42. ECG

Installation Procedure
1. Connect the ECG to the USB port on the system.

Figure 3-43. ECG Installation

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 Peripherals Installation

Installation Procedure (continued)

2. Wait 5 seconds for ECG function start automatically.

Figure 3-44. ECG Mode

ECG Intended Use

ECG is intended to disclose either normal condition or patterns

of arrhythmia, or features of prognostic value in the following
cases:
• Patients with suspected cardiac abnormalities
• Populations of patients at an age or period in which a
routine baseline evaluation of ECG characteristics is
desired.

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Patient Preparation

The ECG traces quality depends very much on the stability and
conductivity of the electrodes during the test, especially during
high stages when the patient movements can cause artifacts.
Here are some basic rules to ensure good electrical contact:
• Shave hair at the electrode contact points.
• Use a special shirt that attached the electrodes and lead
wires to the body.
• Use high quality liquid gel electrodes.
• Make sure that the lead wires do not swing.
Detachable 3 leads each 100cm with clip connectors on the
patient end designed for use with disposable ECG electrodes.
Furthermore, equip 3 repeatable limbs electrode clamps which
can connect with clip connector. Limbs electrodes are white, red
and green (AHA\IEC).

Table 3-19: ECG Lead Placement

Patient Cable Marking

Lead AHA IEC Position on Patient

I RA (White) R (Red) Right Arm

II LA (Black) L (Yellow) Left Arm

III RL (Green) N (Black) Right Leg

Technical Specification of ECG

Table 3-20: ECG Technical Specifications

Feature Specification

ECG

Patient Cable 3 leads conform to AAMI

Defibrillator Protection: Protected against 360 J discharge

Patient leakage current < 10 uA

Ground Isolation 4 kV rms

Input Impedance >100 Mohm

CMMR > 100 dB

DC max.input +/- 300mv

Frequency range (-3db) 0.05 - 150 Hz

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Table 3-20: ECG Technical Specifications (Continued)

Feature Specification

Signal dynamic range 10mV

Power USB 5vdc, 80mA

Ext. ECG

Input Level +/- 1v, Amplification 1000

A2D

A2D resolution 12 bit,2’complement

Full scale range +/- 5 mV

LSB weight 2.44 uV

Full scale + +5 mV (Digital value = 7FF hex)

Midscale 0mV (Digital value =000 hex)

Midscale - LSB -2.44 uV (Digital value = FFF hex)

Full scale - -5 mV (Digital value = 800 hex)

Sample Rate 1000

Communication

USB 2.0 compliant, Full Speed Device Control, Isochronous Transfer Types

Environmental

Operating Temperature Range 0°C to 50°C

Storage Temperature Range: -40°C to 70°C

Relative Humidity 0-85% non-condensing

Regulatory

Safety Standards IEC601-1 , IEC601-1-25

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 Chapter 4

General Procedures and

Functional Checks

This chapter provides procedures for quickly checking

major functions of the LOGIQ e and diagnostics
instructions using the built-in service software and
power supply adjustments.

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General Procedures and Functional Checks

Overview

Contents in this chapter

• ‘Overview’ on page 4-2
• ‘General procedures’ on page 4-3
• ‘Functional checks’ on page 4-17

Special Equipment required

To perform these tests, you'll need any of the sector, linear, or
convex transducers. (Normally you should check all the
transducers used on the system).

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 General procedures

General procedures

Contents in this Section

• ‘Caution and Warning’ on page 4-4
• ‘Power ON/Boot Up’ on page 4-5
• ‘Connect AC/DC to the LOGIQ e’ on page 4-6
• ‘Switch ON the AC Power to LOGIQ e’ on page 4-8
• ‘Power shut down’ on page 4-11
• ‘Removable media’ on page 4-13
• ‘Archiving and loading presets’ on page 4-13
• ‘Where are the User Manuals and the Service Manual?’ on
page 4-15
• ‘How to display or print the PDF files from the Manual
CD-ROM?’ on page 4-15
• ‘Lockout/Tagout (LOTO) requirements’ on page 4-16

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General Procedures and Functional Checks

Caution and Warning

CAUTION Ultrasound system requires all covers.

Operate this Ultrasound system only when all board covers and
frame panels are securely in place. The covers are required for
safe operation, good Ultrasound system performance and
cooling purposes.

WARNING Energy Control and Power Lockout for LOGIQ e.

When servicing parts of the Ultrasound system where there is
exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as
there are no test points to verify isolation.
6. Remove/disconnect the battery, if present.
Ultrasound System components may be energized.

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 General procedures

Power ON/Boot Up

Warnings

DANGER ALWAYS CONNECT THE ULTRASOUND SYSTEM TO A

FIXED POWER SOCKET WHICH HAS THE PROTECTIVE
GROUNDING CONNECTOR.

DANGER NEVER USE A THREE-TO-TWO PRONG ADAPTER; THIS

DEFEATS THE SAFETY GROUND.

DANGER ENSURE THAT THE POWER CORD AND PLUG ARE

INTACT AND THAT THE POWER PLUG IS THE PROPER
HOSPITAL-GRADE TYPE (WHERE REQUIRED).

CAUTION Ultrasound system requires all covers.

Operate this Ultrasound system only when all board covers and
frame panels are securely in place. The covers are required for
safe operation, good Ultrasound system performance and
cooling purposes.

CAUTION Use only power supply cords, cables and plugs provided by or
designated by GE.

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General Procedures and Functional Checks

Connect AC/DC to the LOGIQ e

Connecting AC/DC to the LOGIQ e ultrasound unit, involves

preliminary checks of the power cord, voltage level and
compliance with electrical safety requirements.
1. Ensure that the wall outlet is of appropriate type.
2. Uncoil the power cable, allowing sufficient slack so that the
unit can be moved slightly.
3. Verify that the power cable is without any visible scratches
or any sign of damage.
4. Verify that the on-site mains voltage is within the limits
indicated on the rating label near the Circuit Breaker on the
rear of the unit.
5. Connect the Power Cable to the Power Inlet at the rear of
the unit.
6. Connect the Power Cable’s other end (male plug) to a
hospital grade mains power outlet with the proper rated
voltage, and the unit is ready for Power ON/Boot Up.

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 General procedures

Connect AC/DC to the LOGIQ e (continued)

Lower the handle. Plug the AC adapter output connector into the
system DC input port (located on the system’s rear panel) with
the arrow side upward. Plug the AC adapter power cord into a
grounded, protective earth outlet.
After AC/DC is connected correctly to the scanner, the power is
applied to the scanner. When the Control panel Power On/Off
key is pressed once, the System starts.

UP

Figure 4-1. Connect AC Adapter

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General Procedures and Functional Checks

Switch ON the AC Power to LOGIQ e

When power is applied to the scanner, power is distributed to

the Cooling Unit, Control Panel, LCD, Peripherals and the
Back-end Processor.
1. Press the Power On/Off switch at the front of the system
once.

Figure 4-2. Power On/Off button

When the Power On/Off switch on the Control Panel is

pressed once, the Back-end Processor starts and the
software code is distributed to initiate the scanner.
No status messages are displayed during this process.

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 General procedures

Check System Date and Time

A warning message “Please check the system date and time are
correct” appears on the screen when the system is powered up.
This warning message appears for the possible reasons:
• The system is not boot up for more than 14 days.
• The system time has been changed by 24 hours earlier than
the current system time of last boot-up.
This warning message is to remind the user to check the system
date in case the system date and time is incorrect.

Figure 4-3. Check system date and time message

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General Procedures and Functional Checks

Check System Date and Time (continued)

Move the cursor to OK and press the Cursor Key to select OK.
The system enters scanning mode.

Figure 4-4. Cursor key

Check the system date and time. If it is incorrect, follow below

steps to reset the system date and time.
1. Enter Utility -> System -> General -> Date/Time.
2. Reset the system date and time.
3. Select Apply and select OK.
4. Select Save.

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 General procedures

Power shut down

When you switch off the unit, the system performs an automatic
shutdown sequence.
1. Press the Power On/Off switch at the front of the system
once.
2. The System-Exit window is displayed.

Figure 4-5. System Exit menu

3. Using the Trackball or Select key, select Shutdown.

4. The shutdown process takes 15 seconds and the power off
sequence is complete when the power status LED is turned
off.
5. Disconnect the probes. Clean or disinfect all probes as
necessary. Store them in their shipping cases to avoid
damage.
6. Close LCD cover.

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General Procedures and Functional Checks

Power shut down (continued)

The SYSTEM - EXIT menu, used when switching off the unit,
gives you these choices:
• Logoff
Use this button to log off the current user.
The system remains ON and ready for a new user to log on.
If the Logoff button is dimmed, it indicates that no user is
logged on to the unit at the moment.
• Shutdown
Use this button to shut down the system. The entire system
will shut down. It is recommended to perform a full shutdown
at least once a week.
• Sleep Mode
Use this button when you do a portable exam in order to
reduce the time to start up the system.
• Cancel
Use this button to exit from the System-Exit menu and
return to the previous operation.
• Exit
(Only available when logged in as GE Service with Service
Dongle)
Select this button when you want to exit to the Windows
Desktop.
NOTE: If you need to restart LOGIQ e when logged on to the
Windows Desktop, ensure that you do a complete power
down (Shut Down). This is required to power up the Front
End Processor.

System shutdown

Disconnect the Mains Power Cable is necessary. For example:

Relocating the scanner.

CAUTION DO NOT unplug and/or transport the unit until after the power
off sequence has been completed. Failure to do so may result
in corrupted patient files.

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 General procedures

Removable media
Refer to the latest revision of the User Manual to perform the
following tasks:
• Using Removable Media
• Labeling Removable Media
• Formatting Removable Media
• Verifying Removable Media

Archiving and loading presets

NOTE: Always save presets before any software reload. This ensures
the presets loaded after the software reload are as up–to–date
as possible.
NOTE: If you want to restore the wireless network configuration after
software reload, DO NOT disconnect the wireless adapter
during software reload process.
All user presets except changes to Summary, Anatomy, and
Biometry pages, can be saved on an DVD-R disk (or USB
memory device, SD Card) for reloading on the system.
NOTE: Presets should NOT be saved on the same DVD-R disk (or USB
memory device, SD Card) as images. The Archive Menu lists
the images but does NOT list the presets stored on a DVD-R
disk (or USB memory device, SD Card).

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General Procedures and Functional Checks

Archiving Presets to an DVD-R Disk (or USB memory device, SD Card)

1. Insert an empty (blank) DVD-R disk into the DVD-RW.

2. Access to the Utility/Config Menu, and select System. The
Backup sheet will be shown on the LCD display.

Figure 4-6. Backup Sheet

3. Select the item to Backup/Restore.

4. Enter backup destination or browse through the disk to
locate the destination.
5. Select Backup. The backup status for each item is displayed
on the Result column.

Loading Presets from an DVD-R disk (or USB memory device, SD Card)

1. Insert the DVD-R disk with the archived Presets into the
DVD-RW.
2. Access to Utility->System->Backup/Restore. The Restore
sheet will be shown on the LCD display. See Figure 4-6 on
page 4-14.
3. Select the items needed to be restored.
4. Select Restore. The system performs the restore and
restarts.

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 General procedures

Where are the User Manuals and the Service Manual?

Online versions of the User Manuals are available via the help
function.
Both the User Manuals and the Service Manual are delivered as
PDF files on a CD-ROM. Paper copies may be ordered from
GE.

How to display or print the PDF files from the Manual CD-ROM?
1. Insert the CD-R disk (CD-ROM) into the CD-drive on a PC
or Laptop with Adobe Acrobat Reader.

CAUTION Do not try to use the LOGIQ e to read these files, it will not
work!

2. Follow the instructions on the screen to display the manual

of choice.
3. Before printing the complete manual, or pages from the
manual, select File > Page Setup.
4. Select the paper size and choose Portrait.
5. Select File > Print to start printing. In the pop up window,
you may choose which pages to print and the number of
copies you want to print (usually 1 copy).

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General Procedures and Functional Checks

Lockout/Tagout (LOTO) requirements

Follow OSHA Lockout/Tagout requirements (USA) or local
Lockout/Tagout requirements by ensuring you are in total
control of the AC power plug at all times during the service
process.
To apply Lockout/Tagout:
1. Plan and prepare for shutdown.
2. Shutdown the equipment.
3. Isolate the equipment.
4. Apply Lockout/Tagout Devices.
5. Remove battery.
6. Control all stored and residual energy.
7. Verify isolation.
All potentially hazardous stored or residual energy is
relieved.

WARNING Energy Control and Power Lockout for LOGIQ e

When servicing parts of the system where there is exposure to
voltage greater than 30 volts:
1. Turn off the scanner.
2. Unplug the system.
3. Maintain control of the system power plug.
4. Wait for at least 20 seconds for capacitors to discharge as
there are no test points to verify isolation. The amber light
on the operator panel On/Off button will turn off.
5. Remove the system battery.
All potentially hazardous stored or residual energy is relieved.

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 Functional checks

Functional checks

Contents in this Section

• ‘Overview’ on page 4-18
• ‘Operator Panel’ on page 4-18
• ‘Soft Menu Key Tour’ on page 4-19
• ‘Monitor Display’ on page 4-20
• ‘Performance Tests’ on page 4-21
• ‘B mode Checks’ on page 4-21
• ‘M Mode Checks’ on page 4-25
• ‘Color Flow Mode Checks’ on page 4-28
• ‘Doppler Mode Checks’ on page 4-32
• ‘Tissue Velocity Imaging (TVI) Checks’ on page 4-37
• ‘CWD Functional Check’ on page 4-39
• ‘Basic Measurements’ on page 4-41
• ‘Probe/Connectors Check’ on page 4-42
• ‘Cineloop Check’ on page 4-44
• ‘Image Management’ on page 4-45
• ‘Backup and Restore Database, Preset Configurations and
Images’ on page 4-46
• ‘Restore System Presets and Configurations’ on page 4-48
• ‘Software Configuration Checks’ on page 4-52
• ‘Peripheral Checks’ on page 4-52
• ‘Color Printers’ on page 4-52
• ‘DVD-RW Settings and Check-out’ on page 4-57
• ‘Wireless LAN Adapter Checks’ on page 4-58
• ‘Footswitch Checks’ on page 4-60
• ‘USB memory stick checks’ on page 4-60
• ‘Barcode Scanner Checks’ on page 4-60

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General Procedures and Functional Checks

Overview
In this section, the functional checks for are described.
Functional checks are used to verify that the product works as
intended. Functional checks may also be used during
troubleshooting.

Operator Panel

Figure 4-7. Control Panel Tour

1. Time Gain Compensation (TGC) 9. Imaging/Measurement Keys: Cursor, Clear,

2. New Patient Body Pattern, Measure, M/D Cursor, Scan
3. Mode/Gain/Auto keys: M-Mode, Doppler (PW) Area, Enter
Modes, Color Flow (CF) Mode and B-Mode 10. Depth/Zoom/Ellipse
4. Follow Up 11. Start/Stop (L/R)
5. Steer 12. Freeze
6. Coded Harmonic Imaging (CHI) 13. Programmable Image Store Keys
7. Report 14. Utility
8. Additional Feature Keys: Exam, Needle, PDI 15. Keyboard

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 Functional checks

Soft Menu Key Tour

In general, there are two types of softMenu keys: Paddle Switch
and adjustable knobs.

Figure 4-8. SoftMenu Key Tour

1. Press the adjustable knobs to toggle option menu between

line one and line two.
2. Rotate the adjustable knobs to adjust the corresponding
parameters.
3. The Paddle Switch is used to access and adjust the Sub
SoftMenu.

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General Procedures and Functional Checks

Monitor Display

Figure 4-9. Monitor Display Tour

1. Power Output Readout 12. Imaging Parameters by Mode.

2. Center Mark for all linear and convex probes 13. Focal Zone Indicator
(used for short axis needle guidance) 14. Depth Scale
3. Patient Name, Patient Identification 15. Body Pattern.
4. Institution/Hospital Name, Date, Time, Operator 16. Touch Panel.
Identification, system status (real-time of frozen) 17. Trackball Functionality Status: Scroll, M&A
5. GE Symbol: Probe Orientation Marker (Measurement and Analysis), Position, Size,
6. Measurement Window. Scan Area Width and Tilt
7. Image. 18. Plug icon
8. Measurement Calipers. 19. Start Menu Icon
9. Gray/Color Bar. 20. Caps Lock On
10. Measurement Results Window 21. Time
11. Probe Identifier. Exam Preset

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 Functional checks

Performance Tests

B mode Checks

Introduction
The B Mode is the system’s default mode.

B Mode Screen Example

Figure 4-10. B Mode Screen Image Example

Preparations
1. Connect one of the probes.
For available probes, See ‘Available probes’ on page 3-30
for more information..
See ‘Connect a probe’ on page 3-18 for more information.
for info about connecting the probes.
2. Turn ON the scanner (if it isn’t turned on already).
The B Mode window is displayed (default mode).

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General Procedures and Functional Checks

B mode Checks (continued)

Adjust the B mode controls

Figure 4-11. Controls available in B Mode

1. Press B on the Operator Panel to access B mode.

2. These Image Controls are used to optimize the B picture.
Verify that all the listed controls are working as intended:

Table 4-1: B Mode Operator Panel Controls

Step Task Expected Result(s) Comments

1 Press B Mode key B Mode Starts

2 Adjust Depth Adjust the field of view. Increasing the depth

may view larger/deeper structures rates, and
decreasing the depth may view near the skin
line.Press Up/Down Button to increase/
decrease. Depth displays on the monitor in cm.

3 Adjust Gain Controls the amount of echo information

displayed in an image. Turn B Mode dial to the
left/right to increase/decrease Gain. Gain
displays on the monitor in Gn (dB).

4 Adjust Focus Increases the number of focal zones or moves

the focal zone(s) to tighten up the beam for
specific area. Press the control to toggle
between Focus Position and Focus Number.
Press Up/Down Button to move or adjust the
focal numbers.

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 Functional checks

Table 4-1: B Mode Operator Panel Controls

Step Task Expected Result(s) Comments

5 Activate Auto Optimize the image based upon a specified

Optimize region of interest or anatomy. Press the Center
Button in the Gain Dial to toggle the ATO/ACE
On and Off.

7 Adjust Time Gain Amplifies the returning signals to correct for

Compensation the attenuation caused by tissues at increasing
(TGC) depth. TGC slide pots spaced proportional to
the depth. Move the slide pots to the left/right
to decrease/increase TGC. A TGC curve
appears on the display.

8 Adjust Scan Area Widen or narrow the size of the sector angle to
maximize the image’s region of interest (ROI).
Press Scan Area and move the Trackball to
narrow/widen the angle.

9 Adjust Zoom Changes the location of the focal point(s). A

triangular focus marker indicates the depth of
the focal point.

10 Reverse Toggles the left/right orientation of the scan

image.

B Mode Softmenu Key

Table 4-2: B Mode Softmenu Key

Step Task Expected Result(s) Comments

1 Adjust Rejection Selects a level below which echoes will not be

amplified (an echo must have a certain
minimum amplitude before it will be
processed).

2 Activate Colorize Enables gray scale image colorization. To

deactivate, reselect a Gray Map.

3 Adjust Edge Edge Enhance brings out subtle tissue

Enhance differences and boundaries by enhancing the
gray scale differences corresponding to the
edges of structures. Adjustments to M Mode's
edge enhancement affects the M Mode only.

4 Activate Gray Map Determines how the echo intensity levels

received are presented as shades of gray.

5 Adjust Frequency Multi Frequency mode lets you downshift to the

probe's next lower frequency or shift up to a
higher frequency.

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General Procedures and Functional Checks

Table 4-2: B Mode Softmenu Key

Step Task Expected Result(s) Comments

6 Adjust Frame Temporal filter that averages frames together.

Average This has the effect of presenting a smoother,
softer image.

7 Adjust Rotation Rotates the image by selecting the value from

the pop-up menu.

8 Adjust Line Density Optimizes B Mode frame rate or spatial

resolution for the best possible image.

Adjust Frame Rate Optimizes B Mode frame rate or spatial

resolution for the best possible image.

9 Power output Optimizes image quality and allows user to

reduce beam intensity. 2% increments
between 0-100%. Values greater than 0.1 are
displayed.

10 Dynamic Range Dynamic Range controls how echo intensities

are converted to shades of gray, thereby
increasing the adjustable range of contrast.

11 Focus Number and Increases the number of transmit focal zones

Position or moves the focal zone(s) so that you can
tighten up the beam for a specific area. A
graphic caret corresponding to the focal zone
position(s) appears on the right edge of the
image.

12 Virtual Convex Virtual Convex for linear probe

13 Virtual Apex Virtual Convex for Sector probe

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 Functional checks

M Mode Checks

Introduction
M Mode provides a display format that represents tissue motion
occurring over time along a single vector.

M-Mode Screen Example

Figure 4-12. M Mode Screen Image Example

Preparations
1. Connect one of the probes.
For available probes, See ‘Available probes’ on page 3-30
for more information..
See ‘Connect a probe’ on page 3-18 for more information.
for info about connecting the probes.
2. Turn ON the scanner (if it isn’t turned on already).

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General Procedures and Functional Checks

M Mode Checks (continued)

Adjust the M Mode controls

Figure 4-13. Controls available in M Mode

1. Press M on the Operator Panel to access M mode.

2. These Image Controls are used to optimize the M picture.
Verify that all the listed controls are working as intended:

Table 4-3: M Mode Operator Panel Controls

Step Task Expected Result(s) Comments

1 Press M Mode key M Mode Starts

2 Adjust Gain Controls the amount of echo information

displayed in an image. Turn B Mode dial to the
left/right to increase/decrease Gain. Gain
displays on the monitor in Gn (dB).

3 Display M-Mode Displays the M-Mode cursor on the B-Mode

Cursor image. Press Cursor and Trackball to position
M-Mode Cursor.

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 Functional checks

M Mode Checks (continued)

M Mode Softmenu Key

Table 4-4: M Mode Softmenu key

Step Task Expected Result(s) Comments

1 Adjust Rejection Selects a level below which echoes will not be

amplified (an echo must have a certain
minimum amplitude before it will be
processed).

2 Adjust Sweep Speed Changes the speed at which the time line is
swept. The following speed values are
available, 1, 2, 3, 4, 6, 8, 12, 16.

3 Adjust Edge Edge Enhance brings out subtle tissue

Enhance differences and boundaries by enhancing the
gray scale differences corresponding to the
edges of structures. Adjustments to M Mode's
edge enhancement affects the M Mode only.

4 Activate Gray Map Determines how the echo intensity levels

received are presented as shades of gray.

6 Activate Colorize Enables gray scale image colorization. To

deactivate, reselect a Gray Map.

7 Activate Full Displays only timeline screen. Press the Full

Timeline Timescreen to activate.

8 Select Display Select the format to display B image and M

Format image on the LCD. Press Display Format, and
select from the pop up menu.

9 Adjust Dynamic Dynamic Range controls how echo intensities

Range are converted to shades of gray, thereby
(Compression) increasing the adjustable range of contrast.

10 Power output Optimizes image quality and allows user to

reduce beam intensity. 2% increments
between 0-100%. Values greater than 0.1 are
displayed.

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General Procedures and Functional Checks

Color Flow Mode Checks

Introduction
Color Flow screens are B Mode or M Mode screens with colors
representing blood or tissue movement.

Color Flow Mode Screen Example

Figure 4-14. CFM Mode Screen Image Example

Preparations
1. Connect one of the probes.
For available probes, See ‘Available probes’ on page 3-30
for more information..
See ‘Connect a probe’ on page 3-18 for more information.
for info about connecting the probes.
2. Turn ON the scanner (if it isn’t turned on already).

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Color Flow Mode Checks (continued)

Adjust the Color Mode controls

Figure 4-15. Controls available in Color Flow Mode

1. Press Color on the Operator Panel to access Color mode.

2. These Image Controls are used to optimize the Color
picture. Verify that all the listed controls are working as
intended:

Table 4-5: Color Flow Mode Operator Panel Controls

Step Task Expected Result(s) Comments

1 Press Color Mode Color Flow Mode Starts

key

2 Adjust Gain Amplifies the overall strength of the echoes

processed in the Color Flow window. Turn the
Gain dial (CFM Mode key) to the left/right to
increase/decrease Gain.

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General Procedures and Functional Checks

Color Flow Mode Softmenu Key

Table 4-6: Color Flow Mode Softmenu Key

Step Task Expected Result(s) Comments

1 Threshold Threshold assigns the gray scale level at

which color information stops.

2 Packet Size Controls the number of samples gathered for a

single color flow vector.

3 Select maps Allows a specific color map to be selected.

After a selection has been made, the color bar
displays the resultant map.

4 Adjust Frequency Enables the adjustment of the probe’s

operating frequency. Press Frequency and
select desired value. The selected frequency is
displayed in the status window.

5 Set Frame Average Averages color frames. Press Frame Average

up/down to smooth temporal averaging.

6 Invert Views blood flow from a different perspective.

Press Invert to reverse the color map.

7 Adjust LIne Density Trades frame rate for sensitivity and spatial
resolution. If the frame rate is too slow, reduce
the size of the region of interest, select a
different line density setting, or reduce the
packet size.

Adjust Frame Rate Adjust Frame rate to a higher setting to

improve motion detection, or to a lower setting
to improve resolution.

8 Activate Spatial Filter Adjust Spatial Filter to smooth out the color,
makes it look less pixely.

9 Adjust Dynamic Dynamic Range controls how echo intensities

Range are converted to shades of gray, thereby
increasing the adjustable range of contrast.

10 TIC Analysis/ Time Intensity Curve (TIC) Analysis/

QAnalysis QAanalysis watch the agent flow through the
anatomy of interest and calculates the mean
pixel intensity within that ROI for all frames in
the user designated loop and plots the
resulting data as a function of time. Select a
desired cine loop from the stored images.

11 Adjust Angle Steer Slants the Color Flow region of interest or the
Doppler line to obtain a better Doppler angle.

12 Move Baseline Adjusts the baseline to accommodate faster or

slower blood flows to eliminate aliasing.

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Table 4-6: Color Flow Mode Softmenu Key

Step Task Expected Result(s) Comments

13 Change scale (PRF) Velocity scale determines pulse repetition

frequency. If the sample volume gate range
exceeds single gate PRF capability, the
system automatically switches to high PRF
mode. Multiple gates appear, and HPRF is
indicated on the display.

14 Transparency Map Allows to select specific transparency map

15 Focus Position Increases the number of transmit focal zones

or moves the focal zone(s) so that you can
tighten up the beam for a specific area. A
graphic caret corresponding to the focal zone
position(s) appears on the right edge of the
image.

16 Power output Optimizes image quality and allows user to

reduce beam intensity. 10% increments
between 0-100%. Values greater than 0.1 are
displayed.

17 Wall Filter Wall Filter insulates the Doppler signal from

excessive noise caused from vessel
movement.

18 Map Compress When you increase the value, high velocity

elements in the map are compressed so that
the map darkens. When you decrease the
value, low velocity elements in the map are
compressed so that the map lightens.

19 Accumulation Accumulation enhances the flow in an image.

Off-Infinite: Infinite provides the same result as
applying CINE Capture to a B-Flow CINE clip.

20 Sample Vol Adjust the control to adjust the sample volume

gate on the Color Flow image.

21 Flash Suppression Activates/deactivates Flash Suppression, a

motion artifact elimination process.

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General Procedures and Functional Checks

Doppler Mode Checks

Introduction
PW Doppler are used to measure velocity (most often in blood).
Doppler mode can be done with a special pencil probe or with
an ordinary probe. By using an ordinary probe, you can first
bring up a B Mode picture for navigation purpose and then add
PW Doppler.

Doppler Mode Screen Example

Figure 4-16. Doppler Mode Screen Image Example

Preparations
1. Connect one of the probes.
For available probes, See ‘Available probes’ on page 3-30
for more information..
See ‘Connect a probe’ on page 3-18 for more information.
for info about connecting the probes.
2. Turn ON the scanner (if it isn’t turned on already).

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Doppler Mode Checks (continued)

Adjust the PW Doppler Mode controls

Figure 4-17. Controls available in Doppler Mode

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General Procedures and Functional Checks

Adjust the PW Doppler Mode controls (continued)

1. Press Color on the Operator Panel to access Color mode.
2. Press PW to start Pulsed Wave Doppler (PW).
Use the trackball to select the Area of Interest (Sample
Volume) in PW or direction of interest in CW.
3. These Image Controls are used to optimize the Color
picture. Verify that all the listed controls are working as
intended:

Table 4-7: PW Doppler Mode Operator Panel Controls

Step Task Expected Result(s) Comments

1 Press PW Mode key PW Mode Starts

2 Adjust Gain Amplifies the overall strength of the echoes

processed in the Color Flow window. Turn the
Gain dial (PW Mode key) to the left/right to
increase/decrease Gain.

3 Display M/D-Mode Displays the M/D-Mode cursor on the B-Mode

Cursor image. Press Cursor and Trackball to position
sample volume graphic. Click SV gate to
adjust sample volume gate size.

4 B-Pause/Enter Toggle between simultaneous and update

presentation while viewing Spectral Doppler.
Press B Pause to toggle between
simultaneous and update.

Doppler Mode Soft Menu Key

Table 4-8: PW Doppler Mode Soft Menu Key

Step Task Expected Result(s) Comments

1 Adjust Rejection Selects a level below which echoes will not be

amplified (an echo must have a certain
minimum amplitude before it will be
processed).

2 Adjust Sweep Speed Changes the speed at which timeline is swept.

Press Sweep Speed up/down to increase/
decrease the value.

3 Activate Full Displays only timeline screen. Press the Full

Timeline Timescreen to activate.

4 Select Display Display layout can be preset to have B-Mode

Format and Time-motion side-by-side or over-under.

5 Adjust Frequency Enables the adjustment of the probe’s

operating frequency. Press Frequency and
select desired value. The selected frequency is
displayed in the status window.

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Table 4-8: PW Doppler Mode Soft Menu Key

Step Task Expected Result(s) Comments

6 Trace Direction Allows to select different trace direction.

7 Invert Vertically inverts the spectral trace without

affecting the baseline position. Press invert to
invert the spectral trace. The Plus and Minus
signs on the velocity scale reverse when the
spectrum is inverted.

8 Auto Calcs Enables or disables auto calculation.

9 Modify Auto Calcs Activates the window to modify the auto

calculation items.

10 Trace Method Allows to select different trace method.

11 Activate Colorize Colorize the gray scale image to enhance the

eyes’ discrimination capability. Press the
Cololize, Trackball to cycle through available
maps and press Set to select.

12 Activate Gray Map Displays a map window adjacent to the image.

Move the trackball to select the map. The
image reflects the map as scrolled through the
selections. Press Set to select.

13 Compression Controls how echo intensities are converted to

(Dynamic Range) shades of gray. Click Dynamic Range to
increase/decrease the value.

14 Adjust Angle Correct Estimates the flow velocity in a direction at an

angle to the Doppler vector by computing the
angle between the Doppler vector and the flow
to be measured.

15 Adjust Steer/Fine Slant the Color Flow linear image left or right to
Steer get more information without moving probes.
Click Angle Steer to the left to slant the linear
image.

16 Move Baseline Adjusts the baseline to accommodate faster or

slower blood flows to eliminate aliasing.

17 Change PRF (Pulse Velocity scale determines pulse repetition

Repetition frequency. If the sample volume gate range
Frequencies) - (Wall exceeds single gate PRF capability, the
Filter) system automatically switches to high PRF
mode. Multiple gates appear, and HPRF is
indicated on the display.

Change Scale - (Low Velocity scale determines pulse repetition

Vel Reject) frequency. If the sample volume gate range
exceeds single gate PRF capability, the
system automatically switches to high PRF
mode. Multiple gates appear, and HPRF is
indicated on the display.

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General Procedures and Functional Checks

Table 4-8: PW Doppler Mode Soft Menu Key

Step Task Expected Result(s) Comments

18 Trace Sensitivity Adjusts the sensitivity to get more accurate

envelope trace.

19 PW/CF Ratio Adjust PW/CF Ratio to show Maximum Ratio

and Minimum Ratio of Color (Power) Doppler
Pixels in each ROI.

20 Spectral Avg Optimizes the smoothness of the spectrum.

Different levels can be selected.

21 Power output Optimizes image quality and allows user to

reduce beam intensity. 10% increments
between 0-100%.

22 SV Length Sizes the sample volume gate.

23 Wall Filter Wall Filter insulates the Doppler signal from

excessive noise caused from vessel
movement.

24 Cycles to Average Set the average value over a number of cycles

(from 1-5).

25 Quick Angle Quickly adjusts the angle by 60 degrees. Press

Quick Angle to toggle between Off, Right and
Left.

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 Functional checks

Tissue Velocity Imaging (TVI) Checks

Introduction
TVI calculates and color codes the velocities in tissue. The
tissue velocity information is acquired by sampling of tissue
Doppler velocity values at discrete points. The information is
stored in a combined format with grey scale imaging during one
or several cardiac cycles with high temporal resolution.

Preparation
1. Connect one of the probes.
For available probes, See ‘Available probes’ on page 3-30
for more information..
See ‘Connect a probe’ on page 3-18 for more information.
about connecting the probes.
2. Turn ON the scanner (if it isn’t turned on already).

TVI Mode Screen Example

Figure 4-18. TVI Mode Screen Image Example

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General Procedures and Functional Checks

Tissue Velocity Imaging (TVI) Checks (continued)

Adjust the TVI Controls

1. Set PDI button for TVI mode in Utility -> Imaging -> General.
2. Press the PDI key to activate TVI Mode.

Adjust TVI Mode Softmenu Key

Table 4-9: TVI Mode Softmenu Key

Step Task Expected Result(s) Comments

1 Adjust Visible Select Visible to display TVI Color with TVI.

2 Adjust LIne Density Trades frame rate for sensitivity and spatial
resolution. If the frame rate is too slow, reduce
the size of the region of interest, select a
different line density setting, or reduce the
packet size.

3 Select Color Map Allows a specific color map to be selected.

After a selection has been made, the color bar
displays the resultant map.

4 Threshold Threshold assigns the gray scale level at

which color information stops.

5 Activate Spatial Filter Adjust Spatial Filter to smooth out the color,
makes it look less pixely.

6 TVI Gain Control color transparency. High values display

more color; low values display more tissue.

7 Width Adjust the sizes of ROI.

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CWD Functional Check

Introduction
CW Doppler are used to measure velocity (most often in blood).
Doppler mode can be done with a special pencil probe or with
an ordinary probe. By using an ordinary probe, you can first
bring up a B Mode picture for navigation purpose and then add
CW Doppler.

CWD Mode Screen Example

Figure 4-19. CWD Mode Image Example

Preparation
1. Connect 3Sc-RS/6S-RS Probe to the system.
See ‘Connect a probe’ on page 3-18 for more information.
for info about connecting the probes.
2. Turn ON the scanner (if it isn’t turned on already).

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General Procedures and Functional Checks

CWD Functional Check (continued)

Activating CW Doppler
To activate CW Doppler Mode:
1. Ensure that the appropriate CW probe is connected.
2. Set the hot key (From programmable key F5-F12) for CWD.
3. Press the hot key which is assigned for CWD mode. The
Doppler Spectrum appears, along with the CW Touch Panel
Menu.
The following CW parameters are displayed: Frequency, Gain,
Acoustic Output, Scale, Wall Filter and Dynamic Range.

Exiting CW Doppler
To exit CW Doppler Mode:
Press the hot key which is assigned for CWD Mode.

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 Functional checks

Basic Measurements

NOTE: The following instructions assume that you first scan the patient
and then press Freeze.

Distance and Tissue Depth Measurements

1. Press Measure once; an active caliper displays.
2. To position the active caliper at the start point (distance) or
the most anterior point (tissue depth), move the Trackball.
3. To fix the start point, press Enter. The system fixes the first
caliper and displays a second active caliper.
4. To position the second active caliper at the end point
(distance) or the most posterior point (tissue depth), move
the Trackball.
5. To complete the measurement, press Enter. The system
displays the distance or tissue depth value in the
measurement results window.

Circumference/Area (Ellipse) Measurement

1. Press Measure once; an active caliper displays.
2. To position the active caliper, move the Trackball.
3. To fix the start point, press Enter. The system fixes the first
caliper and displays a second active caliper.
4. To position the second caliper, move the Trackball.
5. Adjust the Ellipse; an ellipse with an initial circle shape
appears
6. To position the ellipse and to size the measured axes (move
the calipers), move the Trackball.
7. To increase the size, rotate the Ellipse button clockwise. To
decrease the size, contrarotate the Ellipse button
8. To complete the measurement, press Enter. The system
displays the circumference and area in the measurement
results window.

Worksheets
Measurement/Calculation worksheets are available to display
and edit measurements and calculations. There are generic
worksheets as well as Application specific worksheets. The
worksheets are selected from the Measurement Touch Panel.

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General Procedures and Functional Checks

Probe/Connectors Check

NOTE: Probes can be connected at any time, whether the unit is ON or

OFF

Connecting a Probe
1. Place the probe's carrying case on a stable surface and
open the case.
2. Carefully remove the probe and unwrap the probe cable.
3. DO NOT allow the probe head to hang free. Impact to the
probe head could result in irreparable damage.
4. Align the connector with the probe port and carefully push
into place.
5. Lock the probe latch upward.
6. Carefully position the probe cord so it is free to move and is
not resting on the floor.

Activating the probe

The probe activates in the currently-selected operating mode.
The probe's default settings for the mode and selected exam are
used automatically.

Deactivating the probe

1. Press the Freeze key.
2. Gently wipe the excess gel from the face of the probe.
(Refer to the Basic User Manual for complete probe
cleaning instructions).
3. Carefully slide the probe around the right side of the
keyboard, toward the probe holder. Ensure that the probe is
placed gently in the probe holder.

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Probe/Connectors Check (continued)

Disconnecting the probe

Probes can be disconnected at any time. However, the probe
should not be selected as the active probe.
1. Unlock the probe latch downward.
2. Pull the probe and connector straight out of the probe port.
3. Carefully slide the probe and connector away from the
probe port and around the right side of the keyboard.
4. Ensure the cable is free.
5. Be sure that the probe head is clean before placing the
probe in its storage box.

WARNING Take the following precautions with the probe cables: Do

not bend. If you have purchased the cart option, be sure
to keep probe cables free from the wheels.

WARNING Be careful not to trip on the probe cables if using the

device without the optional cart.

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General Procedures and Functional Checks

Cineloop Check

Introduction
A cineloop is a sequence of images recorded over a certain time
frame. When using ECG the time frame can be adjusted to
cover one or more heart cycles. When frozen, the System
automatically displays the cineloop boundary markers on either
side of the last detected heart cycle.

Activating CINE
Press Freeze, then roll the Trackball to activate CINE. To start
CINE Loop playback, press Run/Stop. To stop CINE Loop
playback. press Run/Stop.

Adjust the Cineloop controls

Quickly Move to Start/End Frame

Press First to move to the first CINE frame; press Last to move
to the last CINE frame.

Start Frame/End Frame

Press the Start Frame Two-Button Softkey to move to the
beginning of the CINE Loop. Adjust the Start Frame up/down
Two-Button Softkey upward to move forward through the CINE
Loop. Adjust the Softkey downward to move backward through
the CINE Loop.
Press the End Frame Two-Button Softkey to move to the end of
the CINE Loop. Adjust the End Frame up/down Two-Button
Softkey upward to move forward through the CINE Loop. Adjust
the Softkey downward to move backward through the CINE
Loop.

Adjusting the CINE Loop Playback Speed

Adjust the Loop Speed up/down Two-Button Softkey to
increase/decrease the CINE Loop playback speed.

Moving through a CINE Loop Frame By Frame

Adjust the Frame by Frame up/down Two-Button Softkey to
move through CINE memory one frame at a time.

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 Functional checks

Image Management

For Image Management functionality refer to the LOGIQ e User

Manual. It talks about several topics:
• Clipboard
• Printing Images
• Browsing and Managing an Exam’s Stored Image
• Connectivity, and Dataflow Concept and Creation
• Starting an Exam
• Configuring Connectivity
• TCP/IP
• Services (Destinations)
• Buttons
• Views
• Verifying and Pinging a Device

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General Procedures and Functional Checks

Backup and Restore Database, Preset Configurations and Images

Formatting Media
To Format the backup media, DVD:
1. Go to Utility -> Connectivity -> Removable Media.
2. Select the media type from the drop down menu.
3. Enter the label for the media. It is best to use all capital
letters with no spaces or punctuation marks. Press Format.

Figure 4-20. Format and verify media

4. A pop-up message displays to inform operation completed.

Press OK.
5. If desired, verify that the format was successful by selecting
Verify in Utility -> Connectivity -> Removable Media. see
Figure 4-20 on page 4-46.

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 Functional checks

Backup System Presets and Configurations

NOTE: Always backup any preset configurations before a software
reload. This ensures that if the presets need to be reloaded,
after the software update, they will be the same ones the
customer was using prior to service.
1. Insert a formatted DVD-R disk into the drive.
2. Go to Utility -> System -> Backup/Restore
NOTE: If you are not logged in as GE Service or with administrator
privileges, the Operator Login window is displayed. Log on
with administrator privileges.
3. In the Backup list, select Patient Archive, Report Archive
and User Defined Configuration and Service.
4. In the Media field, select DVD(or USB memory device, SD
Card).
5. Select Backup.
The system performs the backup. As it proceeds, status
information is displayed on the Backup/Restore screen.

Figure 4-21. Backup/Restore Menu

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General Procedures and Functional Checks

Restore System Presets and Configurations

CAUTION The restore procedure overwrites the existing database on the

local hard disk drive. Make sure to insert the correct DVD (or
USB memory device, SD Card).

1. Insert the Backup/Restore DVD-R disk (or USB memory

device, SD Card) into the drive.
2. Go to Utility -> System -> Backup/Restore
NOTE: If you are not logged in with administrator privileges, the
Operator Login window is displayed. Log on with
administrator privileges.
3. In the Restore list, select Patient Archive, Report Archive,
User Defined Configuration and Service.
4. In the Media field, select the Backup/Restore DVD-RW (or
USB memory device, SD Card).
5. Select Restore.
The system performs the restore. As it proceeds, status
information is displayed on the Backup/Restore screen.
After the Restore completes, the system need to reboot.

Figure 4-22. Backup/Restore Menu

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 Functional checks

Archiving Images
1. Insert the archive media. To format the archive media,
DVD-R disk, select the Utility button on the Keyboard.
2. Go to Utility -> Connectivity -> Removable.
3. Format the DVD-R disk. Verify the format if desired.
4. Images will be moved from the hard disk drive by date.
Therefore, the best way is to label media by date.
NOTE: Images will be moved from the hard disk drive by date.
Therefore, the best way to label media is by date. When
images are moved to the archive media, they will be deleted
from the system hard disk drive. However, the patient
database (backed up earlier) maintains pointers to the
location of the images on the archive media.

Figure 4-23. Format DVD-RW Screen

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General Procedures and Functional Checks

Archiving Images (continued)

5. Select Utility -> System -> Backup/Restore. Set EZMove
and EZBackup requirements.

Figure 4-24. EZBackup/Move

6. Press Patient on the control pane to enter Patient Screen.

7. Set the Dataflow to Store images directly to DVD-R disk.
8. Press EZBackup/EZMove. The EZBackup Wizard window
displays. Then Press Next

Figure 4-25. Image Archive window

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 Functional checks

Archiving Images (continued)

9. A Storage Size Information window appears. Press Next to
continue.
10. An EZBackup in Progress... window displays. When the
EZBackup is complete, press Next to continue.
11. Press Finish.

Figure 4-26. EZBackup/Move complete

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General Procedures and Functional Checks

Software Configuration Checks

Table 4-10: Software Configuration Checks

Step Task to do Expected Result(s)

1. Check Date and Time setting Date and Time are correct

2. Check that Location (Hospital Location Name is correct

Name) is correct

3. Check Language settings Desired Language is displayed

4. Check assignment of Printer Keys For LOGIQ e, the default function for Print1-3
Keys is P1 (store image); P2 (print); P3 (USB
Quick Save). Print1-3 Keys can also be
assigned as desired by the customer

5. Check that all of the customer’s All authorized functions are enabled
options are set up correct

Peripheral Checks
This section describes the final setup for the Peripherals and the
Operational Check-out. For Peripherals installation information,
See ‘Peripherals Installation’ on page 3-34 for more information.
Check that peripherals work as described below:

Color Printers

The Printers are controlled from the P2 on the system’s control

panel. The factory setting is P2 for the standard print.
Take Sony UP-D25MD Color Printer for an example to show the
control assignment procedure.

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 Functional checks

Control assignment procedure

The Control Assignment for the printers is done in the Utility
Menu.
1. Turn on the Peripherals and power on the system.
2. Select Utility -> Peripherals.
3. Select Sony UP-D25MD for Standard Printer Properties
and Default Printer. Select Save.

Figure 4-27. Select Printer

NOTE: For control assignment on the network printer HP Universal

Printing PCL6,the control can only work when the network of
the system is connected.

Figure 4-28. Network Printer

Select Properties to view the document information and

configure properties for standard printer.

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General Procedures and Functional Checks

Figure 4-29. Standard Printer Properties

• Printer: A printer to be used as Standard Print.

• Rows: Specify rows on print.
• Columns: Specify columns on print.
• Orientation: Specify orientation to print.
• Top Margin: Specify top margin on print.
• Bottom Margin: Specify bottom margin on print.
• Left Margin: Specify left margin on print.
• Right Margin: Specify right margin on print.

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 Functional checks

Color Printers (continued)

4. Select Utility -> Connectivity -> Service.

5. Select the Standard Print. In the Printer field, select Sony
UP-D25MD. Select Save to save the setting.

Figure 4-30. Standard Print

6. Select Utility -> Connectivity -> Button. In the field of

Physical Print Buttons, select Print2.
7. Select Standard Print, press “>>” to add to the Printflow
View.

Figure 4-31. Add Standard Print

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General Procedures and Functional Checks

Color Printers (continued)

8. If another device has been selected, use “<<“to clear
window.

Color Printers Checks

Make sure Printer Function is assigned to P2 key.

Table 4-11: Printer checks

Step Task Expected Result(s)

1 When scanning in B Mode, press Image scanning stops with the last image on
Freeze to stop image acquisition the screen.

2 Press P2 key on the control panel. The image displayed on the screen is
printed on Color printer, depending on the
key assignment configuration.

3 Check if the print quality is of expected

quality.

NOTE: For checking the printer function on HP Universal Printing PCL6

Network Printer, when pressing P2, a pop-up window displays to
require you to input the Printer Address. Contact your network
administrator for local network information.

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DVD-RW Settings and Check-out

1. Connect DVD-RW to the system.

2. Insert the DVD/CD into the DVD-RW.
3. Select Utility -> Connectivity -> Removable Media.

Figure 4-32. Removable Media

4. Click Verify to check the media’s status.

Figure 4-33. Verify Media

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General Procedures and Functional Checks

Wireless LAN Adapter Checks

1. Connect Wireless LAN Adapter to the USB port on the

system. The Wireless Network configuration displays.

Figure 4-34. Wireless configuration

2. Select Configuration. A message pops up to indicate

running Wireless Network Configuration. Wait until Wireless
Network Configuration window appears.

Figure 4-35. Message

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Wireless LAN Adapter Checks (continued)

3. Select the Wireless Networks and select Connect.

Figure 4-36. Wireless Network Configuration

4. The wireless network icon at the left bottom of the screen

shows the wireless network is connected.

Figure 4-37. Wireless Network connected

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Footswitch Checks

Table 4-12: Footswitch Checks

Step Task Expected result(s)

1 Set Freeze for right Pedal. Connect Footswitch Image scanning stops with the latest
to one USB port on the system. When scanning image on the screen.
in B mode, click right button of Footswitch once.

2 Click the right pedal of Footswitch once again. Image scanning starts.

USB memory stick checks

Table 4-13: USB memory stick checks

Step Task Expected result(s)

1 Power on the system.

2 Connect USB memory stick with USB port “New hardware device detector” icon display
on the system. on the status bar.

3 Click the “New hardware device detector” Check whether the device driver installed
icon successfully.

Barcode Scanner Checks

Table 4-14: Barcode scanner check

Step Task Expected result(s)

1 Power on the system.

2 Connect Barcode Scanner via the USB A beep should be heard.

port on the system.

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 Chapter 5

Components and Functions

(Theory)

This chapter explains LOGIQ e’s system concepts,

component arrangement, and subsystem functions.

It also describes the power distribution and the

Common Service Desktop interface.

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Components and Functions (Theory)

Overview

Contents in this chapter

• ‘Overview’ on page 5-2
• ‘Block Diagram and Theory’ on page 5-3
• ‘Power Diagram’ on page 5-5
• ‘Common Service Platform’ on page 5-7

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 Block Diagram and Theory

Block Diagram and Theory

Contents in this Section

• ‘Block Diagram’ on page 5-3
• ‘General Information’ on page 5-4
• ‘Top Console’ on page 5-4

Block Diagram

KBD
F ull S ys
L 6L C D Panel
C ONN

LVDS

L 6DO C K ING L 6IO WMS T: G F I+T R X128

C AR T
C ONN
C O M-E module mS ATA
C ONN
Intel Mobile C PU SSD
Us er P orts 2610u@ 25W
i7@ 2 core, 2 thread
S D C AR D
C ONN

P C I-E

L 6WDC C ONN L 6C W D(O P T)

DS P @ B ridge
TEE

C ONN
LV P S HV P S
E MIF

C harger R F data& S C I
and
S witch
F P GA
F P GA
Mid- RS
B F64 L6P F P C
P roces s ing AF E P uls ers BGA C onn. C onn 128 Conn L 6MultP ort
x128 x128

F P GA
B attery pack (8 cells ) B F 64

Figure 5-1. LOGIQ e System Block Diagram

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Components and Functions (Theory)

General Information
LOGIQ e is an ultrasound imaging scanner.
The system can be used for:
• 2D Black and White imaging
• 2D Color Flow
• M-Mode Black and White imaging
• Doppler
• A number of combinations of the above
LOGIQ e is a digital beam forming system that can handle up to
128 elements linear probes.
Signal flow from the Probe Connector Panel to the Front End, to
the Mid Processors and Back End Processor and finally to the
LCD and peripherals.
System configuration is stored on a hard disk drive and all
necessary software is loaded from the hard disk drive on power
up.

Top Console
The Top Console includes a Standby/On switch, a keyboard,
different controls for manipulating the picture quality, controls for
use in Measure & Analyze (M&A), and loudspeakers for stereo
sound output (used during Doppler scanning).

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 Power Diagram

Power Diagram

Contents in this Section

• ‘Overview’ on page 5-5
• ‘AC Power’ on page 5-5
• ‘Battery Charging’ on page 5-6
• ‘Air Flow Distribution’ on page 5-6

Overview
The AC Power assy’s main tasks are to isolate and output to the
DC/DC unit which is inside the system console. The input of AC
power pack will be the AC outlet and it’s universal, the range is
AC 90V-264V, 47-63Hz. And no main power switch located on
this power pack.

AC Power
The mains cord has plugs in one side end. A male plug connects
to the mains outlet on site.
The mains voltage is routed to the AC power pack through a
Circuit Breaker located on the site.
The Circuit Breaker is of the auto fuse type, if for some reason
the current grows to high, the switch will automatically break the
power.
From the Main Circuit Breaker, the AC power is routed via an
Inrush Current Limiter to a internal outlet connector for the
Mains Transformer.

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Components and Functions (Theory)

Battery Charging
The charging circuit is lithium-Ion battery charge and discharge
controller. This block can switch the power between the battery
and the output of AC Pack. If the output of AC Pack is available,
the power input of Charge Board Unit should be from the AC
Pack and the battery will be charged if it’s not full. This block will
be also in charge of the battery charging monitor to avoid the
battery over heat and over charging, charging will be shut off
automatically if battery is charged fully. The battery will
discharge to provide the power to the system when out of AC
power pack output or AC line.

Air Flow Distribution

Figure 5-2. Air Flow Inside the System

The two air flow passes allow the scanner to be cooled down as
shown in the figure above.
• Path A (Bottom front > CPU Assy > Bottom left) for TMST &
CPU Assy cooling.
• Path B (Bottom front > PWA Assy > Bottom right) for PWA
cooling.

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 Common Service Platform

Common Service Platform

Contents in this Chapter

• ‘Introduction’ on page 5-7
• ‘The usage for security cable’ on page 5-8
• ‘Global Service User Interface (GSUI)’ on page 5-9
• ‘Service Login’ on page 5-9
• ‘Access/Security’ on page 5-10
• ‘Customer Service Home Page’ on page 5-13

Introduction
The Service Platform contains a set of software modules that
are common to all PC backend ultrasound and cardiology
systems. The Common Service Platform will increase service
productivity and reduce training and service costs.

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Components and Functions (Theory)

The usage for security cable

The ultrasound system equipped with Kensington security slot
which is compatible with a Kensington security cable.

Figure 5-3. Security slot

How to prevent unauthorized removal of the ultrasound system?

1. Wrap the cable around the immovable object
2. Make sure and rotate the key to the right (unlocked position)
3. Insert the lock into the Kensington security slot in the
system side cover
4. Rotate the key to the left (locked position).
5. For more information, visit www.kensington.com

Figure 5-4. Security slot and system

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 Common Service Platform

Global Service User Interface (GSUI)

Service Login
Select Utility -> Service. This button links the user or the Field
Engineer (FE) to the service login screen.

Figure 5-5. Service Login Screen

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Components and Functions (Theory)

Access/Security
The service interface has different access and security user
levels. Each user is only granted access to the tools that are
authorized for their use
NOTE: A Service Dongle is necessary for use by GE Service when
performing proprietary level diagnostics. Online Center access
to the scanner requires the password and they must have
“Disruptive” permission and customer input to run diagnostics.

Table 5-1: Service Login User Levels

User Level Access Authorization Password

Operator Authorized access to specified diagnostics, error uls

logs and utilities. Same acquisition diagnostic tests
Administrator as GE Service. uls

External Service gogems

GE Service Knowledge of a service level password. Rotating security

A physical Service Key (Dongle) required password

NOTE: For GE Field Engineer, the password changes at specific

intervals. Access with the password is tied to the service key.
Every access request, whether successful or not, will be logged
into a service access log that is viewable to authorized users.

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 Common Service Platform

Access/Security (continued)
NOTE: If the following window displays unauthorized access prohibited
after input of correct password to try to login, do the followings:

Figure 5-6. Authentication Failure

1. Close the Login window.

2. Enter Utility -> System -> General.
3. Select Date/Time.

Figure 5-7. Date/Time

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Components and Functions (Theory)

Access/Security (continued)
4. Change the Date/Time to the current date. Select OK and
select Save to save the current date.

Figure 5-8. Date/Time

5. Select Utility -> Service and try to login again.

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 Common Service Platform

Customer Service Home Page

Enter customer service home page with customer level and
password.

Figure 5-9. Customer Service Home Page

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Components and Functions (Theory)

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 Chapter 6

Service Adjustments

This chapter describes how to test and make

adjustments to the LOGIQ e. You can use these to test
the system for errors.

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Service Adjustments

LCD Monitor adjustments

Purpose of this section

This section describes how to test and adjust the scanner.
These tests are optional. You may use them to check the
system for errors.

Monitor Adjustments
1. To adjust the brightness and volume:
1. On the alphanumeric keyboard,
• adjust brightness with the Ctrl + Up/Down keys;
• adjust volume with the Ctrl + Left/Right keys

Figure 6-1.

1. Brightness
2. Volume

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 Chapter 7

Diagnostics/Troubleshooting

This chapter describes how to setup and run the tools

and software that help maintain image quality and
system operation. Very basic host, system and board
levels are run whenever power is applied. Some
Service Tools may be run at the application level.

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Diagnostics/Troubleshooting

Overview

Contents in this chapter

• ‘Overview’ on page 7-2
• ‘Gathering Trouble Data’ on page 7-3
• ‘USB Quick Save’ on page 7-7
• ‘Screen Capture’ on page 7-9
• ‘Global Service User Interface (GSUI)’ on page 7-13
• ‘Network Configuration’ on page 7-17

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 Gathering Trouble Data

Gathering Trouble Data

Overview
There may be a time when it would be advantageous to capture
trouble images and system data (logs) for acquisition to be sent
back to the manufacturer for analysis. There are different
options to acquire this data that would give different results

Contents in this Section

• ‘Overview’ on page 7-3
• ‘Collect Vital System Information’ on page 7-3
• ‘Collect a Trouble Image with Logs’ on page 7-5

Collect Vital System Information

The following information is necessary in order to properly
analyze data or images being reported as a malfunction or being
returned to the manufacturer:
Product Name = LOGIQ e
From the Utility>System>About screen:
Applications Software
• Software Version
• Software Part Number
System Image Software
• Image Revision
• Image Part Number

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Diagnostics/Troubleshooting

Collect Vital System Information (continued)

System Hardware
Click and open Additional About Information for hardware
information: Module Name, Revision and Part Number.
• Module Name
This column indicates the hardware modules which are
supported on the system.
• Revision
This column displays the information of the hardware. The
“--” mark in the cell of this column indicates that the
hardware in the same row is not installed on the system.
• Part Number
This column indicates the part number of the hardware. The
“--” mark indicates that there is no part number display for
the hardware in the same row.

Figure 7-1. Hardware Information

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 Gathering Trouble Data

Collect a Trouble Image with Logs

If the system should malfunction, press the Alt+D keys
simultaneously. This will collect a screen capture of the image
monitor, system presets and the following logs:
• Keyboard Shadow Log
• Error Logs
• Crash Log
• Power Supply
• Temperature
NOTE: Power Supply and Temperature logs are not currently being
updated by the LOGIQ e.
This Alt+D function is available at all times.

Figure 7-2. Alt+D Dialog Box

When Alt+D is pressed, a menu box appears that allows for:

• A place to enter a description of the problem
• A choice to store to a pre-formatted DVD-R, RD
(Removable Disk) or to the Export directory D:\SERVICE.

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Diagnostics/Troubleshooting

Collect a Trouble Image with Logs (continued)

Use a log to if the user wants to send information to GE. There
are two methods to follow:
The subsequent file is compressed and time stamped. The
screen capture is a bitmap which eliminates the possibility of
artifacts from compression.
• To save log files and an image snapshot, press Alt+D, select
the save logs function, and fill in the form. Use a USB flash
drive or CD-R to store the log(s). When you fill out the form,
fill in the system behavior you saw, plus any other
comments. Fill in the check box if the system crashed.
• To save log files and an image snapshot, press Alt+D.
Describe the issues, then select to store logs to
D:\SERVICE. Select ContactGE in Service Menu, then
complete the form of Contact Information, Problem Type
and Problem Description and select Send.

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 USB Quick Save

USB Quick Save

Overview
There may be times when the customer or field engineer will
want to directly save images into USB memory. This is
accomplished by saving individual Cine clips (moving images-
avi format) or still images (jpg format) directly to a USB memory
disk by pressing a Print Key.
The P3 key is the factory default print key to accomplish the
USB Quick Save. However, the default is for the Image Area
only or the customer may have customized the default Key
function.

Check and Record the P3 Key Function

Check the function of the default Key in the event that the
customer may have made some customized settings.
1. Click Utility on the keyboard.
2. Select Connectivity from the Utilities Menu.
3. Select the Button tab on the Connectivity screen.
4. In the Physical Print Buttons section, select Print3 key.
The Connectivity/Buttons Screen will be displayed.

Figure 7-3. Buttons Set Up Screen

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Diagnostics/Troubleshooting

Check and Record the P3 Key Function (continued)

P3 is the factory default USB Quick Save key. If it is not set
to Image Area, proceed to step 5 to record the customer’s
customized settings.
5. In the Destinations section, record the service that is
displayed.
6. In the Physical Print Buttons section, record the
parameters related to the service.

Setting the P3 Key to USB Quick Save

If the P3 Key is not set to USB Quick Save:
1. While on the Connectivity screen, with the Buttons tab
displayed, go to the Destinations list.
2. From the list select USB Quick Save. Press [>>] to add the
selection to the Printflow View section.

Figure 7-4. Set P3 Key to USB Quick Save

3. Ensure that the Physical Print Buttons section for capture

Area is set to Image Area and No Image Compression.
4. The P3 Key should now be set up for USB Quick Save,
sending the images directly to the USB memory

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 Screen Capture

Screen Capture

There may be times when the customer or field engineer will

want to capture a presentation on the screen. This is
accomplished by first saving the image(s) to the clipboard using
a Print Key.
There’s no factory default print key to accomplish a secondary
screen capture. However, customer may have customize any of
Print Key function. Print1, Print2 and Print3 are the same.
Therefore, screen capture should involve the following steps:
1. Check and record any custom settings for the Print1 button
2. Set the Print1 button to Whole Screen, Secondary Capture.
3. Capture the required screens to the Hard Disk Drive or
DVD-R.
4. Restore the Print1 button to it’s original settings.

Contents in this Section

• ‘Check and Record the P1 Key Function’ on page 7-10
• ‘Setting the P1 Key to Screen Capture’ on page 7-10
• ‘Capturing a Screen’ on page 7-11
• ‘Reset the P1 Key to Customer’s Functionality’ on
page 7-12

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Diagnostics/Troubleshooting

Check and Record the P1 Key Function

Check the function of the Print1 Key in the event that the
customer may have made some custom settings.
1. Press Utility on the control panel.
2. Select Connectivity from the Utilities Menu.
3. Select the Button tab on the Connectivity screen.
4. In the Physical Print Buttons field, select Print1.
The Connectivity/Buttons Screen will be displayed.
If P1 is not set to Whole Screen, proceed to step 5 to record
the customer’s customized settings.

Figure 7-5. Connectivity/Button screen

5. In the Destinations section, record the service that is

displayed.
6. In the Physical Print Buttons section, record the
parameters related to the service.

Setting the P1 Key to Screen Capture

If the P1 Key is not set to screen capture:
1. While on the Connectivity screen, with the Buttons tab
displayed, go to the Destinations list.
2. From the list select Copy To Dataflow. Press [>>] to add
the selection to the Printflow View section.
3. Ensure that the Physical Print Buttons section for capture
Area is set to Whole Screen, secondary Capture and No
Image Compression.
4. The P1 Key should now be set up for whole screen capture,
sending the screens to the image buffer (clipboard).

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 Screen Capture

Capturing a Screen
The following is a generic process to capture any screen from
the scanner:
1. Navigate to and display the image/screen to be captured.
2. Press P1. This will place a snapshot of the screen on the
“clipboard” displayed at the bottom of the scan image
display.

Figure 7-6. Select Image to Capture

3. Click Freeze to unfreeze the image to view the image

screen and the snapshots displayed on the bottom.
4. Highlight the snapshot to be stored
5. Select Menu on the right side of the image screen, then
highlight and select Save As.

Figure 7-7. Menu > Save As

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Diagnostics/Troubleshooting

Capturing a Screen (continued)

6. A Save dialog box will be opened. Select Save first, and
Select Transfer to CD/DVD to save the image on the CD/
DVD

Figure 7-8. Save Dialog Box

Reset the P1 Key to Customer’s Functionality

If the customer had programmed the P3 Key to a function other
than screen capture, restore that functionality recorded in
section ‘Check and Record the P1 Key Function’ on page 7-10.
Refer to Figure 7-5 on page 7-10.
1. Select Utility on the control panel.
2. Select Connectivity -> Button.
3. In the Physical Print Buttons field, select Print1.
4. In the Destinations list, select the service(s) recorded in step
5, Section ‘Check and Record the P1 Key Function’ on
page 7-10.
5. In the Physical Print Buttons section, select the parameters
related to the service recorded in step 6, section ‘Check and
Record the P1 Key Function’ on page 7-10.

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 Global Service User Interface (GSUI)

Global Service User Interface

(GSUI)

Contents in This Section

• ‘Common Diagnostics’ on page 7-13
• ‘Restart the system after diagnostics’ on page 7-16

Common Diagnostics

Utilities

Provides two selections:

• Disruptive Mode
Allows you to enable or disable disruptive mode
troubleshooting.
• System Shutdown
Allows for system shutdown from the diagnostic menu.
Select to Restart System or Shutdown System. Also, select
to retain Disruptive Mode or Not.
After submitting to restart or shutdown a confirmation
screen gives one last chance to confirm or cancel the
request.

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Diagnostics/Troubleshooting

PC

• Essential Test tests: PCI, PCI Express, CPU, Memory, HD

Disk and Video.
• Hard Drive Long: tests functionality of the hard drive.
• Hard Drive Short: tests functionality of the hard drive.
• Memory: tests the memory on the mother board.
• Network Adapter: Network calbe must be connected.
• System board: tests the real time clock.
• Video: tests functionality of video adapters.

PC Interactive

• AVI playback tests playing back an AVI file.

• Click “Play” to run the test. If the test is successful, you
will see a brief video clipo with audio. For more
information about the test, click “More Information”.
• Click “Pass” if the test successfully reproduces the
video clip.
• Click “Fail” if the test is unable to successfully reproduce
the video clip.
• Click “Cancel” button to quit the test without recording a
test result.
• Keyboard
• Press each key on the keyboard and it will be added to
the History. Hold down a key to test the repeat of that
key. To cancel, click Cancel or press Alt+X.
• Special purpose keys like volume control or Internet
access keys may not be detected. To test the Fn key of
a notebook computer, hold down the Fn key while
pressing another key.
• Note: This diagnostic is intended to verify keyboard
keys are in good working order. It is not intended to
verify that keyboards produce desired characters.

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 Global Service User Interface (GSUI)

PC Interactive (continued)

• Monitor Test Patterns

• This test is composed of various elements that verify a
monitor functions correctly. To test a monitor feature,
click the appropriate button. You can return to this dialog
by clicking the mouse button or pressing any key.
• The Combination Test helps you verify your monitor is
properly aligned, and set at the correct color depth and
resolution. Use the crosshair pattern in each corner of
the screen to visually determine if the monitor aligns
correctly. If the crosshairs appear distorted or out of
focus, a problem may exist with the monitor alignment.
Use the color spectrum array for visually verifying the
monitor color depth capacity. If the colors in the color
spectrum do no blend smoothly together, a problem
may exist with the monitor color depth. Use the
graduated horizontal and vertical alignment bars to
determine the monitor resolution capabilities. The better
you can discern individual lines as they move closer
together, the higher the resolution capabilities of the
monitor.
• The Solid Color Test helps point out malfunctioning or
dysfunctional pixels using five basic colors: red, green,
blue, black, and white. Fill the screen with an
appropriate color by clicking the associated button. If a
pixel is malfunctioning, the pixel color will contrast with
the color of all other pixels.
• The VESA Test Patterns allow you to test the monitor for
proper luminance, geometry and focus. Click the
appropriate button to fill the screen with the associated
test pattern. You can return to this dialog by clicking the
mouse button or pressing any key.

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Diagnostics/Troubleshooting

PC Interactive (continued)

• Trackball
• The Mouse Status Test verifies the cursor position and
mouse button state. When a mouse button is pressed,
the corresponding button on the picture will change
color. If the mouse is a wheel or scroll mouse, an arrow
will indicate the direction the wheel is being rotated.
Clicking the wheel will flash the picture of the mouse in
the Mouse Status Test area.
• The Drag and Drop Test verifies a mouse can
successfully perform drag and drop operations. Left
click the picture of the CD and drag is onto the picture of
the drive. If successful, the picture will change.
• The Double Click Test verifies a mouse can successfully
perform double-click operations. Double-click on the
picture of the monitor. If successful, the picture will
change.
• Sound Test generates sounds for testing the speakers.
• USB Ports Test lists USB Devices.

Figure 7-9. USB Ports Test

Restart the system after diagnostics

Always shutdown the system and reboot after a

diagnostics session.

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 Network Configuration

Network Configuration

Contents in This Section

• ‘Network Configuration’ on page 7-17
• ‘Wire-LAN Network’ on page 7-17
• ‘Wireless LAN Network’ on page 7-19

Network Configuration

Wire-LAN Network

1. Connect system with network.

2. Enter Utility-> Connectivity-> TCP/IP, in IP settings
window, check Enable DHCP, and select the proper
network speed in Network Speed.

Figure 7-10. Enable DHCP

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Diagnostics/Troubleshooting

Network Configuration (continued)

NOTE: If user wants to setup static IP address, uncheck Enable

DHCP option, input static address in IP-Address box,
Subnet Mask and Default Gateway box. In Network
Speed, choose the proper speed available.

Figure 7-11. Input static address

3. Select Save, and a popup window displays. Select OK to

restart the system and activate the changes.

Figure 7-12. System Restart inquiry dialog

4. After the system restarts, the network icon at the left bottom
of screen turns green.

Figure 7-13. Network icon

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 Network Configuration

Wireless LAN Network

1. Connect wireless LAN card with system.

2. Enter Utility -> Connectivity.
3. In the Section of Wireless Network, select Configuration.

Figure 7-14. Wireless Network configuration

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Diagnostics/Troubleshooting

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 Chapter 8

Replacement Procedures

This chapter describes how to remove and install, or

replace, modules and subsystems in the LOGIQ e. It
also includes instructions for installing and re-installing
the software.

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Replacement Procedures

Overview

Contents in this chapter

• ‘Overview’ on page 8-2
• ‘Warnings and important information’ on page 8-3
• ‘Disassembly/Re-assembly’ on page 8-5
• ‘Loading the software’ on page 8-13

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 Warnings and important information

Warnings and important information

Warnings

WARNING Energy Control and Power Lockout for LOGIQ e.

When servicing parts of the Ultrasound system where there is
exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as
there are no test points to verify isolation.
6. Remove/disconnect the battery, if present.
Ultrasound System components may be energized.

WARNING Because of the limited access to cabinets and equipment in the

field, placing people in awkward positions, GE has limited the
lifting weight for one person in the field to 16 KG (35 LBS).
Anything over 16 KG (35 LBS) requires 2 people.

WARNING DO NOT touch any boards with integrated circuits prior to

taking the necessary ESD precautions.
Always connect yourself, via an arm-wrist strap, to the advised
ESD connection point located on the rear of the Ultrasound
system (near the power connector).
Follow general guidelines for handling of electrostatic sensitive
equipment.

NOTE: Use an ESD compatible work space or the ESD-kit during parts
replacement.

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Replacement Procedures

Warnings (continued)

WARNING The waste of electrical and electronic equipment must not be

disposed as unsorted municipal waste and must be collected
separately.
Please contact the manufacturer or other authorized disposal
company to decommission your equipment.

Returning/shipping probes and repair parts

Equipment being returned must be clean and free of blood and
other infectious substances.
GE policy states that body fluids must be properly removed from
any part or equipment prior to shipment. GE employees, as well
as customers, are responsible for ensuring that parts/equipment
have been properly decontaminated prior to shipment. Under no
circumstance should a part or equipment with visible body fluids
be taken or shipped from a clinic or site (for example, body coils
or an ultrasound probe). The purpose of the regulation is to
protect employees in the transportation industry, as well as the
people who will receive or open this package.
NOTE: The US Department of Transportation (DOT) has ruled that
“items that were saturated and/or dripping with human blood
that are now caked with dried blood; or which were used or
intended for use in patient care” are “regulated medical waste”
for transportation purposes and must be transported as a
hazardous material.

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 Disassembly/Re-assembly

Disassembly/Re-assembly

Warning and Caution

WARNING ONLY QUALIFIED SERVICE PERSONNEL SHOULD

REMOVE ANY COVERS OR PANELS. ELECTRICAL
HAZARDS EXISTS AT SEVERAL POINTS INSIDE.
BECOME THOROUGHLY FAMILIAR WITH ALL
HAZARDOUS VOLTAGES AND HIGH CURRENT
LEVELS TO AVOID ACCIDENTAL CONTACT

CAUTION Do not wear the ESD wrist strap when you work on live circuits
and more than 30V peak is present.

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Replacement Procedures

Handle Assy (Part No. 5483188)

Purpose: This is a description on how to remove and replace the
Handle Assy.

Tools

• Common Phillips screwdrivers

• Allen/Unbraco/Torx wrench

Needed Manpower

• 1 person, 5 minutes + travel

Preparation

• Shut down the system, disconnect the AC/DC power cord

and remove the battery.

Removal Procedure

Table 8-1: Removal Procedure for Handle Assy

No. Steps Corresponding Graphic

1. Unscrew 2 handles caps on both sides

of the system by rotating the cap
counterclockwise.

2. Pull out the handle.

Mounting Procedure

1. Install the new parts in the reverse order of removal.

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 Disassembly/Re-assembly

Advanced Isolation Cart Components Replacement

Basket of Advanced Isolation Cart (Part No. 5571410)

Purpose: This is a description on how to remove and replace the

Basket of Advanced Isolation Cart.

Tools
• Common Phillips screwdrivers
• Allen/Unbraco/Torx wrench

Needed Manpower
• 1 person, 2 minute + travel

Preparation
• Power off the Advanced Isolation Cart and disconnect the
AC/DC power cord.

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Replacement Procedures

Removal Procedure

Table 8-2: Removal Procedure for Basket

No. Steps Corresponding Graphic

1. Unscrew the 1 screw under the basket.

2. Hold the basket with both hands and

push it up.

3. Remove the basket from the Upper

Column.

Mounting Procedure
1. Install the new parts in the reverse order of removal.

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 Disassembly/Re-assembly

Drawer of Advanced Isolation Cart (Part No. 5571411)

Purpose: This is a description on how to remove and replace the
Drawer of Advanced Isolation Cart.

Tools
• Common Phillips screwdrivers
• Allen/Unbraco/Torx wrench

Needed Manpower
• 1 person, 2 minute + travel

Preparation
• Power off the Advanced Isolation Cart and disconnect the
AC/DC power cord.

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Replacement Procedures

Removal Procedure

Table 8-3: Removal Procedure for Drawer

No. Steps Corresponding Graphic

1. Unscrew the 1 screw under the drawer.

2. Hold the drawer with both hands and

push it up.

3. Remove the drawer from the Upper

Column.

Mounting Procedure
1. Install the new parts in the reverse order of removal.

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 Disassembly/Re-assembly

3-Probe Port of Advanced Isolation Cart (Part No. 5571412)

Purpose: This is a description on how to remove and replace the
3-Probe Port of Advanced Isolation Cart.

Tools
• Common Phillips screwdrivers
• Allen/Unbraco/Torx wrench

Needed Manpower
• 1 person, 2 minute + travel

Preparation
• Power off the Advanced Isolation Cart and disconnect the
AC/DC power cord.

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Replacement Procedures

Removal Procedure

Table 8-4: Removal Procedure for 3-Probe Port

No. Steps Corresponding Graphic

1. Unscrew the 1 screw under the 3-Probe

Port.

2. Hold the 3-Probe Port with both hands

and push it up.

3. Remove the 3-Probe Port from the

Upper Column.

Mounting Procedure
1. Install the new parts in the reverse order of removal.

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 Loading the software

Loading the software

Contents in This Section

• ‘Purpose of this section’ on page 8-13
• ‘Customer provided prerequisite’ on page 8-13
• ‘Data Management - moving all images’ on page 8-14
• ‘Backing up the Patient Archive and System Configurations’
on page 8-14
• ‘Recording important settings and parameters’ on page 8-15
• ‘Loading the System Software’ on page 8-16
• ‘Loading the System Software with USB memory stick’ on
page 8-16
• ‘Software Version check out’ on page 8-22
• ‘Reload the Correct Preset Region’ on page 8-23
• ‘Option Strings Check’ on page 8-24
• ‘Probe Recognition Check’ on page 8-25
• ‘Peripheral Device Check’ on page 8-25
• ‘Reinstall DICOM Devices’ on page 8-26

Purpose of this section

This section describes how to reinstall software on LOGIQ e.

Customer provided prerequisite

• Formatted and labelled media for Images storage.
• Formatted and labelled media for Patient Archive and
Presets (User Defined Settings).
• Password for the user ADM.

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Replacement Procedures

Data Management - moving all images

CAUTION An error, or a power loss may occur.

Always backup the Patient Archive and the Presets (System
Configurations) before loading the software!
In order to complete a successful restore of the Patient
Database, as needed after a hard disk replacement, or if all the
content on the hard disk has been erased, the images must be
moved away from LOGIQ e before doing backup of the Patient
Database.
Depending on the location set-up, either move the images to a
remote server or to removable media like DVD or CD discs.

• Move the images to a remote server or to removable media.

For instructions, please see “Disk management” in the User
Manual/User Guide.

Backing up the Patient Archive and System Configurations

CAUTION An error, or a power loss may occur.

Always backup the Patient Archive and the Presets (System
Configurations) before loading the software!
In order to complete a successful restore of the Patient
Database, as needed after a hard disk replacement, or if all the
content on the hard disk has been erased, the images must be
moved away from LOGIQ e before doing backup of the Patient
Database.
Depending on the location set-up, either move the images to a
remote server or to removable media like DVD or CD discs.

• Backup the Patient Archive and System Configurations.

For instructions, please see “Data Backup and Restore” in
the User Manual/User Guide.

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 Loading the software

Recording important settings and parameters

Overview

CAUTION An error, or a power loss may occur.

It is considered to be best practice to always keep a record on
paper of the settings for the LOGIQ e. Verify if it is current
before you start to load software!

Always keep a record of the settings for the LOGIQ e on paper.

Verify if it is current before starting a software loading! If needed,
record the settings.
This subsection includes descriptions for recording data from
the following screens:

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Replacement Procedures

Loading the System Software

WARNING While the software install procedure is designed to

preserved data, you should save any patient data,
images, system setups and customer presets to CD,
DVD, USB Flash Drive, or USB Hard Disk before doing a
software upgrade.
NOTE: Before loading the system software, please ensure that the
power can be continuously supplied and there is no risk of
power cut off during loading procedure.
There are two methods to load the system software:
• Load the system software with USB memory stick.

Loading the System Software with USB memory stick

NOTE: Before starting this procedure, remove all probes and

peripherals and remove them from the Docking Cart.
NOTE: While it is believed to be unnecessary, it would not hurt to
disconnect the system from the network and remove all
transducer.
NOTE: Please ensure AC adapter is connected during system upgrade!
1. Insert the USB memory stick labeled “System & Application
Software” to the system.
2. Properly turn off the scanner by momentarily pressing the
Power On/Off Switch. In System-Exit window, select
Shutdown to shutdown the system.
NOTE: If the system will not shutdown normally, hold down the
Power On/Off Switch until the light turns off.
3. Power on the system. The system will detect the USB
memory stick automatically.

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 Loading the software

Loading the System Software with USB memory stick (continued)

4. Press any key to continue when below message displays.

Figure 8-1. Upgrade message

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Replacement Procedures

Loading the System Software with USB memory stick (continued)

5. Select one of the options for loading the system. Select

choice [a] to load the complete disk.

CAUTION If you select [a], ALL existing software and data will be erased.
If backup has not been performed, all data like Patient
Database, System Configuration and User Configurations
(Customer Presets) will be lost.

• To select [a], the complete disk will be loaded. This

option is recommended for application software
upgrade.
NOTE: When to select [a] to load complete disk, please ensure
that any patient data on the disk has been backed up.
• To select [b], only the bootable C: partition is loaded.
This option is intended for recovery of a system that will
not boot up. It is not recommended for application
software upgrade because during upgrade process, the
data on the system would possibly be impacted.
• To select [c] to quit system upgrade process.
• To select [e] to erase the complete disk. This process
will erase all patient data and all existing software on the
system. (For R9.x.x only)
NOTE: Do not select [e] for loading system software.

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 Loading the software

Loading the System Software with USB memory stick (continued)

Figure 8-2. System Software load instruction (For R8.x.x)

Figure 8-3. System Software load instruction (For R9.x.x)

WARNING While the software install procedure is designed to

preserve data, you should select choice [b] to format disk
C only.

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Replacement Procedures

Loading the System Software with USB memory stick (continued)

6. Input “Yes” or “No” and press Enter key to continue.

Figure 8-4. Confirmation on loading the system

7. System USB memory stick will be loading. Wait for the

software installation to complete. (Typical installation time:
5-10 minutes). Status bar on the screen indicates progress.

WARNING Do not interrupt the software loading at any time.

Figure 8-5. Loading status

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 Loading the software

Loading the System Software with USB memory stick (continued)

8. After finish updating system, remove the USB memory stick

and press any key to shut down the system.
NOTE: If you don not remove the USB memory stick, the software
system loading process repeats when the system boots up.

Figure 8-6. System upgrade complete

9. Restart the system.

If you select [a] to load the complete disk, the following
steps are required.
a. Enter the system’s Serial Number and select OK. The
system’s Serial Number is at the bottom of the system.
Press On/Off switch to restart the system.

Figure 8-7. System Serial Number

b. After the system restarts, enter the software license and

select OK. The system will enter into scan mode.

Figure 8-8. Software license

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Replacement Procedures

Software Version check out

Functional Check-out
1. Power on LOGIQ e system and wait until system booting to
main screen.
2. Press Utility on the control panel.
3. Select the About button on the right.

Figure 8-9. About

4. Check whether “Software Version” is the right version for

use.

Figure 8-10. Software version

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 Loading the software

Reload the Correct Preset Region

NOTE: After the system software loading completion, please reload the
correct preset region.
1. Reboot the system.
2. Select Utility -> General.
3. In the Location portion, select the right region in the field of
Preset Region.

Figure 8-11. Preset Region

4. Reboot the system.

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Replacement Procedures

Option Strings Check

NOTE: After the system software loading completion, please check the
option strings to ensure that the options are activated and
working.
1. Reboot the system.
2. Select Utility -> Admin -> System Admin.
3. Enter the option keys into the Enter New Option Key field
and press Add.
4. Ensure that all the install option keys are displayed and the
status of Options are valid.
• The status “Valid” means the option keys are activated
and working.
• The status “disabled” means the option keys are not
activated and not working. Check if the option is
installed and if the serial number and option key are
correct.

Figure 8-12. Option strings

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 Loading the software

Probe Recognition Check

NOTE: After the system software loading completion, please check to

ensure that the system can recognize the probes.
Plug in the probe. In scanning mode, the probe information is
displayed on the right top location of the screen. About the
probe specification for intended use on LOGIQ e.
Plug in at least one of each type of the probes and check if each
of the probes is recognized and the probe information is
displayed correctly.

Figure 8-13. Probe identification

Peripheral Device Check

Check to ensure that all the peripheral devices work properly.

For instruction of peripheral device check, See ‘Peripheral
Checks’ on page 4-52 for more information.

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Replacement Procedures

Reinstall DICOM Devices

Reinstall any DICOM devices used by the customers and check

to ensure these DICOM devices work properly.
The instruction about installing DICOM devices is not
incorporated in this manual. To access the instruction about
installing DICOM devices please refer to another manual Basic
User Manual. Please use the latest revision of this document.

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 Chapter 9

Renewal Parts

This chapter lists the renewal parts available for the

LOGIQ e.

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Renewal Parts

Overview

Contents in this chapter

• ‘Overview’ on page 9-2
• ‘List of Abbreviations’ on page 9-2
• ‘Renewal Parts Lists’ on page 9-3

List of Abbreviations
Table 9-1: List of Abbreviations

ABBREVIATION DESCRIPTION

3D THREE DIMENSIONAL

Assy ASSEMBLY

KBD Keyboard

LCD Liquid Crystal Display

BnV Brightness and Volume

WMST Master Board

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 Renewal Parts Lists

Renewal Parts Lists

Contents in This Section

• ‘Power Cable’ on page 9-4
• ‘Operator Console Assy’ on page 9-5
• ‘LCD Assy’ on page 9-6
• ‘Keyboard Assy’ on page 9-7
• ‘Bottom Assy’ on page 9-9
• ‘E-Isolation Cart and Advanced Isolation Cart’ on page 9-14
• ‘Accessories and Kits’ on page 9-17
• ‘Probe’ on page 9-20
• ‘Manuals’ on page 9-22
NOTE: The part replacement is shown by the “Replaced By” column in
the table. If the part is replaced by a new version, the new
version is shown in the “Replaced By” column in the table. The
item number for the new version will have a letter in the
alphabetical order after the Arabic numerals. For example, the
new version in item 300A will replace the parts or only some
parts in the item 300. The parts in item 300 which are replaced
by item 300A will have the part number of new version in the
“Replaced By” column. The parts in item 300 which are not
replaced do not have a new version in the “Replaced By”
column.
NOTE: The software R8.x.x and R9.x.x which are used to distinguish
the different features of the system in all the manuals only refer
to the systems which are originally installed with the software
version R8.x.x and R9.x.x. Not all the features of R9.x.x will be
supported when upgrading the software from R8.x.x to R9.x.x on
the system which is originally installed with software R8.x.x.

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Renewal Parts

Power Cable
Table 9-2: Power Cable List

Replaced
Item Part Number Description By Qty

1 5460229 ACDC Adapter with Clamp Filter 1

2 5177126-2 ACDC Power Cable for Japan 1

3 5177195-2 ACDC Power Cable for Argentina 1

4 5177154-2 ACDC Power Cable for Switzerland 1

5 5177187-3 ACDC Power Cable for Australia 1

6 5177123-2 ACDC Power Cable for Europe 1

7 5176907-2 ACDC Power Cable for United Kingdom 1

8 5176773-2 ACDC Power Cable for India 1

9 5176753-2 ACDC Power Cable for Israel 1

10 5176304-2 ACDC Power Cable for China 1

11 5177146-2 ACDC Power Cable for USA 1

12 5177153-2 ACDC Power Cable for Denmark 1

13 5400868-2 ACDC Power Cable for Brazil 1

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 Renewal Parts Lists

Operator Console Assy

Figure 9-1. Operator Console Assy

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Renewal Parts

LCD Assy
Table 9-3: LCD Assy

Part Replaced
Item Number Part Name By Corresponding graphic Qty

100 5460119 LOGIQ e LCD Assy 1

102 5483138 LOGIQ e LCD Panel 1

Kits

103 5419292 LOGIQ e LCD Back 1

Cover Assy

104 5418452 LOGIQ e LCD Front 1

Cover

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 Renewal Parts Lists

Keyboard Assy
Table 9-4: Keyboard Assy

Part Replaced
Item Number Part Name By Corresponding graphic Qty

200 5453774 LOGIQ e Keyboard 1

Assy

201 5446052 LOGIQ e KBD Cover 1

Assy

203 5456388 LOGIQ e AN 1

Keyboard

204 5451287 LOGIQ e Trackball 1

Assy

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Renewal Parts

Table 9-4: Keyboard Assy

Part Replaced
Item Number Part Name By Corresponding graphic Qty

205 5483141 LOGIQ e Keyboard 1

PWA Kits

206 5483143 LOGIQ e TGC Keytop 1

Kits

207 5483185 LOGIQ e Depth 1

Keytop Kits

208 5483189 LOGIQ e Speaker 1

Kits

209 5154621-2 LOGIQ e KBD cable 1

kits with new KBD
cable

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 Renewal Parts Lists

Bottom Assy
Table 9-5: Bottom Assy

Part Replaced
Item Number Part Name By Corresponding graphic Qty

300 5482282 Advantech 128G SSD 1

Model:SQF-SMSM4-
128G-S8C

301 5443576 LOGIQ e WDC PWA 1

302 5449310 LOGIQ e CPU 1

Module

303 5452099 LOGIQ e Bottom 1

Cover Assy

304 5462354 LOGIQ e Utility PWA 1

Assy

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Renewal Parts

Table 9-5: Bottom Assy

Part Replaced
Item Number Part Name By Corresponding graphic Qty

305 5454601 LOGIQ e Probe 1

Connector Assy

306 5460069 LOGIQ e Left Fan 1

Assy

307 5458580 LOGIQ e Right Fan 1

Assy

308 5483140 LOGIQ e LCD Hinge 1

and Handle Hinge
Kits

309 5483142 LOGIQ e Main PWA 1

and Heatpipe Kits
(For the system which
is originally installed
with Software R8.x.x)

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 Renewal Parts Lists

Table 9-5: Bottom Assy

Part Replaced
Item Number Part Name By Corresponding graphic Qty

310 5451284 LOGIQ e Battery 1

Pack

311 5483358 LOGIQ e Probe 1

Connect Lock Kits

312 5419298 LOGIQ e Menu Panel 1

Assy

313 5462567 LOGIQ e Rubber Kits 1

314 5422180 LOGIQ e Battery Lock 1

315 5145407 LOGIQ e CMOS 1

Battery

316 5484857 Memory Module 1

317 5490318 OPTKey IC 1

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Renewal Parts

Table 9-5: Bottom Assy

Part Replaced
Item Number Part Name By Corresponding graphic Qty

318 5452120-S LOGIQ e CWD Board 1

319 5483188 LOGIQ e Handle Kits 1

320 5490737 LOGIQ e Heatpipe

Module Kits

321 5483186 LOGIQ e Screw Kits 1

322 5582183 LOGIQ e Main PWA 1

and Heatpipe Kits
(For Software R8.0.5
and above)

323 5589352 LOGIQ e Main PWA 1

and Heatpipe Kits
(For the system which
is originally instatlled
with Software R9.x.x)

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 Renewal Parts Lists

Table 9-5: Bottom Assy

Part Replaced
Item Number Part Name By Corresponding graphic Qty

324 5692065 LOGIQ e Memory 1

SO-DIMM
DDR3-1600-4G for
ADV CPU (For R9.x.x
only)

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Renewal Parts

E-Isolation Cart and Advanced Isolation Cart

Table 9-6: E-Isolation Cart

Part Replaced
Item Number Part Name By Corresponding graphic Qty

1400 5507953 E-Isolation Cart 1

Power Box 220V

1401 5507952 E-Isolation Cart 1

Power Box 110V

1402 5420768-2 Printer Box Assy for 1

E-Isolation Cart

1403 5420771-2 E-Isolation Cart Assy 1

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 Renewal Parts Lists

Table 9-6: E-Isolation Cart

Part Replaced
Item Number Part Name By Corresponding graphic Qty

1404 5561128-S Advanced Isolation

Cart Assy

1405 5439000 Front Castor

MYSD-120R for
Advanced Isolation
Cart

1406 5571410 Basket Kits for

Advanced Isolation
Cart

1407 5571411 Drawer Kits for

Advanced Isolation
Cart

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Renewal Parts

Table 9-6: E-Isolation Cart

Part Replaced
Item Number Part Name By Corresponding graphic Qty

1410 5571412 3-Probe Port Kits for

Advanced Isolation
Cart

1411 5426642 Cable Hook Kit for

Advanced Isolation
Cart

1412 5426645 Locate Block and

Screw Cap for
Advanced Isolation
Cart

1413 5426644 Probe and Gel Holder

Kit for Advanced
Isolation Cart

1414 5461076 Rear Handle Kit for

Advanced Isolation
Cart

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 Renewal Parts Lists

Accessories and Kits

Table 9-7: Accessories and Kits

Part Replaced
Item Number Part Name By Corresponding graphic Qty

400 5483317-3 Software R8.0.3 USB 5483317-6 1

400A 5483317-5 Software R8.0.5 USB 5483317-6 1

400B 5483317-6 Software R8.0.6 USB 5483317-7 1

400C 5483317-7 Software R8.0.7 USB 1

401 5483187 LOGIQ e LOGO Kits 1

402 5491253 SONY UPD25 Color 1

Printer Brazil kit

403 5495509 SONY UPD897 BW 5495509-2 1

Printer Brazil Kit

403A 5495509-2 SONY UPD898MD 1

BW Printer Brazil Kit

404 5499686 LOGIQ e eSmart 1

Trainer Japanese
USB Flash Drive

405 5133106-2 SONY UPD25 Color 1

Printer CHN kit

406 5133107-2 SONY UPD25 Color 1

Printer USA kit

407 5133108-2 SONY UPD25 Color 1

Printer EUP kit

408 5133109-2 SONY UPD25 Color 1

Printer JPN kit

409 5151259 SONY UPD897 BW 5151259-2 1

Printer USA Kit

409A 5151259-2 SONY UPD898MD BW 1

Printer USA Kit

410 5151261 SONY UPD897 BW 5151261-2 1

Printer Europe Kit

410A 5151261-2 SONY UPD898MD BW 1

Printer Europe Kit

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Renewal Parts

Table 9-7: Accessories and Kits

Part Replaced
Item Number Part Name By Corresponding graphic Qty

411 5151262 SONY UPD897 BW 5151262-2 1

Printer China Kit

411A 5151262-2 SONY UPD898MD BW 1

Printer China Kit

412 5151263 SONY UPD897 BW 5151263-2 1

Printer Japan Kit

412A 5151263-2 SONY UPD898MD BW 1

Printer Japan Kit

413 5421913 LOGIQ e 1

eSmartTrainer USB
Flash Drive

414 5449275-2 TWIN LITEON 1

eUAU108 DVDRW
Kit

415 5473920 NetGear WNA1000M 1

Wireless USB Micro
Adapter Kit

416 5151236 USB Foot Switch for 1

LOGIQ e

417 5446188 USB barcode reader 1

Honeywell
1900GHD-2

418 5129487 ECG module from 1

Norav Isral

419 5146056 ECG Detachable 1

cable AHA Type USA

420 5146055 USB Cable for ECG 1

421 5146739 ECG detachable 1

cable IEC type EURO
and ASIA

422 5195563 ECG module with 1

SKD label

423 5177378 SKD ECG Package 1

English Label

424 5446638 Keeber8G USB Stick 1

425 5136239-S Vet caution label (For 1

R9.x.x only)

426 5447716-S Probe Vet label Kit for 1

USA (For R9.x.x only)

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 Renewal Parts Lists

Table 9-7: Accessories and Kits

Part Replaced
Item Number Part Name By Corresponding graphic Qty

427 5720394 LOGIQ e Vet Kits (For 1

R9.x.x only)

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Renewal Parts

Probe
Table 9-8: Probes for LOGIQ e

Part Part Replaced

Item Name Number Description By Illustration Qty

500 L4-12t-RS 5435010 Linear Probe 1

(Frequency
Range: 4.2~13)

501 L10-22-RS 5441887 Linear Probe 1

(Frequency
Range: 10~22)

502 12L-RS 5409291 Linear Probe 1

(Frequency
Range: 4.2~13)

503 3Sc-RS 47237516 Sector Probe 1

(Frequency
Range: 1.7~4)

504 8C-RS 5434194 Convex Probe 1

(Frequency
Range: 4.2~11)

505 C1-5-RS 5499608 Convex Probe 1

(Frequency
Range: 2~5)

506 L8-18i-RS 5499609 Linear Probe 1

(Frequency
Range: 6.3~18)

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 Renewal Parts Lists

Table 9-8: Probes for LOGIQ e

Part Part Replaced

Item Name Number Description By Illustration Qty

507 9L-RS 5499511 Linear Probe 1

(Frequency
Range: 3~9)

508 6S-RS 5394465 Sector Probe 1

(Frequency
Range: 3~7)

509 E8C-RS 5499516 Convex Probe 1

(Frequency
Range: 4.2~10)

510 4C-RS 5488477 Linear Probe 1

(Frequency
Range: 2~15)
(For R9.x.x only)

511 LK760-RS KN10010 Linear Probe 1

6 (Frequency
Range: 3.5~10)
(For R9.x.x only)

512 6Tc-RS 5548914 Sector Probe 1

(Frequency
Range: 3~8)
(For R9.x.x only)

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Renewal Parts

Manuals
Table 9-9: Manuals for LOGIQ e (For R8.x.x)

Item Part Number Description Qty

600 5461614-100 LOGIQ e Service Manual 1

System User Manual

601 5454606-100 LOGIQ e Basic User Manual, English 1

602 5454606-101 LOGIQ e Basic User Manual, French 1

603 5454606-106 LOGIQ e Basic User Manual, Spanish 1

604 5454606-108 LOGIQ e Basic User Manual, German 1

605 5454606-111 LOGIQ e Basic User Manual, Italian 1

606 5454606-127 LOGIQ e Basic User Manual, Brazilian Portuguese 1

607 5454606-140 LOGIQ e Basic User Manual, English 1

608 5437241-141 LOGIQ e User Guide, Chinese Simplified 1

609 5437241-121 LOGIQ e User Guide, Dutch 1

610 5437241-129 LOGIQ e User Guide, Estonian 1

611 5437241-142 LOGIQ e User Guide, Swedish 1

612 5437241-143 LOGIQ e User Guide, Traditional Chinese 1

613 5437241-144 LOGIQ e User Guide, Korean 1

614 5437241-145 LOGIQ e User Guide, Russian 1

615 5437241-150 LOGIQ e User Guide, Polish 1

616 5437241-151 LOGIQ e User Guide, Greek 1

617 5437241-153 LOGIQ e User Guide, Hungarian 1

618 5437241-154 LOGIQ e User Guide, Slovakian 1

619 5437241-155 LOGIQ e User Guide, Czech 1

620 5437241-159 LOGIQ e User Guide, Turkish 1

621 5437241-160 LOGIQ e User Guide, Danish 1

622 5437241-161 LOGIQ e User Guide, Norwegian 1

623 5437241-162 LOGIQ e User Guide, Finnish 1

624 5437241-165 LOGIQ e User Guide, Bulgarian 1

625 5437241-167 LOGIQ e User Guide, Romanian 1

626 5437241-168 LOGIQ e User Guide, Croatian 1

627 5437241-174 LOGIQ e User Guide, Lithuanian 1

9-22 LOGIQ e – Basic Service Manual

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 Renewal Parts Lists

Table 9-9: Manuals for LOGIQ e (For R8.x.x)

Item Part Number Description Qty

628 5437241-175 LOGIQ e User Guide, Latvian 1

629 5437241-176 LOGIQ e User Guide, Serbian 1

630 5437241-177 LOGIQ e User Guide, European Portuguese 1

631 5437241-170 LOGIQ e User Guide, Ukrainian 1

632 5437241-181 LOGIQ e User Guide, Indonesian 1

Table 9-10: Manuals for LOGIQ e (For R9.x.x)

Item Part Number Description Qty

633 5561650-100 LOGIQ e Basic Service Manual 1

System User Manual

634 5561643-100 LOGIQ e Basic User Manual, English 1

635 5561643-101 LOGIQ e Basic User Manual, French 1

636 5561643-106 LOGIQ e Basic User Manual, Spanish 1

637 5561643-108 LOGIQ e Basic User Manual, German 1

638 5561643-111 LOGIQ e Basic User Manual, Italian 1

639 5561643-127 LOGIQ e Basic User Manual, Brazilian Portuguese 1

640 5561643-140 LOGIQ e Basic User Manual, English 1

641 5561645-141 LOGIQ e User Guide, Chinese Simplified 1

642 5561645-121 LOGIQ e User Guide, Dutch 1

643 5561645-129 LOGIQ e User Guide, Estonian 1

644 5561645-142 LOGIQ e User Guide, Swedish 1

645 5561645-143 LOGIQ e User Guide, Traditional Chinese 1

646 5561645-144 LOGIQ e User Guide, Korean 1

647 5561645-145 LOGIQ e User Guide, Russian 1

648 5561645-150 LOGIQ e User Guide, Polish 1

649 5561645-151 LOGIQ e User Guide, Greek 1

650 5561645-153 LOGIQ e User Guide, Hungarian 1

651 5561645-154 LOGIQ e User Guide, Slovakian 1

652 5561645-155 LOGIQ e User Guide, Czech 1

653 5561645-159 LOGIQ e User Guide, Turkish 1

LOGIQ e – Basic Service Manual 9-23

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Renewal Parts

Table 9-10: Manuals for LOGIQ e (For R9.x.x)

Item Part Number Description Qty

654 5561645-160 LOGIQ e User Guide, Danish 1

655 5561645-161 LOGIQ e User Guide, Norwegian 1

656 5561645-162 LOGIQ e User Guide, Finnish 1

657 5561645-165 LOGIQ e User Guide, Bulgarian 1

658 5561645-167 LOGIQ e User Guide, Romanian 1

659 5561645-168 LOGIQ e User Guide, Croatian 1

660 5561645-174 LOGIQ e User Guide, Lithuanian 1

661 5561645-175 LOGIQ e User Guide, Latvian 1

662 5561645-176 LOGIQ e User Guide, Serbian 1

663 5561645-177 LOGIQ e User Guide, European Portuguese 1

664 5561645-170 LOGIQ e User Guide, Ukrainian 1

665 5561645-181 LOGIQ e User Guide, Indonesian 1

666 5561645-184 LOGIQ e User Guide, Kazakh 1

9-24 LOGIQ e – Basic Service Manual

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 Chapter 10

Care and Maintenance

This chapter describes Care and Maintenance on the

Ultrasound system and peripherals. These procedures
are intended to maintain the quality of the Ultrasound
system’s performance. Read this chapter completely
and familiarize yourself with the procedures before
performing a task.

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Care and Maintenance

Overview

Contents in this chapter

• ‘Overview’ on page 10-2
• ‘Protecting Health Information’ on page 10-3
• ‘Warnings’ on page 10-12
• ‘Why do maintenance’ on page 10-13
• ‘Maintenance task schedule’ on page 10-15
• ‘Tools required’ on page 10-17
• ‘System maintenance’ on page 10-21
• ‘Electrical safety tests’ on page 10-30
• ‘When there's too much leakage current …’ on page 10-42
• ‘Inspection Paperwork’ on page 10-44
• ‘Electrical Safety Tests Log’ on page 10-46

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 Protecting Health Information

Protecting Health Information

Hide Patient Data

You can preset to display or remove patient information from the
scanning screen title bar when scanning or storing images.
Select Utility -> System -> General, preset in the field of Hide
Patient Data in the portion of Title Bar. Select Save.

Figure 10-1. Hide Patient Information

• Never. When set to this, the patient information is not

removed from title bar when scanning and when storing
images.
• On Store. When set to this, the patient information is
removed from title bar only when storing the images.
• Always. When set to this, the patient information is always
removed from the scanning screen title bar when scanning
and when storing images.
NOTE: Upon recall of images with measurements, Dual image, the
DICOM image is recalled. In this case, there is no patient data
burned into the DICOM image. If you DO NOT want this to
occur, set this to Never.

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Care and Maintenance

Protecting Health Information

Prevent from copying data including Patient Information to
external storage device.
Select Utility -> Admin -> System Admin and check the box in
the portion of Protecting Health Information (PHI). Select
Save and reboot the system.

Figure 10-2. Protecting Health Information

Prevent writing patient information to external storage:

Media: USB Memory / SD Card / USB HDD / CD-R / DVD-R
Function: Export / MPEGVue / EZBackup / EZMove / Save As /
Save As Images / Report Save As / Backup Patient Archive and
Report Archive from Utility.

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 Protecting Health Information

Software Wiping to Erase Patient Data (For R9.x.x only)

You can erase all the patient data with the software to wipe the
partitions on the system.

WARNING The software wiping procedure will erase all the patient data
and all existing software on the system. While the software
wiping procedure is designed to preserved data, you should
save any patient data, images, system setups and customer
presets to CD, DVD, USB Flash Drive, or USB Hard Disk
before doing a software wiping.

NOTE: Before starting software wiping, please ensure that the power
can be continuously supplied and there is no risk of power cut
off during loading procedure.
Use the software to wipe the partitions of the system to erase
the patient data:
1. Insert USB memory stick labeled “System & Application
Software” to the system.
2. Properly turn off the system by momentarily pressing the
Power/On/Off Switch. In System-Exit window, select
Shutdown to shutdown the system.
NOTE: If the system will not shut down normally, hold down the
Power On/Off Switch until the light turns off.
3. Power on the system. The system will detect the USB
memory stick automatically.

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Care and Maintenance

Software Wiping to Erase Patient Data (For R9.x.x only) (continued)

4. Press any key to continue when below message displays.

Figure 10-3. Software message

5. Select [e] to erase the complete disk.

NOTE: All patient data (if any) will be destroyed! Please backup
patient data before executing erasing patient data!

Figure 10-4. Information of erasing patient data

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 Protecting Health Information

Software Wiping to Erase Patient Data (For R9.x.x only) (continued)

6. Input “Yes” or “No” and press Enter key to continue.

Figure 10-5. Confirmation on erasing patient data

7. The software is wiping the partitions. Wait for the wiping

procedure to complete. On the screen, it displays which
partition is in wiping progress and how much has been
completed.
NOTE: Do not interrupt the wiping process at any time until all the
partitions wiping is completed.

Figure 10-6. Wiping progress

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Care and Maintenance

Software Wiping to Erase Patient Data (For R9.x.x only) (continued)

8. When the all the partitions have been wiped, this message
will display on the screen. Remove the USB memory stick
and press any key to shut down the system.

Figure 10-7. Software wiping complete

9. The software wiping procedure has erased all existing

software. If you want to use the system, you need to load
the system software. Refer to ‘Loading the software’ on
page 8-13 for more information about loading the system
software.

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 Protecting Health Information

Users
The Users screen allows you to define user IDs. It also allows
you to specify operators registration, operator’s rights setting,
and registration of staff related to an examination (for example,
referring and interpreting physicians).
Select Utility -> Admin -> Users.

Figure 10-8. Users Preset Menu

Table 10-1: User List

Preset Parameter Description

User List Lists the user ID for all system users.

Identity Type the operator’s user ID, Password, Prefix, Last Name, First Name, Middle
Name, Suffix, Phone Number.

Group Membership Select the user’s group: Operator (sonographers, doctors, or any person using
the ultrasound system); Ref.Phys. (referring physician can be associated to the
patient examination in the extended Patient information window); Perf.Phys. –
physician performing the exam can be associated to the patient examination in
the extended Patient information window.

Operator Rights Admin – If selected, the operator has extended rights with access to the
administrative setup functionality. The operator can also perform advanced
operations

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Care and Maintenance

Creating a user

1. Press Add and select New.

2. Type the user ID. ENSURE that you DO NOT include the
following characters in a user’s ID: slash (/), dash (-),
asterisk (*), question mark (?), an underscore (_),
ampersand (&), or blank spaces. Also, DO NOT set up a
user with the same initials/signifier.
3. Type the user’s information in the Identity section.
4. Select the user’s group(s).
5. If the user needs full configuration and advanced operations
access, select Admin.
6. Press Save.
NOTE: DO NOT add users with the same initials/signifier. The system
allows you to do this; however, the first user is erased and only
the second remains.
NOTE: When adding a new user, press Add first. Then edit the ID from
the default of “NewUser” and edit the other fields. DO NOT
press Add again unless you actually want to create another
user. Press Save after adding one or more users. The user
listed as NewUser on the list will be updated with the edited ID
when you re-enter this screen.

Changing a user configuration

1. Move the Trackball to a user ID in the User List.

2. Make the desired changes.

Deleting a user

1. Move the Trackball to a user ID in the User List.

2. Select Remove.
The user is removed from the User List

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 Protecting Health Information

Logon
The Logon section defines log on procedures.
Select Utility -> Admin -> Logon.

Figure 10-9. Administrative Logon Preset Menu

Table 10-2: Logon

Preset Parameter Description

Auto Logon Specifies logon procedures:

• When blank, the user must select a user ID and enter a password when
logging on.
• When selected, the system is started automatically, using the last user
logon.

Common Network Login Specifies the user ID and password used to access the network. User – User
ID for network access; Password – Password for network access

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Care and Maintenance

Warnings

DANGER BE SURE TO DISCONNECT THE ULTRASOUND SYSTEM

POWER PLUG AND OPEN THE MAIN CIRCUIT BREAKER
BEFORE YOU REMOVE ANY PARTS. BE CAUTIOUS
WHENEVER POWER IS STILL ON AND COVERS ARE
REMOVED.

CAUTION Practice good ESD prevention. Wear an anti–static strap when

handling electronic parts and even when disconnecting/
connecting cables.

CAUTION Do not pull out or insert circuit boards while power is on.

CAUTION Do not operate this Ultrasound system unless all board covers
and frame panels are securely in place. System performance
and cooling require this.

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 Why do maintenance

Why do maintenance

Periodic maintenance inspections

It has been determined by engineering that your LOGIQ e does
not have any high wear components that fail with use, therefore
no Periodic Maintenance inspections are mandatory.
However, some customers’ Quality Assurance Programs may
require additional tasks and or inspections at a different
frequency than listed in this manual.

Keeping records
It is good business practice that ultrasound facilities maintain
records of periodic and corrective maintenance. The Ultrasound
Periodic Maintenance Inspection Certificate provides the
customer with documentation that the Ultrasound system is
maintained on a periodic basis.
A copy of the Ultrasound Periodic Maintenance Inspection
Certificate should be kept in the same room or near the
Ultrasound system.

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Care and Maintenance

Quality assurance
In order to gain accreditation from organizations such as the
American College of Radiology (USA), it is the customer’s
responsibility to have a quality assurance program in place for
each Ultrasound system. The program must be directed by a
medical physicists, the supervising radiologist/physician or
appropriate designee.
Routine quality control testing must occur regularly. The same
tests are performed during each period so that changes can be
monitored over time and effective corrective action can be
taken.
Testing results, corrective action and the effects of corrective
action must be documented and maintained on the site.
Your GE service representative can help you with establishing,
performing and maintaining records for a quality assurance
program. Contact GE for coverage and/or price for service.

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 Maintenance task schedule

Maintenance task schedule

How often should maintenance tasks be performed?

The Care and Maintenance task schedule (provided in
Table 10-3 on page 10-15) specifies how often your LOGIQ e
should be serviced and outlines items requiring special
attention.
NOTE: It is the customer’s responsibility to ensure the LOGIQ e care
and maintenance is performed as scheduled in order to retain its
high level of safety, dependability and performance.
Your GE Service Representative has an in-depth knowledge of
your LOGIQ e and can best provide competent, efficient service.
Contact GE for coverage information and/or price for service.
The service procedures and recommended intervals shown in
the Care and Maintenance Task Schedule assumes that you
use your LOGIQ e for an average patient load (10-12 per day)
and not use it as a primary mobile Ultrasound system which is
transported between diagnostic facilities.
NOTE: If conditions exist which exceed typical usage and patient load,
then it is recommended to increase the periodic maintenance
frequencies.

Table 10-3: Customer Care Schedule

Per
Facilities
Service at Indicated QA
Time Daily Weekly Monthly Program Notes

Clean Probes •* * or before each use

Inspect AC Mains Cable • Mobile Ultrasound

system: Check
Weekly

Inspect Cables and •

Connectors

Clean Console •

Clean LCD •

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Care and Maintenance

Table 10-3: Customer Care Schedule (Continued)

Per
Facilities
Service at Indicated QA
Time Daily Weekly Monthly Program Notes

Console Leakage Current See Notes Twice Annually

Checks

Peripheral Leakage See Notes Twice Annually

Current Checks

Surface Probe Leakage See Notes Twice Annually

Current Checks

Endocavity Probe Leakage See Notes Quarterly Annually

Current Checks

Surgical Probe Leakage See Notes Quarterly Annually

Current Checks

Measurement Accuracy See Notes Twice Annually

Checks

Functional Checks See Notes also after corrective

maintenance

NOTE: The maintenance may require specialized equipment to

complete.
NOTE: The periodic maintenances are not mandatory. The table above
is for reference only.

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 Tools required

Tools required

NOTE: For a list of required tools for servicing the LOGIQ e, refer to
chapter 8.

Standard GE tool kit

The following is a description of the “Standard” GE tool kit in the
USA. Not all tools are required.

Table 10-4: Overview of GE-1 tool kit contents

Tool ID Description Tool ID Description

9-45358 Pliers Retaining Ring 9-XL9971MM Xcelite-hex Blade 1.27mm

9-4078 Scribe 9-XL9972MM Xcelite-hex Blade 1.5mm

9-44572 Wrench Open End 3/8 - 7/16 9-XL9973MM Xcelite-hex Blade 2 mm

9-44579 Wrench Open End 1/2 - 9/16 9-XL9974MM Xcelite-hex Blade 2.5mm

9-44579 Wrench Open End 1/2 - 9/16 9-XL9975MM Xcelite-hex Blade 3mm

9-45385 Pliers, Arc Joint 7 inch 9-XL9976MM Xcelite-hex Blade 4mm

9-45378 Pliers, Slip Joint 9-XL9977MM Xcelite-hex Blade 5mm

9-4518 Pliers, Long Nose, Miniature 9-XL991CM Handle

9-4518 Pliers, Long Nose, Miniature C2356E Screw starter - Kedman

Quick Wedge

9-44776 Ignition Wrench Set, 10 pc. BLBO Box - 18 Compartment

9-44601 Wrench, Adj., 4 inch DWL4283T Box - 5 Compartment

9-4151 Screwdriver, Blade, Stubby 9-41322 Pickup Tool, Claw type

9-41421 Screwdriver, Blade, Pocket 9-6757 6 pc Needle File Set

clip

9-41594 Screwdriver, Blade 1/8 in. × 4 9-9487 Utility Knife

in.

9-41581 Screwdriver, Blade 3/16 in. × 4 9-45341 Pliers Vice Grip 10 inch
in.

9-39451 20' Steel Tape, locking Spring 9-3001 Xacto Pen Knife
load

LOGIQ e – Basic Service Manual 10-17

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Care and Maintenance

Table 10-4: Overview of GE-1 tool kit contents (Continued)

Tool ID Description Tool ID Description

9-GH807 Ratchet, Offset, Slotted 9-HT62002 Solder Aid, Fork and Hook

68-412 Ratchet, Offset, Phillips 9-4099 Mirror, Round, Telescoping

9-GH130 Tapered Reamer 9-GH3001 Steel Rule Decimal 6 inch

9-41584 Screwdriver, slotted 1/4 in. × 6 9-GH300ME Steel Rule Metric 6 inch
in.

9-4118 Screwdriver, Phillips #2, 9-XL9920 Xcelite-hex Blade.050 inch

Stubby

9-41293 Screwdriver, Phillips #0 9-XL9921 Xcelite-hex Blade 1/16 inch

9-41294 Screwdriver, Phillips #1 9-XL9922 Xcelite-hex Blade 5/16 inch

9-41295 Screwdriver, Phillips #2 9-XL9923 Xcelite-hex Blade 3/32 inch

9-46677 Hex Keys, 20 pc., Metric 9-XL9924 Xcelite-hex Blade 1/8 inch

9-34701 1/4 in. Standard Socket set (19 9-XL9925 Xcelite-hex Blade 5/32 inch
pc)

9-43499 1/2 inch Socket 1/4 inch drive 9-XL9926 Xcelite-hex Blade 3/16 inch

9-4355 Flex Spinner 9-XL99764 Xcelite-hex Blade 7/64

9-43523 Breaker 9-XL99964 Xcelite-hex Blade 9/64

9-43531 6 inch Ext. 9-XLM60 Mini-screwdriver kit

9-65283 Case 8.5 in. × 4.5 in. × 2 in. 9-45072 Pliers 6 inch Diagonal
Deep

9-46696 Hex Keys 9-XL100X Wire Stripper/Cutter 5 inch -

100X

9-39829 Torpedo Level, Magnetic 9-XL87CG Pliers - very fine needle

nose-87CG

9-38461 Hammer, Ball Peen, 4 oz. 9-WEWDT-07 Weller-Soldering-Replacem

ent Tip(1)

9-4280 Universal Joint 1/4 inch 9-WS175-E Wiss - Surgical Scissors

9-WEW60P3 Weller - Soldering Iron, 3 wire KH174 Hemostat 5 inch Straight

9-WECT5B6 Weller - Soldering Iron Tip KH175 Hemostat 5 inch curved

9-WEWDP12 Weller - Desoldering Pump 9-Z9480121 Alignment tool (red)

93383 Flashlight Mini-Mag Lite (AAA

Bat.)

9-GH408 Tweezers

21576 Brush - Bristle

10-18 LOGIQ e – Basic Service Manual

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 Tools required

Table 10-4: Overview of GE-1 tool kit contents (Continued)

Tool ID Description Tool ID Description

9-4516 Pliers 4 1/4 inch Diagonal

GE-2 tool kit

Table 10-5: Overview of GE-2 tool kit contents

GE-2 Sears Kit (#99034)

Tool ID Description Tool ID Description

9-45381 Pliers, Arc Joint 9 1/2 inch 9-44067 Socket 1 1/16 in. for 1/2 in.
drive

9-45092 Pliers, Linesman 8 1/2 inch 9-42679 Socket 10MM Hex for 1/2 in.
drive (2273333)

9-42882 Punch, Pin 3/32 inch 9-44262 Extension 10 inch for 1/2 in.
drive (2273405)

9-42884 Punch, Pin 5/32 inch 9-4258 3/8 inch to 1/2 inch Adapter

9-42886 Punch, Pin 1/4 inch 9-34374 3/8 inch Metric Socket Set -
12 PT

9-42973 Cold Chisel 1/2 inch 9-44311 16mm Socket 12 pt.

9-GH77 Center Punch Automatic 9-33485 Metal Socket Tray

9-GH890 File Handle, Adj. 9-33484 Metal Socket Tray

9-31276 File, Round, Bastard 8 inch 9-33484 Metal Socket Tray

9-31277 File, Half Round, Bastard 8 9-52068 Tap and Drill Set
inch

9-31263 File, Flat Mill 8 inch 9-52722 #6 Tap

21045C Close Quarter Saw 9-52723 #8 Tap

9-44604 Wrench, Adj. 10 inch High Speed Drill Set

9-41587 Screwdriver 5/16 inch × 8 inch #36 Drill

9-41586 Screwdriver, Stubby 5/16 inch #29 Drill

9-GH19512 Countersink 1/2 inch 9-44046 3/8 inch Socket Set

9-44741 12 PC Combination Wrench

Set

LOGIQ e – Basic Service Manual 10-19

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Care and Maintenance

Special tools, supplies and equipment used for maintenance

Table 10-6: Overview of tool requirements for periodic maintenance

Tool / kit Comments

Digital Volt Meter (DVM)

Anti Static Kit Kit includes anti–static mat, wrist strap and cables for 200 to 240V
system
3M #2204 Large adjustable wrist strap
3M #2214 Small adjustable wrist strap
3M #3051 conductive ground cord

Anti Static Vacuum Cleaner 120V

230V

Safety Analyzer Electrical leakage testing may be accomplished with any calibrated
Electrical Safety Analyzer tool compliant with AAMI/ESI 1993 or
IEC 60601 or AS/NZS 3551.

QIQ Phantom RMI Grayscale Target Model 403GS

NOTE! The use of a Phantom is not required during Preventive
Maintenance. Customer may use it as part of their Quality
Assurance Program tests.

B/W Printer Cleaning Sheet See printer user manual for requirements

Color Printer Cleaning Sheet See printer user manual for requirements

Disposable Gloves

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 System maintenance

System maintenance

Contents in This Section

• ‘Preliminary checks’ on page 10-21
• ‘Functional checks’ on page 10-23
• ‘System checks’ on page 10-23
• ‘Peripheral/option checks’ on page 10-24
• ‘Mains cable inspection’ on page 10-24
• ‘Cleaning’ on page 10-25
• ‘Physical inspection’ on page 10-25
• ‘Optional Diagnostic Checks’ on page 10-26
• ‘Probe maintenance’ on page 10-27
• ‘Basic probe care’ on page 10-27
• ‘Basic probe cleaning’ on page 10-28
• ‘Battery Performance Maintenance’ on page 10-29

Preliminary checks
The preliminary checks take about 15 minutes to perform. Refer
to the Ultrasound system user documentation whenever
necessary.

Table 10-7: System preliminary checks

Step Item Description

1. Ask and Listen Ask the customer if they have any problems or questions about the
equipment.

2. Paperwork Fill in the top of Ultrasound Inspection Certificate (see Figure 10-15 on
page 10-44). Record all probes and Ultrasound system options.

3. Power up • Turn the Ultrasound system power on and verify that all fans and
peripherals turn on.
• Watch the displays during power up to verify that no warning or error
messages are displayed.
• Where applicable, confirm that the battery is charged. If no AC Input
present, use the internal battery.

4. Probes Verify that the Ultrasound system properly recognizes all probes.

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Care and Maintenance

Table 10-7: System preliminary checks

Step Item Description

5. Displays Verify proper display on the monitor.

6. InSite Where applicable, for Warranty and Contract Customers only:

• Verify that InSite is functioning properly.
• Ensure two-way remote communications.

7. Review Error Logs Where applicable, Error Logs can be reviewed via system diagnostics.

8. Diagnostics Optional.

9. Presets Backup all Customer Presets to an appropriate media.

10. Image Archive Back up the Image Archive onto appropriate media.

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 System maintenance

Functional checks
NOTE: See also Chapter 4
The functional checks take about 60 minutes to perform. Refer
to the Ultrasound system user documentation whenever
necessary.

System checks

Table 10-8: System functional checks

Step Item Description

1. B-Mode Verify basic B-Mode (2D) operation. Check the basic Ultrasound system
controls that affect this mode of operation.

2. CF-Mode Verify basic CF-Mode (Color Flow Mode) operation. Check the basic
Ultrasound system controls that affect this mode of operation.

3. Doppler Modes Verify basic Doppler operation (PW and CW if available). Check the basic
Ultrasound system controls that affect this mode of operation.

4. M-Mode Verify basic M-Mode operation. Check the basic Ultrasound system
controls that affect this mode of operation.

5. Probe Elements Perform an Element Test on each probe to verify that all the probe
elements and system channels are functional.

6. Applicable Verify the basic operation of all optional modes such as Contrast. Check
Software Options the basic Ultrasound system controls that affect each options operation.

7. Xmit/Recv Use the Visual Channel Utility on the loop connect to verify that all system
Elements xmit/recv channels are functional.

8. Operator Panel Perform the Operator Panel Test Procedure.

test

9. Keyboard Do the interactive keyboard test.

10. LCD Verify basic LCD display functions. Refer to Chapter 3 of the User Manual.

11. Software Menu Verify Software Menu display functions. Refer to Chapter 3 of the User
check Manual.

12. Peripherals See: ‘Peripheral Checks’ on page 4-52.

13. Measurements In measurement mode, make distance measurement, get result in result
window. Verify the distance by graduate rule. Distance Accuracy should
be within ±5%. (Name result from result window Result A, result from
graduate rule Result B; Distance Accuracy = (Result B-Result A)/Result A)

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Care and Maintenance

Peripheral/option checks

If any peripherals or options are not part of the system

configuration, the check can be omitted.
Refer to the User Manual for a list of approved peripherals/
options.

Table 10-9: GE approved peripheral/hardware option functional checks

Step Item Description

1. Media Verify media drive(s) read/write properlty. Clean if necessary.

2. B/W Printer Verify hardcopy output of the B/W video page printer. Clean heads and
covers if necessary.

3. Color Printer Verify hardcopy output of the Color video page printer. Clean heads and
covers if necessary.

4. DICOM Verify that DICOM is functioning properly. Send an image to a DICOM

device.

5. ECG Verify basic operation with customer

6. Footswitch Verify that the footswitch is functioning as programed. Clean as necessary.

7. DVD Verify that the DVD is functioning properly. Clean heads and covers if
necessary.

Mains cable inspection

Table 10-10: Mains Cable Inspection, As Appropriate

Step Item Description

1. Unplug Cord Disconnect the mains cable from the wall and Ultrasound system.

2. Inspect Inspect it and its connectors for damage of any kinds.

3. Verify Verify that the LINE, NEUTRAL and GROUND wires are properly attached
to the terminals, and that no strands may cause a short circuit.

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 System maintenance

Cleaning

Table 10-11: General Cleaning

Step Item Description

1. Console Remove the battery. Use a fluid detergent in warm water on a soft, damp
cloth to carefully wipe the entire system. Be careful not to get the cloth too
wet so that moisture does not enter the console.

2. Probe Holder Clean probe holders. (they may need to be soaked to remove excess gel).

3. LCD Use a soft, non-abrasive folder cloth. Gently wipe the LCD face. DO NOT
use a glass cleaner that has a hydrocarbon base (such as Benzene,
Methy Alcohol or Methy Ethyl Ketone) on LCD with the filter (anti-glare
shield).

Physical inspection
NOTE: These features may not be present on all Ultrasound systems.

Table 10-12: Physical checks

Step Item Description

1. Labeling Verify that all Ultrasound system labeling is present and in readable
condition.

2. Scratches & Dents Inspect the exterior for dents, scratches or cracks.

3. Input Power Refer to: ‘Mains cable inspection’ on page 10-24.

4. Cables & Check all internal cable harnesses and connectors for wear and secure
Connectors connector seating. Pay special attention to footswitch assembly and probe
strain or bend reliefs.

5. Shielding & Check to ensure that all EMI shielding, internal covers, air flow panels and
Covers screws are in place. Missing covers and hardware could cause EMI/RFI
problems while scanning.

6. Control Panel Inspect keyboard and control panel. Note any damaged or missing items.

7. Control Panel Check for proper operation of all operator panel and Freeze Key light.
Lighting

8. LCD Inspect the LCD Display for scratches and bad pixels.
Verify proper operation of Contrast and Brightness controls.
Where applicable, confirm that the LCD arm allows:
• swivelling the screen to the left and to the right
• folding the screen to the locked position
• release and adjustment backwards and forwards
• can be adjusted in the up/down positions.
Note: LCD Arm movement may vary and is not applicable to all Ultrasound
systems.

9. External I/O Check all connectors for damage.

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Care and Maintenance

Table 10-12: Physical checks (Continued)

Step Item Description

10. Power and Check for proper operation of all Power and System Status Indicators.
System Status
Indicators

11. Battery Where applicable, check that the battery is not damaged, does not leak,
does not emit an odor, and is not deformed or discolored. Observe all
warnings and cautions for battery handling, recharging, storing, and/or
disposal,

Optional Diagnostic Checks

Optionally you can access the diagnostic software as described
in Chapter 5 or 7. View the error logs and run desired
diagnostics.

View the Log

1. Review the system error log for any problems.

2. Check the temperature log to see if there are any trends that
could cause problems in the future.
3. Check the Configuration Log; update if needed.

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 System maintenance

Probe maintenance

Probe related checks

Table 10-13: System preliminary checks

Step Item Description

1. Probe Holder Clean probe holders. (they may need to be soaked to remove excess gel).

2. Probes Thoroughly check the Ultrasound system probe connectors and remove
dust from inside the connector sockets if necessary. Visually check for
bent, damaged or missing pins.

3. Probes Verify that the Ultrasound system properly recognizes all probes.

Basic probe care

The Ultrasound system user manuals and various probe

handling cards provide a complete description of probe care,
maintenance, cleaning and disinfection. Ensure that you are
completely familiar with the proper care of GE probes.
Ultrasound probes can be easily damaged by improper
handling. See the User Manual and probe care cards for more
details. Failure to follow these precautions can result in serious
injury and equipment damage. Failure to properly handle or
maintain a probe may also void its warranty.
Any evidence of wear indicates the probe cannot be used.
Do a visual check of the probe pins and Ultrasound system
sockets before plugging in a probe.
The Interoperative probes often have special considerations and
individual probe user manuals. For Interoperative probes also
refer to their separate user manuals.

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Care and Maintenance

Basic probe cleaning

Refer to the User’s Manual for details on probe cleaning.

WARNING To help protect yourself from blood borne diseases, wear

approved disposable gloves. These are made of nitrile derived
from vegetable starch to prevent allergic latex reactions.

CAUTION Failure to follow the prescribed cleaning or disinfection

procedures will void the probe’s warranty.
DO NOT soak or wipe the lens with any product not listed in the
User Manual. Doing so could result in irreparable damage to
the probe.
Follow care instructions that came with the probe.

CAUTION Disinfect a defective probe before you return it. Be sure to tag
the probe as being disinfected.

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 System maintenance

Battery Performance Maintenance

Battery replacement every three years is recommended.
It is recommended to do battery performance maintenance one
time per year.
Please follow the flow chart below to carry out battery
performance maintenance.

Battery discharge

No
>45 minutes?

Yes

Battery charge > 3 hour Battery charge > 3 hour

No No
Battery power > 90%? Battery power > 90%?

Yes Yes

Replace battery Battery is Ok Discharge Replace battery

No
>45 minutes?

Yes

Battery is Ok Replace battery

Figure 10-10. Flow chart of Battery Performance Maintenance

NOTE: Disconnect all probes when discharge battery.

NOTE: Discharge the battery to let the system automatically shut down.

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Care and Maintenance

Electrical safety tests

Contents in This Section

• ‘Safety test overview’ on page 10-30
• ‘Leakage current limits’ on page 10-33
• ‘Outlet test - wiring arrangement’ on page 10-35
• ‘Grounding continuity’ on page 10-36
• ‘Chassis leakage current test’ on page 10-37
• ‘Data Sheet for enclosure Source Leakage Current’ on
page 10-38
• ‘Probe leakage current test’ on page 10-39
• ‘Definition’ on page 10-39
• ‘Tools’ on page 10-39
• ‘Generic procedure on probe leakage current’ on
page 10-40
• ‘Meter Procedure Using Probe Adapter’ on page 10-40
• ‘No Meter Procedure Using Probe Adapter’ on page 10-40
• ‘Data Sheet for Transducer Source Leakage Current’ on
page 10-41

Safety test overview

The electrical safety tests in this section are based on and
conform to IEC 60601-1 Medical Equipment Safety Standards.
They are intended for the electrical safety evaluation of
cord-connected, electrically operated, patient care equipment. If
additional information is needed, refer to the IEC 60601-1
documents

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 Electrical safety tests

WARNING THE USER MUST ENSURE THAT THE SAFETY

INSPECTIONS ARE PERFORMED AT LEAST EVERY 6
MONTHS ACCORDING TO THE REQUIREMENTS OF
THE PATIENT SAFETY STANDARD IEC-EN 60601-1.
ONLY TRAINED PERSONS ARE ALLOWED TO
PERFORM THE SAFETY INSPECTIONS MENTIONED
ABOVE.

DANGER TO MINIMIZE RISK OF ELECTRICAL SHOCK, ONLY

TRAINED PERSONS ARE ALLOWED TO PERFORM THE
ELECTRICAL SAFETY INSPECTIONS AND TESTS.

DANGER TO AVOID ELECTRICAL SHOCK, THE ULTRASOUND

SYSTEM UNDER TEST MUST NOT BE CONNECTED TO
OTHER ELECTRICAL EQUIPMENT. REMOVE ALL
INTERCONNECTING CABLES AND WIRES. THE
ULTRASOUND SYSTEM UNDER TEST MUST NOT BE
CONTACTED BY USERS OR PATIENTS WHILE
PERFORMING THESE TESTS.

CAUTION Possible risk of infection. Do not handle soiled or contaminated

probes and other components that have been in patient
contact. Follow appropriate cleaning and disinfecting
procedures before handling the equipment.

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Care and Maintenance

Safety test overview (continued)

Prior to initiating any electrical test, the Ultrasound system must
be visually inspected. Perform the following visual checks:
• Check for missing or loose enclosure covers that could
allow access to internal live parts.
• Examine the mains cord, mains plug and appliance inlet for
damaged insulation and adequacy of strain relief and cable
clamps.
• Locate and examine all associated transducers. Inspect the
cables and strain relief at each end. Inspect the transducer
enclosure and lens for cracks, holes and similar defects.
Test the system, peripherals and probes for leakage current.
Excessive leakage current can cause injury or death in sensitive
patients. High leakage current can also indicate degradation of
insulation and a potential for electrical failure. Do not use probes
or equipment having excessive leakage current.
To minimize the risk that a probe may shock someone the
customer should:
• Not use a probe that is cracked or damaged in any way.
• Check probe leakage current:
• Based on your facilities QA program for surface probes.
• Based on your facilities QA program for endocavitary
probes.
• whenever probe damage is suspected.

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 Electrical safety tests

Leakage current limits

WARNING Energy Control and Power Lockout for LOGIQ e.

When servicing parts of the Ultrasound system where there is
exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as
there are no test points to verify isolation.
6. Remove/disconnect the battery, if present.
Ultrasound System components may be energized.

CAUTION Compare all safety-test results with safety-test results of

previously performed safety tests (e.g. last year etc). In case of
unexplainable abrupt changes of safety-test results consult
experienced authorized service personnel or GE for further
analysis.

The following limits are summarized for IEC 60601-1 Medical

Equipment Safety Standards. These limits are GEMS standards
and in some cases are lower than the above standards listed.

Table 10-14: Chassis Leakage Current Limits - Accessible Metal Surface

Normal Reverse
Country Condition Open Ground Polarity Open Neutral

All (Except USA & 0.1 mA 0.5 mA 0.5 mA 0.5 mA

Canada)

USA & Canada 0.1 mA 0.3 mA 0.3 mA 0.3 mA

Table 10-15: Type BF Applied Part Leakage Current Limits - Probes Surface

Normal Open Reverse Open *Mains

Country Condition Ground Polarity Neutral Applied

All 0.1 mA 0.5 mA 0.5 mA 0.5 mA 5.0 mA

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Care and Maintenance

Leakage current limits (continued)

Table 10-16: Type CF Applied Part Leakage Current Limits - ECG Connections

Normal Open Reverse Open *Mains

Country Condition Ground Polarity Neutral Applied

All 0.1 mA 0.5 mA 0.5 mA 0.5 mA 5.0 mA

NOTE: *Mains Applied refers to the sink leakage test where mains
(supply) voltage is applied to the part to determine the amount of
current that will pass (or sink) to ground if a patient contacted
mains voltage.
The following tests are performed at the factory and should be
performed at the site. These tests are: chassis leakage current,
and probe leakage current. All measurements are made with an
electrical safety analyzer which should be calibrated and
compliant with AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551.

Table 10-17: Equipment Type and Test Definitions

Applied Parts or accessories that contact the patient to

Parts perform their function. For ultrasound equipment,
(AP) this includes transducers and ECG leads.

Type BF Body Floating or

non-conductive ultrasound
probes which are marked
with the 'man in box' BF
symbol. this includes all
transducers.

Type CF Cardiac Floating or

non-conductive
intraoperative probes for
direct cardiac contact and
isolated ECG connections
so marked with the 'heart in
box' CF symbol.

Sink The current resulting from the application of mains

Leakage voltage to the applied part. This test is required
test for Type CF applied parts.

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 Electrical safety tests

Outlet test - wiring arrangement

Test all outlets in the area for proper grounding and wiring
arrangement by plugging in the neon outlet tester and noting the
combination of lights that are illuminated. Any problems found
should be reported to the hospital immediately and the
receptacle should not be used.

CORRECT WIRING OPEN GROUND WIRE

REVERSED POLARITY OPEN NEUTRAL WIRE

HOT AND GROUND OPEN HOT WIRE

REVERSED

Figure 10-11. Typical alternate outlet tester

NOTE: No outlet tester can detect the condition where the Neutral
(grounded supply) conductor and the Grounding (protective
earth) conductor are reversed. If later tests indicate high leakage
currents, this should be suspected as a possible cause and the
outlet wiring should be visually inspected.

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Care and Maintenance

Grounding continuity

DANGER ELECTRIC SHOCK HAZARD. THE PATIENT MUST NOT BE

CONTACTED TO THE EQUIPMENT DURING THIS TEST.

Measure the resistance from the third pin of the attachment plug
to the exposed metal parts of the case. The ground wire
resistance should be less than 0.2 ohms. Reference the
procedure in the IEC60601-1.

1. GROUND PIN
2. OHMMETER
3. LOGIQ e
4. ACCESSIBLE METAL PART:
• MONITOR HOUSING
• PEAR PANEL CONNECTOR
• ANY CASTER/WHEEL SUPPORT

Figure 10-12. Ground continuity test

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 Electrical safety tests

Chassis leakage current test

DANGER ELECTRIC SHOCK HAZARD. WHEN THE METER'S

GROUND SWITCH IS OPEN, DON'T TOUCH THE
ULTRASOUND SYSTEM!.

CAUTION Equipment damage possibility. Never switch the Polarity and

the status of Neutral when the Ultrasound system is powered
ON. Be sure to turn the Ultrasound system power OFF before
switching them using the POLARITY switch and/or the
NEUTRAL switch. Otherwise, the Ultrasound system may be
damaged.

Generic procedure

The test verifies the isolation of the power line from the chassis.
The testing meter is connected from accessible metal parts of
the case to ground. Measurements should be made with the unit
ON and OFF, with the power line polarity Normal and Reversed.
Record the highest reading of current.

Figure 10-13. Set Up for Chassis Source Leakage Current, IEC 601-1 Clause 19 -
Continuos Leakage Currents and Patient, Auxiliary Currents

When using the Microguard or a similar test instrument, its

power plug may be inserted into the wall outlet and the
equipment under test is plugged into the receptacle on the panel
of the meter. This places the meter in the grounding conductor
and the current flowing from the case to ground will be indicated
in any of the current ranges. The maximum allowable limit for
chassis source leakage is shown in Table 10-14 on page 10-33.

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Care and Maintenance

Data Sheet for enclosure Source Leakage Current

The test passes when all readings measure less than the value
shown in Table 10-14 on page 10-33. Record all data on the PM
Inspection Certificate.

Table 10-18: Typical Data Sheet for enclosure Source Leakage Current

Tester
Neutral
Tester or Test 1 Test 2 Real
Unit Polarity Ground Speaker Panel Metal Optional Optional
Power Switch Switch Cover Parts Test 3 Test 4

Enter Name of tested peripheral here:

ON NORM OPEN

ON NORM CLOSED

ON REV OPEN

ON REV CLOSED

OFF NORM OPEN

OFF NORM CLOSED

OFF REV OPEN

OFF REV CLOSED

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 Electrical safety tests

Probe leakage current test

DANGER DO NOT USE THE PROBE IF THE INSULATING MATERIAL

HAS BEEN PUNCTURED OR OTHERWISE COMPROMISED.
INTEGRITY OF THE INSULATION MATERIAL AND PATIENT
SAFETY CAN BE VERIFIED BY SAFETY TESTING
ACCORDING TO IEC60601-1.

CAUTION Equipment damage possibility. Never switch the Polarity and

the status of Neutral when the Ultrasound system is powered
ON. Be sure to turn the Ultrasound system power OFF before
switching them using the POLARITY switch and/or the
NEUTRAL switch. Otherwise, the Ultrasound system may be
damaged.

Definition

This test measures the current that would flow to ground from
any of the probes through a patient who is being scanned and
becomes grounded by touching some other grounded surface.
NOTE: Some leakage current is expected on each probe, depending on
its design. Small variations in probe leakage currents are normal
from probe to probe. Other variations will result from differences
in line voltage and test lead placement. It is abnormal if no
leakage current is measured. If no leakage current is detected,
check the configuration of the test equipment.

Tools

For needed tools, see: ‘Tools required’ on page 10-17.

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Care and Maintenance

Generic procedure on probe leakage current

Measurements should be made with the ground open and

closed, with power line polarity normal and reversed, and with
the unit Off and On. For each combination, the probe must be
active to find the worst case condition.

POLARITY REVERSING SWITCH

H (BLACK) PROBE

CONSOLE
POWER N (WHITE)
OUTLET

G (GREEN)

MOMENTARY
SWITCH LEAKAGE TEST
METER

Figure 10-14. Set up for probe leakage current

NOTE: Each probe will have some amount of leakage current,

dependent on its design. Small variations in probe leakage
currents are normal from probe to probe. Other variations will
result from differences in line voltage and test lead placement.

DANGER TO AVOID PROBE DAMAGE AND POSSIBLE ELECTRIC

SHOCK, DO NOT IMMERSE PROBES INTO ANY LIQUID
BEYOND THE LEVEL INDICATED IN THE PROBE USERS
MANUAL. DO NOT TOUCH THE PROBE, CONDUCTIVE
LIQUID OR ANY PART OF THE UNIT UNDER TEST WHILE
DOING THE TEST.

Meter Procedure Using Probe Adapter

Follow the Safety Analyzer tool instruction to test each

transducer for leakage current.
The electrical Safety Analyzer tool should be calibrated and
compliant with AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551.

No Meter Procedure Using Probe Adapter

Follow the Safety Analyzer tool instruction to test each

transducer for leakage current.
The electrical Safety Analyzer tool should be calibrated and
compliant with AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551.

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 Electrical safety tests

Data Sheet for Transducer Source Leakage Current

The test passes when all readings measure less than the values
shown in Table 10-15 on page 10-33. Record all data on the PM
Inspection Certificate.

Table 10-19: Typical Data Sheet For Transducer Source Leakage Current

Transducer Tested:

Tester Power Polarity Tester GROUND or

Unit Power Switch NUETRAL Switch Measurement

ON NORM OPEN

ON NORM CLOSED

ON REV OPEN

ON REV CLOSED

OFF NORM OPEN

OFF NORM CLOSED

OFF REV OPEN

OFF REV CLOSED

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Care and Maintenance

When there's too much leakage

current …

AC/DC Fails
Where applicable, check the AC/DC adapter and its cable.
Replace a new one if any portion is defective.

Chassis Fails
Check the ground on the power cord and plug for continuity.
Ensure the ground is not broken, frayed, or intermittent. Replace
any defective part.
Where applicable, tighten all grounds. Ensure star washers are
under all ground studs.
Inspect wiring for bad crimps, poor connections, or damage.
Test the wall outlet; verify it is grounded and is free of other
wiring abnormalities. Notify the user or owner to correct any
deviations. As a work around, check the other outlets to see if
they could be used instead.
NOTE: No outlet tester can detect the condition where the white neutral
wire and the green grounding wire are reversed. If later tests
indicate high leakage currents, this should be suspected as a
possible cause and the outlet wiring should be visually
inspected.

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 When there's too much leakage current …

Probe Fails
Test the probe in another connector to isolate if the fault lies with
the probe or the Ultrasound system. Or Change another probe
to confirm if the fail is caused by console.
NOTE: Each probe will have some amount of leakage, dependent on its
design. Small variations in probe leakage currents are normal
from probe to probe. Other variations will result from differences
in line voltage and test lead placement. The maximum allowable
leakage current for body surface contact probe differs from
inter-cavity probe. Be sure to enter the correct probe type in the
appropriate space on the check list.
If excessive leakage current is slot dependent, inspect the
system connector for bent pins, poor connections, and ground
continuity.
If the problem remains with the probe, replace the probe.

Peripheral Fails
Tighten all grounds. Ensure star washers are under all ground
studs.
Inspect wiring for bad crimps, poor connections, or damage.

Still Fails
If all else fails, begin isolation by removing the probes, external
peripherals, then the on board ones, one at a time while
monitoring the leakage current measurement.

New Unit
If the leakage current measurement tests fail on a new
Ultrasound system and if situation can not be corrected, submit
a Safety Failure Report to document the Ultrasound system
problem. Remove Ultrasound system from operation.

ECG Fails
Inspect cables for damage or poor connections.

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Care and Maintenance

Inspection Paperwork

Ultrasound Inspection Forms

ULTRASOUND INSPECTION CERTIFICATE

C us tome r N a me : S y s te m I D : D is pa tc h N umbe r / Date Performed: Warranty/C ontract/HBS

System Type M ode l N umbe r: S e ria l N umbe r: M a nufa c ture D a te :

P robe 1 : F r e q u e nc y : S c a n F orma t*: M ode l N umbe r: S e ria l N umbe r:

P robe 2 : F r e q u e nc y : S c a n F orma t*: M ode l N umbe r: S e ria l N umbe r:

P robe 3 : F r e q u e nc y : S c a n F orma t*: M ode l N umbe r: S e ria l N umbe r:

P robe 4 : F r e q u e nc y : S c a n F orma t*: M ode l N umbe r: S e ria l N umbe r:

P robe 5 : F r e q u e nc y : S c a n F orma t*: M ode l N umbe r: S e ria l N umbe r:

* Scan Format: Phased Array, Linear Array, Curved Array, Mechanical Array or Other

Figure 10-15. Ultrasound Inspection Certificate

* Scan Format: Phased Array, Linear Array, Curved Array,

Mechanical Array or Other

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 Inspection Paperwork

Ultrasound Inspection Forms (continued)

FUNCTIONAL CHECKS PHYSICAL INSPECTION AND CLEANING

OK? or Physical Inspection and Cleaning
Functional Check (if applicable) N/A (if applicable) Inspect Clean

B -Mode F unc tion C ons ole

D opple r Mode s F unc tion LC D

C F -Mode F unc tion E x te rna l I /O

M-Mode F unc tion C a ble s a nd C onne c tors

Applicable Software Opti ons G E A pprove d P e riphe ra ls (DVD-RW, Printer)

A pplic a ble H a rdwa re O ptions L a be ling (see User Manual for Labeling)

Control Panel

LCD

Measurement Accuracy

GE Approved Peripherals

COMMENTS:
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________

Figure 10-16. Functional Checks

ELECTRICAL SAFETY
Max Value Value
Electrical Test Performed Allowed Measured OK? Comments

Outlet (correct ground &wiring config.)

Type BF Applied Part Leakage Current

Limits- Probe

enclosure Source Leakage Current -

Chassis Leakage Current Limits

Peripheral 1 Leakage Current

Peripheral 2 Leakage Current

PROBES

Probe Number Max Value Max Value

(from previous page) Allowed Measured OK? Comments

Probe 1:

Probe 2:

Probe 3:

Final Check. All system covers are in place. System scans with all probes as expected.

Accepted by: ______________________________________________________________________

Figure 10-17. Electrical Safety

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Care and Maintenance

Electrical Safety Tests Log

Table 10-20: Electrical safety tests log

Electrical test Max Value OK? Comments

performed value measured
allowed

Outlet (correct ground

and wiring config.)

System ground
continuity

Chassis source
leakage current -
probe

Chassis source
leakage current -
wheel

Chassis source
leakage current -
monitor

Patient lead source

leakage (lead to
ground)

Patient lead source

leakage (lead to lead)

Patient lead source

leakage (isolation)

Peripheral 1 leakage
current

Peripheral 1 ground
continuity

Peripheral 2 leakage
current

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 Electrical Safety Tests Log

Table 10-20: Electrical safety tests log (Continued)

Electrical test Max Value OK? Comments

performed value measured
allowed

Peripheral 2 ground
continuity

Peripheral 3 leakage
current

Peripheral 3 ground
continuity

Table 10-21: Electrical safety tests (probes) log

Max Max value OK? Comments

value measured
Probe allowed

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Care and Maintenance

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 Chapter 11

Docking Cart Setup

This chapter describe the docking cart and give

information on how to set up and use it, the concepts,
functional test, troubleshooting of the docking cart.

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Docking Cart Setup

Overview

Contents in this chapter

• ‘Overview’ on page 11-2
• ‘Set Up Docking Cart’ on page 11-4
• ‘Cart Using’ on page 11-39
• ‘Docking Cart Functions (Theory)’ on page 11-43
• ‘Diagnostics/Troubleshooting’ on page 11-45

Introduction

This chapter contains this information:

•
• How to setup Docking Cart. Included are references to a
procedure that describes how to receive and unpack the
equipment and how to file a damage or loss claim.
How to prepare the facility and unit of the actual setup, and
how to check and test the unit and external peripherals for
electrical safety are included in this procedure. Also
included in this section are guidelines for transporting the
unit to a new site.
• The procedures for mounting the system to LOGIQ e and
releasing the system from Docking Cart.
• Explain the Docking Cart’s concepts, component
arrangement, and subsystem function.
• Describes how to test and adjust the functions. These tests
are optional. You may use them to check the system for
errors.
• Describes how to setup and run the tools that help Docking
Cart operation. Cart and board level diagnostics are run
whenever power is applied. Some Service Tools may be run
at the application level.

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 Overview

Safety Consideration

NOTE: Please refer to Chapter 1 and Chapter 2 for the safety

information and site requirement for the Docking Cart. Chapter 1
and Chapter 2 should be read before conducting any installation
work on Docking Cart.

CAUTION The Docking Cart weighs 59 kg (130.1 lb.) or more, depending

on installed peripherals, when ready for use. Care must be
used when moving it or replacing its parts.
Failure to follow the precautions listed below could result in
injury, uncontrolled motion and costly damage.
ALWAYS:
• be sure the pathway is clear
• use slow, careful motions
• Limit movement to a slow careful walk.
• use two people when moving on inclines or lifting more
than 16 kg (35 lbs)

WARNING When the docking cart is raised for a repair or moved along any
incline, use external caution since it may become unstable and
tip over.

CAUTION Do not move Docking Cart with big incline angle.

Do

CAUTION The Docking Cart is not water proof. Do not expose the
Docking Cart to water or any kind of liquid.
Never set liquids on the Docking Cart to ensure that liquid does
not drip into the unit.

CAUTION Put peripherals in correct position to avoid Docking Cart

overload.

NOTE: Special care should be taken when transporting the Docking

Cart in a vehicle.

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Docking Cart Setup

Set Up Docking Cart

Contents in This Section

• ‘Setup Reminders’ on page 11-5
• ‘Average Setup Time’ on page 11-5
• ‘Setup Warnings’ on page 11-5
• ‘Safety Reminders’ on page 11-7
• ‘Receiving and Unpacking the Equipment’ on page 11-8
• ‘Unpacking Docking Cart’ on page 11-8
• ‘Moving into Position’ on page 11-11
• ‘Product Locator Installation Card’ on page 11-11
• ‘Preparing for Installation’ on page 11-12
• ‘Verify Customer Order’ on page 11-12
• ‘Electrical Specifications’ on page 11-12
• ‘EMI Protection’ on page 11-12
• ‘Physical Dimension and Weight’ on page 11-13
• ‘Peripheral Installation’ on page 11-14
• ‘On-Board Optional Peripherals’ on page 11-14
• ‘Connect USB Printer to Docking Cart’ on page 11-14
• ‘Connect DVD-RW to Docking Cart’ on page 11-19
• ‘Connect ECG to Docking Cart’ on page 11-22
• ‘Options Installation’ on page 11-24
• ‘Install Extended Life Battery to Docking Cart’ on page 11-24
• ‘Install 3-Probe Port to Docking Cart’ on page 11-28
• ‘Install Color Printer Shelf to Docking Cart’ on page 11-32
• ‘Top Support DVD/Print Shelf Assy’ on page 11-34
• ‘Paperwork’ on page 11-38
• ‘Product Locator Installation’ on page 11-38
• ‘User Manual’ on page 11-38

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Setup Reminders

Average Setup Time

Table 11-1: Average Installation Time

Description Average Setup Time Comments

Unpacking the cart 0.5 hour

Cart options 0.5 hour Dependant on the configuration that

is required

The Docking Cart has been designed to be setup and checked

out by an experienced service technician in approximately four
hours. Docking Cart consoles with optional equipment may take
slightly longer.

Setup Warnings

• Since the Docking Cart weighs approximately 53 kg.(116 lb)

without options, preferably two people should unpack it.
Two people are also preferable for setting up any additional
bulky items.
• There are no operator serviceable components. To prevent
shock, do not remove any covers or panels. Should
problems or malfunctions occur, unplug the power cord.
Only qualified service personnel should carry out servicing
and troubleshooting.
NOTE: For information regarding packing labels, refer to LABELS
ON PACKAGE.

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Setup Warnings (continued)

• After being transported, the unit may be very cold or hot. If

this is the case, allow the unit to acclimate before you turn it
on. It requires one hour for each 2.5°C increment it's
temperature is below 10°C or above 30°C.

CAUTION Equipment damage possibility. Turning the system on without

acclimation after arriving at site may cause the system to be
damaged.

Table 11-2: Acclimation Time

°C 60 55 50 45 40 35 30 25 20 15 10

°F 140 131 122 113 104 95 86 77 68 59 50

hrs 8 6 4 2 0 0 0 0 0 0 0

°C 5 0 -5 -10 -15 -20 -25 -30 -35 -40

°F 41 32 23 14 5 -4 -13 -22 -31 -40

hrs 2 4 6 8 10 12 14 16 18 20

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 Set Up Docking Cart

Safety Reminders

DANGER WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE

OF OPENING THE AC GROUND LINE (I.E., METER’S
GROUND SWITCH IS OPEN), DON’T TOUCH THE UNIT!

CAUTION Two people should unpack the unit because of its weight. Two
people are required whenever a part weighing 19kg (42 lb.) or
more must be lifted.

CAUTION If the unit is very cold or hot, do not turn on its power until it has
had a chance to acclimate to its operating environment.

CAUTION To prevent electrical shock, connect the unit to a properly

grounded power outlet. Do not use a three to two prong
adapter. This defeats safety grounding.

CAUTION Do not use a 20 Amp to 15 Amp adapter on the 120 Vac unit’s
power cord. This unit requires a dedicated 20 A circuit and can
have a 15A plug if the on board peripherals do not cause the
unit to draw more than 14.0 amps.

CAUTION Do not operate this unit unless all board covers and frame
panels are securely in place. System performance and cooling
require this.

CAUTION OPERATOR MANUAL(S)

The User Manual(s) should be fully read and understood
before operating the Docking Cart and kept near the unit for
quick reference.

Figure 11-1. Environmental Labels

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Docking Cart Setup

Receiving and Unpacking the Equipment

When a new Docking Cart arrives, check that any components
are not damaged and are not in short supply. If shipping
damage or shortage occurs, contact the address shown in
Chapter 1.

CAUTION The crate with the Docking Cart weighs approximately 59 kg.
Be prepared for a sudden shift of weight as the unit is removed
from its base (pallet).

Unpacking Docking Cart

Table 11-3: Procedure to take out Docking Cart

No. Steps Corresponding Graphic

1. Cut off the two packing strap

(1-2) and remove them.
Then remove the two
reinforce cardboards and
remove the top cover.

2. Rotate the knob

counterclockwise until it is
loose and remove it.

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Table 11-3: Procedure to take out Docking Cart

No. Steps Corresponding Graphic

3. Remove the ring from the

carton.

4. Open the carton and remove

it.
Remove the PE bag from the
top.

5. Remove the top foam.

Remove the plastic film and
the bottom foam from the
Docking Cart.

6. Cut off the reinforce strap and

remove the pads on the four
castors.
Two people lift up the docking
cart and move it off the
platform.

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Unpacking Docking Cart (continued)

Figure 11-2. Remove Foam

1. Lateral
2. Bottom Foam
3. Platform
4. Top cover

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 Set Up Docking Cart

Moving into Position

CAUTION Do not tilt the unit more than 5 degrees to avoid tipping it over.

In general, a single adult can move the LOGIQ e along an even

surface with no steep grades. At least two people should move
the machine when large humps, grooves, or grades will be
encountered. (It is better to pull from the rear rather than push
from the front of the unit). Before moving, store all loose parts in
the unit. Wrap transducers in soft cloth or foam to prevent
damage.
LOGIQ e is a compact and mobile machine, two people should
move it over rough surfaces or up and down grades.

Product Locator Installation Card

NOTE: The Product Locator Installation Card shown in this manual may
not be same as the provided Product Locator card.

Figure 11-3. Product Locator Installation Card

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Preparing for Installation

Verify Customer Order

Compare items received by the customer to that which is listed

on the delivery order. Report any items that are missing, back
ordered or damaged.

Electrical Specifications

Verify that Docking Cart is set to the correct voltage.

The Voltage settings for the Docking Cart is found on a label to
the left of the Power switch and External I/O, on the rear of the
system.

CAUTION Connecting a Docking Cart to the wrong voltage level will most
likely destroy it.

Table 11-4: Electrical requirements for Docking Cart

PARAMETER AREA LIMITS

Voltage Range 100-240V~ 350VA

Power All applications More than or equal to 750 VA

Line Frequency All applications 50/60Hz (±2Hz)

Power Transients All applications Less than 25% of nominal peak voltage for less
than 1 millisecond for any type of transient,
including line frequency, synchronous,
asynchronous, or aperiodic transients.

Decaying Oscillation All applications Less than 15% of peak voltage for less than 1
millisecond.

EMI Protection

This Unit has been designed to minimize the effects of Electro

Magnetic Interference (EMI). Many of the covers, shields, and
screws are provided primarily to protect the system from image
artifacts caused by this interference. For this reason, it is
imperative that all covers and hardware are installed and
secured before the unit is put into operation.

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 Set Up Docking Cart

Physical Dimension and Weight

The physical dimension of the Docking Cart is summarized in

Table 11-5 on page 11-13 including the size of Docking Cart, 3
probe ports and speakers.

Table 11-5: Physical Dimensions of Docking Cart

Height Width Depth Unit

Tall 950 470 617 mm

Tall 31.2 15.4 240.2 inch

Short 810 470 617 mm

Short 37 15.4 240.2 inch

The weight of Docking Cart is 59 kg (130.1 lbs) with 3 probe

ports.

Figure 11-4. Overall Dimensions

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Docking Cart Setup

Peripheral Installation

On-Board Optional Peripherals

Table 11-6: Peripherals Validate for Docking Cart

Device Manufacturer Model Interface Video Signal

B/W Printer SONY UP-D897MD USB Interface N/A (* USB

Interface)

SONY UP-D898MD USB Interface N/A (* USB

Interface)

Color Printer SONY UP-D25MD USB Interface N/A (* USB

Interface)

DVD-RW LITEON LITEON eUAU108 USB Interface N/A (* USB

Interface)

ECG NORAV GE ECGUSB1D-EX USB Interface N/A (* USB

Interface)

See each option setup instructions for installation and

connection procedures.

Connect USB Printer to Docking Cart

Tools
• Common Allen Screwdriver
• common Phillips screwdriver

Needed Manpower
• 1 person, 8 minutes+travel

Preparations
• Shut down the system and switch off the main breaker

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 Set Up Docking Cart

Connect USB Printer to Docking Cart (continued)

Mounting Procedure

Table 11-7: Mounting Procedure of B/W USB Printer

No. Step Corresponding Graphic

1. Remove the rear panel from

Docking Cart.
Place the DC/AC adapter in the
cabinet of Docking Cart. Let the
cable of DC/AC adapter come out
from the back of Docking Cart.
Note: The printer DC/AC adapter
is optional. It is ordered separately.

2. Connect the power cable from the

Docking Cart to the DC/AC
adapter.

Note: When connecting the power

cable to DC/AC adapter, align the
embossing on the power cable
connector with the groove on the
DC/AC adapter connector port
edge. Then push the cable
connector into the port.

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Table 11-7: Mounting Procedure of B/W USB Printer

No. Step Corresponding Graphic

3. Connect the DC/AC cable to the

printer (3). Connect USB cable to
the printer (1) and to the USB HUB
(2). Then install the rear panel of
Docking Cart.

Table 11-8: Mounting Procedure of B/W USB Printer on Top Support DVD/Print Shelf

No. Step Corresponding Graphic

1. Be sure Top DVD/Print Shelf has

been installed.
See ‘Top Support DVD/Print Shelf
Assy’ on page 11-34 for more
information.

2. Place the DC/AC adapter in the

cabinet of Docking Cart. Let the
cable of DC/AC adapter come out
from the back of Docking Cart.
Refer to Table 11-7 on page 11-15
for this information.

Connect the power cable from the

Docking Cart to the DC/AC
adapter. Refer to Table 11-7 on
page 11-15 for the information

3. Connect USB Cable and Power

Cable of DC/AC adapter to the
printer and let the cables go down
through Monitor Support Space.

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Table 11-8: Mounting Procedure of B/W USB Printer on Top Support DVD/Print Shelf

No. Step Corresponding Graphic

4. Connect the USB Cable to the

USB HUB.

5. Connect the power cable from the

Docking Cart to the DC/AC
adapter. See Table 11-7 on
page 11-15 for more information.

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Docking Cart Setup

Removal Procedure
Remove the new parts in the reverse order of installation.
NOTE: When disconnecting the power cable from the DC/AC adapter,
grab the handle of the cable with fingers and pull the cable.

Figure 11-5. Disconnect Power Cable

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 Set Up Docking Cart

Connect DVD-RW to Docking Cart

Tools
• NA

Needed Manpower
• 1 person, 3 minutes+travel

Preparations
• Shut down the system and switch off the main breaker.

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Docking Cart Setup

Connect DVD-RW to Docking Cart (continued)

Mounting Procedure

Table 11-9: Mounting Procedure of DVD-RW

No. Step Corresponding Graphic

1. Connect the USB Y Cable to the DVD-RW.

2. Unscrew the 4 screws to remove the real panel.

3. Place the DVD-RW on the DVD-RW shelf and

let the USB Y cable come out from the back of
the docking cart.

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 Set Up Docking Cart

Table 11-9: Mounting Procedure of DVD-RW

No. Step Corresponding Graphic

4. Connect the two USB Connectors on the USB Y

cable to the USB ports on the docking cart.
Note: Be sure the two connectors on the USB Y
cable are connected to the USB ports on the
Docking Cart at the same time.

5. Mount the rear panel to the docking cart and

tighten the 4 screws.

Table 11-10: Mounting Procedure of DVD-RW to Top support DVD/print shelf

No. Step Corresponding Graphic

1. Be sure Top DVD/Print Shelf has been

installed.
See ‘Top Support DVD/Print Shelf Assy’ on
page 11-34 for more information.

2. Place the DVD-RW on the TOP DVD Shelf

and connect the USB cable to the USB HUB.
Refer to Table 11-9 on page 11-20 for the
information.

Removal Procedure
Remove the new parts in the reverse order of installation.

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Connect ECG to Docking Cart

Tools
• No special tools needed

Needed Manpower
• 1 person, 3 minutes+travel

Preparations
• Shut down the system and switch off the main breaker.

Mounting Procedure

Table 11-11: Mounting Procedure of ECG

No. Step Corresponding Graphic

1. Install ECG..

2. Put ECG in the ECG bracket.

3. Connect the ECG to the USB port on the

Docking Cart.

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 Set Up Docking Cart

Connect ECG to Docking Cart (continued)

NOTE: If the ECG is not in use, hang the cable in the ECG cable hook.

Figure 11-6. Hang the cable

Removal Procedure
Remove the new parts in the reverse order of installation.

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Options Installation

Install Extended Life Battery to Docking Cart

NOTE: Before installing the Extended Life Battery, switch off the circuit
breaker on the power box to power off the Docking Cart

Mounting Procedure

CAUTION Use caution to avoid injuring hands when installing the

Extended Life Battery.

Table 11-12: Mounting Procedure of Extended Life Battery

No. Step Corresponding Graphic

1. Flip down the 2 cover latches on the

battery cover.

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 Set Up Docking Cart

Table 11-12: Mounting Procedure of Extended Life Battery

No. Step Corresponding Graphic

2. Remove the battery cover.

3. Insert the Battery into the power box.

4. Push the battery into the power box.

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Docking Cart Setup

Table 11-12: Mounting Procedure of Extended Life Battery

No. Step Corresponding Graphic

5. Flip up the 2 latches on the battery.

6. Try pulling the battery to check if the

battery is fixed in the power box.
• If the battery can not be pulled out, it
means the battery is well installed.
• If the battery can be pulled out, it
means the battery is not well installed.
Reinstall the battery until it can not be
pulled out from power box.

Removal Procedure
Remove the new parts in the reverse order of installation. See
‘Extended Life Battery (Part No. 5486499)’ on page 12-9 for
more information.

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Extended Life Battery Diagram

Figure 11-7. Diagram

Extended Life Battery Usage

Review the Extended Life Battery User Instruction (5494921)
that is packed with the Extended Life Battery. Please be sure to
use the latest revision of the document.

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Docking Cart Setup

Install 3-Probe Port to Docking Cart

1. Pull out the lock on the 3-Probe Port bracket and rotate the
lock 90° clockwise. Refer to picture 1.

Figure 11-8.

2. Do not slant the 3-Probe Port and hold it with both hands.
Aligning the two hooks on the 3-Probe Port with the two
holes at the Docking Cart bottom, mount the 3-Probe Port to
the Docking Cart. Refer to picture 2.
NOTE: Be sure that the 3-Probe Port is not slanted when mounting it to the
Docking Cart.

Figure 11-9.

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 Set Up Docking Cart

Install 3-Probe Port to Docking Cart (continued)

3. While holding the 3-Probe Port with both hands, install it by

aligning the two attachment pins (1-2) with the two slots on
the bracket, then push up the 3-Probe Port. The two
attachment pins on 3-Probe Ports move up along the two
slots on the bracket. Refer to picture 3.

Figure 11-10.

4. Make sure the 3-Probe Port is not slanted, then push it to

the right. The two attachment pins (1-2) on the 3-Probe Port
are clamped on the bracket. The hook (3) on the 3-Probe
Port and the hook on the bracket are interlocked. Refer to
picture 4.

Figure 11-11.

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Docking Cart Setup

Install 3-Probe Port to Docking Cart (continued)

5. Rotate the lock 90° counterclockwise and release your

hand, the lock automatically springs in the lock position.
Refer to picture 5.

Figure 11-12.

6. Mount the probe connector to the Docking Cart. Refer to

picture 6.

Figure 11-13.

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 Set Up Docking Cart

Install 3-Probe Port to Docking Cart (continued)

7. Stick 3-Probe Port label on Docking Cart.

Take out the label which is provided with 3-Probe Port in the
Kit. Remove the backing tape on the label. Stick it at this
location on the top cover of Docking Cart. See picture 7.

Figure 11-14.

Removal Procedure
Remove the new parts in the reverse order of installation. See
‘3-Probe Port Assy (Part No. 5423182-2)’ on page 12-5 for more
information.

3-Probe Port Usage

Review the 3-Probe Port User Instruction (5494922) that is
packed with the 3-Probe Port. Please be sure to use the latest
revision of the document.

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Docking Cart Setup

Install Color Printer Shelf to Docking Cart

Tools
• Common Phillips screwdrivers
• Allen/Unbraco/Torx wrench

Preparation
• Shut down the system and switch off the main breaker.

Table 11-13: Mounting Procedure for Color Printer Shelf Assy

No. Steps Corresponding Graphic

1. Remove the rear panel. See ‘Rear

Panel Assy (Part No. 5422978)’ on
page 12-8 for more information.

2. Remove the storage rack. See ‘Storage

Rack (Part No. 5219976-2)’ on
page 12-7 for more information.

3. Remove the 3 screw pads and unscrew

the 3 screws on the cabinet top cover.

4. Unscrew the 2 screws at the back of the

cabinet.

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 Set Up Docking Cart

Table 11-13: Mounting Procedure for Color Printer Shelf Assy

No. Steps Corresponding Graphic

5. Slightly lift up the cabinet top cover with

one hand and pull out the DVD and B/W
printer shelf with another hand from the
front of the Docking Cart.

6. Place the color printer shelf in to the

cabinet from the front of Docking Cart.

7. Install the 8 screws to fix the shelf on

Docking Cart.

8. Fix the cabinet top cover and Install the

Rear Panel.

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Docking Cart Setup

Top Support DVD/Print Shelf Assy

Tools
• Common Hex driver
• common Phillips screwdriver

Needed Manpower
• 1 person, 2 minutes+travel

Preparations
• Turn off all the power supply.

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Mounting Procedure

Table 11-14: Mounting Procedure of Top Support DVD/Printer Shelf Assy

No. Step Corresponding Graphic

1. Remove the rear panel. See ‘Rear Panel

Assy (Part No. 5422978)’ on page 12-8 for
more information.

2. Remove Storage Rack. See ‘Storage Rack

(Part No. 5219976-2)’ on page 12-7 for more
information.

3. Remove the cover of the Monitor Support

Space Cap.

4. Turn over the Top DVD/Print Shelf. Turn over

B/W Printer and push it into the Top DVD/
Print Shelf.

5. Put the Support DVD/Print Shelf above the

Top DVD/Print Shelf with the roll upwards.

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Docking Cart Setup

Table 11-14: Mounting Procedure of Top Support DVD/Printer Shelf Assy

No. Step Corresponding Graphic

6. Align the four screws holes to make sure the

screw holes in B/W Printer and two shelves
should superpose. Screw 4 screws. When
screwing, slightly lift up the printer with hands
to make the printer close to Top DVD/Print
Shelf.

7. Place the Top DVD/Printer shelf on the top of

the cabinet and install it with the Support
Shelf snapped to the top of the cabinet.

8. Screw the 2 screws.

9. Screw the 2 screws.

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Table 11-14: Mounting Procedure of Top Support DVD/Printer Shelf Assy

No. Step Corresponding Graphic

10. Install the rear panel.

Removal Procedure
Remove the new parts in the reverse order of installation.

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Paperwork
NOTE: During and after setup, the documentation (i.e. User Manuals...)
for the peripheral units must be kept as part of the original
system documentation. This will ensure that all relevant safety
and user information is available during the operation and
service of the complete system.

Product Locator Installation

User Manual

Check that the correct User Manual(s) for the Docking Cart is
included with the installation. Specific language versions of the
User Manual may also be available. Check with your GE Sales
Representative for availability.

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 Cart Using

Cart Using

Contents in This Section

• ‘Introduction’ on page 11-39
• ‘Height Adjustment’ on page 11-39
• ‘Locking the Wheels’ on page 11-40
• ‘Mounting the System to Cart’ on page 11-40
• ‘Release the System from Docking Cart’ on page 11-41
• ‘Switch the Three Probes’ on page 11-42
• ‘System Operation’ on page 11-42

Introduction
Docking Cart supports the ultrasound system as below:
• LOGIQ e (Software version R8.x.x)
The docking cart can supply power for the system and
peripherals which are mounted to the docking cart.

Height Adjustment
To adjust the height of the mounting-platform, raise the Release
lever and pull the platform up or push it down with both hands,
the traveling distance is 140mm.
When the lever is released the platform remains at the adjusted
height.

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Locking the Wheels

Depress the front of the Brake Lever with your foot. With the
Brake Lever down the rolling and swivel function are locked.

Figure 11-15. Released and Locked position

Mounting the System to Cart

The system can be mounted to Docking Cart either while the
display screen is closed with the system fully shut-down or in
standby mode, or while the display screen is open with the
system powered On or Off.
NOTE: A battery or an empty battery-shell should always be attached to
the system before mounting system to the cart.

CAUTION Use caution when mounting system while it is turned-on to

avoid shocks or vibrations which may be harmful to the
hard-drive.

To mount the system to the cart:

Figure 11-16. Mounting System to Cart

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 Cart Using

Mounting the System to Cart (continued)

1. Hold the system slightly tilted towards you and place the
front bottom part over the front sliding guides.
NOTE: When put the system on docking cart top cover ,aviod
injuring the fingures and hands.
2. Lower the rear part of the system to sit over the rear sliding
guides. Push the system towards the rear until you feel that
it stops and you hear a click (While pushing the system to
the rear, prop the vertical plane behind the handles with
fingers so that the cart does not move)
3. Rotate the system handle to the rear of LCD stoppers to
lock the system. At this stage the system should be locked
well on all four comers.Gently pull the system up to verify
that it is locked well and can not be easily released.
4. Connect the probe connector of Three-probe Port to the
system, press the probe connector locking lever up.

Release the System from Docking Cart

The system can be mounted to Docking Cart either while the
display screen is closed with the system fully shut-down or in
standby mode, or while the display screen is open with the
system powered On or Off.

CAUTION Before dismounting the system while it is powered ON, be sure

to check availability and charge of battery, as system will
switch-over to battery operation as it is released.

To release the system from mounting platform:

Figure 11-17. Release the System from Cart

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Docking Cart Setup

Release the System from Docking Cart (continued)

1. Disconnect the probe connector of Three-Probe Port from
the system.
2. Rotate the handle to unlock system
3. Place palm of one hand on the handle and push the system
release button toward you with the other hand until it stops,
then release the button back to it’s normal position.
4. Lift up the system from the platform.

Switch the Three Probes

The system can switch the probe between the three probe which
are connected in the Docking Cart Three Probes Box.
From the keyboard, press the Exam key. The Probe screen
appears. Select the probe which you want.

Figure 11-18. Probe Screen

NOTE: If the docking cart loses power, the factory default probe is the
probe which is connected to the port.

System Operation
LOGIQ e is supported on Docking Cart.
NOTE: To upgrade the system, release the system from the Docking
Cart and connect the USB Memory Stick or SD Card to the
system directly.
NOTE: To power off Docking Cart, open the circuit breaker and then
pull out the AC Power Cord from the wall AC outlet.
NOTE: Do not plug the AC Power into the wall in the state of closing the
circuit breaker.

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 Docking Cart Functions (Theory)

Docking Cart Functions (Theory)

Overview
The section explains Docking Cart's system concepts,
component arrangement, and subsystem function.

Block Diagram

Figure 11-19. Docking Cart Function Diagram

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Docking Cart Setup

Information
• Docking Connection Board
DockBoard is a PWA, it has a Docking Port, which is
responsible for docking and connecting to the LOGIQ e.
• Power Box
The DC20V Power is transferred via this PWA Board and is
extended from this board to USB HUB and peripherals.
• Rear Board
It is a PWA, which take most charge of the Docking Cart
electric system: Network, USB connection, DVI.

Supported External Interface/Port

Table 11-15: Supported external interface/port

Item Interface/Port Description

1 DVI Support to 1024x768,60Hz

2 Network 10M/100M auto-adaptive

3 USB 2.0 4 USB 2.0 ports

Figure 11-20. Supported external Interface/Port

1. Network 2. DVI 3. USB port

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 Diagnostics/Troubleshooting

Diagnostics/Troubleshooting

Overview
This section describes how to setup and run the tools that help
Docking Cart operation. Cart and board level diagnostics are run
whenever power is applied. Some Service Tools may be run at
the application level.

Troubleshooting
There is a troubleshooting tool available that the customer can
use as a first step to investigate failure issues. It gives the
current status of failure and provides some relative ways to
figure out.

Gathering Trouble Data

There may be a time when it would be advantageous to capture

trouble information for acquisition through remote diagnostics or
to be sent back to the manufacturer for analysis. There are
different options to acquire this data that would give different
results.
• Product Name: Docking Cart
• Docking Cart S/N Number:

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Docking Cart Setup

Troubleshooting Trees

System Does Not Boot

System doesn’t boot!

Is the AC power cable

NO
seated to the Scanner and
to the wall power outlet?

Connect the AC power cable

YES between the Scanner and the wall
power outlet in right way.

Is the main breaker turned NO

ON?

Turn ON the main breaker of

YES the Scanner.

Has the ON/OFF

NO
key on the Control Panel
been pressed once?

Press the ON/OFF button on the

YES Control Panel.

End

Figure 11-21. System Does Not Boot

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 Diagnostics/Troubleshooting

Can Not Charge the Extended Life Battery

Figure 11-22. Can not Charge the Extended Life Battery

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Docking Cart Setup

Extended Life Battery Has No OUTPUT

Figure 11-23. Extended Life Battery Has No OUTPUT

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 Chapter 12

Docking Cart Servicing

This Chapter describes replacement procedure and lists

the renewal parts available for Docking Cart. The Care
and Maintenance on Docking Cart is also provided.

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Docking Cart Servicing

Overview

Contents in this chapter

• ‘Overview’ on page 12-2
• ‘Replacement Procedure’ on page 12-3
• ‘Disassembly/Re-assembly’ on page 12-3
• ‘Renewal Parts’ on page 12-12
• ‘Care & Maintenance’ on page 12-23

Introduction

This chapter contains this information:

• Describes replacement procedures for the modules and
subsystems of Docking Cart.
• Provides an overview of Renewal Parts for Docking Cart.
• Describes Care & Maintenance on Docking Cart and
peripherals. These procedures intended to maintain the
quality of Docking Cart systems performance.

Safety consideration

NOTE: Please refer to Chapter 1 and Chapter 2 for the safety

information and site requirement for the Docking Cart. Chapter 1
and Chapter 2 should be read before conducting any service
work on Docking Cart.

List of Abbreviations
• Assy - Assembly
• Ctrl - Control
• Int - Internal
• I/O - Input/Output
• LCD - Liquid Crystal Display
• PAT - Patient
• PC - Personal Computer (Back End Processor)

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 Replacement Procedure

Replacement Procedure

Introduction
This section describes how to remove and install, or replace,
modules and subsystems in the Docking Cart.

Contents in this Section

• ‘Introduction’ on page 12-2
• ‘Disassembly/Re-assembly’ on page 12-3
• ‘Warning and Caution’ on page 12-3
• ‘Storage Rack (Part No. 5219976-2)’ on page 12-7
• ‘Rear Panel Assy (Part No. 5422978)’ on page 12-8
• ‘Extended Life Battery (Part No. 5486499)’ on page 12-9

Disassembly/Re-assembly

Warning and Caution

WARNING DO NOT service or disassemble parts under FRU unit level at

any circumstances.

CAUTION DO NOT wear the ESD wrist strap when you remove a part of
power supply unit. Turn OFF power and unplug the power cord
before removing a part of power supply unit. However be sure
to turn off power and wear the strap before you remove a circuit
boards.

WARNING Only Qualified service personnel should remove any covers or

panels. Electrical hazards exists at several points inside.
Before thoroughly familiar with all hazardous voltages and high
current levels to avoid accidental contact.

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Docking Cart Servicing

Disassembly/Re-assembly (continued)

WARNING Because of the limited access to cabinets and equipment in the

field, placing people in awkward positions, GE has limited the
lifting weight for one person in the field to 16 KG (35 LBS).
Anything over 16 KG (35 LBS) requires 2 people.

WARNING DO NOT touch any boards with integrated circuits prior to

taking the necessary ESD precautions.
Always connect yourself, via an arm-wrist strap, to the advised
ESD connection point located on the rear of the Ultrasound
system (near the power connector).
Follow general guidelines for handling of electrostatic sensitive
equipment.

WARNING The waste of electrical and electronic equipment must not be

disposed as unsorted municipal waste and must be collected
separately.
Please contact the manufacturer or other authorized disposal
company to decommission your equipment.

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 Replacement Procedure

3-Probe Port Assy (Part No. 5423182-2)

Purpose: This is a description on how to remove and replace the

Docking Cart 3-Probe Port Assy.

Tools
• Common Phillips screwdrivers
• Allen/Unbraco/Torx wrench

Needed Manpower
• 1 person, 1minutes + travel

Preparation
• Shut down the system and switch off the main breaker.

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Docking Cart Servicing

Removal Procedure

Table 12-1: Removal Procedure for 3-Probe Port Assy

No. Steps Corresponding Graphic

1. Disconnect the probe

connector

2. Pull out the lock and rotate

the lock 90° clockwise.

3. Hold the 3-Probe Port with

both hands, meanwhile use
one finger of the right hand to
push up the lock on 3-Probe
Port and move the 3-Probe
Port to the right, then remove
the 3-Probe Port.
The two screws on the
3-Probe Port are released
from the bracket.
Take down the 3-Probe Port.

Mounting Procedure
Install the new parts in the reverse order of removal.
See ‘Install 3-Probe Port to Docking Cart’ on page 11-28 for
more information.

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 Replacement Procedure

Storage Rack (Part No. 5219976-2)

Purpose: This is a description on how to remove and replace the

Storage Rack.

Tools
• Common Phillips screwdrivers
• Allen/Unbraco/Torx wrench

Needed Manpower
• 1 person, 1 minutes + travel

Preparation
• NA

Removal Procedure

Table 12-2: Removal Procedure for Storage Rack

No. Steps Corresponding Graphic

1. Unscrew the 2 screws.

2. Remove the storage rack from the top

cabinet.

Mounting Procedure
1. Install the new parts in the reverse order of removal.

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Docking Cart Servicing

Rear Panel Assy (Part No. 5422978)

Purpose: This is a description on how to remove and replace the

Rear Panel Assy.

Tools
• No special tools

Needed Manpower
• 1 person, 1 minutes + travel

Preparation
• Shut down the system and switch off the main breaker.

Removal Procedure

Table 12-3: Removal Procedure for Rear Panel Assy

No. Steps Corresponding Graphic

1. Loose the 4 screws.

2. Remove the rear panel Assy.

Mounting Procedure
1. Install the new parts in the reverse order of removal.

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 Replacement Procedure

Extended Life Battery (Part No. 5486499)

Purpose: This is a description on how to remove and replace the

Extended Life Battery.

Tools
• No special tools.

Needed Manpower
• 1 person, 1 minutes + travel

Preparation
• Shut down the system and switch off the main breaker.

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Docking Cart Servicing

Extended Life Battery (Part No. 5486499) (continued)

Removal Procedure

Table 12-4: Removal Procedure Extended Life Battery

No. Steps Corresponding Graphic

1. Flip down the two handle locks on the

Extended Life Battery.

2. Pull out the Extended Life Battery.

3. While pressing the two spring lockings

on both side of the battery with fingers,
then move out the battery.

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 Replacement Procedure

Table 12-4: Removal Procedure Extended Life Battery

No. Steps Corresponding Graphic

4. Take out the battery with both hands.

Mounting Procedure
1. Install the new parts in the reverse order of removal.
See ‘Install Extended Life Battery to Docking Cart’ on
page 11-24 for more information.
After the battery is installed, try pulling the battery to check if the
battery is fixed in the power box.
• If the battery can not be pulled out, it means the battery is
well installed.
• If the battery can be pulled out, it means the battery is not
well installed. Reinstall the battery until it can not be pulled
out from power box.

CAUTION Use caution to avoid injuring hands when installing the

Extended Life Battery.

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Docking Cart Servicing

Renewal Parts

Contents in This Section

• ‘Introduction’ on page 12-12
• ‘Power Cable’ on page 12-13
• ‘Operator Console Assy’ on page 12-14
• ‘Docking Station’ on page 12-15
• ‘Probe Holder’ on page 12-17
• ‘Shelf Service’ on page 12-19
• ‘Bottom and Wheels’ on page 12-20
• ‘Panel and Cabinet’ on page 12-21
• ‘Gas Spring and Gas Spring Lever’ on page 12-21
• ‘Power Box and Extended Life Battery’ on page 12-21

Introduction
This chapter lists the renewal parts available for Docking Cart.

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 Renewal Parts

Power Cable
Table 12-5: Docking Cart Power Cable List

Item Part Number Description Quantity

1 5177126-2 Power Cable for Japan 1

2 5177195-2 Power Cable for Argentina 1

3 5177154-2 Power Cable for Switzerland 1

4 5177187-3 Power Cable for Australia 1

5 5177123-2 Power Cable for Europe 1

6 5176907-2 Power Cable for United Kingdom 1

7 5176773-2 Power Cable for India 1

8 5176753-2 Power Cable for Israel 1

9 5176304-2 Power Cable for China 1

10 5177146-2 Power Cable for USA 1

11 5177153-2 Power Cable for Denmark 1

12 5400868-2 Power Cable for Brazil 1

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Docking Cart Servicing

Operator Console Assy

Figure 12-1. Operator Console Assy

1. Lever 7. Three-probe connector

2. Up/Down 8. Ethernet port, DVI, USB ports
3. DVD-RW shelf 9. Storage rack
4. B/W Printer shelf 10. Cable hook
5. Speaker 11. Power box
6. Probe holder

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 Renewal Parts

Docking Station
Table 12-6: Docking Station

Part
Item Number Part Name Corresponding graphic Qty

700 5422689-2 LOGIQ e Top Support 1

701 5423180-2 LOGIQ e DS Top Cover Assy 1

702 5423191-2 LOGIQ e DS Main PWA 1

703 5444585 LOGIQ e Multiport board 1

cable

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Docking Cart Servicing

Table 12-6: Docking Station

Part
Item Number Part Name Corresponding graphic Qty

704 5421742 Docking Cart Monitor Support 1

Space Cap

705 5422460 Docking Cart DS Bottom 1

Cover

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 Renewal Parts

Probe Holder
Table 12-7: Docking Probe Holder

Part
Item Number Part Name Corresponding graphic Qty

800 5423182-2 LOGIQ e 3-probe Box Assy 1

801 5422462-2 LOGIQ e Docking Cart 1

3-probe box left cover

802 5422461 LOGIQ e Docking Cart 1

3-probe box right cover

803 5240778-2 Probe Holder Service Kit 1

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Docking Cart Servicing

Table 12-7: Docking Probe Holder

Part
Item Number Part Name Corresponding graphic Qty

804 5483613 3-probe Box Supporter 1

Bracket Assy

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 Renewal Parts

Shelf Service
Table 12-8: Shelf Service

Part
Item Number Part Name Corresponding graphic Qty

900 5255346-2 Support shelf with package 1

901 5219976-2 Storage Rack 1

902 5255345-2 Peripheral shelf with package 1

903 5423171-2 Top DVD Shelf Assy 1

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Docking Cart Servicing

Bottom and Wheels

Table 12-9: Bottom and Wheels

Part
Item Number Part Name Corresponding graphic Qty

1000 5441308 USB HUB Assy 1

1001 5443853 Black white Rear Castor 1

N125 from Secure

1002 5454032 Black white Front Castor 1

N125 from Secure

1003 5458670 DCAC adapter for printer 1

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 Renewal Parts

Panel and Cabinet

Table 12-10: Panel and Cabinet

Part
Item Number Part Name Corresponding graphic Qty

1100 5422978 Cart Rear Panel Assy 1

Gas Spring and Gas Spring Lever

Table 12-11: Gas Spring and Gas Spring Lever

Part
Item Number Part Name Corresponding graphic Qty

1200 5423168 Gas Spring Lever Assy 1

1201 5245175 Gas Spring Service Kit 1

Power Box and Extended Life Battery

Table 12-12: Power Box and Extended Life Battery

Part
Item Number Part Name Corresponding graphic Qty

1300 5439693 LOGIQ e Power Box for 1

Docking Cart

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Docking Cart Servicing

Table 12-12: Power Box and Extended Life Battery

Part
Item Number Part Name Corresponding graphic Qty

1301 5440512 Extended Life Battery for 1

Docking Cart Power Box

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 Care & Maintenance

Care & Maintenance

Contents in This Section

• ‘Overview’ on page 12-23
• ‘Purpose’ on page 12-23
• ‘Periodic Maintenance Inspections’ on page 12-24
• ‘Why do Maintenance’ on page 12-25
• ‘Maintenance Task Schedule’ on page 12-26
• ‘Tools Required’ on page 12-28
• ‘Safety Test’ on page 12-30
• ‘Inspection Paper Work’ on page 12-35

Overview

Purpose

This section describes Care & Maintenance on Docking Cart.

These procedures are intended to maintain the quality of
Docking Cart. Read this chapter completely and familiarize
yourself with the procedures before performing a task.

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Docking Cart Servicing

Periodic Maintenance Inspections

It has been determined by engineering that your Docking Cart

system does not have any high wear components that fail with
use, therefore no Periodic Maintenance Inspections are
mandatory. Some Customers Quality Assurance Programs may
require additional tasks and or inspections at a different
frequency than listed in this manual.

CAUTION Practice good ESD prevention. Wear an anti–static strap when

handling electronic parts and even when disconnecting/
connecting cables.

DANGER THERE ARE SEVERAL PLACES ON THE BACKPLANE, THE

AC DISTRIBUTION, AND DC DISTRIBUTION THAT ARE
DANGEROUS. BE SURE TO DISCONNECT THE SYSTEM
POWER PLUG AND OPEN THE MAIN CIRCUIT BREAKER
BEFORE YOU REMOVE ANY PARTS. BE CAUTIOUS
WHENEVER POWER IS STILL ON AND COVERS ARE
REMOVED.

CAUTION Do not pull out or insert circuit boards while power is ON.

CAUTION Do not operate this unit unless all board covers and frame
panels are securely in place. System performance and cooling
require this.

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 Care & Maintenance

Why do Maintenance

Keeping Records

It is good business practice that ultrasound facilities maintain

records of quality checks and corrective maintenance. The
Ultrasound Inspection Certificate (provided on ‘Inspection Paper
Work’ on page 12-35) provides the customer with
documentation that the ultrasound scanner is maintained on a
periodic basis.
A copy of the Ultrasound Periodic Maintenance Inspection
Certificate should be kept in the same room or near the scanner.

Quality Assurance

In order to gain accreditation from organizations such as the

American College of Radiology (USA), it is the customer’s
responsibility to have a quality assurance program in place for
each scanner. The program must be directed by a medical
physicists, the supervising radiologist/physician or appropriate
designee.
Routine quality control testing must occur regularly. The same
tests are performed during each period so that changes can be
monitored over time and effective corrective action can be
taken.
Testing results, corrective action and the effects of corrective
action must be documented and maintained on the site.
Your GE service representative can help you with establishing,
performing and maintaining records for a quality assurance
program. Please contact us for coverage information and/or
price for service.

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Docking Cart Servicing

Maintenance Task Schedule

How often should care & maintenance tasks be performed?

The Care & Maintenance Task Schedule (provided on

Table 12-13 on page 12-26) specifies how often your Docking
Cart should be serviced and outlines items requiring special
attention.
NOTE: It is the customer’s responsibility to ensure the Docking Cart
care & maintenance is performed as scheduled in order to retain
its high level of safety, dependability and performance.
Your GE Service Representative has an in-depth knowledge of
your LOGIQ e ultrasound scanning system and can best provide
competent, efficient service. Please contact us for coverage
information and/or price for service.
Your GE Service Representative has an in-depth knowledge of
your LOGIQ e ultrasound scanning system and can best provide
competent, efficient service. Please contact us for coverage
information and/or price for service.
NOTE: If conditions exist which exceed typical usage and patient load,
then it is recommended to increase the maintenance
frequencies.

Table 12-13: Customer Care Schedule

Service at Indicated Per Facilities

Time Daily Weekly Monthly QA Program Notes

Clean Probe Holders X

Clean Air Filter X more frequently

depending on your
environment

Inspect AC Mains Cable X Mobile Unit Check

Weekly

Inspect Cables and X

Connectors

Clean Console X

Inspect Wheels, Casters, X Mobile Unit Check

brakes and Swivel Locks Daily

Check Control Panel X Mobile Unit Check

Movement Daily

Console Leakage Current X also after

Checks corrective
maintenance

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 Care & Maintenance

Table 12-13: Customer Care Schedule

Service at Indicated Per Facilities

Time Daily Weekly Monthly QA Program Notes

Peripheral Leakage X also after

Current Checks corrective
maintenance

Surface Probe Leakage X also after

Current Checks corrective
maintenance

Endocavity Probe X also after

Leakage corrective
Current Checks maintenance

Transesphongeal Probe X also after

Leakage corrective
Current Checks maintenance

Surgical Probe Leakage X also after

Current Checks corrective
maintenance

Functional Checks X also after

corrective
maintenance

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Docking Cart Servicing

Tools Required

Standard GE Tool Kit

The following is a description of the “Standard” GE tool kit in the

USA. Not all tools are required for PMs.
Please refer to ‘Standard GE tool kit’ on page 10-17 for the
information.

Special Tools, Supplies and Equipment

Table 12-14: Overview of Requirement for Care & Maintenance

Tool Part Number Comments

Digital Volt Meter (DVM)

Leakage Current Ultrasound 2113015 For 120V and 220V Units

Kit

Anti Static Kit 46–194427P231 Kit includes anti–static mat, wrist strap and
46–194427P279 cables for 200 to 240 V system
46–194427P369 3M #2204 Large adjustable wrist strap
46–194427P373 3M #2214 Small adjustable wrist strap
46–194427P370 3M #3051 conductive ground cord

Anti Static Vacuum Cleaner 46–194427P278 120V

46–194427P279 230V

Air Filter air intake

Safety Analyzer The safety Analyzer tool should be calibrated

and compliant with AAMI/ESI 1993 or IEC
60601 or AS/NZS 3551.

CD-RW Media For LOGIQ e

B/W Printer Cleaning Sheet See printer user manual for requirements

Color Printer Cleaning Sheet See printer user manual for requirements

Disposable Gloves

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 Care & Maintenance

Cleaning Dusk Screen

The dusk screen requires weekly cleaning in order to retain its
performance. Power off the Power Box when the dusk screen is
removed for cleaning.
1. Pull out the Dusk Screen from the power box.

Figure 12-2. Pull out the Dusk Screen

2. Dust the Dusk Screen with a vacuum cleaner and/or wash it

with a mild soapy solution. If washed, rinse and dry the Dusk
Screen before re-installation.

Figure 12-3. Clean the Dusk Screen

3. Re-install the Dusk Screen on the power box.

Figure 12-4. Re-install the Dusk Screen

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Docking Cart Servicing

Safety Test

Input Power

Table 12-15: Main Cable Inspection

Step Item Description

1 Unplug Cord Disconnect the mains cable from the wall and system.

2 Inspect Inspect it and its connectors for damage of any kind.

3 Verify Verify that the LINE, NEUTRAL and GROUND wires are properly attached
to the terminals, and that no strands may cause a short circuit.

4 Verify Inlet connector retainer is functional.

Cleaning

Table 12-16: General Cleaning

Step Item Description

1 Console Use a fluid detergent in warm water on a soft, damp cloth to carefully wipe
the entire console. Be careful not to get the cloth too wet so that moisture
does not enter the console.

2 Probe Holder Clean probe holders (they may need to be soaked to remove excess gel).

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 Care & Maintenance

Safety Test (continued)

Physical Inspection

Table 12-17: Physical Checks

Step Item Description

1 Labeling Verify that all system labeling is present and in readable condition. refer to
the LOGIQ e User Manual for details.

2 Scratches & Inspect the console for dents, scratches or cracks.

Dents

3 Wheels & Check all wheels and casters for wear and verify operation of foot brake, to
Brakes stop the unit from moving, and release mechanism. Check all caster locks
and caster swivel locks for proper operation.

4 Cables & Check all internal cable harnesses and connectors for wear and secure
Connectors connector seating. Pay special attention to footswitch assembly and probe
strain or bend reliefs.

5 Shielding & Check to ensure that all EMI shielding, internal covers, air flow panels and
Covers screws are in place. Missing covers and hardware could cause EMI/RFI
problems while scanning.

6 External I/O Check all connectors for damage and verify that the labeling is good.

7 Op Panel Lights Check for proper operation of all operator panel and TGC lights.

8 Monitor Light Check for proper operation of any monitor lights if available.

9 External Check for proper operation of any external microphones by recording an

Microphone audio test.

Outlet Test - Wiring Arrangement - USA & Canada

Please refer to ‘Outlet test - wiring arrangement’ on page 10-35

for the information.

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Docking Cart Servicing

Safety Test (continued)

Grounding continuity

DANGER ELECTRIC SHOCK HAZARD. THE PATIENT MUST NOT BE

CONTACTED TO THE EQUIPMENT DURING THIS TEST.
Measure the resistance from the third pin of the attachment plug
to the exposed metal parts of the case. The ground wire
resistance should be less than 0.2 ohms. Reference the
procedure in the IEC60601-1.

1. GROUND PIN
2. OHMMETER
3. LOGIQ e
4. ACCESSIBLE METAL PART:
• MONITOR HOUSING
• PEAR PANEL CONNECTOR
• ANY CASTER/WHEEL SUPPORT

Figure 12-5. Ground continuity test

Meter Procedure
Follow these steps to test the ground wire resistance.
• Turn the LOGIQ e unit OFF.
• Plug the unit into the meter, and the meter into the tested
AC wall outlet.
• Plug the black chassis cable into the meter's “CHASSIS”
connector and attach the black chassis cable clamp to an
exposed metal part of the LOGIQ e unit.
• Set the meter's “FUNCTION” switch to the RESISTANCE
position.
• Set the meter's “POLARITY” switch to the OFF (center)
position.
• Measure and record the ground wire resistance.

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 Care & Maintenance

Safety Test (continued)

Chassis Leakage Current Test

Please refer to ‘Chassis leakage current test’ on page 10-37 for

the information.

Isolated Patient Lead (Source) Leakage - Lead to Lead

Refer to the procedure in the IEC 60601-1.

Isolated Patient Lead (Sink) Leakage-Isolation Test

Refer to the procedure in the IEC 60601-1.

CAUTION Line voltage is applied to the ECG leads during this test. To
avoid possible electric shock hazard, the system being tested
must not be touched by patients, users or anyone while the
ISO TEST switch is depressed.

NOTE: It is not necessary to test each lead individually or power

condition combinations as required in previous tests.
Data Sheet for ECG Leakage Current:
The test passes when all readings measure less than the value
shown in the table below. Record all data on the PM Inspection
Certificate.

Table 12-18: Maximum Allowance Limit for ECG Leakage Current

Maximum Allowance Limit

AC Power Ground Ground

Source Open Closed

Patient Lead to Ground Leakage Current Test 115V 10uA 10uA

and
Patient Lead to Lead Leakage Current Test 220/240V 500uA 10uA

Table 12-19: Maximum Allowance Limit for ECG Leakage Current

AC Power
Source Maximum Allowance Limit

Patient Lead Isolation Current Test 115V 20uA

220/240V 5mA

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Docking Cart Servicing

Isolated Patient Lead (Sink) Leakage-Isolation Test (continued)

Table 12-20:

Tester Tester Tester Lead Selector

ECG Polarity Ground
Power Switch Switch RL RA LA LL C

ON NORM CLOSED

ON REVERSE CLOSED

ON NORM OPEN

ON REVERSE OPEN

OFF NORM CLOSED

OFF REVERSE CLOSED

OFF NORM OPEN

OFF REVERSE OPEN

Probe Leakage Current Test

Please refer to ‘Probe leakage current test’ on page 10-39 for

the information.

When There’s Too Much Leakage Current...

Please refer to ‘When there's too much leakage current …’ on
page 10-42 for the information.

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 Care & Maintenance

Inspection Paper Work

ULTRASOUND INSPECTION CERTIFICATE

Customer Name: System ID: Dispatch Number / Warranty/Contract/HBS
Date Performed:

System Type Model Number: Serial Number: Manufacture Date:

Probe 1: Frequency: Scan Format*: Model Number: Serial Number:

Probe 2: Frequency: Scan Format*: Model Number: Serial Number:

Probe 3: Frequency: Scan Format*: Model Number: Serial Number:

Probe 4: Frequency: Scan Format*: Model Number: Serial Number:

Probe 5: Frequency: Scan Format*: Model Number: Serial Number:

Probe 6: Frequency: Scan Format*: Model Number: Serial Number:

Probe 7: Frequency: Scan Format*: Model Number: Serial Number:

Probe 8: Frequency: Scan Format*: Model Number: Serial Number:

Probe 9: Frequency: Scan Format*: Model Number: Serial Number:

*Scan Format: Phased Array, Linear Array, Curved Array,

Mechanical Array or Other

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Docking Cart Servicing

Inspection Paper Work (continued)

FUNCTIONAL CHECKS PHYSICAL INSPECTION AND CLEANING

Functional Check (if applicable) OK? Physical Inspection and Inspect Clean
or N/A Cleaning
(if applicable)

B-Mode Function Console

Doppler Modes Function Monitor

CF-Mode Function Touch Panel

M-Mode Function Air Filter

Applicable Software Options Probe Holders

Applicable Hardware Options External I/O

Control Panel Wheels, Brakes & Swivel Locks

Measurement Accuracy Cables and Connectors

GE Approved Peripherals GE Approved Peripherals

(CD-RW, MOD, Printers)

COMMENTS:

12-36 LOGIQ e – Basic Service Manual

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 Care & Maintenance

Inspection Paper Work (continued)

ELECTRICAL SAFETY
Electrical Test Performed Max Value OK? Comments
Value Measured
Allowed

Outlet (correct ground &wiring

config.)

System Ground Continuity

Chassis Source Leakage Current -

Probe

Chassis Source Leakage Current -

Caster

Chassis Source Leakage Current - CRT

Patient Lead Source Leakage

(Lead to Ground)

Patient Lead Source Leakage

(Lead to Lead)

Patient Lead Source Leakage

(Isolation)

Peripheral 1 Leakage Current

Peripheral 1Ground Continuity

Peripheral 2 Leakage Current

Peripheral 2Ground Continuity

Peripheral 3 Leakage Current

Peripheral 3Ground Continuity

PROBES
Probe Number Max Max OK? Comments
(from previous page) Value Value
Allowed Measured

Probe 1:

Probe 2:

Probe 3:

Probe 4:

Probe 5:

Probe 6:

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Docking Cart Servicing

Probe 7:

Probe 8:

Probe 9:

Final Check. All system covers are in place. System scans with all probes as expected.

Accepted by:______________________________________________________________________

12-38 LOGIQ e – Basic Service Manual

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 Index

A D
abbrevations, 9-2 damage in transport, i-11
acclimate time, 2-3 dangerous procedure warnings, 1-29
Admin screen data network setup requirements, 2-16
Logon, 10-11 desirable features, 2-14
approved DICOM network function, 2-16
internal peripherals, 3-22 DICOM setup requirements, 2-17
approved internal peripherals, 3-22 disconnect
average setup time, 3-3 probe, 3-19
display PDF files
B from manual CD-ROM
print PDF files
before installation (site preparations), 2-1 from manual CD-ROM, 4-15
Boot Up, 3-15
E
C
electrical requirements, 2-6
cable inspection EMI limitations
mains cable inspection, 10-24 EMI limitations, 2-9
care and maintenance, 10-1 general requirements, 2-6
warnings, 10-12 power stability requirements
CE compliance, 1-32 power stability requirements, 2-7
change history, i-1 power transients
chapter 1 power transients, 2-7
introduction, 1-1 site circuit breaker
chassis leakage current test, 10-37 site circuit breaker, 2-7
cold or hot site power outlets
if the unit is very cold or hot, 2-3 site power outlets, 2-7
compatibility specific requirements for the unit, 2-6, 3-22
hardware/software, 9-3 unit power plug
completing the setup, 3-13 unit power plug, 2-7
compliance, 1-32 voltage drop-out
configuration, 3-20 voltage drop-out, 2-7
connect electrical safety, 1-24
probe, 3-18 electrical safety tests, 10-30
console environmental requirements, 2-3 electrical specification, 3-14
console requirements, 2-3 electromagnetic interference
contact information, 1-34 abatement, 2-10
contents in this manual, 1-3 prevention, 2-10
conventions used in book, 1-7 electrostatic discharge prevention, 1-33
copyrights, i-14 EMC, 1-32
customer assistance, 1-34 compliance, 1-32
phone numbers, 1-35 what is EMC?, 1-32
customer order EMI, 1-32
verification, 3-12 abatement, 2-10
customer provided prerequisite, 8-13 prevention, 2-10
protection, 3-12

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5561650-100 English Rev. 3
environmental dangers, 2-19 L
environmental specifications for the unit, 2-4
errors, i-12 legal notes, i-14
ESD, 1-32 lighting, 2-5
ESD prevention, 1-33 list of abbrevations, 9-2
exam study, display location, 4-20 loading software, 8-13
examine packages, 3-6 lockout/tagout (LOTO) requirements, 1-30
log on procedures
F defining, 10-11
Logon
facility needs, 2-12 Admin screen, 10-11
desirable features, 2-14 LOTO
DICOM network function, 2-16 lockout/tagout requirements, 1-30
DICOM setup requirements, 2-17
network setup requirements, 2-16 M
purchaser responsibilities, 2-12
required facility needs, 2-13 mains cable inspection, 10-24
suggested floor plan maintenance
scanner and EchoPAC in same room, 2-15 physical inspection, 10-25
floor plan suggestion preliminary checks, 10-21
scanner and EchoPAC in same room, 2-15 system maintenance, 10-21
focal zone, display location, 4-20 maintenance task schedule, 10-15
functional checks, 10-23 manufacturer, 1-35
mains cable inspection, 10-24 mass
system checks, 10-23 with monitor and peripherals, 3-13
Measurement Summary window, display location,
G 4-20
mechanical safety, 1-22
GE Healthcare leakage current limits, 10-33 model designations, 1-7
general console requirements, 2-3 models covered by this manual, 1-5
generic procedure on probe leakage current, 10-40
grounding continuity, 10-36, 12-32 N
H network setup requirements, 2-16

hardware/software compatibility, 9-3 O

hardware-software
compatibility, 5-3 omission and errors, i-12
hot or cold operational and storage temperature for probes, 2-11
if the unit is very cold or hot, 2-3
how often should maintenance tasks be performed?, P
10-15
human safety, 1-19 P4 Key Function, 7-10
paperwork
I after setup, 3-33
PDF files
icons, 1-7 display and print, 4-15
icons indicating a special procedure to be used, 1-10 periodic maintenance inspection (PM), PM (periodic
if the unit is very cold or hot, 2-3 maintenance inspection), 10-13
imaging parameters, display location, 4-20 phone numbers
important precautions, i-2 customer assistance, 1-35
installation physical dimensions, 3-13
see "system setup", 3-1 physical inspection
installation warnings at arrivel, 3-12
see "setup warnings", 3-3 Power On, 3-15
introduction (chapter 1), 1-1 precautions
certified electrical contractor statement, i-11
damage in transport, i-11
important precautions, i-2

Index-2 LOGIQ e – Basic Service Manual

5561650-100 English Rev. 3
 service safety considerations, i-13 electrical specifications, 3-14
translation policy, i-2 physical dimensions, 3-13
prepeare for setup, 3-12 standard GE tool kit, 10-17
prerequisite standard hazard icons, 1-9
provided by customer, 8-13 statement
probe certified electrical contractor statement, i-11
connect, 3-18 system
disconnect, 3-19 specifications, 3-13
probe cleaning, 10-28 system checks, 10-23
probe identifier, locating, 4-20 system maintenance, 10-21
probe leakage current test, 10-39 physical inspection, 10-25
probe maintenance, 10-27 preliminary checks, 10-21
basic probe care, 10-27 system manufacturer, 1-35
basic probe cleaning, 10-28 system requirements verification, 3-13
probe related checks, 10-27 system setup, 3-1
probe related checks, 10-27
probes environmental requirements, 2-11 T
operational and storage temperature for probes,
2-11 tools required, 10-17
product icons, 1-11 special tools, supplies and equipment, 10-20
product locator installation card, 3-33 standard GE tool kit, 10-17
products covered by this manual, 1-5 trademarks, i-14
proprietary to GE Healthcare, i-14 translation policy, i-2
Purchaser responsibilities, 2-12 transport
purpose of operator manual, 1-5 damage, i-11
typical users of the service manual, 1-4
R
U
receiving and unpacking, 3-6
receiving the product, 3-6 unpacking, 3-6
required facility needs, 2-13 unpacking instructions, 3-7
requirements, 2-3
requirements verification, 3-13 V
returning/shipping probes and repair parts, 1-31
revision history, i-1 verification
system requirements, 3-13
S verify customer order, 3-12
voltage settings, 3-14
safety
human, 1-19 W
safety precaution messages, 1-8
warnings, 10-12
safety test overview, 10-30
service safety considerations, i-13 dangerous procedures, 1-29
what is EMC?, 1-32
setup
when there’s too much leakage current, 10-42
completion, 3-13
preparations, 3-12 chassis fails, 10-42
ECG fails, 10-43
reminders, 3-3
new unit, 10-43
setup time, 3-3
setup warnings, 3-3 peripheral fails, 10-43
probe fails, 10-43
shipping/returning probes and repair parts, 1-31
still fails, 10-43
site preparations, 2-1
software loading, 8-13
software option
configuration, 3-31
software/hardware compatibility, 9-3
software-hardware
compatibility, 5-3
specifications, 3-13

LOGIQ e – Basic Service Manual Index-3

5561650-100 English Rev. 3
Index-4 LOGIQ e – Basic Service Manual
5561650-100 English Rev. 3
GE