Medrad MK 7 Arterion
Medrad MK 7 Arterion
Mark 7 Arterion™
Injection System
3027921 Rev. G
Serial numbers and date of installation information must be supplied when ordering replacement parts, or
inquiring about servicing. For convenience, record the following information below:
Owner:
Date Installed:
The information and specifications included in this publication were in effect at the time of approval for
printing. MEDRAD, reserves the right, however, to discontinue or otherwise change specifications or
design at anytime without notice, and without incurring any obligation whatsoever.
MEDRAD
Service Manual
Mark 7 Arterion Injection System
Nihon MEDRAD KK
Breeze Tower
2-4-9, Umeda,
Kita-ku, Osaka
530-0001, Japan
Phone: +81(0)66-133-6250
Fax: +81(0)66-344-2395
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Mark 7 Arterion Injection System
ii
Table of Contents
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Mark 7 Arterion Injection System
iv
Table of Contents
9.4.6 Display Control Unit Desk Stand Mount Weight and Dimensions.......................................................... 9 - 118
9.4.7 Display Control Unit Wall Mount Weight and Dimensions..................................................................... 9 - 119
9.4.8 Power Unit Floor Mount Weight and Dimensions ................................................................................. 9 - 120
9.5 ISI Technical Specifications ........................................................................................................................... 9 - 120
9.5.1 ISI Output Specifications ..................................................................................................................... 9 - 120
9.5.2 ISI Input Specifications........................................................................................................................ 9 - 121
9.5.3 ISI Connector Specifications................................................................................................................ 9 - 122
9.6 Fuses ............................................................................................................................................................ 9 - 126
9.7 Environmental Specifications......................................................................................................................... 9 - 126
9.7.1 Operating............................................................................................................................................ 9 - 126
9.7.2 Non-Operating: (Transportation and Storage) ...................................................................................... 9 - 127
9.7.3 EMI/RFI............................................................................................................................................... 9 - 127
9.7.4 Equipment Classification..................................................................................................................... 9 - 127
9.7.5 Class I Product.................................................................................................................................... 9 - 127
9.7.6 Type CF Defibrillation-proof Applied Par.............................................................................................. 9 - 127
9.7.7 IPX1.................................................................................................................................................... 9 - 127
9.7.8 Continuous Mode of Operation ............................................................................................................ 9 - 127
9.7.9 EU Directive........................................................................................................................................ 9 - 127
10 Options and Accessories ........................................................................................ 10 - 129
10.1 Mark 7 Arterion System Mount Options ..................................................................................................... 10 - 129
10.1.1 Injector Head Mount Options........................................................................................................... 10 - 129
10.1.2 Power Unit Mount Options .............................................................................................................. 10 - 129
10.1.3 Display Control Unit Mount Options ................................................................................................. 10 - 129
10.1.4 Cable Brackets ............................................................................................................................... 10 - 129
10.2 Mark 7 Arterion Accessory Devices and Kits .............................................................................................. 10 - 130
10.2.1 Switches......................................................................................................................................... 10 - 130
10.2.2 Accessory Devices and Kits ............................................................................................................ 10 - 130
10.3 Mark 7 Arterion Cords and Cables ............................................................................................................. 10 - 130
10.3.1 Power Cords ................................................................................................................................... 10 - 130
10.3.2 Head Power and Communication Extension Cables ......................................................................... 10 - 130
10.3.3 Display Cables ................................................................................................................................ 10 - 131
10.4 OCS Mounting Systems ............................................................................................................................. 10 - 131
10.4.1 Stationary Ceiling Mount................................................................................................................. 10 - 131
10.4.2 Mobile Ceiling Mount ..................................................................................................................... 10 - 131
10.4.3 Wall Mount .................................................................................................................................... 10 - 131
10.4.4 Ceiling Mount Plate......................................................................................................................... 10 - 131
10.5 OEM Imaging System Interface Cables ...................................................................................................... 10 - 132
10.5.1 General Electric .............................................................................................................................. 10 - 132
10.5.2 Phillips............................................................................................................................................ 10 - 132
10.5.3 Siemens ......................................................................................................................................... 10 - 132
10.5.4 Universal Imaging System Interface Cables..................................................................................... 10 - 132
10.5.5 Equipotential Cables ....................................................................................................................... 10 - 133
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Mark 7 Arterion Injection System
vi
1 Introduction
This manual applies to the Mark 7 Arterion Injection System.
Read all of the information contained in this manual. Understanding this information will assist in
operating the Mark 7 Arterion Injection System ina safe manner.
This device is intended to be used by medical professionals with adequate training and experience in
cardiac catheterization procedures and techniques
1.2 Purpose
This manual is intended to provide instructions for servicing the Mark 7 Arterion Injection System
(herein referred to as “the injection system” safely and accurately. It is intended for those qualified to
service the injection system, whether they be MEDRAD Service Personnel, Laboratory Service
Technicians, or MEDRAD Authorized Dealers.
The information in this manual is intended for people with adequate backgrounds and experience in
electronics and electromechanical devices. Any attempt to repair a sophisticated medical device such
as the injector may result in personal injury, property damage, or patient injury.
For instructions on operating this equipment and associated warnings and cautions please reference
the operation manual
1.3 Contraindications
This device is not intended to be used for chemotherapy and is not intended to administer fluids other
than intravascular contrast agents and common flushing solutions.
1.4 Certifications
This device is equipped to operate at 100-240 VAC, 50/60 Hz, and is designed to comply with
EN 60601-1 / IEC 60601-1 Second/Third Edition and EN 60601-1-2/IEC 60601-1-2 Third edition.
1-1
Mark 7 Arterion Injection System
NOTICE
Electro-Mechanical Hazard-Equipment Damage may result.
• For proper operation, use only accessories and options provided by MEDRAD that are
designed specifically for the injector system. Other non-MEDRAD approved accessories or
options may cause equipment damage or may result in increased emissions or decreased
immunity of the injector system. Injector system accessories listed in it’s operation man-
ual comply with the requirements of electromagnetic emissions and immunity standards
IEC-60601-1-2 / 2007 3rd edition.
• Injector may disarm or fail to operate when exposed to high magnetic fields. Portable and
mobile RF communications equipment can affect the injector.
• Do not use injector adjacent to or stacked with other equipment. If adjacent or stacked
use is necessary, the injector should be observed to verify normal operation in the config-
uration in which it will be used.
Table 1 - 1: Recommended separation distances between portable and mobile RF communications equipment and the
injector
The injector is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the
user of the injector can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF
communications equipment (transmitters) and the injector as recommended below, according to the maximum output power of the com-
munications equipment
1-2
Introduction
Table 1 - 1: Recommended separation distances between portable and mobile RF communications equipment and the
injector
150 KHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
3.5 3.5 7
d = ------- p d = ------- p d = ------ p
V1 E1 E1
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m)
can be estimated using the equation applicable to the frequency of the transmitter, where p is the maximum output power
rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from
structures, objects and people.
INJECTOR REQUIRES SPECIAL PRECAUTIONS REGARDING EMC. Install and put into service
according to the EMC information provided below:
The injector is intended for use in the electromagnetic environment specified below. The customer or user of the injector should assure
that it is used in such an environment.
RF emissions The injector uses RF energy only for its internal function. There-
CISPR 11 Group 1 fore, its RF emissions are very low and are not likely to cause any
interference in nearby electronic equipment.
Voltage fluctuations/flicker
emissions Complies
IEC 61000-3-3
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Mark 7 Arterion Injection System
The injector is intended for use in the electromagnetic environment specified below. The customer or user of the injector should assure
that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Surge +1 kV differential mode +1 kV differential mode Mains power quality should be that of a typical
IEC 61000-4-5 +2 kV common mode +2 kV common mode commercial or hospital environment
<5% UT <5% UT
(>95% dip in UT) (>95% dip in UT)
for 0.5 cycle for 0.5 cycle
40% UT 40% UT
Voltage dips, short (60% dip in UT) (60% dip in UT) Mains power quality should be that of a typical
interruptions and volt- commercial or hospital environment. If the user
for 5 cycles for 5 cycles
age variations on of the injector requires continuous operation
power supply input during power mains interruptions, it is recom-
70% UT 70% UT mended the injector be powered from an unin-
lines
IEC 61000-4-11 (30% dip in UT) (30% dip in UT) terruptible power supply or battery
for 25 cycles for 25 cycles
<5% UT <5% UT
(>95% dip in UT) (>95% dip in UT)
for 5 sec for 5 sec
Power frequency
Power frequency magnetic fields should be at
(50/60 Hz)
3 A/m 3 A/m levels characteristic of a typical location in a
magnetic field
typical commercial or hospital environment.
IEC 61000-4-8
NOTE: UT is the a.c. mains voltage prior to application of the test level.
The injector is intended for use in the electromagnetic environment specified below. The customer or user of the injector should assure
that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
1-4
Introduction
Conducted RF 3 V rms
3 V rms d = 1.17 p
IEC-61000-4-6 150 kHz to 80 MHz
Radiated RF 3 V/m
IEC 61000-4-3 80 MHz to 2.5 GHz 3 V/m 80 MHz to 800 MHz
d = 1.17 p
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from
structures, objects and people.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur
radio, AM and FM radio broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed
RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the injector is
used exceeds the applicable RF compliance level above, the injector should be observed to verify normal operation. If abnormal performance
is observed, additional measures may be necessary, such as reorienting or relocating the injector.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
1.8 Disclaimers
MEDRAD makes no warranties on the contents of this manual, and specifically disclaims any implied
warranties of merchantability or fitness for any purpose.
MEDRAD reserves the right to change specifications and the contents of this manual without
obligation.
External wiring modification disclaimer: MEDRAD disclaims liability for any modifications or interfaces
with other equipment which are not in conformity with the specifications and information contained
within this manual. Such unauthorized action could jeopardize injector operation, safety, or reliability.
Accessory equipment connected to the MEDRAD Mark 7 Arterion Injection System must be certified
according to EN 60601-1 / IEC 60601-1 standard. Furthermore, all configurations shall comply with
system standard EN 60601-1-1/IEC 60601-1-1 Second Edition and EN 60601-1/IEC 60601-1 Third
Edition. Anyone who connects additional equipment to the signal input or output part configures a
1-5
Mark 7 Arterion Injection System
medical system and is therefore responsible that the system complies with the requirements of the
standard EN 60601-1-1/IEC 60601-1-1 Second Edition and EN 60601-1/IEC 60601-1 Third Edition. To
obtain on-site consulting or consulting references, contact MEDRAD Service.
All drawings in this manual are for reference purposes only, and may not reflect the construction of
units produced prior to the publication of this manual. Reproduction quality of these drawings may
have been effected by the level of reduction required. Call MEDRAD Service if assistance in drawing
interpretation is required.
1.10 Trademarks
MEDRAD, FluiDot, and MEDRAD Mark 7 Arterion Injection System are trademarks of MEDRAD, INC.
Other trademarks which appear in this manual are the property of their respective companies.
1-6
2 Symbols and Icons
The symbols and icons discussed in the sections below describe the requirements to which the Mark 7
Arterion Injection System conforms, how warnings are displayed in manual, and the icons used on the
equipment and equipment packaging.
IPX1 Code that specifies the degree of protection against vertically falling water
drops (IEC 60529).
Indicates separate collection for Electrical and Electronic Equipment per Direc-
tive 2002/96/EC .
2.3 Warnings
Indicates hot surface. Item can be hot and should not be touched without taking
care.
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Mark 7 Arterion Injection System
Purged Air Confirmation icon - indicates that the operator has confirmed that all
air has been purged.
2-8
Symbols and Icons
The hand switch connection location found on the back of the Display Control
Unit.
The Power Unit cable connection location found on the back of the Display Con-
trol Unit.
Operators use the End Case button to end the injection for a patient case, to
retract the syringe plunger, to clear the Total Contrast number, and to create a
record of the case.
The Enable button activates the Fill Strip and Auto-Fill button.
The Fill Strip allows operators to retract and advance the piston from the Injec-
tor Head.
The Auto-Fill button fills the syringe with a user defined contrast volume and at
a user defined speed.
2-9
Mark 7 Arterion Injection System
Indicates Alternating Current and identifies the Power Unit power cord connec-
tion.
Identifies a connection for Display Control Unit1. The Power Unit has two con-
nection points.
Identifies a connection for Display Control Unit2. The Power Unit has two con-
nection points.
Identifies the Earth Ground point (this terminal is meant for supplementary
grounding please contact MEDRAD prior to using this terminal)
Identifies an Injector Head connection. The Power Unit has two connection
points.
2 - 10
3 System Warnings, Precautions, and Notices
3.1 Warnings
WARNING
Air Embolism Hazard - Serious patient injury or death may result.
• Inspect pressure jacket and replace when signs of damage are evident.
• Use only accessories and options provided by MEDRAD which are designed specifically
for the injection system.
• Injector head shall be mounted on Articulating Arm.
• Inspect system and do not use when signs of damage are evident.
Electric Shock Hazard - Serious patient and/ or worker injury or death may result.
• The system should be opened and serviced by MEDRAD Service or MEDRAD trained
service personnel.
• Use only power cord approved for use on Mark 7 Arterion.
• For U.S installations, equipment shall only be connected to Hospital Grade or Hospital Only
outlets.
• Disconnect the system from line power before cleaning or attempting to perform any
maintenance or repairs.
• Avoid contact with pins.
• Ensure that connector covers are in place or cables are connected.
3.2 Cautions
CAUTION
Electric Shock Hazard - Minor or moderate patient and/ or worker injury may result.
• Verify that the voltage and frequency marked on the serial tag on the Power Unit matches
the voltage and frequency of the electrical outlet.
• Do not use extension cord or power adaptor with the system.
Mechanical Hazard - Minor or moderate patient and/ or worker injury may result.
• Do not use injector head handle to move injector system.
• Do not use the cabling or syringe to position injector system.
• Do not use system in the presence of flammable or combustible gases or other agents.
• Turn off power system and disconnect patient when system malfunction occurs.
• Follow installation procedures including use of proper screws and plugging all unused
holes.
• Move Articulating Arm to upper position prior to removing head.
• Do not mount DCU to Articulating Arm.
• Ensure that the retention knob is secure when mounting the head.
• Do not create a trip hazard when installing cable bracket.
• Do not create a trip hazard when routing cables.
3.3 Notices
NOTICE
Mechanical Hazard - Equipment Damage may result.
• Do not hang items on the Display Control Unit or Wall Mounting Bracket.
• Do not oil the friction plate on the Wall Mount Bracket.
3 - 11
Mark 7 Arterion Injection System
NOTICE
Electro-Mechanical Hazard - Equipment damage may result.
• Do not use tools to over tighten connections or to assist in the removal of disposables.
• Do not roll pedestal over cables.
• Regular preventive maintenance is recommended to ensure that the system stays
calibrated and functions properly. Refer to maintenance section of this manual or contact
MEDRAD for additional information.
• Allow the injector to stabilize at room temperature before use.
• Follow Electrostatic Discharge (ESD) protection practices.
• Disconnect the power cord before removing or replacing PC boards.
• Do not apply voltage to ISI connector.
• Provide only a switch closure if the injector is being started by an external start
connection.
• Do not block Power Unit vents.
• Installation clearance should be a minimum of 3 to 5 inches (8 to 13 cm).
• Before installing the Table Mount, ensure the table rail can withstand a minimum vertical
static load of 18 kg (40 lbs.) Refer to the table manufacturer documentation for weight
load information.
• Do not over tighten Table Mount knob.
• Do not force the Table Mount onto the table rail.
• Loosen Table Mount knob prior to removal of components.
3 - 12
4 Cleaning and Maintenance
WARNING
Cross Contamination Hazard - Serious patient and/or worker injury or death may result.
• Do not contact disposables with cleaning agent during cleaning.
• Do not conduct cleaning process during injection procedure.
NOTICE
Electro-Mechanical Hazard - Equipment Damage may result.
• Disconnect power before cleaning.
• Use a wipe or dampened cloth for cleaning.
• Do not soak or immerse components.
• Do not use strong cleaning agents.
• Perform routine cleaning and maintenance.
• Remove power when connecting or disconnecting cables.
• Do not clean the syringe.
This chapter identifies the proper methods for cleaning the injection system, the recommended main-
tenance schedule, and an operational checkout of the injection system.
The injection system must be properly maintained to ensure it is in peak operating condition. The indi-
vidual maintenance schedule depends upon how your injection system is used, the type of procedures
performed, and frequency of use.
Failures which occur due to lack of proper maintenance will not be covered under warranty.
NOTE: MEDRAD Service will make available for purchase upon request:
• Service and schematic manuals that will assist qualified technicians to repair
components classified as repairable.
• On-site consulting services.
4.1 Daily
CAUTION
Mechanical Hazard - Minor or moderate patient and/or worker injury may result.
• Do not use an autoclave to sterilize the Pressure Jacket.
• Refer to Pressure Jacket cleaning instructions.
The following procedures are recommended for daily cleaning and inspection of all components on the
injection system. If any defects are detected, either repair the system, or call the local MEDRAD office
or the local authorized dealer for service. Do not use the system until the problem is corrected.
4.1.1 Cleaning the Injector Head, Syringe Heat Maintainer, Pressure Jacket, Piston,
Syringe Interface, and Table Bracket
Clean the product by wiping with a cloth dampened with warm water.
Disinfect components, except Pressure Jacket, with:
• Germicical Disposable Wipe, or
• Bleach Wipe, for isolation patients
4 - 13
Mark 7 Arterion Injection System
5. Clean the Pressure Jacket with a soft cloth or a paper towel dampened with a cleaning solu-
tion to remove contrast media and other contamination.
Some cleaning agents react with the plastic material and may cause structural degradation.
MEDRAD recommends that the Pressure Jacket be washed in a solution of warm tap water
(35° – 45° C) and mild non-abrasive detergent (neutral grade low pH, enzymatic cleaner),
and then rinsed thoroughly and dried with a soft towel.
A solution of dish washing detergent and water is compatible with the Pressure Jacket. If a
germicidal cleaning agent is desired, contact the germicide manufacturer to check the rec-
ommended dilution and compatibility with polycarbonates. If the solution is acceptable, fol-
low the manufacturer’s directions exactly. Do not clean the Pressure Jacket with an
automatic dishwasher. The Pressure Jacket is not dishwasher safe. Do not leave the Pres-
sure Jacket in germicide for extended periods of time.
Do not expose the Pressure Jacket to fluorocarbons (such as Freon), or other solvents (ace-
tone, benzol, carbon tetrachloride, MEK, MIBK, toluol, trichlor, and triclene). Gasses used to
pressurize aerosol cans can be damaging to the Pressure Jacket. Therefore, do not use aero-
sols in or around the Pressure Jacket.
6. Fully advance the piston
7. Turn off the system at the Power Unit.
8. Clean the piston.
9. Clean the inner area of the syringe interface.
10. Clean the Drop Front. The drop front cone should pivot freely back and forth. If it does not, it
may be contaminated with contrast.
11. Clean the Injector Head case.
12. Re-install the clean Pressure Jacket.
13. Re-install the clean Syringe Heat Maintainer.
14. Clean any spilled contrast media from the Table Bracket and table rail to assure free move-
ment of the bracket along the rail.
4 - 14
Cleaning and Maintenance
Rotate the Pressure Jacket while looking through it to view all areas. This includes the front edges and
the entire cylindrical surface.
A Pressure Jacket should be rejected for cracks, crazing, scratches (if a fingernail can catch on the
scratch), and opacity. These conditions indicate that the Pressure Jacket has been weakened and may
fracture during a high pressure injection. The Pressure Jacket should NOT BE USED if any of these con-
ditions exist.
Cracks are usually the result of a sharp impact (such as from dropping). A crack may appear simply as
a line, usually originating at the radius or edge and may also appear in conjunction with crazing.
Figure 4 - 1: Cracks
Stress Cracks may appear after the Pressure Jacket has been subjected to a number of pressure
cycles. These tiny cracks appear around the front area of the Pressure Jacket, and usually form a pat-
tern around the jacket’s circumference. Stress cracks are easiest to see while rotating the Pressure
Jacket in front of a light source.
Figure 4 - 3: Crazing
Scratches result from objects striking or scraping the inside or outside surface of the Pressure Jacket.
Scratches may occur when the Pressure Jacket is improperly handled. Check depth of scratches by
pulling your finger across the scratch, perpendicular to the surface. If your fingernail catches on a
scratch, the Pressure Jacket should NOT BE USED.
Figure 4 - 4: Scratches
Normally the Pressure Jacket is transparent, enabling you to clearly see through the barrel.
4 - 15
Mark 7 Arterion Injection System
Figure 4 - 5: Opacity
4.2 Monthly
Once a month, the entire system should be thoroughly inspected and cleaned, and an Operation
Checkout should be performed using the procedures outlined in “14.2.3 Performing an Operational
Checkout”.
4.2.1 Cleaning the Display Control Unit, Pedestal, Power Unit, and Table Bracket
NOTICE
Electro-Mechanical Hazard - Equipment Damage may result.
• Remove power when connecting or disconnecting cables.
• Do not spray cleaning solutions directly onto the DCU touch screen.
Clean the product by wiping with a cloth dampened with warm water.
4 - 16
Cleaning and Maintenance
4.2.2 Inspecting and Cleaning the Internal Air Filter (Power Unit)
1. Turn off the system at the Power Unit.
2. Remove the two screws shown in the drawing below.
A basic functional checkout of the injection system should be included as part of monthly maintenance.
Verify proper operation of the injection system to help detect any problems that may not be noticed in
day-to-day operation. The following procedure represents a suggested series of activities which
encompasses typical operation of the system. Read the following procedure carefully before beginning
the checkout. If problems are detected or any step fails this checkout, contact your MEDRAD Service
Representative.
An empty Syringe is required to perform this checkout.
1. Plug in the injection system.
2. Press the Main Power Switch on the Power Unit, and press the On/Off Switch on the Dis-
play Control Unit. All power switches should illuminate green.
4 - 17
Mark 7 Arterion Injection System
a. Ensure that the system passes self-test with no error messages. When self-test com-
pletes, a safety screen displays.
b. Press Continue to acknowledge the safety information and proceed to the Home tab.
c. Ensure that the Home tab displays.
3. Press the brightness controls to ensure that the controls vary the display brightness without
completely obscuring information at either extreme. Adjust to a suitable brightness.
4. Use the handle and the back of the Injector Head (but not the Manual Knob) to rotate the
Injector Head to the Purge position (upright).
a. Ensure that the Volume Remaining display on the Injector Head (orange digits) is active
and is properly oriented.
b. Ensure that the Flow Rate, Volume, and Pressure Limit are not active.
5. Use the handle and the back of the Injector Head (but not the Manual Knob) to the Inject posi-
tion (downward).
a. Ensure that the Volume Remaining display inverts.
b. Ensure that the Flow Rate, Volume, and Pressure Limit display and are properly ori-
ented.
6. Insert an empty syringe into the syringe interface.
a. Completely close the drop front.
b. Ensure that the Volume Remaining icon on the Injector Head illuminates.
7. Press the Forward and Reverse on the Fill Strip.
a. Ensure the piston does not move.
8. Press the Enable button.
a. Ensure the green indicator near the enable key illuminates.
b. Ensure the green indicator goes out after approximately five seconds.
9. Press the Enable button, and press Forward on the Fill Strip within five seconds.
a. Ensure that the piston extends.
b. Vary the position of your finger on the Fill Strip to ensure the piston load speed varies.
c. Ensure that the Volume Remaining display on the head decreases.
10. Press the Enable button, and press Reverse on the Fill Strip within five seconds.
a. Ensure that the piston retracts.
b. Vary the position of your finger on the Fill Strip to ensure the piston load speed varies.
c. Ensure that the Volume Remaining display on the head increases.
d. Retract the piston to its rear limit. The Volume Remaining should read “150mL”.
11. From the Home tab, enter a protocol with the following parameters:
Volume - 20 ml
Flow Rate - 10 ml/s
Pressure Limit - 500 PSI
a. Ensure the Injector Head displays these value.
12. Select Arm Single to Arm the injector.
a. Ensure that the display indicates that the injector is in the Armed state.
b. Ensure that the Armed light on the injector head is on solid.
13. Using the hand switch or foot switch, initiate an injection.
a. Ensure that the Display Control Unit display indicates that the injector is in the “Inject-
ing” state and the Armed light on the injector head flashes.
b. Confirm that the injection completes in approximately two seconds.
c. Ensure that the Armed light on the Injector Head goes out.
d. When the injection is complete, release the switch.
e. Ensure the Actuals window on the Display Control Unit indicates that 20 ml volume was
delivered at a rate of 10 ml/s.
14. From the Display Control Unit touch screen, change the Volume to 50mL.
4 - 18
Cleaning and Maintenance
4.3 Annually
MEDRAD offers Preventative Maintenance Programs. These annual programs greatly assist in main-
taining accuracy and reliability, and can also extend the life of the system. Contact your local MEDRAD
office or your local authorized dealer for further information. See Chapter 1 “Information” for address,
telephone, fax and website information.
Manufacturer Model
Bio-Tek Instruments, Inc. Model 601 PRO
4 - 19
Mark 7 Arterion Injection System
Manufacturer Model
Bapco IEC601L
1. With power applied, and the line at normal, leakage should be less than 300 micro amps.
2. With power applied and the line reversed, leakage should be less than 300 micro amps.
3. Disconnect the leakage test device.
4 - 20
5 Troubleshooting
5.1 System Malfunction Codes
Conditions can occur which will prevent the injection system from being armed, or interrupt an injec-
tion that is in progress. These conditions may be operator induced or caused by a system malfunction.
The system displays Error Codes to inform the operator of these conditions.
Consider the following guidelines before troubleshooting any condition. These guidelines may help in
quickly resolving the condition. Try the simpler things first.
• Remove the power cord from the power source for one minute, then reapply power. The con-
dition could be intermittent, or caused by a voltage transient. If the condition persists, con-
tinue troubleshooting.
• To verify the existence of a condition, try to recreate the problem. Follow the Checkout Proce-
dure outlined in this manual for proper/improper operation of the system Refer to “Perform-
ing an Operational Checkout” on page 4 - 17.
• Some faults can be caused by a noisy electrical environment. If these conditions persist, con-
tact MEDRAD Factory Service* for further assistance.
* Indicates contact MEDRAD Factory Service or an Authorized Dealer. Refer to “Information” on page 1
- 1 for address, phone, and Fax information.
5 - 21
Mark 7 Arterion Injection System
CAUTION
Mechanical Hazard - Minor or moderate patient and/or worker injury may result.
• Remove power and disconnect patient when system malfunction occurs.
Type 3 messages are system malfunction messages which require power to be removed from the sys-
tem. Type three messages are accompanied by three beeps. Some Type 3 messages provide sugges-
tions to prevent the condition from recurring. If the condition cannot be corrected, record the code and
number from the lower left corner of the dialog box, then call MEDRAD Service for assistance.
Type 3 errors are divided into categories of function level. Each category is also divided into specific
errors. Below is a list of the categories and suggested repair sequences. These are to be tried in order,
not to be performed all at once. For further assistance, contact MEDRAD Service or an authorized
dealer.
NOTE: Before replacing any parts, cycle power to the system. This initiates a system self-
test. If this does not correct the problem, replacement of serviceable components
as needed may be required.
5 - 22
Troubleshooting
MOTA Motor A
Errors with a prefix of MOTA indicate a problem with the motor or the associated circuitry.
• Ensure the connection to Motor Drive card is fully seated.
• Replace Motor.
• Replace Motor Drive Card.
POTA Pot A
Errors with a prefix of POTA indicate a problem with the potentiometer or the associated circuitry.
• Ensure the connector is fully seated on the interface card.
• Realign potentiometer.
• Replace potentiometer.
• Replace Signal Management Card.
• Replace the Servo/CPU card.
POWR Motor Drive Card
Errors with a prefix of POWR indicate a problem with the Motor Drive card or the associated circuitry.
• Verify power supply voltages are at the Power Drive card.
• Ensure that connectors are fully seated.
• Replace the Motor Drive card.
• Replace the Servo/CPU Card.
SBC Single Board Computer (SBC)
Errors with a prefix of SBC indicate a problem with the Single Board Computer or associated circuitry.
• Ensure the card has all the connectors fully seated.
• Replace the SBC card.
• Replace the Display Interface Card.
SER Servo/CPU Card
Errors with SER typically indicate the Head Card. This may be either a condition that must be corrected,
or an electrical transient that disrupted the system.
• Replace the Servo/CPU card.
• If the condition persists, call MEDRAD Factory Service.
SYRSENA Syringe Sensor A
Errors with a prefix of SYRSENA indicate a problem with the syringe sensor or associated circuitry.
• Ensure no syringe is present during self test.
• Ensure the connector between the Syringe sensor and the Signal Management Card is fully
seated.
• Replace the Syringe Sensor Switch.
• Replace the Signal Management Card.
• Replace the CPU/Servo Card.
SW Software Problem
Errors with SW typically indicate a problem with internal software. This may be either a condition that
must be corrected, or an electrical transient that disrupted the system.
• Contact MEDRAD to reload software.
• Replace the SBC card.
• Replace the Servo/CPU card.
5 - 23
Mark 7 Arterion Injection System
5 - 24
6 Theory of Operation
The system consists of three basic parts:
• Display Control Unit
• Power Unit
• Injector Head
Each component in the system is interconnected with an external cable from the Power Unit, the sys-
tem center.
This section explains basic circuit block diagrams of each of the sub-systems. A block diagram of each
primary component is followed by a functional block description for each of the sub-systems.
• "System Interconnect"
• "DCU"
• "Power Unit"
• "Head"
• "Head Display/Armed Light Card"
• "ISI"
Effects on Pressure
Factors
Decrease Increase
Consider the above factors when setting pressure limit to achieve the desired injection flow rate.
Proper pressure limit setting optimizes the angiographic images.
The injector applies the minimum pressure needed to achieve the programmed flow rate. If the pres-
sure from the injector exceeds the programmed pressure limit, the system cannot achieve the flow rate
and a Sentinel message displays.
Pressure information can be found in the History tab.
6 - 25
Mark 7 Arterion Injection System
6 - 26
Theory of Operation
6 - 27
Mark 7 Arterion Injection System
6 - 28
Theory of Operation
3032670
3032670
30
6 - 29
Mark 7 Arterion Injection System
6 - 30
Theory of Operation
3032056
6 - 31
Mark 7 Arterion Injection System
6 - 32
Theory of Operation
6.4.2.2 DCU
The DCU serves three main functions.
Display - All functions of the System are displayed on the DCU. This includes Operating values, Warn-
ings and Cautions, and Error messages.
Input - When information is to be placed into the System, the selected value is entered on the face of
the DCU.
Monitor - The DCU monitors the safety, and functionality of the System.
6.4.2.4 Accessories
The accessories listed in this section are listed on the System Block Diagram.
6.5 DCU
The Display interface board is the primary PCB in the Display enclosure. Support circuits are placed on
this PCB including the physical support for the SBC. All connectors and switches, such as the start
switch and interface cable from the Base are terminated at the Display interface card.
6 - 33
Mark 7 Arterion Injection System
6 - 34
Theory of Operation
6 - 35
Mark 7 Arterion Injection System
6.5.2.12 LCD
The primary visual interface to the operator is a 640 x 480 Color Liquid Crystal Display (LCD) panel with
a physical dimension of 10.4” diagonally. This is driven directly from the SBC card.
6 - 36
Theory of Operation
6 - 37
Mark 7 Arterion Injection System
6 - 38
Theory of Operation
6.7 Head
6.7.1 Head Overview Block Diagram
6 - 39
Mark 7 Arterion Injection System
6.7.2.5 Potentiometer
Provides absolute piston positioning information.
6.7.2.7 Servo/CPU
Contains a microprocessor that manages card power, data, footswitch control, motor drive, network
communications.
6 - 40
Theory of Operation
TO POWER UNIT
P321
5V 5V 15 V
5V
CPU 5V
PHASE
AI_DSPA_PHASEA_I CURRENT
AI_DSPA_PHASEB_I FEEDBACK
AI_DSPA_PHASEC_I U11, U13,
U14
6
CPU 5V P334 P335 P332
AGND
TO SERVO/CPU CARD
DGND
CABLE #3036502
4
AGND Drive Inhibit
Control SHUTDOWN
P301
DO_nDRIVE Isolation
INHIBIT CONTROL U9 HALL
ENCODER MOTOR GEAR
SENSORS
DI_DRIVE 5 BOX
INHIBIT STATUS Drive Inhibit
Status
Isolation
U9 MOTOR
ASSEMBLY
DI_DSPA_EIA
DI_DSPA_EIB
S1
P335
DI_DSPA_COMM_A
S2
DI_DSPA_COMM_B
S3
DI_DSPA_COMM_C
6 - 41
Mark 7 Arterion Injection System
6. Bridge Current Test Feedback - Measuring, isolating and filtering Power Amplifier bridge
voltage.
7. 5 VDC Regulator - 5 VDC power to the servo motor.
CPU/SERVO CARD
3011677
3026498 3032056
3026385
To Signal
Cable
Cable
P/J 4
P/J 2
Network
Management Power Comunications To Tower
Card
To Signal
3026500
Cable
P/J 3
SAX
3026502
Management
Cable
To Motor
P/J 1
Card Display Motor
Drive Drive Card
3026499
To Signal
Cable
P/J 7
P/J 5
Management Standard
JTAG
I/O
Card
P/J 9
Debug
To Signal
3026501
Cable
P/J 6
Management Expansion
Card IO
6 - 42
Theory of Operation
6 - 43
Mark 7 Arterion Injection System
6 - 44
Theory of Operation
tainer Controller within the CPLD, which in turn provides the drive signal for control of the
amount of heat generated.
15. The External Interfaces Card (EIC) provides ESD protection and filtering for the various signals
from devices outside of the Head before connecting to the SMC. The addition of this board
allows for better shunting of potential noise sources away from the system components as
well as helps to simplify cabling and servicing. The four interfaces on the EIC are:
a. The RJ45 Service and Calibration port allows for connection of Service SWIFT to the
Head and also includes the simultaneous connection of the calibration device. ESD pro-
tection is provided on the calibration signal. The Ethernet connection simply passes
straight through the EIC and provides attachment to the bulkhead cable.
b. The Heat Maintainer signals have ESD protection and filtering as they pass through the
EIC. A wiring harness connects the panel mounted 6-pin DIN connector for the Heat
Maintainer to the EIC.
c. The future Air Detector signals have ESD protection and filtering as they pass through
the EIC. A wiring harness connects the panel mounted 8-pin DIN connector for the Air
Detector to the EIC.
d. (Future Item) The RJ11 connector provides the direct interface to the Hand Controller.
The Hand Controller signals have ESD protection and filtering as they pass through the
EIC.
16. The CPLD contains the logic for controlling the Heat Maintainer and Air Detection interfaces.
17. (Future Item) The Air Detection and Hand Controller interfaces are connected to the External
Interfaces Card and then provided to the CPLD and SAX card. The power to the Air Detector is
fused and controlled by the SAX card.
P506 P504
nFILL HDC_TX
nENABLE
P HDC_RX
nFWD1:5 5 KEYPRESS
FROM / TO
J
SIGNAL
5 PWR_FAIL MANAGEMENT
5
nREV1:5 CARD
HEAD OVERLAY 1 +15V
0 DGND
nENA_LED
1
+5V
Shield ground HEAD
layer on
DGND
P ICD2 TEST /
overlay DISPLAY 5 PROGRAMMING
CARD 0 PORT
2
P
5 REAL ICE
0 DEBUGGING
3
P
DGND PORT
nARMLT1
6 - 45
Mark 7 Arterion Injection System
6 - 46
Theory of Operation
6.8.2.2 Microcontroller
The Microcontroller is a Microchip PIC18F87J11 general purpose 8-bit microcontroller.
This particular PIC device has an 80 pin TQFP package, features 128K of program flash memory, 3904
bytes of internal system RAM and operates over a voltage range of 2-3.6VDC
The PIC is clocked with an external 9.216MHz oscillator, chosen primarily for parts reuse with existing
designs and minimal baud error with the UART.
The PIC peripherals used in this design are the extended memory interface, the UART, A/D Converter
and a PWM output.
This design utilizes this particular PIC devices External Memory Interface function, in which the nvRAM
/ RTC memory and 7-segment LED displays are interfaced using traditional parallel data / addressing.
The board will be equipped with ports to program and debug the PIC from the In-Circuit Debugger
(ICD2/3) or the In-Circuit Emulator (RealICE).
6 - 47
Mark 7 Arterion Injection System
6 - 48
Theory of Operation
6.9 ISI
6.9.1 ISI Basic Functionality
The MEDRAD Mark 7 Arterion ISI supports the following functions on the Injector as depicted in the
figure below.
• Allows the Injector to be Disarmed when Armed or Injecting.
• Prevents the Injector from being Armed.
• Allows the Injector to be Started from an Imaging System input when the Injector is in an
armed state.
• Allows the Injector Hand Controller and Footswitch to be disabled from directly initiating a
contrast injection
6 - 49
Mark 7 Arterion Injection System
6 - 50
Theory of Operation
6 - 51
Mark 7 Arterion Injection System
CPU/Servo
3012611 / 3011677/ 3032056
ISI Power
Processing, Management
Conversion, Head SMB
P 208
J 203
P/J 5
P 103
3007258 SMC
and 3007265
Serilization
P 105
Imaging
P 401 System
ISI Card
P 404
P 403
3011562
Head
Power Unit
3007255
3027770
24V
5V 15V 24V
15V 15V to 24V
Isolation Power
24V
Supply
T1, U2, U3 1 Opto- Universal
Isolated Connector
Inputs P403
15V to 5V
Converter 5V 5
Harness - 3011596
7
U1 2
5V 24V
Harness
3011597
To SMB
P 401
5V 5V 15V 24V
RS 485 Relay
Transceiver Microcontroller Outputs Siemens
U4 U5 with Connector
3 Readback P404
6
4
7
ISI Card
P 402
3011562 8
3032782
6 - 52
Theory of Operation
6.9.4.4 4 - Microcontroller
Receives data from RS-485 transceiver, isolated input signals from the Imaging System and transmits
data to RS-485 transceiver and drivers for relay outputs. The microcontroller provides the control of the
ISI interface and provides the status of the inputs in these messages.
6 - 53
Mark 7 Arterion Injection System
6 - 54
Theory of Operation
6 - 55
Mark 7 Arterion Injection System
Figure 6 - 11: Universal ISI Cable (XMC 906i) - For use with Toshiba and Shimadzu
6 - 56
Theory of Operation
Figure 6 - 14: Philips Integris ISI Cable - Table Connection (XMC 925A)
6 - 57
Mark 7 Arterion Injection System
Figure 6 - 15: Philips Integris ISI Cable - Remote Power Unit (XMC 945S and XMC 945 40)
Figure 6 - 16: Philips Allura Xper ISI Cable - Remote Power Unit (XMC 947R)
6 - 58
Theory of Operation
Figure 6 - 17: Philips Allura Xper ISI Cable - Table Connection (XMC 927A)
6 - 59
Mark 7 Arterion Injection System
6 - 60
7 Disassembly/Assembly
WARNING
Electric Shock Hazard - Serious patient and/ or worker injury or death may result.
• Perform calibration when specific components listed below are replaced in the system.
NOTICE
Mechanical Hazard - Minor or moderate patient and/or worker injury may result.
• Ensure all gaskets are properly seated and not damaged upon re-assembly.
NOTE: Electronic assemblies contain potentially hazardous materials. Dispose of system
components or accessories properly. Follow all local regulations for the recycling or
disposal of electronic assemblies, or contact MEDRAD Service for assistance.
When troubleshooting the MEDRAD Mark 7 Arterion Injection System, it may be necessary to order
replacement parts for a given assembly. This section contains information regarding individual assem-
blies of the system. Each primary assembly has a corresponding Parts Diagram and Parts List, specify-
ing components that may require replacement. To order replacement parts, contact MEDRAD Service,
or your authorized MEDRAD dealer.
This chapter shows disassembly and assembly for the following sub-assemblies:
• "Display Control Unit"
• "Head"
• "Power Unit"
Inverter
Touchscreen
Inverter Display
7 - 61
Mark 7 Arterion Injection System
9. Remove the four screws securing the interface card, and fold the card to side with white con-
nector.
10. Remove the eight screws securing the clear plastic display cover and lift off the display cover.
11. Remove copper tape from the display to cover, leaving it attached to cover.
12. Lift out the display.
13. Lift out the touch screen.
To install new touch screen:
1. Ensure the new touch screen is clean before installing.
2. Set touch screen into the cover. Ensure it lays flat (the metal tabs on the connector face
upwards and the label faces down).
3. Set the display into cover. Ensure it lays flat.
4. Install the white connector to display.
5. Install the copper tape back onto display.
6. Install the display cover over the display, and secure it with eight screws.
7. Install interface card into assembly, and secure it with four screws.
8. Attach the two connectors from the display to the inverter card.
9. Install the touch screen cable to interface card.
10. Connect the two power switch connectors and speaker connector from rear cover to board.
11. Install the cover, and secure it with four screws.
12. Reconnect any removed cables or covers.
Inverter
Touchscreen
Inverter Display
7 - 62
Disassembly/Assembly
9. Remove the four screws securing the interface card, and fold the card to side with white con-
nector.
10. Remove the eight screws securing the clear plastic display cover and lift off the display cover.
11. Remove copper tape from the display to cover, leaving it attached to cover.
12. Lift out the display.
To replace LCD display:
1. Ensure the new display is clean before installing.
2. Set display into cover. Ensure it sits flat.
3. Install the white connector to display.
4. Install the copper tape back onto display.
5. Install the display cover over the display, and secure it with eight screws.
6. Install the interface card into assembly, and secure with four screws.
7. Attach two connectors from the display to the inverter card.
8. Install the touch screen cable to the interface card.
9. Connect the two power switch connectors and speaker connector from rear the cover to the
board.
10. Install the cover, and secure it with four screws.
11. Reconnect any removed cables or covers.
7 - 63
Mark 7 Arterion Injection System
7 - 64
Disassembly/Assembly
2. Set the card onto the display interface card, and secure it with the four screws
3. Install the connectors removed (the two ribbon cables, the Ethernet cable, and the three con-
nectors) from the CPU card.
4. Connect the power switch connectors (2) and speaker connectors from the rear cover to the
board.
5. Install the cover, and secure it with the four screws.
6. Reconnect any removed cables or covers.
3. Connect the two power switch connectors and speaker connector from rear cover to board.
4. Install the cover, and secure it with the four screws.
5. Reconnect any cables removed.
7 - 65
Mark 7 Arterion Injection System
3. Connect the two power switch connectors and speaker connector from the rear cover to the
board.
4. Install the cover, and secure it with the four screws.
5. Reconnect any removed cables or covers.
7.2 Head
7.2.1 Top Head Cover 3026093
To remove old head cover:
1. Remove the four screws from the bottom cover.
7 - 66
Disassembly/Assembly
Overlay
Connector
Arm Light
Connector
7 - 67
Mark 7 Arterion Injection System
Locked Unlocked
7 - 68
Disassembly/Assembly
Locked Unlocked
3. Remove the screw holding the ground tab.
4. Peel off the overlay from the top of the cover.
To install the top overlay:
1. Clean the cover of any residue from the old overlay.
2. Feed the ribbon connector through the top cover.
3. Remove the backing from the new overlay.
4. Feed the ground strap cable through the cover before securing the overlay.
5. Insert the overlay connector, and slide the locker into place to lock the connector.
6. Secure the ground strap with the screw.
7. Install the top cover.
7 - 69
Mark 7 Arterion Injection System
Signal Management
Board P211
Ground Wire
P331
9. Tilt the cover down, and remove the three connectors from the external interface card.
7 - 70
Disassembly/Assembly
10. Remove the two screws holding the head cable clamp to the rear plate 5/64 hex key.
11. Lift off the cover and cable.
To install bottom head cover:
1. Position the head cover so that the head cable can be secured to the rear plate.
2. Secure the head cable to the rear plate with the cable clamp over the exposed copper tape
on the cable.
3. Route the wires under the handle, and connect the three connectors to external interface
card.
4. Route the Ethernet connector wires under the handle, and connect it to the Servo CPU card.
5. Route the wires under the handle, and connect P331 connector to power card.
7 - 71
Mark 7 Arterion Injection System
3. Once nut is off of the inside cover, slide the cable out of the cover.
To install head cable:
1. Remove the nut from the new cable.
2. Slide the cable into the cover.
3. Replace the nut onto the cable, and seat it into the bottom cover.
7 - 72
Disassembly/Assembly
4. Rotate the cable to secure the nut. Tighten the nut with 7/8 wrench.
5. Install the top and bottom covers.
7 - 73
Mark 7 Arterion Injection System
6. Use a 1/8 hex key to remove the two screws securing the arms into the front plate.
7. Lift off the drop front arms and the metal ring.
8. Remove the drop front and syringe sensor switch.
9. Use a 3/16 hex key to remove the four bolts securing the front plate to the frame.
10. Slide the front plate off of the piston.
To install drop front:
1. The new drop front comes with a front plate attached to metal ring.
2. Remove the four screws holding the metal ring to front plate, and slide the metal ring forward
onto arms.
3. Install the front plate onto the piston, and secure it onto the head with the four bolts.
4. Slide the metal plate back against the front plate.
5. Secure the two bottom screws onto metal plate.
6. Set the handle onto the front plate, and secure the handle. Apply Loctite 242 to the screws.
7. Install the screw holding the handle to the side of the head. Apply Loctite 242 to the screws.
8. Install the drop front and the syringe sensor switch.
9. Install the top and bottom covers.
7 - 74
Disassembly/Assembly
Syringe Sensing
Switch
Drop Front
Switch
2. Remove the four screws holding the interface card, and slide the card back to gain access to
the switch.
3. Use a 3/32 hex key to remove the screw holding the drop front switch into the front plate.
4. Remove the four screws securing the power card, and slide the card back to gain access to
the switch.
5. Use a 3/32 hex key to remove the screw securing the syringe sensing switch onto front plate.
6. Lift out the switches.
7. Disconnect the cable from the interface card.
To install drop front switch and syringe sensor switch:
1. Thread the screw into the new drop front switch and into front plate.
2. Rotate switch until it fully seats into the front plate.
3. Secure the screw.
4. Thread the screw into the new syringe sensor switch and into front plate.
5. Rotate switch until it fully seats into the front plate.
6. Secure the screw.
7. Connect the cable to the interface card.
8. Secure the screws onto the power card and the interface card.
9. Install the top and bottom covers.
7 - 75
Mark 7 Arterion Injection System
Encoder
Connector
Power
Connector
Ferrite
7. Remove four screws holding motor to rear plate 9/64 hex key.
8. Lift motor out.
To install the motor:
1. Install motor into rear frame with cables facing toward ball screw and away from handle.
2. Make sure motor is fully seated to rear plate. Secure with four screws.
3. Install belt onto small gear and them big gear.
4. Install board support as shown above, wire cables run under support. Secure with two
screws without lock washers.
5. Install four other screws.
6. Connect encoder wires to power card.
7. Connect power connector.
8. Install ferrite onto power wires.
9. Install top and bottom covers.
10. Electrically recalibrate Pressure.
7 - 76
Disassembly/Assembly
Blue
White
Brown
Red Strip
Faces Up
Connector
Under Ribbon
Cable
7 - 77
Mark 7 Arterion Injection System
4. Remove card.
To install Servo CPU:
1. Install card and secure with four screws.
2. Install five ribbon cables.
3. Install top and bottom covers.
4. Electrically Recalibrate Head.
7 - 78
Disassembly/Assembly
Connector
Under Handle
Connector
Under Ribbon
3. Remove two bolt holding pivot knuckle to head frame (5/32 hex key).
4. Slowly lift knuckle away from head. There is still a cable attached to the assembly.
5. Disconnect cable from position sensor card.
6. Remove screw securing card and lift card off.
To install the position sensor:
1. Rotate sensor on new card to match “D” location in shaft.
2. Set card onto shaft and alignment hole.
3. Secure with screw.
4. Connect cable to position card.
7 - 79
Mark 7 Arterion Injection System
5. Set assembly onto frame and secure with two screws (loctite screws with loctite 242).
6. Install top and bottom covers.
7. Electrically Recalibrate position sensor.
Combo Gear
Mark 2
Mark 1
7 - 80
Disassembly/Assembly
5. Remove cover.
7 - 81
Mark 7 Arterion Injection System
To install cover:
1. Install connectors into connector bodies in top cover. They are keyed to be installed one way.
Push till they snap into place.
2. Install cover and secure with fourteen screws previously removed.
Red
Goes to Red/White
Display 2
Yellow
Yellow/White
7 - 82
Disassembly/Assembly
7 - 83
Mark 7 Arterion Injection System
#8-32 x 1/4”
#8-32 x 1/4”
#8-32 x 1/4”
#8-32 x 1/4”
#8-32 x 1/4”
#8-32 x 1/4”
#8-32 x 1/4”
#8-32 x 1/4” #8-32 x 1/4”
#8-32 x 1/4”
3. Lift and tilt the top of the Power Unit.
NOTE: Do not lift the top of the Power Unit too high to avoid disconnecting other wires in
the Power Unit.
4. Press the two metal clips (A) on the side of the Display Control Unit 1 connector and Injector
Head housing to disconnect the housing from the shell.
5. Remove the two screws for each of the shells. Retain the screws.
6. Lift the shells out of the top of the Power Unit.
7. Remove the port covers for Display Control Unit 1 and the Injector Head from the back plate
of the Power Unit.
8. Place the port covers removed in step 7 over the empty ports on the top of the Power Unit.
Use the screws removed in step 7.
9. Insert the shells into the corresponding holes in the back of the Power Unit.
NOTE: The smaller shell goes into the Display Control Unit 1 hole and the larger shell goes
into the Injector Head hole.
7 - 84
Disassembly/Assembly
10. Use the screws removed in step 5 to secure the shells into the holes.
11. If relocating Display Control Unit 2 proceed to the Optional Steps. Otherwise proceed to step
12.
E
D
VIII. Disconnect cable from the back of the Service Port (B).
IX. Remove the four screws from the ISI Card (C). Retain the screws.
X. Remove the nut from the ground screw (D). Retain the nut.
XI. Lift the ground wire for the Display Control Unit 2 connector off of the ground screw.
XII. Replace the ground screw nut (D) removed in step X.
XIII. Gently lift the ISI card and reroute the Display Control Unit2 connector so that no longer sits
under the ISI card.
XIV. Replace the ISI card and secure it with the four screws (C) removed in step IX.
XV. Plug the cable removed in step VIII into the back of the Service Port.
XVI. Remove the nut from the ground screw (E). Retain the nut.
XVII.Place the ground wire for the Display Control Unit 2 connector onto the ground screw.
XVIII.Replace the ground screw nut (E) removed in step XVI.
7 - 85
Mark 7 Arterion Injection System
XIX. Align the grooves on the Display Control Unit 2 connector with the corresponding notches on
the Display Control Unit 2 shell.
XX. Snap the Display Control Unit 2 connector into place.
End Optional Steps
12. Align the grooves on the Display Control Unit 1 connector with the corresponding notches on
the Display Control Unit 1 shell.
NOTE: The smaller connector is Display Control Unit 1.
13. Snap the Display Control Unit 1 connector into place.
14. Repeat steps 12 and 13 for the Injector Head connector.
15. Replace the top of the Power Unit onto the base.
16. Secure the six side screws, two top screws, and six back screws removed in step 2.
7 - 86
Disassembly/Assembly
2. Install cover plate and secure with two screws removed in step 1.
3. Slide four of the wires removed from power supply through holes in plate. The green yellow
wire does not go through a hole in the plate.
4. Remove four screws that secure the power supply from bottom cover.
5. Remove four nuts (11/32) securing the mounting plate.
6. Lift up on plate and pull towards the front of the case with the wires to the front connectors
still attached.
7 - 87
Mark 7 Arterion Injection System
7. Unplug AC power inlet from front of power supply and power sense connector.
NOTE: If the power sense connector cannot be removed, remove other end of the wire
from Power card and then remove from power supply once out of module.
Red
Yellow
Yellow/White
Red/White
Extra
Ground Wire
Ground Wire
6. Reinstall cover.
7 - 88
Replacement Parts
8 Replacement Parts
• Display Control Unit Assembly Drawings and Bill of Material
• Injector Head Assembly Drawings and Bill of Material
• Power Unit Assembly Drawings and Bill of Material
• Pedestal Assembly Drawing and Bill of Material
17 4X
3
7
17 8X
4
18 2X
6
18 4X
8 - 89
Mark 7 Arterion Injection System
22
14
12
13
19 2X
16
16 10
20
11
20 4X
21 3X
15
8
17 6X
9
11
11
3018832/
2 ASSY, PCB, DISPLAY INTERFACE, MARK 7 / STELLANT 1
3032670
3011679/
6 PCB,GRAPHICS,STELLANT,PHOENIX 1
3034402
8 - 90
Replacement Parts
18 SCREW,MACH,PNH,PHL,ZP,4-40X1/4 602-0440-140 6 ZP
19 SCREW,MACH,PNH,PHL,ZP,6-32X1/8 602-0632-180 2 ZP
20 SCREW,MACH,PNH,PHL,ZP,8-32X5/8 602-0832-580 5 ZP
21 SCREW,MACH,PNH,PHL,ZP,8-32X1/2 602-0832-120 3 ZP
22 SCREW,MACH,FLH,PHL,ZP,8-32X3/8 603-0832-380 3 ZP
8 - 91
Mark 7 Arterion Injection System
18 29
38 61 4X 12
79 66 17 65
68 22 67
32
1 16
58 28
20
77 25 35
38 61 4X 7 10
19 33 78
31 80
37 11
4 5 80
30 34 4X
6
4X 80 3
8 33 78
9 4X 33
4X 34
63
76 21
24
75 27
2 38 61 4X
74 36 62
78 59
26
38 2X
23
8 - 92
Replacement Parts
4X 38 61
44
72 73 49
15
48
43
70
40
42 69 45
39
52
46 50
14 13
47
53
54
71 41
51 62 8X
8 - 93
Mark 7 Arterion Injection System
64
(NOT SHOWN)
ALL AROUND GROOVE
56 4X
81
55
60 4X
57
8 - 94
Replacement Parts
8 - 95
Mark 7 Arterion Injection System
34 SCREW,MACH,SKTCAP,HEX,BO,1/4-20X1 614-1420-100 8
36 SCREW,MACH,PNH,PHL,SST18-8,6-32X1/4 3006128 1
37 SCREW,MACH,SKTCAP,HEX,BO,10-24X5/8 1
38 SCREW,MACH,PNH,PHL,SST,6-32X3/8,YEL HD 3005960 18
51 SCREW,MACH,PNH,PHL,SST18-8,4-40X1/4 3009880 8
52 SCREW,MACH,BTNHD,HEX,BO,4-40X1/4 614-0440-140 2
53 SCREW,MACH,PNH,PHL,BO,6-32X1/2 3008623 2
56 SCREW,MACH,PNH,PHL,ZP,8-32X2 3011293 4
58 SCREW,MACH,SKTCAP,LOW,HEX,8-32X1/2,SST 2
59 SCREW,MACH,SKTFLH,HEX,1/4-20X1-1/8,SST 2
60 SCREW,MACH,FLH,PHL,SST18-8,6-32X3/4 3006049 4
8 - 96
Replacement Parts
61 WASHER,ITL,ZP,#6 605-0006-000 16
62 WASHER,ITL,ZP,#4 605-0004-000 9
65 SCREW,MACH,SKTCAP,HEX,SST,6-32X1/2 3011294 2
66 SCREW,MACH,SKTCAP,HEX,SST,10-32X1/2 3011722 1
80 SUPERLUBE 3000603 AR
8 - 97
Mark 7 Arterion Injection System
4 32 33
36
37
41 2X 3X
36
37 3X
8 - 98
Replacement Parts
23
18
17
22
16
21
9 29
10 30 2X
15
39 8X
12 11
13
14 31
20
2X
1
46
8
7
38 2X 47 8
40 2X
2X 9 44 1
8 - 99
Mark 7 Arterion Injection System
4X 39 22 34
24 34
2X
5 25 26 27 28 36
36
37 3X
3X 37
45 14X
6 29
4X 35
42 43
3011562/
2 ASSEMBLY, PCB, IMAGING SYSTEM INTERFACE (ISI), TOWER 1
3032782
8 - 100
Replacement Parts
8 - 101
Mark 7 Arterion Injection System
45 CREW,MACH,PNH,PHL,ZP,6-32X1/4 602-0632-140 14
46 NUT,MACH,HEX,ZP,4-40 604-0440-140 2
8 - 102
Replacement Parts
24
14
9
37
15
16
19
1
23
27
2 38
18 32
6
12
5
7
11
29
13
17
21
30
10
26
4
40
39
22
28
20 25 35
8 - 103
Mark 7 Arterion Injection System
8 - 104
Replacement Parts
31 SCREW,6-32X3/8,PFH,Z 3030097 2
8 - 105
Mark 7 Arterion Injection System
8 - 106
9 Specifications
This chapter provides specifications for the Mark 7 Arterion Injection System and its components.
This chapter lists:
• "System Technical Specifications"
• "High Pressure Connector Tubing Specifications"
• "System Component Weight and Dimensions"
• "Mounting Components Weight and Dimensions"
• "ISI Technical Specifications"
• "Environmental Specifications"
9 - 107
Mark 7 Arterion Injection System
9 - 108
Specifications
47.3 in
120.1 cm
90°
180° 22.0 in.
180° 55.9 cm
150°
45°
170°
8.6 in
21.8 cm
70°
90°
55.8 in
141.7 cm
57.4 in 53.1 in
145.8 cm 134.8 cm 48.2 in
122.4 cm
23.5 in
59.6 cm
26.1 in
66.2 cm
Weight: 146 lbs. (66.22kg)
9 - 109
Mark 7 Arterion Injection System
3.040 in.
7.7 cm
12.62 in.
32.1 cm
11.042 in.
28 cm
5.470 in.
13.9 cm
9 - 110
Specifications
9.765 in.
24.8 cm
9 - 111
Mark 7 Arterion Injection System
12.375 in.
31.4 cm 29.486 in.
74.9 cm
20.200 in.
51.3 cm
45.338 in.
115.3 cm
39.364 in.
100 cm
36.633 in.
93 cm
29.586 in.
75.1 cm 22.036 in.
56 cm
Weight*: 100lbs. (45.35 kg)
*Pedestal weight is total weight of the pedestal and does not include the Injector Head, Display Control
Unit, or Power Unit weights.
9 - 112
Specifications
2 in.
5.08 cm
48.5 in.
123.19 cm
35.6 in.
90.42 cm 26.75 in.
67.95 cm
9 - 113
Mark 7 Arterion Injection System
12 in.Compressed
17 in.Extended
5.375 in.
1.438 in.
Weight*: 5.4 lbs
*Table Mount weight is total weight of the table mount and does not include the Injector Head weight.
9 - 114
Specifications
29.5 in.
o 74.9 cm
360
360 o
50 o
360 o
System Weight*: Short Column 89.58 lbs (40.63 kg)
Medium Column 96.18 lbs (43.63 kg)
Long Column 100.66 lbs (45.66 kg) 360o
32 in.
81 cm
*System weight is total weight of OCS system and does not include Injector Head weight.
9 - 115
Mark 7 Arterion Injection System
70.5 in.
179 cm
Required for fully
extended rotation
50 °
4.5 in. 57 in.
11.4 cm 145 cm
28 in.
71 cm
80 in.
203 cm
Floor
System Weight*: 43.28 lbs (19.63 kg)
*System weight is total weight of OCS system and does not include Injector Head weight.
9 - 116
Specifications
*System weight is total weight of OCS system and does not include Injector Head weight.
1.99 in.
8.06 in.
5.375 in.
1.438 in.
Weight*: 3.8 lbs
*Table Mount weight is total weight of the table mount and does not include the Display Control Unit
weight.
9 - 117
Mark 7 Arterion Injection System
9.4.6 Display Control Unit Desk Stand Mount Weight and Dimensions
8.76 in.
22.3 cm
8.09 in.
20.5 cm
Weight*: 2.6 lbs. (1.17kg)
*Desk stand weight is total weight of the desk stand and does not include the Display Control Unit
weight.
9 - 118
Specifications
12.56 in.
31.9 cm
11.87 in.
13.08 in. 30.1 cm
33.2 cm
1 in.
(1.00)
2.5 cm
1.83 in.
4.6 cm
*Wall Mount weight is total weight of the wall mount and does not include the Display Control Unit
weight.
9 - 119
Mark 7 Arterion Injection System
This signal is a pair of relay contacts output from the Injector. When active,
it indicates that the Injector is in an armed state and is ready to accept the
start input from the Imaging System. This signal operates as an Extended
Arm; it becomes active with the arming of the Injector and remains active
Extended_Arm after an injection until the signal that initiated the injection (e.g.
INJ_START signal from the Imaging System) is deactivated.
NOTE: The Injector still disarms at the completion of the
injection; only this ISI armed signal is extended.
This signal is a pair of relay contacts output from the Injector. It indicates
Injecting
that the piston on the Injector is in motion.
9 - 120
Specifications
This signal is a pair of relay contacts output from the Injector. When the
Injector X-ray delay has expired, this signal becomes active and notifies
X-Ray Trigger the Imaging System to start the X-ray. Like the Extended Arm signal, the
X-RAY_TRIGGER signal remains active until the signal initiating the injec-
tion (e.g. INJ_START signal from the Imaging System) is deactivated.
This signal is a pair of relay contacts output from the Injector. When the
INJ_HAND_SWITCH_DISABLE input is active and the Injector is armed,
Inj_Hand_Switch_On
this signal indicates when the Injector hand switch (contrast activation
only) or foot switch is in an “on” position; otherwise, this signal is inactive.
This signal is an input to the Injector and is generated by the Imaging Sys-
tem. Once the Injector is armed and the EXTENDED_ARM signal is active,
Inj_Start activating this signal enables the Injector to start. Deactivating this signal
during an injection will abort any injection in progress and disarm the
Injector.
This signal is an input to the Injector and is generated by the Imaging Sys-
tem. This signal must be inactive to allow the Injector to be armed. When
Inj_Disarm
the Injector is armed or is injecting, activating this signal will disarm the
Injector and abort any injection in progress.
This signal is an input to the Injector and is generated by the Imaging Sys-
tem. This signal must be inactive to allow the Injector hand switch and
Inj_Hand_Switch_- foot switch to function normally when in ISI mode. When this signal is
Disable active, the Injector hand switch (contrast activation only) and foot switch
are disabled from directly starting the Injector and the Injector can only be
started from a remote INJ_START control.
9 - 121
Mark 7 Arterion Injection System
Signal Description
Output signal to Imaging System that shorts pins 1 and 2 together when
Injecting
the system is injecting. When not injecting, pins 1 and 2 are open.
Output signal to Imaging System that shorts pins 3 and 4 together when
Extended_Arm
the system is armed. When not armed, pins 3 to 4 are open.
Input signal from Imaging System; when pins 5 and 6 are shorted, the
injector hand switch and/or foot switch is disabled from directly initiating
Handswitch Disable
an injection. When open, the injector hand switch and/or foot switch func-
tions normally.
Input signal from Imaging System; when pins 7 and 9 are shorted, the
Remote Start
injector is commanded to start the injection.
9 - 122
Specifications
Signal Description
Input signal from Imaging System; when pins 8 and 6 are shorted, the
Remote Disarm
injector is commanded to disarm.
Output signal to Imaging System that shorts pins 10 and 11 together when
X-Ray Trigger
active.
9 - 123
Mark 7 Arterion Injection System
ISOLATED
+24Vdc
INJ_START
9
ISOLATED
GROUND RELAY
ISOLATED
+24Vdc
INJ_DISARM
8
ISOLATED RELAY
GROUND
ISOLATED
+24Vdc
INJ_HAND_
SWITCH_DISABLE 5
RELAY
3
EXTENDED_ARM
4
RELAY
1
INJECTING
2
RELAY
10
X-RAY_TRIGGER
11
RELAY
14
A closed relay contact
INJ_HAND_SWITCH_ON indicates the corresponding
15
signal is active
RELAY
9 - 124
Specifications
INJ_START
RELAY
ISOLATED
GROUND
ISOLATED
+24Vdc
INJ_DISARM
8
ISOLATED RELAY
GROUND
ISOLATED
+24Vdc
INJ_HAND_
SWITCH_DISABLE 5
RELAY
ISOLATED
+24Vdc
EXTENDED_ARM
4
RELAY
3
ISOLATED
GROUND
ISOLATED
+24Vdc
INJECTING 2
ARMED_RETURN
ISOLATED
GROUND
10
X-RAY_TRIGGER
11
RELAY
14 A closed relay contact
INJ_HAND_SWITCH_ON indicates the corresponding
15 signal is active
RELAY
9 - 125
Mark 7 Arterion Injection System
9.6 Fuses
Table 9 - 10: 15
Fuse Value P/N Purpose LED
F1 1A 3016255 15V To head display card None*
F2 .75A 3013605 48 V to heater None
F3 .125A 3030037 5V to air sensor None
*Indirectly indicated by LED 15 on the Head Display Card.
9 - 126
Specifications
Air Pressure: 57 kPa to 106 kPa after it has stabilized to ambient conditions.
9.7.3 EMI/RFI
The injector system is classified as Group 1, Class B equipment per the requirements of EN 60601-1-2.
Accessories provided by MEDRAD will also comply with this standard.
9.7.7 IPX1
IEC 60529 classification of degree of protection (IP Code) provided by enclosures of electrical equip-
ment against ingress of vertically dripping water with harmful effects.
9.7.9 EU Directive
The MEDRAD Mark 7 Arterion Injection Systemcomplies with the essential requirements of the Medical
Device Directive 93/42/EEC and bears the CE Mark to show conformity with the provisions of this
Directive.
9 - 127
Mark 7 Arterion Injection System
9 - 128
10 Options and Accessories
The sections below list catalog numbers for:
• "Mark 7 Arterion System Mount Options"
• "Mark 7 Arterion Accessory Devices and Kits"
• "Mark 7 Arterion Cords and Cables"
• "OCS Mounting Systems"
• "OEM Imaging System Interface Cables"
Adjustable Table Mount Kit (includes adjustable table mount and dis-
ART 700 DCU TM A N/A
play mount fulcrum)
Fixed Table Mount Kit (includes fixed table mount and display mount
ART 700 DCU TM N/A
fulcrum)
10 - 129
Mark 7 Arterion Injection System
Dual Display Option (Does not include Mounting.) ART 700 2DCU 3030114
Power Cord - North America and Japan - Standard Length ART 700 PC110V 3011249
Power Cord - North America and Japan - 20 ft. (6.096 m) ART 700 PP 3015600
10 - 130
Options and Accessories
Portegra - Stationary Ceiling Mount - 22.8 in. (58 cm) Post OCS CEIL 58-P 3016424
Portegra - Stationary Ceiling Mount - 33.5 in. (85 cm) Post OCS CEIL 85-P 3016426
Portegra - Stationary Ceiling Mount - 39.4 in. (100 cm) Post OCS CEIL 100-P 3016423
Portegra 2 - Track Ceiling Mount - 22.8 in. (58 cm) Post OCS Track 58-P 3016427
Portegra 2 Track Ceiling Mount - 33.5 in, (85 cm) Post OCS Track 85-P 3016425
Portegra 2 - Wall mount - 33.5 in. (85 cm) Post OCS Wall-P 3016482
10 - 131
Mark 7 Arterion Injection System
GE Innova, 20 ft. (6 m) Remote Power Unit, ISI Signals Only XMC 917A 3016024
10.5.2 Phillips
Integris (Including Integris Allura), 15 ft. (4.5 m) ISI Equipotential XMC 925A 3012643
MultiDiagnostic (MD) and Integris, ISI Signals Only, Remote Power Unit XMC 945-S XMC 945-S
Multidiagnostic (MD) and Integris, ISI SIgnals Only, Remote Power Unit XMC 945 40 3008776
XPER, 80 ft. (24 m) ISI Signals, Remote Power Unit XMC 947R 3009602
10.5.3 Siemens
Axiom Artis, 16.5 ft. (5 m) ISI, Power, Equipotential XMC 977A 3012642
Multistar, Angiostar 13 ft. (4 m) ISI, Power, Equipotential XMC 970A with 3016360 3016359
Universal Synchronization Cable, 50 ft. (15 m) XMC 906 50I XMC 906 50I
Universal Synchronization Cable, 75 ft. (23 m) XMC 906 75I XMC 906 75I
Universal Synchronization Cable, 100 ft. (31 m) XMC 906 100I XMC 906 100I
10 - 132
Options and Accessories
10 - 133