Alaris® GS Syringe Pump Directions For Use

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 Contents

Page
Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
About This Manual. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Quick Start Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Features of the Alaris® GS Syringe Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Controls and Indicators. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Symbol Definitions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Main Display Features. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Operating Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Getting Started . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Basic Features. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Alarms and Warnings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Configured Options. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Alaris® GS Syringe Pump Configured Options Record. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Compatible Syringes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Associated Products. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Compatible Extension Sets. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Occlusion Pressure Limits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
IrDA, RS232 and Nurse Call Specification. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Trumpet Curves and Start-up Curves. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Products and Spare Parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Service Contacts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30

1000DF00327 Issue 3 1/30

 Introduction
The Alaris® GS Syringe Pump (herein after referred to as "pump") is a fully featured syringe pump suitable for critical care and general
infusion applications.

The Alaris® GS Syringe Pump is compatible with a wide range of standard, single-use, disposable Luer-lock syringes. It accepts syringe sizes
from 5 ml to 50 ml. See the 'Compatible Syringes' section for a full list of compatible syringes.

Intended Purpose
The Alaris® GS Syringe Pump is intended for use by medical staff for purposes of controlling infusion rate and volume.
Conditions of Use
The Alaris® GS Syringe Pump should only be operated by a clinician competent in use of automated syringe pumps and
post-placement management of intravenous catheters.
CareFusion cannot guarantee the continued system accuracy with other manufacturer’s syringes as identified in the
A ‘Compatible Syringes’ table. Manufacturers may change syringe specification significant to system accuracy without
prior notification.

Indications
The Alaris® GS Syringe Pump is indicated for infusion of therapeutics including:
• analgesics
• antimicrobials
• blood products
• chemotherapy
• subcutaneous
• nutrition

Contraindications
The Alaris® GS Syringe Pumps is contraindicated for:
• enteral therapies
• epidural

About This Manual

The user must be thoroughly familiar with the Alaris® GS Syringe Pump described in this manual prior to use.

All illustrations used in this manual show typical settings and values which may be used in setting up the functions of the pump. These
settings and values are for illustrative use only. Where stated, a minimum infusion rate refers to a nominal rate of 1.0ml/h, and an
intermediate infusion rate refers to a nominal rate of 5.0ml/h. The complete range of infusion rates, settings and values are shown in the
Specifications section.

Quick Start Guide

1. Press the a button to turn the pump on.

2. CLEAR SETUP? - NO retains previous data. YES clears previous data.

3. Load syringe.

4. Confirm correct size and brand of syringe.

5. Ensure extension set is attached to syringe, but disconnected from patient.

If the PURGE SYRINGE option has been enabled then the prompt to purge screen is displayed and the set can be purged as
required.

6. INFUSION RATE - Change rate if necessary using the f keys.

7. PURGE - Press the i button followed by the PURGE softkey.

8. Connect extension set to the patient access device.

9. Press the b button to start the infusion.

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 Features of the Alaris® GS Syringe Pump
ON/OFF Release lever for High visibility
RUN Display MDI Alarm Indicator

PURGE/
BOLUS

MUTE

OPTION

Finger
Grips

Extension HOLD Shelf for chevron Syringe Clamp Positive Plunger

set hook keys and softkeys Grippers

Rating Plate (see Symbol Definitions for

an explanation of the symbols used)

Release
lever for
Rotating
Cam

M e dic
al D ev
ice Int
erface
(M D I )

Rotating Cam to
lock on to horizontal
rectangular bars IR Communications
port
Carrying Potential Folded Pole RS232 Extension set
Handle Equalisation Clamp Connector hook
(PE) connector (optional)

1000DF00327 Issue 3 3/30

 Controls and Indicators
Controls:

Symbol Description

a ON/OFF button - Press once to switch the pump ON. Press and hold down for 3
seconds to switch the pump OFF.

b RUN button - Press to start the infusion. The green LED will flash during infusion.

h HOLD button - Press to put the infusion on hold. The amber LED will be lit while on
hold.

c MUTE button - Press to silence alarm for 2 minutes (configurable). Press and hold
until 3 beeps are heard for 15 minutes silence.

PURGE/BOLUS button - Press to access PURGE or BOLUS soft keys. Press and hold
down soft key to operate.
PURGE the extension set during set up.
l Pump is on hold

i
l Extension set is not connected to the patient
l Volume Infused (VI) is not added
BOLUS - fluid or drug delivered at an accelerated rate.
l Pump is infusing
l Extension set is connected to the patient
l VI is added

d OPTION button - Press to access optional features (see Basic Features).

f CHEVRON keys - Double or single for faster/slower increase or decrease of values

shown on display.

g BLANK SOFTKEYS - Use in conjunction with the prompts shown on the display.

Indicators:

Symbol Description

j BATTERY indicator - When illuminated the pump is running on the internal battery.
When flashing the battery power is low with less than 30 minutes of use remaining.

S AC POWER indicator - When illuminated the pump is connected to an AC power

supply and the battery is being charged.

1000DF00327 Issue 3 4/30

 Symbol Definitions

Labelling Symbols:

Symbol Description

w Attention (Consult accompanying documents)

x Potential Equalisation (PE) Connector

y RS232/Nurse call Connector (Optional)

l Defibrillation-proof type CF applied part (Degree of protection against electrical

shock)

O Protected against vertically falling drops of water

r Alternating Current

s Device complies with the requirements of Council Directive 93/42/EEC as amended

by 2007/47/EC.

T Date of Manufacture

t Manufacturer

U Not for Municipal Waste

A Important information

W Fuse Rating

EC REP Authorised representative in the European Community

1000DF00327 Issue 3 5/30

 Main Display Features

Pressure Information
(if enabled)

Volume Infused
Infusion Volume
Option
Rate Infused

Screen Icons

Symbol Description

BATTERY icon - Indicates battery charge level to highlight when the battery will require recharging.
N This feature can be accessed by pressing the d button, scroll through the options using the
f keys, select BATTERY ICON and this icon will be shown.

1000DF00327 Issue 3 6/30

 Operating Precautions

Disposable Syringes and Extension Sets

• Always clamp or otherwise isolate the patient line before unclamping or removing a syringe from the
pump.  Failure to do so may result in unintended administration.

• This Alaris® GS Syringe Pump has been calibrated for use with single-use disposable syringes. To ensure

m correct and accurate operation, only use 3 piece Luer-Lock versions of the syringe make specified on
the pump or described in this manual. Use of non-specified syringes or extension sets may impair the
operation of the pump and the accuracy of the infusion.

•
n
Uncontrolled flow or syphoning may result if the syringe is located incorrectly in the pump, or if it is
removed from the pump before the extension set is properly isolated from the patient. Isolation may
include closing a tap in the patient line or activating a flow stop clamp.

•
o Secure the extension set to the pump using the extension set hook at the rear of the pump. This provides
protection against accidental dislodging of the syringe from the pump.

G • When combining several apparatus and/or instruments with extension sets and other tubing, for example
via a 3-way tap, the performance of the pump may be impacted and should be monitored closely.

Mounting the Pump

•
H
The pump must be mounted within 1.0m above or below the patient’s heart. The most accurate pressure
monitoring in the extension set is achieved when the pump is positioned close to the patients heart
level.

• Do not mount the pump in a vertical position with the syringe pointing upwards as this could lead to

I an infusion of air which may be in the syringe. To protect against the introduction of air the user should
regularly monitor the progress of the infusion, syringe, extension line and patient connections and follow
the priming procedure specified herein.
Operating Environment

• When using any infusion pump in conjunction with other pumps or devices requiring vascular access,
extra care is advised. Adverse delivery of medication or fluids can be caused by the substantial variation in
pressures created within the local vascular system by such pumps. Typical examples of those pumps are
used during dialysis, bypass or cardiac assist applications.

• This pump is suitable for use in Hospital and clinical environments other than domestic establishments
and those directly connected to the public single phase AC mains power supply network that supplies
buildings used for domestic purposes. However, it may be used in domestic establishments under the
supervision of Medical professionals with additional necessary appropriate measures. (Consult Technical
Service Manual, appropriately trained technical personnel or CareFusion for further information).

• This pump is not intended to be used in the presence of a flammable anaesthetic mixture with air or
oxygen or nitrous oxide.

Operating Pressure

• This is a positive pressure pump designed to achieve very accurate fluid administration by automatically
compensating for resistance encountered in the infusion system.

• The pumping pressure alarm system is not designed to provide protection against, or detection of, IV
complications which can occur.

Alarm Conditions

•
J
Several alarm conditions detected by this pump will stop the infusion and generate visual and audible
alarms. Users must perform regular checks to ensure that the infusion is progressing correctly and no
alarms are operating.

1000DF00327 Issue 3 7/30

 Operating Precautions (continued)

Electromagnetic Compatibility and Interference

• This pump is protected against the effects of external interference, including high energy radio frequency

M •
emissions, magnetic fields and electrostatic discharge (for example, as generated by electrosurgical and
cauterising equipment, large motors, portable radios, cellular telephones etc.) and is designed to remain
safe when unreasonable levels of interference are encountered.
Therapeutic Radiation Equipment: Do not use the pump in the vicinity of any Therapeutic Radiation
Equipment. Levels of radiation generated by the radiation therapy equipment such as Linear Accelerator,
may severely affect functioning of the pump. Please consult manufacturer’s recommendations for
safe distance and other precautionary requirements. For further information, please contact your local
CareFusion representative.
• Magnetic Resonance Imaging (MRI): The pump contains ferromagnetic materials which are susceptible
to interference with magnetic field generated by the MRI devices. Therefore, the pump is not considered
an MRI compatible pump as such. If use of the pump within an MRI environment is unavoidable, then
CareFusion highly recommends securing the pump at a safe distance from the magnetic field outside
the identified ‘Controlled Access Area’ in order to evade any magnetic interference to the pump; or
MRI image distortion. This safe distance should be established in accordance with the manufacturers’
recommendations regarding electromagnetic interference (EMI). For further information, please refer to
the product technical service manual (TSM). Alternatively, contact your local CareFusion representative for
further guidance.
• Accessories: Do not use any non-recommended accessory with the pump. The pump is tested and
compliant with the relevant EMC claims only with the recommended accessories. Use of any accessory,
transducer or cable other than those specified by CareFusion may result in increased emissions or
decreased pump immunity.
• This pump is a CISPR 11 Group 1 Class A device and uses RF energy only for its internal function in the normal
product offering. Therefore, its RF emissions are very low and are not likely to cause any interference with
the nearby electronic equipment. However, this pump emits a certain level of electromagnetic radiation
which is within the levels specified by IEC/EN60601-1-2 and IEC/EN60601-2-24. If the pump interacts with
other equipment, measures should be taken to minimise the effects, for instance by repositioning or
relocation.
• In some circumstances the pump may be affected by an electrostatic discharge through air at levels close
to or above 15kv; or by radio frequency radiation close to or above 10v/m. If the pump is affected by
this external interference the pump will remain in a safe mode; the pump will duly stop the infusion and

K alert the user by generating a combination of visual and audible alarms. Should any encountered alarm
condition persist even after user intervention, it is recommended to replace that particular pump and
quarantine the pump for the attention of appropriately trained technical personnel. (Consult Technical
Service Manual for further information).
Hazards

B • An explosion hazard exists if the pump is used in the presence of flammable anaesthetics. Exercise care to
locate the pump away from any such hazardous sources.

A •

•
Dangerous Voltage: An electrical shock hazard exists if the pump’s casing is opened or removed. Refer all
servicing to qualified service personnel.

When connected to an external power source, a three-wire (Live, Neutral, Earth) supply must be used. If the
integrity of the external protective conductor in the installation or its arrangement is in doubt, the pump
should be operated from the battery.
• Do not open the RS232/Nurse Call protective covering when not in use. Electrostatic discharge

V (ESD) precautions are required when connecting RS232/Nurse Call. Touching the pins of the
connectors may result in ESD protection failure. It is recommended that all actions must be taken by
appropriately trained personnel.
• If this pump is dropped, subjected to excessive moisture, fluid spillage, humidity or high temperature, or
otherwise suspected to have been damaged, remove it from service for inspection by a qualified service

L engineer. When transporting or storing the pump, use original packaging where possible, and adhere
to temperature, humidity and pressure ranges stated in the Specifications section and on the outer
packaging.

1000DF00327 Issue 3 8/30

 Getting Started
Initial Set-up

Before operating the pump read this Directions For Use manual carefully.

A
1. Check that the pump is complete, undamaged and that the voltage rating specified on the label is compatible with your AC power
supply.
2. Items supplied are:
l Alaris® GS Syringe Pump
l User Support CD (Directions For Use)
l AC Power Cable (as requested)
l Protective Packaging
3. Connect the pump to the AC power supply for at least 2½ hours to ensure that the internal battery is charged (verify that the S is
lit).

Language Selection
1. On initial start-up the pump will display the Select Language screen.
2. Select the required language from the list displayed using the f keys.
3. Press the OK softkey to confirm your selection.

The pump will automatically operate from its internal battery if the pump is switched on without being connected to

A the AC power supply.

Should the pump fail to perform correctly, replace in its original protective packaging, where possible and contact a
qualified service engineer for investigation.

1000DF00327 Issue 3 9/30

 Getting Started (continued)
Do not mount the pump with the AC power inlet or the syringe pointing upwards. This could affect the electrical

A safety in the event of a fluid spill or lead to the infusion of air which may be in the syringe.

Pole Clamp Installation

The pole clamp is fitted to the rear of the pump and will provide secure fixing to vertical I.V. poles of a diameter between 15 and 40 mm.

Recessed area

1. Pull the folded pole clamp towards you and unscrew the clamp to
leave enough room for the size of the pole.
2. Place pump around pole and tighten screw until the clamp is
secured to the pole.

* *

Ensure the pole clamp is folded away and stored

A within the recessed area at the rear of the

pump before connecting to a Docking Station/
Workstation* or when not in use.
Never mount the pump such that the IV infusion
stand becomes top heavy or unstable.

Docking Station/Workstation* or Equipment Rail Installation

Rectangular bar Release lever (push to release)

Rotating cam

The rotating cam can be fitted to the rectangular bar on the Docking Station/Workstation* or the equipment rail measuring 10 by 25 mm.
1. Align the rotating cam on the rear of the pump with the rectangular bar on the Docking Station/Workstation* or the equipment rail.
2. Hold the pump horizontally, push the pump firmly onto the rectangular bar or equipment rail.
Ensure that the pump 'clicks' securely into position onto the bar.
3. To release, push the release lever and pull the pump forwards.

*Alaris® DS Docking Station and Alaris® Gateway Workstation.

1000DF00327 Issue 3 10/30

 Getting Started (continued)

Loading and Confirming a Syringe

Warning: To securely load and confirm a syringe carefully follow the steps below. An incorrect loading of a syringe may
A result in misidentification of the syringe type and size. If then confirmed, this may lead to significant inaccuracy of the
infusion rate and may also affect pump performance.
Only use a syringe of the type stated on the pump or in this manual. Using an incorrect syringe could adversely affect the
accuracy of the infusion rate and may also affect pump performance.
When drawing fluid into the syringe, draw enough to compensate for any 'dead space' volume in the extension set and
syringe at the end of infusion as this cannot be fully infused.

 
Finger
Grips

Plunger
Plunger Flange
Grippers Plunger Plunger
Holder

Syringe
Barrel

Barrel
Flange

Syringe
Clamp

Syringe Flange Clamp

Place the pump on a stable horizontal surface or secure as described previously.
Prepare, load and prime the single-use disposable syringe and extension set using standard aseptic techniques.
1. Squeeze the finger grips together on the plunger holder and slide the mechanism to
the right.
2. Pull the syringe clamp forward and down.

1000DF00327 Issue 3 11/30

3. Insert the syringe ensuring that the barrel flange is located in the slots on the syringe
flange clamp.
To ensure the syringe is loaded correctly, place the barrel flange in the space
A between the syringe clamp and the syringe flange clamp. This is correct if the
syringe remains in position before the syringe clamp is closed.

4. Lift the syringe clamp until it locks against the syringe barrel.

5. Squeeze the finger grips on the plunger holder and slide the mechanism to the left
until it reaches the plunger end.
6. Release the finger grips. Ensure that the plunger grippers are securing the plunger in
place and the finger grip returns to its original position.

7. Ensure that the syringe type and size match those displayed on the pump then press CONFIRM. If required, the make
of syringe can be changed by pressing the TYPE softkey.

IVAC 50

CONFIRM TYPE

Note: If the PURGE SYRINGE option has been enabled then the prompt to purge screen is displayed and the exten-
sion set can be purged as required, however ensure that the extension set is not connected to the patient dur-
ing this process.
CareFusion recommends to limit the number of configured syringe types and sizes available for selection on the pump.
A Secure the extension set using the extension set hook at the rear of the pump. This provides protection against accidental
dislodging of the syringe from the pump.
Ensure that both plunger grippers are fully locked onto the plunger flange and the upper finger grip has returned to its
original position.

1000DF00327 Issue 3 12/30

 Getting Started (Continued)

Starting the Pump

1. Connect the pump to an AC power supply using the AC power cable.
Press the a button.
l The pump will run a short self-test. Ensure that two beeps are activated during this test.
l Check the display test pattern and ensure that no rows are missing.
l Check that the displayed time and date are correct.
Note: A warning - REPAIRING LOGS, may be displayed if event log information was not completely stored at the previous power down.
This is for information only, the pump will continue to power up as normal.

2. CLEAR SETUP? - Answering NO will retain all previous rate and volume settings. YES will automatically reset the rate and volume
settings to zero.

3. LOAD SYRINGE - Load the syringe according to the procedure in this manual.

4. CONFIRM SYRINGE - Check that the syringe type and size being used matches the display. If required, the make of syringe can be
changed by pressing the TYPE button. Press CONFIRM when the correct type and size are shown.

If the PURGE SYRINGE option has been enabled then the prompt to purge screen is displayed and the set can be purged as
required.

5. INFUSION RATE - Check the rate shown if old patient data has been retained and change the rate if necessary using the f
keys.

6. PURGE (if required) - Press the i button and then press and hold the PURGE softkey until fluid flows and the purging of the syringe
extension line is complete. Release the softkey. The volume used during purging will be displayed.

7. CONNECT TO PATIENT - Connect the extension set to the patient access device.

8. START - Press b to commence operation. The AMBER STOP light will be replaced by the flashing GREEN START light to indicate that the
pump is in operation.

9. STOP - Press h to halt the operation. The amber light will replace the green light.

1000DF00327 Issue 3 13/30

 Basic Features

Purge
The i button allows the delivery of a limited volume of fluid in order to purge the extension set prior to being connected to a patient or
after changing a syringe.
1. Press the i button when the pump is not infusing. Ensure that the extension set is not connected to the patient.
2. Press and hold the PURGE softkey until fluid flows and the purging of the IV infusion set is complete. The volume used during purging
will be displayed, but it is not added to the volume infused.
3. When purging is complete release the PURGE softkey. Press the QUIT softkey to exit back to the main display.

The pump will not purge if the rate lock has been enabled. During PURGE the pressure limit alarms are temporarily

A increased to their maximum level.

Bolus Infusion

The bolus feature can be used at the start of an infusion or during an infusion.
If the bolus volume reaches the set limit the bolus will stop and the pump will revert to infuse at the set rate.
1. During infusion press the i button once to display the bolus screen.
2. Use the f keys to set the bolus rate required.
3. To deliver the bolus press the BOLUS softkey. During the bolus the volume being infused is displayed.
4. When the desired bolus has been delivered, release the softkey. The bolus volume is added to the total volume infused.

A bolus cannot be administered if the rate lock is enabled or if the feature is disabled in General Options. During

A BOLUS the pressure limit alarms are temporarily increased to their maximum level.

Clear Volume
This option enables the volume infused to be cleared.
1. Press the VOLUME softkey to display the CLEAR VOLUME option.
2. Press the YES softkey to clear the volume. Press the NO softkey to retain the volume.
Selecting YES resets the volume infused in the 24H LOG option.

Rate Lock
If Rate Lock is enabled, when the infusion rate has been set and the infusion started (or following a bolus infusion) the rate lock prompt
will appear on the main display.
To select the rate lock function press the YES softkey. Press the NO softkey if the rate lock is not required.
When rate lock is enabled, the following are unavailable:
l Bolus / purge
l Switching the pump off
To disable the rate lock if selected:
1. Press the d button to access the options menu.
2. Select the UNLOCK RATE option using the f keys and press the OK softkey.
To enable the rate lock if not selected:
1. Press the d button to access the options menu.
2. Select RATE LOCK and press the OK softkey.

1000DF00327 Issue 3 14/30

 Basic Features (Continued)
Pressure Display

This feature can be enabled / disabled within the General Options menu (see 'Configured Options'). When

q
enabled, a Pressure Icon appears on the display indicating the current pressure level and the pressure alarm
level. The pressure alarm level can be set within the General Options menu.

? 24 Hour Log
This option allows the 24 hour log of volume infused to be reviewed.
1. Press the d button to access the options menu.
2. Select the 24H LOG option using the f keys and press the OK softkey.
The display shows the hourly volume infused. The volume infused shown in brackets is the total volume infused since the volume was
last cleared. See example below:
07:48 - 08:00 4.34ml (4.34ml)
08:00 - 09:00 2.10ml (6.44ml)
09:00 - 10:00 2.10ml (8.54ml)
VOLUME CLEARED
3. Press the QUIT softkey to exit the log.

? Event Log
This option allows the event log to be reviewed. It can be enabled/disabled.
1. Press the d button to access the options menu.
2. Select the EVENT LOG option using the f keys and press the OK softkey.
3. Scroll through the log using the f keys. Press the QUIT softkey to exit the log.

1000DF00327 Issue 3 15/30

 Alarms and Warnings
Alarms are indicated by a combination of an audible alarm, flashing alarm indicator and a descriptive message in the display.
1. First press the c button to silence the alarm for a maximum of 2 minutes*, then check the display for an alarm message. Press CANCEL
to cancel the alarm message.
2. If the infusion has stopped, rectify the cause of the alarm then press the b button to resume the infusion.

If the pump initiates a safety processor alarm condition (an audible high pitched continuous shrill accompanied with a red
A alarm indicator) and there is no error message displayed on the pump, remove the pump from service for examination by
a qualified service engineer.

Display Description and Troubleshooting Guide

DRIVE DISENGAGED The drive system has been disengaged during operation. Check the finger grips and the position
of the syringe.

OCCLUSION Excessive pressure measured at the syringe plunger exceeding the alarm limit. Identify and
remove the cause of the blockage in the drive, syringe, or administration system before restarting
the infusion.

CHECK SYRINGE Incorrect size of syringe has been fitted, the syringe has not been positioned correctly or has
been disturbed during operation. Check the syringe location and the position.

BATTERY LOW Battery charge low with 30 minutes operation remaining. Battery indicator will flash and after 30
minutes a continuous audible alarm will indicate that the battery is exhausted. Reconnect to the
AC power supply to continue operation and charge the internal battery.

BATTERY EMPTY The internal battery is exhausted. Connect the pump to the AC power supply.

NEAR END OF INFUSION The pump is nearing the end of the infusion. This value can be configured.

END OF INFUSION The pump has reached the end of the infusion. A pre-set volume will remain in the syringe to
minimise the risk of the infusion of air bubbles into the set. This value can be configured.

AC POWER FAIL AC Power has been disconnected and the pump is operating on battery power, if this occurs
when the pump is infusing the message "INFUSION CONTINUES" will be displayed. Reconnect
AC power supply or press the c button to silence the alarm and continue with battery operation.
The alarm will automatically cancel if the AC power supply is reconnected.

Error Code and Message The alarm system has detected an internal malfunction. Note the malfunction code. Remove
pump from service for examination by a qualified service engineer.

ATTENTION (with “3 Beeps”) Three beeps will sound if the pump has been left ON for more than 2 minutes* (referred to as
CALLBACK in the log) without starting the operation. Press the c button to silence the alarm
for a further 2 minutes*. Alternatively press and hold down the c button and wait for 3 beeps
in succession, this will put the warning alarm on standby for 15 minutes.

Alarm Indicator Colour Alarms indicated

AMBER AC POWER FAIL; NEAR END OF INFUSION; ATTENTION; BATTERY LOW.

RED All others.

*Configurable option.

1000DF00327 Issue 3 16/30

 Configured Options
This menu comprises a list of options which are configurable by the user.
1. Turn the pump OFF.
2. Whilst holding down the b button turn the pump ON.
3. The main display will show 000. Enter the access code for Configured Options using the f keys, pressing NEXT to move through
the digits. A full list of access codes can be found in the Technical Service Manual.
4. When the complete code shows on screen, press OK to enter. The Configured Options menu will be displayed.
General Options
1. Select GENERAL OPTIONS from the menu using the f keys and press the OK softkey.
2. Select the option you wish to enable/disable or adjust and press the MODIFY softkey.
3. When all the desired modifications have been carried out press the QUIT softkey.
4. Either select the next configuration option from the menu or turn the pump OFF, returning it to operation as required.

NURSE CALL FITTED Enables Nurse Call (hardware option).

NURSE CALL INVERT When enabled, the nurse call output is inverted.
RS232 SELECTED Sets the pump's communications to use RS232 (hardware option).
NEOI WARNING Sets the Near End Of Infusion warning time, as time left to End Of Infusion.
EOI POINT Sets the End Of Infusion point.
KVO AT EOI When enabled the pump will switch to running at the KVO rate when EOI is reached.
KVO RATE Sets the Keep Vein Open (KVO) rate at which the pump will operate if KVO at EOI is enabled.
BACK OFF When enabled the motor will reverse to relieve line pressure when an occlusion occurs.
AUTO SAVE When disabled the infusion information is cleared on power up.
RATE LOCK When enabled the rate can be locked to prevent unwanted changes of the set infusion rate.
QUIET MODE When enabled the button beeps are muted.
AC FAIL When enabled the AC Power Failure Alarm will sound if the AC power is disconnected.
PRESSURE DISPLAY Enables / disables the Pressure Icon on the main display.
PRESSURE DEFAULT Sets the default occlusion alarm level.
CAP RATE Sets the maximum value for infusion rate.
PURGE RATE Sets the purge rate.
PURGE VOLUME LIMIT Sets the maximum permissible purge volume.
PURGE SYRINGE Prompt to purge syringe after confirmation.
BOLUS Enables / disables the bolus feature.
DEFAULT BOLUS Sets the default bolus rate.
CAP BOLUS RATE Sets the maximum value for bolus rate.
BOLUS VOL LIMIT Sets the maximum permissible bolus volume.
MANUAL BOLUS Volume infused will be increased if plunger is manually moved in and syringe remains confirmed.
CALL BACK TIME Adjusts the time for the pump to sound the call back alarm.
EVENT LOG DISPLAY Enables / disables the event log.
BATTERY ICON Enables / disables the Battery Icon feature availability via the d button.
AUDIO VOLUME Sets the alarm volume of the pump at high, medium or low.
AUTO NIGHT MODE Backlight dims between hours 21:00 and 06:00.

1000DF00327 Issue 3 17/30

 Configured Options (Continued)
Clock Set

1. Select CLOCK SET from the Configured Options menu using the f keys and press the OK softkey.
2. Use the f keys to adjust the date displayed, pressing the NEXT softkey to access the next field.
3. When the correct time and date are displayed press the OK softkey to return to the Configured Options menu.

Hospital Name

This option allows the user to programme in the name of the hospital, ward or department. This will appear during the power-up display
sequence.
1. Select HOSPITAL NAME from the Configured Options menu using the f keys and press the OK softkey.
2. Use the keys to adjust the character displayed, pressing NEXT to access the next position.
3. When the correct name is displayed press OK to return to the Configured Options menu.

Enable Syringes

This option is used to pre-configure the type and size of syringe permitted for use on the pump. Select all possible syringes which may be
used and disable any that should not be used.
1. Select ENABLE SYRINGES from the Configured Options menu using the f keys and press the OK softkey.
2. Use the f keys to scroll through the list of syringes, pressing MODIFY to enable/disable a syringe brand and individual models
within the brand.
3. When all modifications are complete press QUIT to return to the Configured Options menu.

Language

This option is used to set the language of messages shown on the pump display.
1. Select LANGUAGE from the Configured Options menu using the f keys and press the OK softkey.
2. Use the f keys to select the language.
3. When the desired language has been selected press SELECT softkey to return to the Configured Options menu.

Contrast
This option is used to set the contrast on the pump display.
1. Select CONTRAST from the Configured Options menu using the f keys and press the OK softkey.
2. Use the f keys to select a contrast ratio value. The contrast of the display will change when scrolling through the numbers.
3. When the desired value has been reached press the OK softkey to return to the Configured Options menu.

1000DF00327 Issue 3 18/30

 Alaris® GS Syringe Pump Configured Options Record
General Options Enter the pump-specific information for your records on a copy of this page.

Option Default Range Setting

1.9.x and
Software Version 1.5.10 and 2.0.0
2.3.x and above

NURSE CALL FITTED Disabled Disabled Enabled/Disabled

NURSE CALL INVERT Disabled Disabled Enabled/Disabled
RS232 SELECTED Disabled Disabled Enabled/Disabled
NEOI WARNING 1min 5mins 1min - 15mins
EOI POINT 1.0% 1.0% 0.1% - 5% of syringe volume
KVO AT EOI Enabled Enabled Enabled/Disabled
KVO RATE 1.0ml/h 1.0ml/h 0.1ml/h - 2.5ml/h
BACK OFF Disabled Enabled Enabled/Disabled
AUTO SAVE Enabled Enabled Enabled/Disabled
RATE LOCK Disabled Disabled Enabled/Disabled
QUIET MODE Disabled Disabled Enabled/Disabled
AC FAIL Enabled Enabled Enabled/Disabled
PRESSURE DISPLAY Disabled Enabled Enabled/Disabled
PRESSURE DEFAULT L3 L3 L0 - L10 (50mmHg - 1000mmHg)
CAP RATE Max infusion rate 200ml/h 1.0ml/h - 200ml/h
PURGE RATE 200ml/h 200ml/h 100ml/h - 500ml/h
PURGE VOLUME LIMIT 2.0ml 2.0ml 0.5ml - 5.0ml
PURGE SYRINGE Disabled Enabled/Disabled
BOLUS Enabled Enabled Enabled/Disabled
DEFAULT BOLUS Max bolus rate 500ml/h 10ml/h - 500ml/h
CAP BOLUS RATE Max bolus rate 500ml/h 10ml/h - 500ml/h
BOLUS VOL LIMIT 5.0ml 5.0ml 0.5ml (0.1ml)* - 25.0ml
MANUAL BOLUS Disabled Enabled/Disabled
CALL BACK TIME 2mins 0.1mins - 15mins
EVENT LOG DISPLAY Disabled Enabled Enabled/Disabled
BATTERY ICON Enabled Enabled/Disabled
AUDIO VOLUME Medium Medium Low, medium, high
AUTO NIGHT MODE Enabled Enabled Enabled/Disabled
* For software versions 1.9.x and 2.3.x and above

Syringes Enabled
Make Size(s) Make Size(s)

Hospital Name Serial No. Software Version

Approved by Configured by
Date Date

1000DF00327 Issue 3 19/30

 Specifications
Infusion Specifications - System Accuracy -
Maximum infusion rate can be set as part of the configuration. Volumetric Mean +/- 2% (nominal).
0.1ml/h - 150ml/h 5ml syringes
Derating -
0.1ml/h - 200ml/h All other syringes
Temperature +/- 0.5% (5 - 40ºC)
The Volume Infused range is 0.0ml - 9990ml.
High Rates +/-2.0% (rates > syringe volume/h eg.
Bolus Specifications -
>50ml/h in a 50ml syringe.)
Maximum Bolus rates can be set as part of the configuration. Bolus
Important: System accuracy is +/-2% typical by volume as measured
rates are user adjustable, in increments of 10ml/h.
using the trumpet curve test method defined in IEC/EN60601-2-24 at
10 ml/h - 150ml/h 5ml syringes rates of 1.0ml/h (23ºC) and above when the pump is used with the
10 ml/h - 300ml/h 10ml syringes recommended syringes. Caution: Infusion volume accuracy may be
10 ml/h - 500ml/h All other syringes compromised at rates below 1.0ml/h. Differences in factors such as
The bolus volume limit can be set as part of the configuration. size and plunger force in compatible syringes can cause variations
Minimum: 0.5ml (0.1ml - v2.3.x and above or v1.9.x); in accuracy and trumpet curves. See also trumpet curves section in
this manual.
Maximum 25.0ml
Increments of 0.1ml; default 5.0ml Battery Specifications -
During BOLUS the pressure limit alarms are temporarily increased to Rechargeable sealed NiMH. Automatically charges when the pump is
their maximum level. connected to AC power.
Critical Volume - Mean Time To Battery Empty from fully charged @ 5ml/h and 23°C ± 2°C
The bolus which can occur in the event of a single internal fault under normal conditions is 6 hours*
condition with a 50 ml syringe is : *95% lower confidence interval of 5 hours 50 minutes
Maximum Overinfusion - 0.5ml Charging takes 2½ hours from discharge to 90% charge.
Purge Specifications - Memory Retention -
The purge rate is limited to the maximum rate for the syringe and can The electronic memory of the pump will be retained for more than 6
be set as part of the configuration. months when not powered up.
100ml/h - 500ml/h. Fuse Type -
The purge volume range is 0.5ml - 5ml. 2 x T 1.25A, slow blowing.
During PURGE the pressure limit alarms are temporarily increased to AC Power Supply -
their maximum level. 115 - 230VAC, 50 - 60Hz, 20VA (nominal).
Keep Vein Open (KVO) Rate - Dimensions -
0.1 ml/h - 2.5ml/h. 310 mm (w) x 121 mm (h) x 200 mm (d). Weight: 2.7 kg (excluding
End Of Syringe Rate - power cable).
Stop, KVO (0.1ml/h to 2.5ml/h), or set rate if lower than KVO. Protection against fluid ingress -
Near End Of Infusion Alarm - IPX1 - Protected against vertically falling drops of water.
1min - 15min to end of infusion, or 10% of syringe volume, whichever Alarm Conditions -
is smaller.
Drive Disengaged Occlusion
End Of Infusion (EOI) Alarm -
Check Syringe Battery Low / Battery Empty
0.1% - 5% of syringe volume
Near End Of Infusion End of Infusion
Electrical Classification -
Class I product. Continuous Mode Operation, Transportable AC Power Fail Internal Malfunction
Maximum Pumping Pressure Limit - Attention (Nurse Callback)
Highest alarm level 1000mmHg (nominal at L-10) Environmental Specifications -
Occlusion Accuracy (% of full scale)* - Operating Temperature +5°C - +40°C
Pressure mmHg Operating Relative Humidity 20% - 90%
Operating Atmospheric Pressure 700hPa - 1060hPa
L-0 L-3 L-5 L-10
Transport and Storage Temperature -30°C - +50°C
approx. approx. approx. approx.
Transport and Storage Relative Humidity 10% - 95%
50 mmHg 300 mmHg 500 mmHg 1000 mmHg Transport and Storage Atmospheric Pressure 500hPa - 1060hPa
Temp. 23°C ±18% ±21% ±23% ±28% Electrical/Mechanical Safety -
Complies with IEC/EN60601-1 and IEC/EN60601-2-24.
* - Using most common 50ml syringes under normal conditions EMC -
(95% confidence / 95% of pumps).
Complies with IEC/EN60601-1-2 and IEC/EN60601-2-24.

1000DF00327 Issue 3 20/30

 Compatible Syringes

The pump is calibrated and labelled for use with single-use disposable Luer-lock syringes. Only use the size and type of syringe specified
on the pump display. The full list of permitted syringe models is dependent on the software version of the pump.

5ml 10ml 20ml 30ml 50ml

IVAC® ü
AstraZeneca ü
B Braun Omnifix ü ü ü ü ü
B Braun Perfusor ü ü
BD Perfusor ü
BD Plastipak ü ü ü ü ü
BD Precise ü ü
Codan ü ü ü ü
Codan Perfusion ü
Fresenius Injectomat ü ü
Monoject** ü ü ü ü ü
Nipro ü ü ü ü
Pentaferte ü ü ü ü
Rapiject* ü
Terumo ü ü ü ü ü
* - The Rapiject 50ml syringe is a specialised syringe with a large diameter barrel. To provide protection against accidental dislodging always
ensure the infusion line is secured using the infusion set hook - see Loading a Syringe section.
** - TYCO / Healthcare KENDALL - MONOJECT.

Associated Products

The Alaris® DS Docking Station The Alaris® Gateway Workstation

1000DF00327 Issue 3 21/30

 Compatible Extension Sets

The pump uses standard, single-use, disposable extension sets and syringes with Luer-lock connectors. The user is responsible for verifying
the suitability of a product used, if it is not recommended by CareFusion.

Standard Sets
G40015 Standard PVC Syringe Extension Set (150 cm).
Priming Volume: 2.6ml

G40020B Standard PVC Syringe Extension Set (200 cm).

Priming Volume: 1.5ml

G402EP Extension set, luer lock connectors. Kink resistant DEHP free PVC yellow striped tubing. Bore 1mm. Length 200cm.
Priming volume 1.6ml.

Light Protected Sets

G40215 Amber PE Syringe Extension Set (150 cm).
Priming Volume: 1.2ml

G40320 White PVC Syringe Extension Set (200 cm).

Priming Volume: 3.6ml

Low Sorbing Sets

G40615 Polyethylene Syringe Extension Set (150 cm).
Priming Volume: 1.5ml

G40620 Polyethylene Syringe Extension Set (200 cm).

Priming Volume: 2ml

G40720 Polyethylene Lined Syringe Extension Set with clamp. (200 cm).
Priming Volume: 1.5ml

04105010509 Polyethylene Syringe Extension Set (100 cm).

Priming Volume: 1ml

For availability please contact your local CareFusion representative because new sets are continuously being developed for our

A customers.

It is recommended that extension sets are changed in accordance with the Directions for Use.
Carefully read the Directions For Use supplied with the extension set prior to use.

Please note these drawings are not to scale

1000DF00327 Issue 3 22/30

 Compatible Extension Sets (Continued)

The pump uses standard, single-use, disposable extension sets and syringes with Luer-lock connectors. The user is responsible for verifying
the suitability of a product used, if it is not recommended by CareFusion.

Patient Controlled Analgesia (PCA) Sets

30822 PVC Syringe Extension Set with clamp (152 cm).
Priming Volume: 0.5ml

30832 PVC ‘Y’ Syringe Extension Set with back check valve and 2 clamps (178 cm).
Priming Volume: 1.5ml

30842E PVC Syringe Extension Set with back check valve, SmartSite® Needle-Free Valve Port and clamp (30 cm).
Priming Volume: 1.4ml

30852 PVC ‘Y’ Syringe Extension Set with anti-siphon valve, back check valve and 2 clamps (183 cm).
Priming Volume: 1.8ml

30862 PVC Syringe Extension Set with anti-siphon valve and clamp (156 cm).
Priming Volume: 0.6ml

04102215162 PVC Syringe Extension Set with rotating luer. (150 cm).
Priming Volume: 2.9ml

04100010162 PVC Syringe Extension Set (105 cm).

Priming Volume: 7.2ml

For availability please contact your local CareFusion representative because new sets are continuously being developed for our

A customers.

It is recommended that extension sets are changed in accordance with the Directions for Use.
Carefully read the Directions For Use supplied with the extension set prior to use.

Please note these drawings are not to scale

1000DF00327 Issue 3 23/30

 Maintenance

Routine Maintenance Procedures

To ensure that this pump remains in good operating condition, it is important to keep it clean and carry out the routine maintenance
procedures described below.

Interval Routine Maintenance Procedure

As per Hospital Policy Thoroughly clean external surfaces of the pump before and after prolonged period of storage.
Each usage 1. Inspect AC power supply plug and cable for damage.
2. Inspect case, keypad and plunger for damage.
3. Check Start up self test operation is correct.
Before the transfer of the pump to a Clean the pump by wiping over with a lint-free cloth lightly dampened with warm water and a
new patient and as required standard disinfectant / detergent solution.

If the pump is dropped, damaged, subjected to excessive moisture or high temperature, immediately take it out of

A service for examination by a qualified service engineer.

All preventative and corrective maintenance and all such activities shall be performed at a compliant work place in
accordance with the information supplied. CareFusion will not be responsible should any of these actions be performed
outside the instructions or information supplied by CareFusion. For Preventative and Corrective Maintenance
instructions please refer to the Technical Service Manual (TSM).
All servicing should only be performed by a qualified service engineer with reference to the TSM.

Please refer to Technical Service Manual for calibration procedures. The units of measurement used in the

A calibration procedure are standard SI (The International System of Units) units.

Battery Operation

The internal rechargeable battery allows continued operation when the AC power is unavailable, for example during patient transfer or AC
power failure. Mean Time To Battery Empty from fully charged @ 5ml/h and 20°C under normal conditions is 6 hours*. From the battery low
alarm it will take about 2½ hours to 90% charge when reconnected to the AC power supply, whether the pump is in use or not.
The battery is maintenance free, sealed Nickel Metal Hydride and requires no routine servicing. However, to achieve optimum operation,
ensure that the battery is fully recharged after full discharge, before storage, and at regular 3 month intervals during storage.
It is recommended that only a qualified service engineer replaces the battery. For further information regarding the replacement of
batteries refer to the Technical Service Manual.
The battery pack used in this Alaris® Syringe Pump is manufactured by CareFusion and includes a proprietary PCB (printed circuit board)
designed specifically for the Alaris® Syringe Pump, and in conjunction with Alaris® Syringe Pump software, controls battery use, charge
and temperature. Any use of battery packs that are not manufactured by CareFusion in the Alaris® Syringe Pump is at your sole risk, and
CareFusion does not provide any warranty for or endorsement on any battery packs that are not manufactured by CareFusion. CareFusion’s
product warranty shall not apply in the event the Alaris® Syringe Pump has suffered damage or premature wear, or malfunctions or
otherwise operates incorrectly, as a result of use with a battery pack that is not manufactured by CareFusion.
*95% lower confidence interval of 5 hours 50 minutes

1000DF00327 Issue 3 24/30

 Maintenance (continued)
Cleaning and Storage
Before the transfer of the pump to a new patient and periodically during the use, clean the pump by wiping over with a lint-free cloth lightly
dampened with warm water and a standard disinfectant / detergent solution.
Recommended cleaners are:
Brand Concentration
Hibiscrub 20% (v/v)
Virkon 1% (w/v)
Do not use the following disinfectant types:
• Disinfectants which are known to be corrosive to metals must not be used, which include:
• NaDcc (such as Presept),
• Hypochlorites (such as Chlorasol),
• Aldehydes (such as Cidex),
• Cationic Surfactants (such as Benzalkonium Chloride).
• Use of Iodine (such as Betadine) will cause surface discoloration.
• Concentrated Isopropyl alcohol based cleaners will degrade plastic parts.
The syringe and extension sets are disposable single use items and should be discarded after use according to their manufacturers’
instructions.
If the pump is to be stored for an extended period it should be first cleaned and the internal battery fully charged. Store in a clean, dry
atmosphere at room temperature and, if available, employ the original packaging for protection.
Once every 3 months during storage, carry out functional tests as described in the Technical Service Manual and ensure that the internal
battery is fully charged.

Before cleaning always switch OFF and disconnect from the AC power supply. Never allow liquid to enter the casing

A and avoid excess fluid build up on the pump. Do not use aggressive cleaning agents as these may damage the exterior
surface of the pump. Do not steam autoclave, ethylene oxide sterilise or immerse this pump in any fluid.

Disposal

Information on Disposal for Users of Waste Electrical and Electronic Equipment

This U symbol on the product and/or accompanying documents means that used electrical and electronic products should
not be mixed with household waste.
If you wish to discard electrical and electronic equipment, please contact your CareFusion affiliate office or distributor for
further information.
Disposing of this product correctly will help to save valuable resources and prevent any potential negative effects on human
health and the environment which could otherwise arise from inappropriate waste handling.
Information on Disposal in Countries outside the European Union
This symbol is only valid in the European Union. The product should be disposed of taking environmental factors into
consideration. To ensure no risk or hazard, remove the internal rechargeable battery and the Nickel Metal Hydride battery
from the control board and dispose of as outlined by the local country regulations. All other components can be safely
disposed of as per local regulations.

1000DF00327 Issue 3 25/30

 Occlusion Pressure Limits

Time to alarm following occlusion is achieved in less than 30 minutes at rates of 1 ml/h and higher by the appropriate selection of occlusion
levels.
The following graphs show the typical values for time to alarm and bolus volume that can be expected in the event of an occlusion when
the BD Plastipak 50 ml syringe is selected with a G40020B standard extension set.

Time to alarm - 1.0 ml/h Time to alarm - 5.0 ml/h

typical typical

hr:min:sec
hr:min:sec

Occlusion Level Occlusion Level

Bolus Volume without back off Bolus Volume with back off

typical typical
ml

ml

Occlusion Level Occlusion Level

Tests at low alarm levels may alarm immediately - the force at these levels is commonly less than the friction in the syringe (with no
additional fluid pressure). The result is that the pressure relating to the low forces will be less than the nominal quoted occlusion pressure.

Bolus volume following occlusion will be minimised by the back off feature if enabled. The back off will reduce the line pressure by removing
the volume stored in the occluded line and deducting this volume from the volume infused.

1000DF00327 Issue 3 26/30

 IrDA, RS232 and Nurse Call Specification

IrDA / RS232 / Nurse Call Feature RS232 / Nurse Call Connection Data

The RS232 / Nurse call feature is an optional feature on Alaris® Nurse call Specification -
Syringe Pumps. It allows the pump to be monitored remotely
Connector D Type - 9 Pin
and/or controlled via a suitable central monitoring or computer
system. TXD/RXD EIA RS232-C Standard
When the pump is started by a command from the serial interface, TXD Output Voltage Range Minimum: -5V (mark), +5V
communication must take place over the serial interface, a (space)
communication must take place every 15 seconds or the pump Typical: -7V (mark), +7V (space)
will alarm, display communications failure and stop infusing. This with 3kΩ load to ground
failure protects against failure of the communications, including
the removal of the RS232 cable. RXD Input Voltage Range -30V - +30V max.
RXD Input Thresholds Low: 0.6V minimum / High: 3.0V
maximum
The nurse call interface provides a remote

A
RXD Input Resistance 3kΩ minimum
backup to the internal audible alarm. It should
not be relied upon to replace monitoring of the Enable Active, Low:-7V to -12V
internal alarm. Active, High:+7V to +12V,
powers up the isolated RS232
Refer to the Technical Service Manual for further
circuitry
information regarding the RS232 interface.
Since it is possible to control the syringe pump Inactive: Floating/open circuit,
using the RS232 interface at some distance from allows isolated RS232 circuitry
the pump and hence remote from the patient, to power down.
responsibility for the control of the pump is Isolation Socket/Pump 1.5kV (dc, or ac peak)
vested in the software run on the computer
control system. Baud Rate 38.4 kBaud

The assessment for the suitability of any software Start Bits 1 Start Bit
used in the clinical environment to control or Data Bits 8 Data Bits
receive data from the pump lies with the user
Parity No Parity
of the equipment. This software should include
detection of the disconnection or other failure Stop Bits 1 stop bit
of the RS232 cable. The protocol is detailed in Nurse Call Relay Contacts Pins 1, 8 + 9, 30V dc, 1A rating
the Technical Service Manual and is for general
information only.
Any connected analogue and digital components Typical Connection Data -
are required to meet IEC/EN60950 for data 1 Nurse call (Relay) Normally Closed (NC C)
processing and IEC/EN60601 for medical devices.
2 Transmit Data (TXD) Output
Anyone connecting additional devices to the
signal input or output is a system configurator 3 Received Data (RXD) Input
and responsible for meeting the requirements 4 Power Input (DSR)
of the system standard IEC/EN60601-1-1.
5 Ground (GND)
6 Not used
7 Power Input (CTS)
IrDA
8 Nurse call (Relay) Normally open (NC O)
Baud Rate 38.4 kBaud 9 Nurse call (Relay) Common (NC COM)
Start Bits 1 Start Bit
Data Bits 8 Data Bits
Parity No Parity
Stop Bits 1 stop bit

1000DF00327 Issue 3 27/30

 Trumpet Curves and Start-up Curves
In this pump, as with all infusion systems, the action of the pumping mechanism and variations in individual syringes cause short-term fluctuations
in rate accuracy.
The following curves show typical performance of the system in two ways: 1) the delay in onset of fluid flow when infusion commences (start-up
curves), and 2) the accuracy of fluid delivery over various time periods is measured (trumpet curves).
The start-up curves represent continuous flow versus operating time from the start of the infusion. They exhibit the delay in onset of delivery due
to mechanical compliance and provide a visual representation of uniformity. Trumpet curves are derived from the second hour of this data. Tests
performed per IEC/EN60601-2-24 standard.
Trumpet curves are named for their characteristic shape. They display discrete data averaged over particular time periods or 'observation windows',
not continuous data versus operating time. Over long observation windows, short term fluctuations have little effect on accuracy as represented
by the flat part of the curve. As the observation window is reduced, short term fluctuations have greater effects as represented by the "mouth" of
the trumpet.
Knowledge of system accuracy over various observation windows may be of interest when certain drugs are being administered. Short term
fluctuations in rate accuracy may have clinical impact depending on the half-life of the drug being infused, therefore the clinical effect cannot be
determined from the trumpet curves alone.
Start-up and trumpet curves may not be indicative of operation under negative pressure.

A Differences in factors such as size and plunger force in compatible syringes produced by other manufacturers can cause
variations in accuracy and trumpet curves as compared to those represented. Additional curves for compatible syringes are
available upon written request.
For applications where flow uniformity is a concern, rates of 1.0 ml/h or above are recommended.

Start-up Trend. BD Plastipak 50ml @ 0.1ml/h Trumpet Curve. BD Plastipak 50ml @ 0.1ml/h
Rate (ml/h)

Error (%)

Time (mins) Observation Window (mins)

Start-up Trend. BD Plastipak 50 ml @ 1.0 ml/h

Trumpet Curve. BD Plastipak 50 ml @ 1.0 ml/h
Rate (ml/h)

Error (%)

Time (mins) Observation Window (mins)

Trumpet Curve. BD Plastipak 50 ml @ 5.0 ml/h

Start-up Trend. BD Plastipak 50 ml @ 5.0 ml/h
Rate (ml/h)

Error (%)

Time (mins) Observation Window (mins)

1000DF00327 Issue 3 28/30

 Products and Spare Parts

Alaris® Infusion System

Range of products in the Alaris® Infusion System product family are:

Part Number Description

80023UN01 Alaris® GH Syringe Pump
80033UND1 Alaris® CC Syringe Pump
80043UN01 Alaris® TIVA Syringe Pump
80053UN01 Alaris® PK Syringe Pump
80033UND1-G Alaris® CC Guardrails® Syringe Pump
80023UN01-G Alaris® GH Guardrails® Syringe Pump
80263UN01-G Alaris® GP Guardrails® Volumetric Pump
274 Alaris® Transporter
80083UN00-xx1 Alaris® DS Docking Station
80203UNS0x-xx1 Alaris® Gateway Workstation

1 For Docking Stations and Workstation contact local customer services representative to obtain configurations availability and part numbers.

Spare Parts
A comprehensive list of spare parts for this pump is included within the Technical Service Manual.
The Technical Service Manual (1000SM00001) is now available in electronic format on the World Wide Web at :-
www.carefusion.co.uk/alaris-technical/
A username and password are required to access our manuals. Please contact local customer services representative to obtain login details.

Part Number Description

1000SP01122 Internal Battery Pack
1001FAOPT91 AC Power Lead - UK
1001FAOPT92 AC Power Lead - European

1000DF00327 Issue 3 29/30

 Service Contacts
For service contact your local Affiliate Office or Distributor.

AE CN GB NZ
CareFusion, CareFusion, CareFusion, CareFusion,
PO Box 5527, 上海代表机构，中国上海市张杨路 The Crescent, Jays Close, 14B George Bourke Drive,
Dubai, United Arab Emirates. 500 号， Basingstoke, Mt Wellington 1060,
上海时代广场办事处大楼， Hampshire, RG22 4BS, PO Box 14-518,
A 座，24 层， United Kingdom. Panmure 1741, Auckland,
邮编：200122。 New Zealand
Tel: (971) 4 28 22 842 电话：(86) 21 58368018 Tel: (44) 0800 917 8776 Tel: 09 270 2420
Freephone: 0508 422734
Fax: (971) 4 28 22 914 传真：(86) 21 58368017 Fax: (44) 1256 330860 Fax: 09 270 6285
AU DE HU PL
CareFusion, CareFusion, CareFusion, CareFusion,
3/167 Prospect Highway, Pascalstr. 2, Döbrentei tér 1, ul. Rzymowskiego 53,
PO Box 355 52499 Baesweiler, H-1013 Budapest, 02-697 Warszawa,
Seven Hills, NSW 2147, Deutschland. Magyarország. Polska.
Australia.
Tel: (61) 1800 833 372 Tel: (49) 931 4972 837 Tel: (36) 1 488 0232 Tel: (48) 225480069
Tel: (36) 1 488 0233
Fax: (61) 1800 833 518 Fax: (49) 931 4972 318 Fax: (36) 1 201 5987 Fax: (48) 225480001
BE DK IT SE
CareFusion, CareFusion, CareFusion, CareFusion,
Leuvensesteenweg 248 D, Firskovvej 25 B, Via Ticino 4, Hammarbacken 4B,
1800 Vilvoorde, 2800 Lyngby, 50019 Sesto Fiorentino, 191 46 Sollentuna,
Belgium. Danmark. Firenze, Italia. Sverige.
Tel: (32) 2 267 38 99 Tlf. (45)70 20 30 74 Tél: (39) 055 30 33 93 00 Tel: (46) 8 544 43 200
Fax: (32) 2 267 99 21 Fax. (45)70 20 30 98 Fax: (39) 055 34 00 24 Fax: (46) 8 544 43 225
CA ES NL US
CareFusion, CareFusion, CareFusion, CareFusion,
235 Shields Court, Edificio Veganova, De Molen 8-10, 10020 Pacific Mesa Blvd.,
Markham, Avenida de La Vega, nº1, 3994 DB Houten, San Diego, CA 92121,
Ontario L3R 8V2, Bloque 1 - Planta 1, Nederland. USA.
Canada. 28108 Alcobendas, Madrid,
España.
Tel: (1) 905-752-3333 Tel: (34) 902 555 660 Tel: +31 (0)30 2289 711 Tel: (1) 800 854 7128
Fax: (1) 905-752-3343 Fax: (34) 902 555 661 Fax: +31 (0)30 2289 713 Fax: (1) 858 458 6179
CH FR NO ZA
CareFusion Switzerland 221 Sàrl CareFusion, CareFusion, CareFusion,
Critical Care Parc d’affaire le Val Saint Quentin Solbråveien 10 A, Unit 2 Oude Molen Business Park,
A-One Business Centre 2, rue René Caudron 1383 ASKER, Oude Molen Road, Ndabeni,
Zone d’activitiés Vers-la-Pièce 78960 Voisins le Bretonneux Norge. Cape Town 7405, South Africa.
n° 10 France
1180 Rolle / Switzerland
Ph.: 0848 244 433 Tél: (33) 1 30 05 34 00 Tel: (47) 66 98 76 00 Tel: (27) (0) 860 597 572
Tel: (27) 21 510 7562
Fax: 0848 244 100 Fax: (33) 1 30 05 34 43 Fax: (47) 66 98 76 01 Fax: (27) 21 5107567
Rev. B

1000DF00327 Issue 3 30/30

Alaris, Guardrails, SmartSite and IVAC are registered
trademarks of CareFusion Corporation or one of its
subsidiaries. All rights reserved.
All other trademarks are property of their
respective owners.

© 2000-2012 CareFusion Corporation or one of its

subsidiaries. All rights reserved.

This document contains proprietary information of

CareFusion Corporation or one of its subsidiaries,
and its receipt or possession does not convey any
rights to reproduce its contents, or to manufacture
or sell any product described. Reproduction,
disclosure, or use other than for the intended
purpose without specific written authorization of
CareFusion Corporation or one of its subsidiaries is
strictly forbidden.

CareFusion Switzerland 317 Sarl,

t A-One Business Centre, Z.A Vers –La-
Pièce n° 10, CH-1180, Rolle

CareFusion UK 305 Ltd., The Crescent,

EC REP Jays Close, Basingstoke, Hampshire,
RG22 4BS, UK
1000DF00327 Issue 3

carefusion.com