BD Alaris 8002TIG03 Manual

s
Alaris™ Syringe Pump
(with Plus Software) MK4
Models: 8002TIG03, 8003TIG03, 8002TIG03-G, 8003TIG03-G
Directions For Use
en

BDDF00001 Issue 5 1/56
Alaris™ Syringe Pumps
Contents
Page
Introduction ..............................................................................................4
Intended Purpose......................................................................................4
Conditions of Use ......................................................................................4
Indications ............................................................................................4
Contraindications......................................................................................4
About This Manual ........................................................................................5
Conventions used in this manual .......................................................................5
Creating a Data Set........................................................................................6
Features of the Pump......................................................................................7
Controls and Indicators ...................................................................................8
Controls:...............................................................................................8
Indicators: .............................................................................................8
Symbol Definitions ........................................................................................9
Labelling Symbols:.....................................................................................9
Main Display Features ....................................................................................10
Alaris CC Syringe Pump and Alaris CC Guardrails Syringe Pump Display ................................10
Alaris GH Syringe Pump and Alaris GH Guardrails Syringe Pump Display ................................10
Screen Icons ..........................................................................................10
Operating Precautions ...................................................................................11
Disposable Syringes and Extension Sets ...............................................................11
Mounting the Pump ..................................................................................11
Operating Environment ...............................................................................11
Operating Pressure ...................................................................................12
Alarm Conditions .....................................................................................12
Guardrails Safety Software ............................................................................12
Hazards ..............................................................................................12
Electromagnetic Compatibility & Interference. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13
Getting Started ..........................................................................................14
Initial Set-up..........................................................................................14
Language Selection...................................................................................14
Pole Clamp Installation................................................................................15
Docking Station/Workstation* or Equipment Rail Installation ...........................................15
Securing the Syringe with Optional Lock box..............................................................16
Lock box operation ...................................................................................16
Syringe Loading..........................................................................................17
Prepare Syringe and Administration Set ...............................................................17
Loading and Confirming a Syringe.....................................................................18
Starting the Pump........................................................................................20
Basic Features ............................................................................................22
Bolus Infusion ........................................................................................22
Purge.................................................................................................23
Volume to be Infused (VTBI) ..........................................................................23
Clear Volume .........................................................................................23
Rate Lock .............................................................................................23
Rate Titration .........................................................................................23

BDDF00001 Issue 5 2/56
Alaris™ Syringe Pumps
Dosing Summary .....................................................................................24
Set VTBI over Time ....................................................................................24
24 Hour Log ..........................................................................................24
Event Log.............................................................................................24
Data Set Details.......................................................................................24
Infusion Setup ........................................................................................24
Pump Details .........................................................................................24
Add Drug.............................................................................................25
Adjust Alarm Volume .................................................................................25
Profile Filter...........................................................................................25
Standby ..............................................................................................25
Pressure Features ........................................................................................26
Auto Set Pressure (If enabled)* ........................................................................26
Pressure Level with pressure set fitted* ................................................................26
Pressure Level* .......................................................................................26
Alarms and Warnings.....................................................................................27
Original Alarms .......................................................................................27
3rd Edition Alarms ....................................................................................29
Prompts .................................................................................................31
Configured Options ......................................................................................32
Alarm Presets .........................................................................................32
Configured Options...................................................................................32
Alaris Editor Software Profile Configuration ............................................................33
Dosing Only Units ....................................................................................35
Alaris Editor Software Profile Drug library ..............................................................36
Profile Syringe Library ................................................................................36
Specifications ............................................................................................37
Recognised Syringes .....................................................................................40
Associated Products......................................................................................41
The Alaris Gateway Workstation .......................................................................41
The Alaris DS Docking Station .........................................................................41
Compatible Extension Sets ...............................................................................42
Standard Sets.........................................................................................42
Blood Sets ............................................................................................42
TPN Sets..............................................................................................43
Low Sorbing Sets .....................................................................................43
Light Protected Sets ..................................................................................44
NICU Sets.............................................................................................44
Patient Controlled Analgesia (PCA) Sets................................................................45
Maintenance.............................................................................................46
Routine Maintenance Procedures .....................................................................46
Battery Operation.....................................................................................46
Cleaning and Storage .................................................................................47
Disposal ..............................................................................................47
Occlusion Pressure Limits ................................................................................48
With a Pressure Extension Set fitted, G30402M - Standard disposable extension set* ....................48
Without a Pressure Extension Set fitted, G40020B - Standard disposable extension set ..................49
IrDA, RS232 and Nurse call Specification ..................................................................50
IrDA / RS232 / Nurse call Feature.......................................................................50

BDDF00001 Issue 5 3/56
Alaris™ Syringe Pumps
IrDA ..................................................................................................50
RS232 / Nurse call Connection Data ...................................................................51
Trumpet Curves and Start-up Curves .....................................................................52
Alaris CC Syringe Pump and Alaris CC Guardrails Syringe Pump ........................................52
Alaris GH Syringe Pump and Alaris GH Guardrails Syringe Pump ........................................53
Products and Spare Parts .................................................................................54
Spare Parts and Accessories ...........................................................................54
Alaris Editor Software .................................................................................54
Document History........................................................................................55
Contact Us ...............................................................................................56
Customer Service Information.........................................................................56

BDDF00001 Issue 5 4/56
Alaris™ Syringe Pumps
Introduction
Introduction
This Directions for use can be used with the following Mark 4 (MK4) Pumps:-
• Alaris™ CC Guardrails™ Syringe Pump (8003TIG03-G)
• Alaris™ CC Syringe Pump (8003TIG03)
• Alaris™ GH Guardrails™ Syringe Pump (8002TIG03-G)
• Alaris™ GH Syringe Pump (8002TIG03)
Note: All the above products are hereinafter referred to as Pump except where different features are applicable then the specific
Pump will be stated or symbol used, see 'Conventions used in this Manual' section.
Note: The Pumps can be identified as MK4 version by the MK4 on the
label on the rear case, see image right, or by verifying the software
version as 4.x.x or above on power up.
All the Pumps above mentioned function with a wide range of standard, single-use, disposable Luer lock syringes together with
extension sets. The Pump accepts syringe sizes from 5ml to 50ml. A full list of recognised syringes can be found in the 'Recognised
Syringes' section. A list of recommended extension sets can be found in the 'Compatible Extension Sets' section. The Alaris Editor
software for the Pump allows the hospital to develop a best-practice data set of intravenous (IV) medication dosing guidelines for
patient-specific care areas, referred to as profiles. Each profile contains a specific library of drugs, as well as Pump configurations
appropriate for the care area. A profile also contains Hard Limits that cannot be overridden during infusion programming.
The Alaris CC Guardrails Syringe Pump and the Alaris GH Guardrails Syringe Pump profiles also contain Guardrails Soft Alerts that can
be overridden, based on clinical requirements. The hospital defined data set is developed and approved through pharmacy and clinical
input, and then configured into the Pump by qualified technical personnel.
The Alaris CC Guardrails Syringe Pump and the Alaris GH Guardrails Syringe Pump, with a data set loaded, provides automatic alerts
when a dosing limit, bolus limit, concentration limit, or weight limit has been exceeded. These safety alerts are provided without the
need for the Pump to be connected to a PC or network.
The Alaris CC Guardrails Syringe Pump and the Alaris CC Syringe Pump feature an in-line pressure sensor technology, capable of highly
accurate, real time pressure monitoring. Improving the early detection of occlusions, by reducing time to alarm, and preventing the
potential risk of post occlusion bolus.
Intended Purpose
The Alaris Syringe Pump is intended for use by medical staff for purposes of controlling infusion rate and volume.
Conditions of Use
The Alaris Syringe Pump should only be operated by a clinician competent in use of automated syringe pumps and post-placement
management of intravenous catheters.
wBD cannot guarantee the continued system accuracy with other manufacturer’s syringes as identified in the
‘Recognised Syringes’ table. Manufacturers may change syringe specification significant to system accuracy without
prior notification.
Indications
The Alaris Syringe Pump is indicated for infusion of therapeutics including:
• analgesics
• antimicrobials
• blood products
• chemotherapy
• nutrition
• subcutaneous
Contraindications
The Alaris Syringe Pumps are contraindicated for:
• enteral therapies

BDDF00001 Issue 5 5/56
Alaris™ Syringe Pumps
About This Manual
About This Manual
Users are advised to read, to understand this manual and to be thoroughly familiar with the Pumps prior to operating.
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.
wKeep this Manual for future reference during the Pump’s operational life.
It is important to ensure that you only refer to the most recent version of the Directions for Use and Technical Service
Manual for your BD products. These documents are referenced on bd.com. Paper copies of the Directions For Use can
be obtained free of charge by contacting your local BD representative. An estimated delivery time will be provided
when the order is placed.
Conventions used in this manual
BOLD Used for Display names, software commands, controls and indicators referenced in this manual, for
example, Battery Indicator, PURGE, ON/OFF button.
'Single quotes' Used to indicate cross-references made to another section of this manual.
Italics Used to refer to other documents or manuals and also used for emphasis.
This symbol indicates that the option is relevant for the Alaris CC Syringe Pump and the Alaris CC
Guardrails Syringe Pump only.
GH
This symbol indicates that the option is relevant for the Alaris GH Syringe Pump and the Alaris GH
Guardrails Syringe Pump only.
Guardrails This symbol indicates that the option is relevant for the Alaris CC Guardrails Syringe Pump and the Alaris
GH Guardrails Syringe Pump only.
Caution: Wherever this symbol is shown an Important note is found. These notes highlight an aspect of
use that is important for the user to be aware of when operating the Pump.

BDDF00001 Issue 5 6/56
Alaris™ Syringe Pumps
Creating a Data Set
Creating a Data Set
To create a data set for the Pump, first the hospital will need to develop, review, approve and upload a data set according to the
following process. Refer to the Alaris Editor help file for further details and operating precautions.
1. Create a new Data Set (Using the Alaris Editor)
• Select new data set type: a) Plus Data Set - to create a new data set for the Alaris GH Syringe Pump
or the Alaris CC Syringe Pump
b) Plus Guardrails Data Set - to create a new data set for the Alaris GH
Guardrails Syringe Pump or the Alaris CC Guardrails Syringe Pump
2. Master Lists (Using the Alaris Editor)
• Master Drugs A predefined list of drug names and concentrations. This list, as well as
alternate names and concentrations defined in the Master Drug List, will be
accessible when creating a Profile Drug Library
• Master Syringe Library A predefined list of the currently supported syringes available for selection
within the profile
3. Create Care Area Profiles (Using the Alaris Editor)
• Drug Library Drugs and concentrations for a Profile with defaults, minimum limits, maximum
limits and occlusion alarm level. Up to 100 drug set-ups can be entered for
each of the available 30 Profiles.
• Configuration Pump configuration settings, General Options and Units for Dosing Only.
4. Review, Approve and Export Data Set (Using the Alaris Editor)
• Review and Approve It is recommended that the entire data set report is printed, reviewed and
signed as proof of approval by an authorised person, according to hospital
protocol. A signed copy of the data set report should be archived by the
hospital for future reference. Once a data set has been agreed it must be
approved within the Alaris Editor using a secure password.
• Export Export data set to allow data set to be uploaded to a Pump by the Alaris
Transfer Tool.
5. Upload data set to the Pump (Using the Alaris Transfer Tool)
Note: Selection of one profile will be required when uploading the data set to the Alaris GH Syringe Pump or the Alaris CC Syringe
Pump.
6. Prior to clinical use, check that the Data Set ID on the approved data set report matches the Data Set ID shown on the Pump.
7. Switch the Pump off.
8. Switch the Pump on and verify that the data set details screen displays the correct data set name and version. The Pump is now
ready to use.
Note: For Alaris Communication Engine (ACE) work flow see ACE user manual.
wDrug parameters have to be in accordance to local protocols and prescribed information.
Data set transfers should only be performed by Qualified Service Personnel.

BDDF00001 Issue 5 7/56
Alaris™ Syringe Pumps
Features of the Pump
Features of the Pump
High visibility
Alarm Indicator
Release lever
for MDI
Shelf for chevron
keys and softkeys
Positive Plunger
Grippers
Display
Syringe Clamp
ON/OFF
RUN
HOLD
PURGE/BOLUS
MUTE
PRESSURE
OPTION
Extension set
hook
Pressure transducer
Finger
Grips
Extension set
hook
Release
lever for
Rotating
Cam
Carrying
Handle
IR Communications
port
RS232
Connector
Folded Pole
Clamp
Potential
Equalisation (PE)
connector
Rating Plate (see Symbol Definitions for an
explanation of the symbols used)
Pressure transducer
Rotating Cam to
lock on to horizontal
rectangular bars
M
e
d
i
c
a
l
D
e
v
i
c
e
I
n
t
e
r
f
a
c
e
(
M
D
I
)

BDDF00001 Issue 5 8/56
Alaris™ Syringe Pumps
Controls and Indicators
Controls and Indicators
Controls:
Symbol Description
aON/OFF button - Press once to switch the Pump on. Press and hold down for 3 seconds to switch the
Pump off.
Note: Logs are maintained for power down events including when the pump is powered down or
unexpected power loss.
bRUN button - Press to start the infusion. The green LED will flash during infusion.
hHOLD button - Press to put the infusion on hold. The amber LED will be lit while on hold.
RMUTE button - Press to silence alarm for two minutes. To re-enable the alarm audio press the MUTE
button a second time.
Note: Attention alarm only: when not in alarm press and hold until four audible beeps are heard for
15 minutes silence.
i
PURGE/BOLUS button - Press to access PURGE or BOLUS soft keys. Press and hold down soft key to
operate.
PURGE - primes the extension set with fluid or drug during initial set up.
• Pump is on hold
• Extension set must not be connected to the patient
• Volume Infused (VI) is not added
BOLUS - fluid or drug delivered at an accelerated rate.
• Pump is infusing
• Extension set should be connected to the patient
• VI is added
dOPTION button - Press to access optional features, see 'Basic Features' section.
ePRESSURE button - Use this button to display the pumping pressure and alarm level.
This button will also display the pressure trend display.
fCHEVRON keys - Double or single for faster/slower increase or decrease of values shown on display.
gBLANK SOFTKEYS - Use in conjunction with the prompts shown on the display.
Indicators:
Symbol Description
jBATTERY 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.
SAC POWER indicator - When illuminated the Pump is connected to an AC power supply and the battery
is being charged.

BDDF00001 Issue 5 9/56
Alaris™ Syringe Pumps
Symbol Definitions
Symbol Definitions
Labelling Symbols:
Symbol Description
Consult accompanying documents
xPotential Equalisation (PE) Connector
yRS232/Nurse call Connector
lDefibrillation-proof type CF applied part (Degree of protection against electrical shock)
IP32 Protected against direct sprays of water up to 15° from vertical and protected against solid objects greater than
2.5mm.
Note: IP33 applies if AC power cable retainer kit, part number 1000SP01294, is fitted.
rAlternating Current
sDevice complies with the requirements of Council Directive 93/42/EEC as amended by 2007/47/EC.
TDate of Manufacture
tManufacturer
UNot for Municipal Waste
WFuse Rating

+40°C
0°C Operating Temperature Range - Pump can be used between 0 and 40 degrees centigrade.

BDDF00001 Issue 5 10/56
Alaris™ Syringe Pumps
Main Display Features
Main Display Features
Alaris CC Syringe Pump and Alaris CC Guardrails Syringe Pump Display
Pump
Status
Syringe type fitted /
Profile / Drug name Pressure
Information
Infusion Rate Volume
Infused
Volume Infused
Option VTBI
Option
Alaris GH Syringe Pump and Alaris GH Guardrails Syringe Pump Display
GH
Pump
Status
Syringe type fitted /
Profile / Drug name Pressure
Information
Infusion
Rate
Volume
Infused
Volume Infused
Option
VTBI
Option
Screen Icons
Symbol Description
lTime remaining display icon - Indicates time before syringe will require replacement.
N
BATTERY icon - Indicates battery charge level to highlight when the battery will require recharging or
re-connection to AC power supply.
Note: This can be enabled/disabled with the Alaris Editor software
INFUSING Guardrails Soft Alert icons - Indicates the Pump is running at a rate or dose above (pointing up) or below
(pointing down) a Guardrails Soft Alert.
Guardrails
INFUSING
Hard limit Warning icon - Indicates the setting entered is not permitted as it is under or exceeds a Hard
Limit.

BDDF00001 Issue 5 11/56
Alaris™ Syringe Pumps
Operating Precautions
Operating Precautions
Disposable Syringes and Extension Sets
m• The Pump has been calibrated for use with single-use disposable syringes. To best ensure 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.
• The user must be thoroughly familiar with instructions in this Directions For Use and understand how to
load and confirm the syringe on the Pump. Incorrect syringe loading may result in misidentification of the
syringe type and size leading to significant under or over infusion.
• 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.
• 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.
• 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.
Mounting the Pump
• When more than one pump is being used on a patient, those containing high risk, critical medications
must be positioned as close to the patient's heart level as possible to avoid the risk of variations in flow or
siphoning.
• Raising a Pump whilst infusing may result in a bolus of the infusate, whereas lowering a Pump whilst
infusing may result in a delay in the infusion (an underinfusion).
I• Do not mount the Pump in a vertical position with the syringe pointing upwards as this could lead to
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
• Intended environments include general wards, critical and intensive care, operating rooms, accident
and emergency rooms. The Pump may be used in an ambulance environment. Ensure that the Pump
is appropriately attached using the provided pole clamp. The Pump is designed to withstand possible
bumps and vibrations whilst being used in an ambulance, complying with the standard EN 1789. If
the Pump is dropped or experiences any severe physical disturbances, arrange a thorough inspection
by appropriately trained technical personnel as soon as is practically possible. The Pump may also be
used outside the ambulance as long as the temperature is within the specified range as stated in the
'Specifications' section and on the Pump label.
• When using any infusion pump in conjunction with other pumps or devices requiring vascular access,
extra care is necessary. Adverse delivery of medication or fluids can be caused by the substantial variation
in pressures created within the infusion system by such pumps. Typical examples of those pumps are
used during dialysis, bypass or cardiac assist applications.
• The pump is suitable for use in hospital and clinical environments other than domestic establishments
that have access to single phase AC power supply.
• The Pump is not intended to be used in the presence of a flammable anaesthetic mixture with air or
oxygen or nitrous oxide.

BDDF00001 Issue 5 12/56
Alaris™ Syringe Pumps
Operating Precautions
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.
• Alarm tone settings are preserved in the case of power loss, however some system faults will result in loss
of alarm settings. The new alarm tone settings will be stored when powering down from tech mode after
a change. The settings will be lost if a cold-start is performed, but should be saved for faults that don't
require a cold start.
Guardrails Guardrails Safety Software
• The Guardrails Safety Software incorporates soft dosing limits and Pump configuration parameters based
on hospital protocol. The software adds a test of reasonableness to drug programming based on the
limits defined by the hospital. Qualified personnel must ensure the appropriateness of the drug dosing
limits, the compatibility of the drugs, and the performance of each Pump, as part of the overall infusion.
Potential hazards include drug interactions, and inappropriate delivery rates and pressure alarms.
• When loading a data set with the Guardrails Safety Software, the user must ensure the correct profile is
selected prior to starting an infusion.
Hazards
• 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.
V• Do not open the RS232/Nurse Call protective covering when not in use. Electrostatic discharge (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.
L
• If the 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 Qualified Service
Personnel. 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.
• Warning: Alaris Syringe Pumps should not be modified or altered in any way, except where explicitly
directed or authorised by BD. Any use of Alaris Syringe Pumps which have been altered or modified
otherwise than in strict application of directions provided by BD, is at your sole risk, and BD does not
provide any warranty for or endorsement on any Alaris Syringe Pump that has been so modified or
altered. BD 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 unauthorised
modification or alteration of the Alaris Syringe Pump.
• Care must be taken when removing covers or handling moving mechanisms.
• All pumps in a single care area should be configured with the same alarm tones to avoid User confusion.

BDDF00001 Issue 5 13/56
Alaris™ Syringe Pumps
Operating Precautions
Electromagnetic Compatibility & Interference
M• The Pump is protected against the effects of external interference, including high energy radio frequency
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 BD
representative.
MR
• 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 BD
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 BD 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 BD 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.
K
• 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
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).

BDDF00001 Issue 5 14/56
Alaris™ Syringe Pumps
Getting Started
Getting Started
Initial Set-up
wBefore operating the Pump read this Directions For Use manual carefully.
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:
• Alaris Syringe Pump
• User Support CD (Directions For Use)
• AC Power Cable (as requested)
• 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 Sis
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 fkeys.
3. Press the OK softkey to confirm your selection.
w• The Pump may be used safely with the pre-installed default data set. Any data set created for installation must be
approved by an appropriately qualified person with clinical authority in accordance with hospital protocol prior
to upload and activation.
• The Pump will automatically operate from its internal battery if the Pump is switched on without being connected
to the AC power supply.
• Should the Pump fail to perform correctly, replace in its original protective packaging, where possible and contact
Qualified Service Personnel for investigation.

BDDF00001 Issue 5 15/56
Alaris™ Syringe Pumps
Getting Started
wDo not mount the Pump with the AC power inlet or the syringe pointing upwards. This could affect the electrical 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.
wEnsure the pole clamp is folded away and stored
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 I.V. infusion stand
becomes top heavy or unstable.
wPrior to each use, check the pole clamp:
• does not show any signs of excessive wear,
• does not show any signs of excessively loose movement in the extended, mountable position.
If these signs are observed, the Pumps should be taken out of service for examination by Qualified Service Personnel.
Docking Station/Workstation* or Equipment Rail Installation
The rotating cam can be fitted to the rectangular bar on the Docking Station/Workstation* or the equipment rail measuring 10 by
25mm.
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.
3. The Pump should click into position when fitted to the bar.
4. Ensure that the Pump is positioned securely. Verify Pump is secure by gently pulling the Pump away from the Docking Station/
Workstation* without using the release lever. When the Pump is securely attached, it should not come off the Docking Station/
Workstation*.
5. To release, push the release lever and pull the Pump forwards.
Warning: Pump may fall off the Docking Station/Workstation* if not properly mounted which could result in user and/or
patient harm.
Rectangular bar
Rotating cam
Release lever (push to release)
* Alaris Gateway Workstation and Alaris DS Docking Station

BDDF00001 Issue 5 16/56
Alaris™ Syringe Pumps
Securing the Syringe with Optional Lock box
Securing the Syringe with Optional Lock box
Lock box operation
The optional lock box is a available in two configurations:
• Rate Unlocked lock box - is designed to allow the user to
adjust rate whilst infusing.
• Rate Locked lock box - is designed to prevent rate change
whilst infusing. If using this lock box users would need to
put the Pump on hold and open the lock box to change the
rate.
wWhen mounting a Pump with lock box ensure that there is sufficient clearance for the cover to be fully opened, a gap
of 130mm minimum below the Pump is recommended.
Open Lock box:
1. Insert the key into the lock and turn key either way to unlock. 2. Lock box will move to the right and can then be opened.
Close Lock box:
1. Load the syringe according to the instructions in the 'Loading and Confirming a Syringe' section.
2. Ensure the extension set is connected to the syringe and threaded through the lock box.
Note: For the Alaris CC Syringe Pump models the pressure disc must be fitted prior to closing the lock box.
3. Set up the Pump according to the instructions in the 'Starting the Pump' section prior to closing the lock box for the Rate Locked
version only.
4. Close the cover until it makes contact with the Pump case. 5. Push the lock box from right to left until a click is heard.
6. Remove the key.
w• Pumps with lock box fitted should only be used when fitted to an Alaris Gateway Workstation, Alaris DS Docking
Station or an I.V. Pole.
• When transporting the Pump with lock box fitted it is recommended that two hands are used when holding or
carrying the Pump.
• If lock or lock box appears to be damaged, remove the Pump from service for examination by Qualified Service
Personnel.
• When the Pump is not in use ensure the lock box is locked.
• Lock box keys should be stored separately and take care not to lock keys inside lock box.
• Refer to the 'Routine Maintenance' section for instructions on cleaning and maintenance.

BDDF00001 Issue 5 17/56
Alaris™ Syringe Pumps
Syringe Loading
Syringe Loading
Prepare Syringe and Administration Set
To decrease potential start-up delays, delivery inaccuracies and delayed generation of occlusion alarms each time a new syringe is
loaded:
• Use smallest syringe size possible, for example, if infusing 9 ml of fluid, use a 10 ml syringe.
• Use the PURGE SYRINGE or PURGE option on the Pump to decrease the delay in the start of the infusion , see Starting the Pump
section.
wWarning: Use the smallest compatible syringe size necessary to deliver the fluid or medication; this is especially
important when infusing high risk or life-sustaining medications at low infusion rates, especially flow rates < 0.5 ml/h.
wWarning: Purge the Pump system before starting an infusion or after replacing a near-empty syringe with a
replacement syringe. When Purging ensure that the extension set is not connected to the patient.
Practice Recommendations:
• Tubing internal diameter: Smallbore or microbore tubing is recommended when infusing at low rates
• Filters: Internal volume, dead space, of in-line filters should be minimized
• Connection sites: Critical drugs should be connected as close to the vascular access site as possible
Positioning of Pump
Ensure that the Pump is as close to level of
patient’s heart as possible.
Patient’s heart level should be in line with
the middle of the Pump or the pressure disc
for the Alaris CC Syringe Pumps.
wWarning: Adjusting the Pump's height relative to the patient's heart level can lead to temporary increases or
decreases in fluid delivery
wCaution: If using multiple syringe pumps and it is not clinically feasible to have all Pumps level with the patient’s
heart, place the high risk or life-sustaining medications as close to the patient’s heart level as possible.
wCaution: When infusing multiple high risk or life-sustaining medications, consider placing the Pumps infusing at the
lowest rates as close to the level of the patient’s heart as possible.

BDDF00001 Issue 5 18/56
Alaris™ Syringe Pumps
Syringe Loading
Loading and Confirming a Syringe
wWarning: To securely load and confirm a syringe carefully follow the steps below. An incorrect loading of a syringe
may 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.
Syringe Flange Clamp
Syringe
Clamp
Barrel
Flange

Plunger
Grippers
Plunger
Flange
Plunger
Holder
Plunger
Finger
Grips
Syringe
Barrel
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.
3. Insert the syringe ensuring that the barrel flange is located in the slots on the syringe flange
clamp.
wTo ensure the syringe is loaded correctly, place the barrel flange in the space
between the syringe clamp and the syringe flange clamp. This is correct if the
syringe remains in position before the syringe clamp is closed.

BDDF00001 Issue 5 19/56
Alaris™ Syringe Pumps
Syringe Loading
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.
CONFIRM TYPE
IVAC 50
ON HOLD
Note: If the PURGE SYRINGE option has been enabled then the prompt to purge screen is displayed and the extension set can be
purged as required, however ensure that the extension set is not connected to the patient during this process.
wBD recommends limiting the number of configured syringe types and sizes available for selection on the Pump using
the Alaris Editor.
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.
Note: Fast Start is a Pump feature to automatically reduce the mechanical slack between the plunger mechanism and syringe at the
start of an infusion, as required.