Alaris IVAC P7000 Mk II Manual

Manufacturer’s Address:
ALARIS Medical UK Ltd
The Crescent
Jays Close
Basingstoke
Hampshire
RG22 4BS
United Kingdom
www.alarismed.com
P7000 Mk II
7001FAOPT73 Iss 13
Directions for Use
Manual del Usuario
P7000 GB/E
7001FAOPT73 Colour cover.qxd 12-09-2003 9:07 Page 2

i/ii
English
Getting Started Page
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Features of the IVAC®P7000 Syringe Pump . . . . . . . . . . . . . . . . . . . . . 2
Controls and Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Front Panel and Main Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Operating Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5
Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Pole Clamp . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Replacing the Mains Fuse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Loading a Syringe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Starting the Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Power ON/OFF . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Purge . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Bolus Infusions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Review . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Pressure Level with Pressure Set fitted . . . . . . . . . . . . . . . . . . . . . . . . 10
Pressure Level without Pressure Set fitted . . . . . . . . . . . . . . . . . . . . . 10
Drugs and Dosing - Drug Name Only . . . . . . . . . . . . . . . . . . . . . . . . . 11
Drugs and Dosing - Using Pre-configured Drug Dosing Protocol . . . . . 11
Drugs and Dosing - Using User-programmed Drug Dosing . . . . . . . . . 11
Volume to be Infused (VTBI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Set VTBI Over Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Set by Doserate / Set by ml/h . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Selecting the Set by Doserate Option . . . . . . . . . . . . . . . . . . . . . . . . . 13
Selecting the Set by ml/h Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Clear Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Induction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Multidose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Clear multidose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
24 H Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Event Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Rate Lock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Disable Rate Lock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Re-Enable Rate Lock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Alarm Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18 - 19
Configured Options
Drug Set-up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20 - 21
General Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 - 23
Clock Set . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Hospital Name . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Enable Syringes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Enable Units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Specifications
RS232 / Nursecall Feature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
Self Test Routine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59 - 62
Configuration Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
Symbol Definition and Equipment Classifications . . . . . . . . . . . . . . . . 65
Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66 - 71
Routine Maintenance Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72
Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72
Cleaning and Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72
Battery Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
Occlusion Pressure Limits for IVAC®50ml Syringes . . . . . . . . . . . . . 76 - 77
Spare Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
Service Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
Trumpet and Start-up Curves . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 80 - 82
Technical Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83
Service Contacts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86
Contents
7001FAOPT73 ISS 13

Español
Puesta en marcha Página
Introducción . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .30
Características de la bomba de jeringa P7000 de IVAC®. . . . . . . . . . .30
Controles e indicadores . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Panel frontal y pantalla principal . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Precauciones de funcionamiento . . . . . . . . . . . . . . . . . . . . . . . . . . . 32 - 33
Instalación . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Pinza de sujeción al palo de goteo . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Sustitución de fusibles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Carga de la jeringa . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Puesta en marcha de la bomba . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Conexión ON/OFF . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Purgado . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Infusión de un bolo . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Revisión . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Nivel de presión con el equipo de presión acoplado (dedicado) . . . . . 38
Nivel de presión sin equipo de presión acoplado (no dedicado) . . . . . 38
Fármacos y dosificaciones - Solo nombre del fármaco . . . . . . . . . . . . . 39
- Uso de protocolos de dosificación de fármacos previamente configurados 39
- Uso de dosificación de fármacos programados por el usuario . . . . . 40
Volumen a infundir (VAI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Programar VAI por tiempo . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Programar por dosis / programar por ml/h . . . . . . . . . . . . . . . . . . 42
Selección de la opción Programar por dosis . . . . . . . . . . . . . . . . . . 42
Selección de la opción Programar por ml/h . . . . . . . . . . . . . . . . . . 42
Borrar el volumen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Inducción . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Multidosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Borrar Multidosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Registro de 24 horas . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Registro de sucesos . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Bloqueo de flujo . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Desactivar el bloqueo de flujo . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Permitir de nuevo Bloqueo Flujo . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Procedimientos de alarmas . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47 - 48
Opciones configuradas
Programación de fármacos . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49 - 50
Opciones generales . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51 - 52
Ajuste del reloj . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
Nombre del hospital . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Jeringas permitidas . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Unidades permitidas . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Especificaciones
Opción RS232/Llamada de enfermera . . . . . . . . . . . . . . . . . . . . . . . . 58
Autocomprobación de rutina . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .59 - 62
Registro de configuración . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64
Definición de los símbolos y clasificación del equipo . . . . . . . . . . . . . 65
Especificaciones . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66 - 71
Procedimientos rutinarios de mantenimiento . . . . . . . . . . . . . . . . . . . 73
Desecho . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
Limpieza y almacenamiento . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
Funcionamiento con batería . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
Límites de la presión de oclusión para las jeringas de 50 ml de IVAC
®
76 - 77
Piezas de repuesto . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
Equipo de mantenimiento . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
Curvas de trompeta y de arranque . . . . . . . . . . . . . . . . . . . . . . . . . 80 - 82
Descripción técnica . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
Servicios técnicos . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
Garantía . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87
ii / ii 7001FAOPT73 ISS 13
Contenido

Getting Started
1/87
7001FAOPT73 ISS 13
Page
English
Getting Started 2 - 19
Configured Options 20 - 28
Specifications 57 - 86
Español
Puesta en marcha 30 - 48
Opciones configuradas 49 - 56
Especificaciones 58 - 87

Getting Started
2/87 7001FAOPT73 ISS 13
Rate range 0.1 to 1200ml/hr.
In-line pressure monitoring 0 to 750mmHg.
Optional auto setting of pressure alarm.
Large graphics format display includes pressure
trending.
24 hour logging of volume and mass.
Event logging records operation of the P7000.
Optional auto bolus reduction following occlusion
alarm.
Optional fast start facility reduces infusion start-up
delays.
Communications and nurse call interfaces.
Multi-position pole clamp.
Configurable drug protocols for simplified drug dosing.
Programmable multidose and induction protocols.
Introduction
The IVAC®P7000 is a fully featured high end variable pressure syringe pump
suitable for critical care applications.
The IVAC®P7000 variable pressure pump is one of the IVAC®family of "P"
Series syringe pumps. Many aspects of general operation, performance,
accuracy and safety checking systems designed into the P7000 unit are
common throughout the range.
The IVAC®P7000 functions with a range of standard, single use, disposable
Luer-lock syringes of various types and accepts sizes from 5ml to 100ml.
Features of IVAC®P7000

Getting Started
3/87
7001FAOPT73 ISS 13
Controls and Indicators
STOP Button - Press to stop the
infusion. The Amber light will
flash to indicate an alarm.
START Button - Press to start the
infusion.
AC POWER - When
illuminated the unit is
connected to AC power and
the internal battery is being
charged.
Use “Double Chevron” for fast increase / decrease and
the “Single Chevron” for slower increase / decrease of
values shown on the display in set-up and configuration.
Are also referred to as the rate keys.
MAIN DISPLAY - For screen information see Front Panel
and Main Display.
Use “Blank Soft Keys” in
conjunction with the
prompts shown on the
display.
OPTIONS button - Press
the OPTIONS button to
access drug name and
other optional features.
Press PURGE/BOLUS to purge the extension line
during set up while the pump is stopped or to bolus
at an accelerated rate while an infusion is running.
PRESSURE - Use the
PRESSURE button to
display the pumping
pressure.
BATTERY - When illuminated the
pump is running on the internal
battery. When flashing the battery
power is low, less than 30 minutes of
use remains.
ON/OFF - Press once
to switch the pump ON.
Press and hold down
for 3 seconds to switch
the pump OFF.
Front Panel and Main Display
Infusion Rate
Time
Syringe Type
Review Data
Pump Status
PRESSURE TRANSDUCER
- Detects if an infusion line
with a pressure disc is fitted.
The pressure transducer will
measure positive infusion line
pressures.

Getting Started
4/87 7001FAOPT73 ISS 13
Operating Precautions
This IVAC®pump has been calibrated for use
with single use disposable syringes. To ensure
correct and accurate operation, only use Luer-
Lock versions of the syringe make and size
specified on the pump or described in the
directions for use. Use of non-specified
syringes or administration sets may impair the
operation of the pump and the accuracy of the
infusion.
Uncontrolled flow or syphoning may result if
the syringe is located on the pump without its
finger grips and plunger correctly located in the
slots provided, or if it is removed from the
pump before the extension line is properly
isolated from the patient. Isolation may include
closing a tap in the patient line or activating a
flow stop clamp.
When combining several apparatus and/or
instruments with administration sets and other
tubing, for example via a 3 way tap, the
performance of the pump may be impacted
and should be monitored closely.
Do not mount the pump in a vertical position
with the AC power inlet or the syringe pointing
upwards. This could affect electrical safety in
the event of a fluid spill over the unit or 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 in the purge procedure in Getting
Started.
This is a positive pressure device 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, infiltration conditions which can
occur at low pressures.
Several alarm conditions detected by this
pump will stop the infusion and generate
audible alarms. Users must perform regular
checks to ensure that the infusion is
progressing correctly and no alarms are
operating.

Getting Started
5/87
7001FAOPT73 ISS 13
This instrument 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 fail
safe if unreasonable levels of interference are
encountered.
In some circumstances the unit may be
affected by an electrostatic discharge of above
8kV. At test levels lower than these values the
unit will operate normally. In rare
circumstances the unit may be affected by
radio frequency radiation above a level of
3V/m. If the unit is affected by this external
interference the unit will fail safe or reset, (a
call back alarm will occur after 2 minutes).
Should false alarm conditions be encountered
either, remove the source of the interference,
or regulate the infusion by another appropriate
means.
This unit emits a certain level of
electromagnetic radiation which is within the
levels specified by IEC60601-2-24 and
IEC60601-1-2. If however the unit interacts
with other equipment measures should be
taken to minimise the effects, for instance by
repositioning or relocation.
If this instrument is dropped, subjected to
excessive moisture, humidity or high
temperature, or otherwise suspected to have
been damaged, remove it from service for
inspection by a qualified service engineer.
An explosion hazard exists if the instrument is
used in the presence of flammable
anaesthetics. Exercise care to locate the unit
away from any such hazardous sources. An
electrical shock hazard exists if the units
casing is opened or removed. Refer all
servicing to qualified service personnel.
A comprehensive service manual containing
circuit descriptions, servicing and testing
information is available for this unit. It can be
ordered from your ALARIS Medical Systems®
authorised distributor (Technical Service
Manual Part Number 6000PB00001).
Operating Precautions

Getting Started
6/87 7001FAOPT73 ISS 13
Installation
Check that the pump is complete, undamaged and that the voltage rating specified on the base
plate is compatible with your AC power supply. Items supplied with this ALARIS Medical Systems®
syringe pump are;
IVAC®P7000 SYRINGE PUMP
MULTI-POSITION POLE CLAMP
DIRECTIONS FOR USE
AC POWER CABLE (AS REQUESTED)
PROTECTIVE PACKAGING
Connect the unit to the AC power supply for 24 hours to ensure that the internal battery is fully
charged.
Should the pump fail to perform correctly, replace it in its original protective packaging and contact
a qualified service engineer for investigation.
Pole Clamp
The pole clamp is supplied fitted to the rear of the unit and will provide secure fixing to standard
I.V. poles of a diameter of up to 40mm.
The pole clamp can also be fitted in a choice of 4 fixing positions allowing the unit to be mounted
to vertical and horizontal poles, equipment rails and hospital furniture in a variety of convenient
operating orientations.
The pole clamp may be adjusted for use with horizontal fittings by using the existing fixings screws
with the alternative fixing holes in the pole clamp.
The multi position pole clamp hinge will support the unit at a range of angles on an I. V. pole. To
adjust the angle the unit needs to be secured to a pole; using a hand at either end of the
instrument, change the screen viewing and syringe access angle of the instrument.
Important:
Do not mount the unit 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.
Replacing the Mains Fuse
If the pump continually illuminates the battery symbol and the AC power indicator light does not
illuminate when the pump is connected to the AC power supply and switched ON, suspect that,
either the power supply fuse in the AC power plug, or, the internal fuse has blown.
First check the power supply fuse in the AC mains plug, if the AC power indicator light does not
illuminate remove the pump from service. It is recommended that the mains fuse is only replaced
by a qualified service engineer. For further information regarding the replacement of the internal
fuses refer to the technical service manual.

Getting Started
7/87
7001FAOPT73 ISS 13
Loading a Syringe
Place the pump on a stable horizontal surface or secure using the pole clamp fitted.
Prepare, load and prime the single use disposable syringe and extension line using standard
aseptic techniques.
1. Squeeze the finger grips on the plunger
holder and slide the mechanism to the left.
Lift the syringe clamp and rotate to the left.
2. Insert the syringe into the slots on the
plunger holder.
3. Squeeze the finger grips on the plunger
holder and slide the mechanism to the right
until the syringe finger flanges locates in
the V slot.
4. Release the finger grips. Apply gentle
pressure on the plunger holder to ensure
that the drive is engaged. Rotate the
syringe clamp forward until it locks onto the
syringe barrel.
5. Check that the syringe plunger and finger
flanges are correctly located in their slots.
Important:
Advance the syringe until the finger
flanges touch the front of the V slot
closest to the syringe clamp. This is
important to prevent delay at the
start of the infusion.
Important:
Only use a syringe of the type stated on the pump labelling.
Important:
Only use a syringe of the type and size indicated on the pump or in this manual.
Using an incorrect syringe could adversely affect the accuracy of the infusion and
the performance of the pump.
When initially loading the syringe, allow for the volume of fluid contained in the
extension line and retained in the syringe at the end of infusion as this “dead-
space” will not be infused.

Getting Started
8/87 7001FAOPT73 ISS 13
Starting the Pump
1. Connect the pump to an AC power supply
using the AC power cable. Press the
ON/OFF button
2. NEW PATIENT? - Answering NO will retain
all previous patient history. YES will
automatically reset the patient history to
zero, press the CONFIRM softkey to
confirm selection. Check time and date is
correct.
3. CONFIRM SYRINGE - Check that the
syringe type and size being used matches
the display. If required, the type of syringe
can be changed by pressing the TYPE
button.
4. Press CONFIRM when the correct type
and size are shown.
5. SET A RATE - Check the rate shown if old
patient data has been retained and change
the rate if necessary using the ADJUST
buttons.
6. PURGE (if required) - Press the
PURGE/BOLUS button then the two
PURGE softkeys together until fluid flows
and priming of the syringe extension line is
complete. The audible alarm will operate
during use of the PURGE softkeys and the
volume used during priming will be shown
on the display.
7. CONNECT PATIENT - Connect the
extension line to the patient access device,
and insert the pressure disc into the
pressure transducer.
8. START - Press START to commence
operation. INFUSING will be displayed.
The AMBER STOP light will be replaced by
the flashing GREEN START light to
indicate that the pump is operating.
Important:
The unit will automatically operate from its internal battery if the pump is
switched on without being connected to the AC power supply.
Each time the unit is switched ON, check that the alarm beeps twice and that all
the segments of the display, the green and amber lights are illuminated during
the self test routine.

Getting Started
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7001FAOPT73 ISS 13
Important:
Alarms are not disabled during the operation of the bolus feature. The pressure alarms are
temporarily increased to their maximum levels during the operation of the bolus feature.
A bolus cannot be administered if the rate lock is enabled or if a multidose set-up is in use.
Purge
1. To use the purge option stop the pump and
press the PURGE button.
2. The display will change and show two purge
softkeys. Press the two PURGE softkeys
simultaneously.
The purged volume is not added to the
volume infused.
3. When the purging function has been
completed press the QUIT softkey to exit the
menu.
The PURGE button allows the delivery of a limited volume of fluid in order to purge the extension line
prior to being connected to a patient or after changing a syringe. The purge function cannot be used if
the rate lock is enabled.
Power ON/OFF
To power up the unit press the power on/off button
once.
To power off the unit press and hold down the
power ON/OFF button for 3 seconds. The display
will count down and switch the unit OFF.
Bolus Infusions
1. During infusion press the BOLUS button once
to display the bolus screen.
2. Use the chevron keys to set the bolus dose
required.
3. To deliver the bolus press the two BOLUS
softkeys simultaneously. During the bolus the
unit will display the volume being infused.
4. When the desired bolus has been delivered,
release the two bolus softkeys. The bolus
volume will be added to the total volume
infused. Press QUIT to exit the bolus screen.
The bolus feature can be used during induction as well as during infusion.
If the volume of the bolus reaches the bolus volume limit the bolus will stop and the pump will
automatically revert to infuse at the set rate. If the volume to be infused is reached during a bolus, the
volume to be infused complete alarm will operate and the unit will revert to its previous state. Press
MUTE to stop the alarm or CANCEL to acknowledge the alarm.

10 / 87
Getting Started
7001FAOPT73 ISS 13
Review
REVIEW
1. To review the protocol data press the
REVIEW softkey.
2. The protocol data will be displayed in the
main display.
3. Press the REVIEW softkey to toggle
between the pressure setting and the VTBI
status.
4. Repeat until the protocol data required is
displayed in the main display.
Pressure level with pressure set fitted (dedicated)
1. To check and adjust the pressure level
press the PRESSURE button. The display
will change and a bar graph will show the
pressure alarm level and current pressure
level.
2. To adjust the alarm level press the rate
keys to increase or decrease the level. The
new level will be indicated on the display.
3. When the pressure level has been selected
press QUIT to exit the screen.
4. If the Auto Pressure Option has been
enabled (see General Options) an
automatic pressure alarm level can be
calculated and set by pressing the AUTO
softkey.
Pressure level without pressure set fitted (non-dedicated)
1. To check and adjust the pressure level
press the PRESSURE button. The display
will change and a bar graph will show the
pressure alarm level and current pressure
level.
2. To adjust the alarm level press the rate
keys to increase or decrease the level. The
new level will be indicated on the display.
3. When the pressure level has been selected
press QUIT to exit the screen.

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7001FAOPT73 ISS 13
When a protocol is used the drug name will be
followed by a *. The set by ml/h / set by doserate
option is now available.
1. Press the ?button to access the options menu.
2. Select the DRUGS AND DOSING option using the
chevron keys
3. Press the OK softkey indicated on the screen to
confirm the selection.
4. Select the drug name from the list displayed using
the chevron keys, press the YES softkey indicated
on the display to confirm the selection.
5. Press the YES softkey indicated on the screen to
select DOSING.
6. Press the YES softkey indicated on the screen to
select PROTOCOL. This will select the predefined
protocol for the drug name selected.
7. Enter the dosing information prompted on the
screen for the drug selected using the OK softkey.
8. Press the CONFIRM softkey to enter the drug
name, dosing information and the protocol
selected.
1. Press the ?button to access the options menu.
2. Select the DRUGS AND DOSING option using the
chevron keys
3. Press the OK softkey indicated on the screen to
confirm the selection.
4. Select the drug name from the list displayed using
the chevron keys, press the YES softkey indicated
on the display to confirm the selection.
5. Press the YES softkey indicated on the screen to
select DOSING.
6. Press the NO softkey indicated on the screen to
not select PROTOCOL.
7. Enter the required dosing information via the
screen prompts, using the chevron keys and the
OK softkey.
8. Press the CONFIRM softkey to enter the drug
name, dosing information and the protocol entered.
These options enable the unit to be set-up for use with a specific drug and/or dosing protocol. Drugs are pre-
configured (see configured options) to enable rapid selection of the drug name, dosing units and default rate.
For increased security using a configured drug maximum and minimum safety limits are programmable for
concentration and dose rates.
Drugs and Dosing - Using pre-configured drug dosing protocol
Drugs and Dosing - Using user-programmed drug dosing
1. Press the ?button to access the options menu.
2. Select the DRUGS AND DOSING option using the
chevron keys
3. Press the OK softkey indicated on the screen to
confirm the selection.
4. To select a drug name press the YES softkey
indicated on the display.
5. Press the NO softkey to not select dosing or drug
protocols.
Caution :
The mass infused display is a sum of all drug masses infused which may be of different concentrations
and even drug type. Therefore it should be noted that the relationship between currently displayed
volume infused and mass infused may not directly relate to the current concentration.
Drugs and Dosing - Drug name only
Getting Started

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12 / 87 7001FAOPT73 ISS 13
Set ‘VTBI Over Time’ must have been
activated in the Configured Options.
This option allows a VTBI and delivery time to
be specified. The rate necessary to deliver the
required volume within the required time will be
calculated and displayed. Infusion must be
stopped to select this option.
1. Press the “?” button to access the options
menu.
2. Select the SET VTBI OVER TIME option
using the chevron keys and press the OK
softkey indicated on the screen.
3. Adjust the volume to be infused using the
chevron keys, when the volume to be infused
has been entered press the OK softkey.
4. Enter the time over which the volume is to be
infused. The infusion rate will automatically
be calculated. Press the OK softkey to enter
the value.
5. Select the rate at VTBI end and press the OK
softkey. The default is STOP.
Set VTBI Over Time
This option allows you to set a specific volume
to infuse, and rate at the end of the volume to
be infused, from stop, 1ml/h, 2ml/h and
continuous infusion at the set rate.
Volume To Be Infused (VTBI)
1. Press the “?” softkey to access the options
menu.
2. Select the SET VTBI option using the
chevron keys and press the OK softkey
indicated on the screen.
3. Enter the volume to be infused using the
chevron keys. When the volume to be infused
has been entered, press the OK softkey.
4. Select the rate at the end of the VTBI using the
rate selection chevrons. The default is STOP.
5. Press the OK softkey to exit the VTBI menu.
6. When the pump has delivered the set volume
it will alarm. Press the CANCEL softkey to
clear the alarm.
7. Press the CLEAR softkey to turn the VTBI
function off, or set a new VTBI using the
chevron keys.

Getting Started
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7001FAOPT73 ISS 13
Set by Doserate / Set by ml/h
To set rates accurately in doserate or flowrate increments it may be necessary to switch between
the rate adjust options SET BY DOSERATE and SET BY ml/h. An arrow to the left of the rate
display indicates the rate that will change when the chevron buttons are used to
increase/decrease the infusion rate.
To set a doserate precisely the arrow must be pointing to the doserate (mg/kg/h); the flowrate will
be calculated from the doserate.
To accurately set a flowrate the arrow must be pointing to flowrate (ml/h); the doserate will be
calculated from the flowrate.
Selecting the Set By Doserate Option
1. Press the ?button to access the options
menu.
2. Select the SET BY DOSERATE option
using the chevron keys.
3. Press the OK softkey. This will select the
set by doserate option and an arrow will
automatically point to the doserate on the
display. If necessary the doserate can be
increased or decreased using the chevron
keys.
Selecting the Set By ml/h Option
1. Press the ?button to access the options
menu.
2. Select the SET BY ml/h option using the
chevron keys.
3. Press the OK softkey. This will select the
set by flowrate option and an arrow will
automatically point to the flowrate on the
display. If necessary the flowrate can be
increased or decreased using the chevron
keys.

Getting Started
7001FAOPT73 ISS 13
14 / 87
Clear Volume
1. Press the ?button to access the options
menu.
2. Select the CLEAR VOLUME option using
the chevron keys and press the OK softkey
indicated on the screen.
3. The volume infused will be displayed.
4. Press the YES softkey to clear the volume
infused displayed. Press the NO softkey to
retain the volume.
Induction
The induction option is enabled within the general options. See General Options in this user
manual.
1. Press the ?button to access the options
menu.
2. Select the INDUCTION option using the
chevron keys
3. Press the OK softkey indicated on the
screen to confirm the selection.
4. Adjust the induction RATE using the
chevron keys, then press the OK softkey.
5. Select the induction VOLUME using the
chevron keys, then press the OK softkey. If
an incorrect value has been entered, press
the BACK softkey to return to the previous
stage.
6. Enter the MAINTENANCE infusion rate
using the chevron keys, then press the OK
softkey.
7. Review the induction data on screen, then
press CONFIRM. If necessary use the
BACK softkey to return to the data. Once
confirmed, the pump will return to the main
display.
8. The induction can be cleared. Stop the
infusion then press the ?button. Select
CLEAR INDUCTION with the chevron keys
and press the OK softkey to confirm.

Getting Started
15 / 87
7001FAOPT73 ISS 13
1. Press the ?button to access the options
menu.
2. Select the MULTIDOSE option using the
chevron keys
3. Press the OK softkey indicated on the
screen to confirm the selection.
4. Adjust the multidose RATE using the
chevron keys, then press the OK softkey.
5. Select the multidose VOLUME to be
infused using the chevron keys, then press
the OK softkey. If an incorrect value has
been entered, use the BACK softkey to
return to the previous stage.
6. Enter the MAINTENANCE infusion rate
using the chevron keys, then press the OK
softkey.
7. Select the FREQUENCY (hr:mins) of each
multidose using the chevron keys, then
press the OK softkey.
8. Review the multidose data on screen, then
press CONFIRM. If necessary use the
BACK softkey to return to the data. Once
confirmed, the pump will return to the main
display. The review section of the display
will show either multidose volume
remaining or time between multidoses
remaining.
Multidose
The multidose function is enabled within the general options. See General Options in this user
manual.
Clear Multidose
1. Stop the infusion then press the ?button.
2. Select CLEAR MULTIDOSE with the
chevron keys and press the OK softkey to
confirm.

Getting Started
16 / 87 7001FAOPT73 ISS 13
Event Log
1. Press the ? button to access the options
menu.
2. Select the EVENT LOG option using the
chevron keys.
3. Press the OK softkey indicated on the
screen.
4. Press the QUIT softkey indicated on the
screen to exit the menu.
24H Log
This option allows the 24H log of volume infused to be reviewed.
1. Press the “?” button to access the options
menu.
2. Select the 24H LOG option using the
chevron keys and press the OK softkey
indicated on the screen.
3. Press the NEXT softkey indicated on the
screen to access the hourly volume infused
log.
4. Press the QUIT softkey indicated on the
screen to exit the log.