Alaris Medical Systems Asena CC Manual

Service Equipment
This Asena®CC has been designed to allow simple and low
cost servicing. Standard components are employed where
possible so that no special test or calibration tools are required.
However, the following items may be useful for general
servicing.
Part
Number Description Quantity
1000PB00991 Directions for Use (English)
ALARIS®Asena®CC
1000SM00001 Technical Service Manual ALARIS®
Asena®Series Syringe Pumps
1000SP01122 Internal Battery Pack
1001FAOPT91 AC Power Lead - UK
1001FAOPT92 AC Power Lead - European
1001FAOPT93 AC Power Lead - Unterminated
Part
Number Description Quantity
0000TG00020 Occlusion Test Gear
0000TG00080 Linear Speed Test Gear
0000JG00047 Cradle, Support (front)
0000TG00095 Asena®Syringe Pump, Calibration tool
1000SP00172 Programming Kit Asena®
Pumps, Accessories and Spare Parts
Please complete the details below and either fax or post this form to ALARIS Medical Systems®or your nearest authorised
distributor (see page 22).
ALARIS®Asena®Infusion System
The complete range of syringe pump products in the ALARIS®
Asena®product family are:
Spare Parts
A comprehensive list of spare parts for this pump is included
within the Technical Service Manual. For the part number
please refer to summary parts list below:
Visit our website: www.alarismed.com
Part
Number Description Quantity
80013UN01 ALARIS®Asena®GS Syringe Pump
80023UN01 ALARIS®Asena®GH Syringe Pump
80033UND1 ALARIS®Asena®CC Syringe Pump
80043UN01 ALARIS®Asena®TIVA Syringe Pump
80083UN00 ALARIS®Asena®DS (no comms)
80093UN00 ALARIS®Asena®IDS Docking Station
274 ALARIS®Asena®Transporter
Syringes and Extension Sets
The Asena®CC uses standard, single-use, disposable
extension lines and syringes with Luer-lock connectors, of type
designed for use on syringe pumps.
Part
Number Description Quantity
30602N IVAC®50ml Luer-lock Syringe
G30402M Standard PVC Syringe Extension Set with
occlusion sensing disc. (200 cm).
G30653M Opaque White PVC Syringe Extension Set
with occlusion sensing disc. (200 cm).
G30303M Polyethylene Syringe Extension Set with
occlusion sensing disc.(200 cm).
G30453M Opaque White PVC low sorbing Syringe
Extension Set with occlusion sensing
disc. (200 cm).
G30302M Polyethylene Lined Syringe Extension
Set with occlusion sensing disc
and clamp. (200 cm).
G40015 Standard PVC Syringe Extension Set
(150 cm).
G40020B Standard PVC Syringe Extension Set
(200 cm).
G40215 Opaque Amber PVC Syringe Extension
Set (150 cm).
G40320 Opaque White PVC Syringe Extension
Set (200 cm).
G40615 Polyethylene Syringe Extension Set
(150 cm).
G40620 Polyethylene Syringe Extension Set
(200 cm).
G40720 Polyethylene Lined Syringe Extension
Set (200 cm).
Name: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Company Name: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
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Address: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
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. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Postcode: . . . . . . . . . . . . . . . . . . .
Telephone: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Facsimile: . . . . . . . . . . . . . . . . . . . . . . . . . . .
Signature: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Date: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
24/24
1000PB00991 Iss. 5.0 1000PB00991 Iss. 5.0 1/24
Visit our website: www.alarismed.com
Contents Introduction
Page
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Features of the Asena®CC syringe pump . . . . 2 - 3
Operating Precautions . . . . . . . . . . . . . . . . . . . . . 4
Getting Started . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Basic Features . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 8
Alarms and Warnings . . . . . . . . . . . . . . . . . . . . . . 9
Configured Options . . . . . . . . . . . . . . . . . . . . . 10 - 12
Drug Protocol Record . . . . . . . . . . . . . . . . . . . . . 13
Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Compatible Accessories . . . . . . . . . . . . . . . . . 15 - 17
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Occlusion Pressure Limits . . . . . . . . . . . . . . . . . 19
Self Test Routine . . . . . . . . . . . . . . . . . . . . . . . . . . 20
RS232/Nursecall Specification . . . . . . . . . . . . . . 20
Trumpet Curves . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Service Contacts . . . . . . . . . . . . . . . . . . . . . . . . . 22
Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Pumps, Accessories and Spare Parts . . . . . . . . 24
The ALARIS®Asena®CC is a fully featured high end variable
pressure syringe pump suitable for critical care applications.
The Asena®CC syringe pump functions with a wide range of
standard, single-use, disposable Luer-lock syringes. It accepts
syringe sizes from 5ml to 50ml. A full list of compatible syringes
can be found on page 15.
Simple to set up and easy to operate.
Large graphics format display including pressure
trending.
Medical Device Interface (MDI) - a unique mounting
mechanism.
Rate Range from 0.1 to 1200ml/h.
In-line pressure monitoring from 0 to 1000 mmHg.
24 hour logging of volume infused.
Event logging records operation of pump.
Advanced Communications and Nursecall interfaces.
Configurable drug protocols for simplified drug
dosing.
Asena®CC Syringe Pump - A Member of the Asena®Infusion System
Directions For Use - English
1000PB00991 Iss. 5 Colour cover.qxd 08/08/2003 08:29 Page 23

1000PB00991 Iss. 5.0 23/24
ALARIS®Medical Systems, Inc. (hereinafter referred to as "ALARIS Medical Systems") warrants that:
(A) Each new infusion instrument (pump, controller or peripheral instrument) is free from defects in material and workmanship
under normal use and service for a period of two (2) years from the date of delivery by ALARIS Medical Systems to the
original purchaser.
(B) Each new accessory is free from defects in material and workmanship under normal use and service for a period of ninety
(90) days from the date of delivery by ALARIS Medical Systems to the original purchaser.
(C) Each Mains Cable, Battery, Flow Sensor (ECD) and non-disposable probe is free from defects in material and workmanship
under normal use and service for a period of ninety (90) days from the date of delivery by ALARIS Medical Systems to the
original purchaser.
(D) Each new Thermometer is free from defects in material and workmanship under normal use and service for a period of one
(1) year from the date of delivery by ALARIS Medical Systems to the original purchaser.
If any product requires repair during the applicable warranty period, the purchaser should communicate directly with its local
ALARIS Medical Systems service centre to determine the appropriate service facility. Except as provided otherwise in this
warranty, repair or replacement will be carried out at ALARIS Medical Systems' expense. The product requiring service should
be returned promptly, properly packaged, and postage prepaid by purchaser. Loss or damage in return shipment to ALARIS
Medical Systems shall be at purchaser's risk.
In no event shall ALARIS Medical Systems be liable for any incidental, indirect or consequential damages in connection with the
purchase or use of any ALARIS Medical Systems product. This warranty shall apply solely to the original purchaser. This
warranty shall not apply to any subsequent owner or holder of the product.
Furthermore, this warranty shall not apply to, and ALARIS Medical Systems shall not be responsible for, any loss or damage
arising in connection with the purchase or use of any ALARIS Medical Systems product which has been:
(A) repaired by anyone other than an authorised ALARIS Medical Systems service representative;
(B) altered in any way so as to affect, in ALARIS Medical System's judgement the stability or reliability of the product or has
had the product's serial or lot number altered, effaced or removed;
(C) subjected to misuse or negligence or accident; or
(D) improperly maintained or used in any manner other than in accordance with the written instructions furnished by ALARIS
Medical Systems.
This warranty is in lieu of all other warranties, express or implied, and of all other obligations or liabilities of ALARIS Medical
Systems, and ALARIS Medical Systems neither assumes nor authorises any representative or other person to assume for it any
other liability in connection with the sale of ALARIS Medical Systems products.
ALARIS MEDICAL SYSTEMS DISCLAIMS ALL OTHER WARRANTIES, EXPRESS OR IMPLIED, INCLUDING ANY
WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE.
Warranty
1000PB00991 Iss. 5.0
2/24
PRESSURE - Use this button to display the
pumping pressure trend display and alarm
level.
Controls and Indicators
ON/OFF - Press once to switch the pump ON.
Press and hold down for 3 seconds to switch
the pump OFF.
RUN button - Press to start the infusion. The
green LED will flash during infusion.
HOLD button - Press to put the infusion on
hold. The amber LED will be lit while on hold.
OPTION button - Press to access optional
features (see pages 7 and 8).
PURGE/BOLUS - Press to access PURGE or
BOLUS soft keys. Press and hold down soft
key to operate. PURGE the extension set
during set up. Pump on hold, extension set not
connected to patient, VI not added. BOLUS
delivered at an accelerated rate. Pump infusing,
extension set connected to patient, VI added.
MUTE - Press to silence alarm for 2 minutes.
Press and hold until 3 beeps are heard for 15
minutes silence.
CHEVRONS - Double or single for
faster/slower increase or decrease
of values shown on display.
BLANK SOFTKEYS - Use in conjunction with
the prompts shown on the display.
BATTERY - 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.
AC POWER - When illuminated the unit is
connected to an AC power supply and the
battery is being charged.
Features of the ALARIS®Asena®CC - Front View
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
TIME REMAINING DISPLAY - Indicates time
before syringe will require replacing.
Pressure
transducer
BATTERY ICON - Indicates battery charge
level to highlight when the battery will require
recharging.
1000PB00991 Iss. 5 Colour cover.qxd 08/08/2003 08:29 Page 25

1000PB00991 Iss. 5.0 3/24
Attention (Consult accompanying
documents)
Potential Equalisation (PE) Connector
RS232/Nursecall Connector (Optional)
Type CF Equipment (Degree of protection
against electrical shock)
Protected against vertically falling drops
of water
Alternating Current
Device complies with the requirements of
the EC Directive 93/42/EEC. Registered
with the CE Mark.
Date of Manufacture
Symbol Definitions
IPX1
Quick Start Guide
1. Press to turn the pump on.
2. CLEAR SETUP? - NO retains previous data.
YES clears previous data.
3. Load syringe.
4. Insert pressure disc into pressure transducer.
5. Confirm correct size and brand of syringe.
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 .
7. PURGE - Press followed by the PURGE
softkey.
8. Connect extension set to the patient.
9. START - Press .
Extension set
hook
Features of the ALARIS®Asena®CC - Rear View
Release
lever for
MDI
Carrying
Handle
Medical Device
Interface (MDI) -
rotating cam to lock
on to horizontal
rectangular bars.
IR Comms port
RS232
Connector
(optional)
Folded
Pole Clamp
Potential
Equalisation
(PE) connector
Rating Plate (see
Symbol Definitions
for an explanation of
the symbols used)
Pressure
transducer

1000PB00991 Iss. 5.0
4/24
This ALARIS®syringe pump has been
calibrated for use with single-use disposable
syringes. To 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 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 incorrectly in the pump, 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.
Secure the infusion line to the pump using the
infusion 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 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.
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 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.
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 and lights. Users must perform regular
checks to ensure that the infusion is
progressing correctly and no alarms are
operating.
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.).
When using any infusion device in conjunction
with other instruments 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 instruments.
Typical examples of those instruments are used
during dialysis, bypass or cardiac assist
applications.
?
Operating Precautions
?
?
?
In some circumstances the unit 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 unit is affected by this external interference
the unit will fail safe or reset (after which a call
back alarm will occur). 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
IEC60601-1-2:1993. 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, fluid spillage, humidity or
high temperature, or otherwise suspected to
have been damaged, remove it from service for
inspection by a qualified service engineer.
When transporting or storing the pump, use
original packaging where possible, and adhere
to temperature, humidity and pressure ranges
stated on page 14 and on the outer packaging.
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.
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 equipment should
be operated from the battery.
A comprehensive Technical Service Manual is
available for this pump. The part number is
1000SM00001.
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.
The complete range of settings and values are
specified on page 14. 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 are shown on
page 14.

1000PB00991 Iss. 5.0 5/24
Place the pump on a stable horizontal surface or secure as
described above.
Prepare, load and prime the single-use disposable syringe and
extension line using standard aseptic techniques.
Important: 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 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.
1. Squeeze the finger grips together on the plunger holder and
slide the mechanism to the right. Pull the syringe clamp
forwards and down.
2. Insert the syringe ensuring that the finger flanges are
located in the slots on the syringe holder.
3. Lift the syringe clamp until it locks against the syringe barrel.
4. Squeeze the finger grips on the plunger holder and slide the
mechanism to the left until it reaches the plunger end.
5. Release the finger grips. Ensure that the plunger grippers
are securing the plunger in place and the finger grip returns
to its original position.
Important: Secure the infusion line using the infusion set
hook at the rear of the pump. This provides protection
against accidental dislodging of the syringe from the
pump.
Important: Ensure that both plunger grippers are fully
locked onto the plunger flange and the upper finger grip
has returned to its original position.
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:
ALARIS®Asena®CC syringe pump
User Support CD
AC Power Cable (as requested)
Protective Packaging
Connect the unit to the AC power supply for 2½ hours to ensure
that the internal battery is fully charged prior to use.
Should the pump fail to perform correctly, replace in its original
protective packaging and contact a qualified service engineer
for investigation.
A pole clamp is fitted to the rear of the unit and will provide
secure fixing to standard vertical I.V. poles of a diameter of
between 15 and 40 mm. It should be folded away when not in
use.
Getting Started
Installation
Loading a Syringe
+ ADJUST -
SYRINGE NAME
VOLUME
VOLUME VTBI
PRESSURE
0
300mmHg
Front Panel and Main Display
Pump Status Syringe type fitted / Drug name Pressure InformationTime Remaining Icon
Infusion Rate Volume Infused Volume Infused
Option
VTBI Option
There is a Medical Device Interface (MDI) at the rear of the
pump used for mounting the pump onto horizontal rectangular
bars, for instance the ALARIS®Asena®Docking Station.
Holding the pump horizontally push the pump firmly on to the
bar. Ensure that the pump clicks securely into position on the
bar. To release, push the release lever and pull the pump
forwards.
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.
The unit will automatically operate from its internal battery
if the pump is switched on without being connected to the
AC power supply.
Battery Icon
Important : To 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.
Syringe Flange
Clamp
Syringe
Clamp
Barrel
Flange
32

1000PB00991 Iss. 5.0
Note: PRESSURE TRANSDUCER - Detects if an infusion
line with a pressure disc is fitted. The pressure transducer
will measure positive infusion line pressures.
Note: Warning - To remove or insert pressure disc from or
into pressure transducer assembly, insert finger into the
recess in the pressure disc and pull forward or push back
with care. DO NOT PULL THE INFUSION LINE TO REMOVE
OR TO INSERT THE PRESSURE DISC.
FULLY DEDICATED Asena®CC - to start an infusion a
pressure disc must be fitted.
SEMI DEDICATED Asena®CC - to start an infusion with
Drugs and Dosing set a pressure disc must be fitted.
9. START - Press 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 in operation.
10.STOP - Press to halt the operation. ON HOLD will be
displayed. The amber light will replace the green light.
The 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.
1. Stop the pump and press the button.
2. Press and hold the PURGE softkey until fluid flows and the
purging of the syringe extension line 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.
Important: The pump will not purge if the rate lock has
been enabled. During PURGE the pressure limit alarms are
temporarily increased to their maximum level.
Basic Features
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. If the volume to be
infused is reached during a bolus, the volume to be infused
(VTBI) complete alarm will sound and the pump will revert to its
previous state. Press to stop the alarm or CANCEL to
acknowledge the alarm and continue normal rate infusion.
1. During infusion press the button once to display the
bolus screen.
2. Use the keys to set the bolus rate required.
3. To deliver the bolus press and hold 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.
Bolus Infusion
Purge
1. Connect the pump to an AC power supply using the AC
power cable. Press the button. The pump will run a
short self-test. Ensure that two beeps are activated during
this test. Check the display test pattern and ensure that no
coloured rows are missing. Finally 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.
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. Insert the pressure disc into the pressure transducer.
5. 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.
6. INFUSION RATE - Check the rate shown if old patient data
has been retained and change the rate if necessary using
the keys.
7. PURGE (if required) - Press the 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.
Important: Prime extension set, massaging pressure
disc to prevent ballooning and ensuring all air
removal.
8. CONNECT TO PATIENT - Connect the extension set to the
patient access device.
Starting the Pump
6/24
Important: If the handsfree bolus option is configured,
then this feature will be cancelled following any
interruption in delivery, even if the bolus delivery is
incomplete. If hands free bolus is permitted a screen will
be displayed allowing the selection of hands free or hands
on bolus.
1. During infusion press the button. This will display
the handsfree bolus screen.
2. Use the to set the bolus dose/volume required.
If necessary press the RATE softkey to adjust the bolus
delivery rate.
3. Press the BOLUS softkey once to begin the delivery of
the bolus. The display will show the bolus being delivered,
the bolus counts down on the screen and will count down
to zero upon completion of the bolus.
On completion of the bolus the pump will automatically
revert to the set infusion rate.
4 To exit the bolus feature press the QUIT softkey.
5. To terminate a bolus being delivered either press the
STOP button or press the button and press the
STOP softkey. This will stop the bolus and continue
infusing at the set rate.
Important: A bolus and handsfree bolus cannot be
administered if the rate lock is enabled, if the feature is
disabled in General Options or when using a selected Drug
Protocol. During BOLUS the pressure limit alarms are
temporarily increased to their maximum level.
Handsfree Bolus Infusion

1000PB00991 Iss. 5.0
Basic Features
Pressure Level with pressure set fitted
Pressure Level without pressure set fitted
(not applicable when FULLY DEDICATED)
This option allows you to set a specific volume to be infused.
Rate at the end of this VTBI can also be set, selecting from
stop, KVO, or continuous infusion at the set rate.
1. Press the VTBI softkey to select the volume to be infused
option.
2. Enter the volume to be infused using the keys
and press the OK softkey.
3. Select the rate at the end of the VTBI using the
keys to scroll through the on-screen choices. The default is
stop.
4. Press OK to enter the rate and exit the VTBI menu.
Volume to be Infused (VTBI)
This option allows you to specify a VTBI and delivery time. The
rate necessary to deliver the required volume within the
specified time is calculated and displayed.
1. Stop the infusion. Press the ?button to access the options
menu.
2. Select the SET VTBI OVER TIME option using the
keys and press the OK softkey.
3. Adjust the volume to be infused using the keys.
When the desired volume has been reached 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 from the list using the
keys and press the OK softkey. The default is STOP.
?Set VTBI over Time
1. To check and adjust the pressure level press the button.
A bar graph will be displayed showing the pressure alarm
level and the current pressure level.
2. Press the keys to increase or decrease the alarm
level. The new level will be indicated on the display.
3. Press OK to exit the screen.
?Event Log
This option allows the event log to be reviewed. It can be
enabled/disabled within General Options.
1. Press the ? button to access the options menu.
2. Select the EVENT LOG option using the keys
and press the OK softkey.
3. Scroll through the log using the keys. Press the
QUIT softkey to exit the log.
?24 Hour Log
This option allows the 24 hour log of volume infused to be
reviewed.
1. Press the ? button to access the options menu.
2. Select the 24H LOG option using the 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:
1. To check and adjust the pressure level press the button.
The display will change to show a 20 minute trend graph
displaying the pressure alarm level and the current pressure
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.
Resets the volume infused in the 24H LOG option.
2. Press the keys to increase or decrease the
pressure alarm level. The new level will be indicated on the
display.
3. The AUTO Pressure feature may be used when a stable
pressure has been achieved over a short period of infusion.
If AUTO Pressure has been enabled (see General Options)
the automatic pressure alarm level is calculated and set by
pressing the AUTO softkey.
4. Press the TREND softkey to view the pressure trend of the
previous 12 hours. The pressure trend can be viewed at 15
minute intervals by using the -/+ keys. The pressure trend
graph displays the pressure at a given time.
5. Press OK to exit the pressure screen.
_+OK
20mmHg
07:45
7/24
3. Press the QUIT softkey to exit the log.
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
If the Auto Set Pressure Option is enabled then the pump
AUTOMATICALLY adjusts the pressure occlusion limit
An AUTO OFFSET value (15-100mmHg) is configured
(Refer to General Options)
After 15 minutes of infusion the pump AUTOMATICALLY
adjusts the occlusion pressure limit to X mmHg (the
AUTO OFFSET value), above the average infusion
pressure since the start of the infusion.
Auto Set Pressure (If enabled)

1000PB00991 Iss. 5.0
Drug Name Only: (available if Drugs are configured)
1. Select a drug name from the list and press the OK softkey.
2. If no protocol is required press the NO softkey.
3. If no dosing is required press the NO softkey.
Pre-configured drug dosing protocol: (available if Drugs are
configured)
1. Select the drug name from the list displayed using the
keys. Press the OK softkey to confirm the
selection.
2. Press the YES softkey to select PROTOCOL. This will
select the pre-defined protocol for the selected drug.
3. Enter the dosing information prompted on the display for the
selected drug using the OK softkey.
See note below *.
User-programmed drug dosing: (available if Drugs are
configured)
1. Select the drug name from the list displayed using the
keys. Press the OK softkey to confirm the
selection.
2. Press the NO softkey to avoid selecting PROTOCOL.
3. Press the YES softkey to select DOSING. This now enables
user-programmed information to be entered.
4. Enter the required dosing information as prompted on the
display, using the keys and the OK softkey.
See note below *.
* Note: Rate values will flash if either the rate (ml/h) or dose
rate are outside the permitted range; and confirmation will not
be possible.
The following options enable the unit to be set-up for use with
a specific drug and/or dosing protocol. Drugs are pre-
configured in a drug library (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.
Note: The dose infused display is the product of the volume
infused and the confirmed concentration. If dosing is confirmed
while the volume infused is greater than 0.0ml or a drug was
previously selected the dose could be inaccurate. If the dose
displayed could be inaccurate the digits will flash on screen. To
reset the flashing, the volume needs to be cleared.
? Drugs and Dosing
Basic Features
Dosing Only:
1. Select DOSING ONLY from the list and press OK.
2. Enter the dosing information as prompted on the display.
3. Press the OK softkey to confirm the dosing information.
4. The BACK softkey may be used at any time to return to the
previous screen.
See note below *.
To access the Drugs and Dosing menu:
1. Press the ? button to first access the options menu.
2. Select DRUGS AND DOSING from the list using the
keys.
3. Press the OK softkey to confirm the selection.
? Dosing Summary
To review currently selected dosing information:
1. Press the ? button to first access the options menu.
2. Select DOSING SUMMARY.
3. Review the information and then press QUIT.
Clear drugs and/or dosing: (available if a drug is selected)
1. Select CLEAR DRUGS AND DOSING or CLEAR DRUG
NAME (displayed if a name only is selected) using the
keys. Press the OK softkey to confirm the
selection.
? Drugs and Dosing (cont.)
Rate Lock
The rate lock feature is enabled/disabled within the General
Options of this pump.
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.
1. 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:
Changing the infusion rate / titration
Bolus / purge
Switch the pump off
VTBI over time infusions.
To disable the rate lock if selected:
1. Press the ?button to access the options menu.
2. Select the UNLOCK RATE option using the keys
and press the OK softkey.
To enable the rate lock if not selected:
1. Press the ?button to access the options menu.
2. Select RATE LOCK and press the OK softkey.
If Rate Titration is enabled the rate can be adjusted while
infusing:
1. Select the new rate using keys.
The message < START TO CONFIRM> will flash on
screen and pump continues to infuse at the original
rate.
2. Press button to confirm the new infusion rate and
resume infusion.
If Rate Titration is disabled the rate can only be adjusted
whilst on hold:
1. Press button to put the pump on hold.
2. Select the new rate using keys.
3. Press button to start infusing at the new rate.
Rate Titration
8/24
? Drug Name
To display selected drug name:
1. Press the ? button to first access the options menu.
2. Select DRUG NAME.
3. Press the OK softkey to confirm the drug name or press
QUIT to exit the option.

1000PB00991 Iss. 5.0
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 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 button to resume the infusion.
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 Pumping pressure has reached the alarm limit. Squeeze the finger grips on the
plunger holder to release the drive mechanism and relieve any excessive pressure in
the syringe and extension set. 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.
PRESSURE DISC OUT The pressure disc has been removed from the pressure transducer during the
infusion. The infusion will stop. Replace the pressure disc then restart the infusion.
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. To modify the time at which the pump will
alarm see the General Options section of this manual.
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 modified. See the General Options section of this manual.
TITRATION NOT CONFIRMED The infusion rate has been changed, but has not been confirmed and 2 minutes* has
expired without any operation. Press key to silence the alarm, then press CANCEL
to clear this message and silence the alarm. Check infusion rate and confirm by
pressing the button or press button to revert to the previous rate. Press
button to start infusion.
(This alarm only occurs if rate titration is enabled)
VTBI DONE The pre-set Volume To Be Infused is complete.
AC POWER FAIL AC Power has been disconnected and the pump is operating on battery power.
INFUSION CONTINUES Reconnect AC power supply or press 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 unit from service for examination by a qualified service engineer.
ATTENTION (with “3 Beeps”) Three beeps will sound if the unit has been left ON for more than 2 minutes* (referred
to as CALLBACK in the log) without starting the operation. Press to silence the
alarm for a further 2 minutes*. Alternatively press and hold down 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; VTBI DONE (KVO or CONTINUE),
ATTENTION; TITRATION NOT CONFIRMED; BATTERY LOW.
RED All others.
*Configurable option.
9/24

1000PB00991 Iss. 5.0
10/24
Configured Options
NURSE CALL FITTED Enables Nurse Call (hardware option).
NURSE CALL INVERT When enabled, the nursecall output is inverted.
RS232 SELECTED Sets the pumps 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.
RATE TITRATION When enabled the rate can be changed whilst the pump is infusing.
PRESSURE DISPLAY Enables / disables the Pressure Icon on the main display.
AUTO PRESSURE Enables / disables the automatic pressure alarm level option.
AUTO SET PRESSURE Automatically sets the line occlusion pressure to a specified amount above the current pressure.
AUTO OFFSET Adjusts the automatic offset value used by auto pressure and auto set pressure. Adjustable from 15
to 100mmHg.
PRESSURE DEFAULT Sets the default occlusion alarm level.
MAX PRESSURE Sets the maximum pressure limit.
WEIGHT Sets the default patient weight in kg.
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.
VTBI CLEAR RATE Rate will be set to zero when VTBI has been set-up with stop as the end rate.
EVENT LOG DISPLAY Enables / disables the event log.
BATTERY ICON Enables / disables the Battery Icon on the main display.
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.
General Options
1. Select GENERAL OPTIONS from the menu using the 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 OK softkey.
4. Either select the next configuration option from the menu or turn the pump OFF, returning it to operation as required.
This menu comprises a list of options which are configurable by the user.
1. Turn the pump OFF.
2. Whilst holding down the button turn the pump ON.
3. The main display will show 000. Enter the access code for Configured Options using the 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.

1000PB00991 Iss. 5.0 11/24
Asena®CC Syringe Pump Configured Options Record
General Options
Syringes Enabled
Make Size(s) Make Size(s)
Enter the pump-specific information for your
records on a copy of this page.
Option Default Range Setting
Software Version 1.5.10 & 2.0.0 1.8.x & 2.2.x
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
RATE TITRATION Disabled Disabled Enabled/Disabled
PRESSURE DISPLAY Disabled Enabled Enabled/Disabled
AUTO PRESSURE Disabled Enabled Enabled/Disabled
AUTO SET PRESSURE Disabled Enabled/Disabled
AUTO OFFSET 30mmHg 15mmHg - 100mmHg
PRESSURE DEFAULT 300mmHg 300mmHg 1mmHg - 1000mmHg
MAX PRESSURE 1000mmHg 1000mmHg 1mmHg - 1000mmHg
WEIGHT 70Kg 1.00Kg 0.01Kg - 250Kg
CAP RATE Max infusion rate 1200ml/h 1.0ml/hr - 1200ml/h
PURGE RATE 200ml/hr 200ml/h 100ml/hr - 500ml/hr
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/hr - 1200ml/h
CAP BOLUS RATE Max bolus rate 1200ml/h 10ml/hr - 1200ml/h
BOLUS VOL LIMIT 5.0ml 5.0ml 0.5ml - 25.0ml
MANUAL BOLUS Disabled Enabled/Disabled
CALL BACK TIME 2.0mins 0.1mins - 15mins
VTBI CLEAR RATE Disabled Enabled/Disabled
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
Hospital Name Serial No.
Configured by
Date
Software Version
Approved by
Date
Units Enabled
ng/min,
ng/kg/min
µg/min,
µg/kg/min,
µg/h,
µg/kg/h,
µg/24h,
µg/kg/24h
mg/min,
mg/kg/min,
mg/h,
mg/kg/h,
mg/24h,
mg/kg/24h,
g/h
g/24h,
U/min,
U/kg/min,
U/h
U/kg/h,
U/24h,
U/kg/24h,
kU/24h,
mmol/h

1000PB00991 Iss. 5.0
5. Review the drug set-up
data on the display, then press the OK softkey to confirm.
6. To delete a drug from the drug library, select the drug using
the keys. Press MODIFY then select YES twice
to delete the drug from the list.
Note: to set a FIXED PROTOCOL set the:-
Max Doserate = Default Doserate = Min Doserate;
Max Conc. = Default Conc. = Min Conc.
Note: use of a protocol in which the Max Bolus is set
OFF will prevent bolus delivery.
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 keys and press the OK softkey.
2. Use the 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 OK to return to
the Configured Options menu.
Configured Options
Drug Library Clock Set
1. Select CLOCK SET from the Configured Options menu
using the keys and press the OK softkey.
2. Use the keys to adjust the date displayed,
pressing NEXT to access the next field.
3. When the correct time and date are displayed press OK 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 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.
Contrast
This option is used to set the contrast on the pump display.
1. Select CONTRAST from the Configured Options menu
using the keys and press the OK softkey.
2. Use the 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 OK 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 keys and press the OK softkey.
2. Use the keys to select the language.
3. When the desired language has been selected press OK to
return to the Configured Options menu.
1. Select the DRUG LIBRARY option from the Configured
Options menu and press the OK softkey.
2. To enter a new drug in the library press the NEW softkey.
3. To enter the name of the new drug use the keys
to scroll through the alphabet. To select a letter press the
NEXT softkey. On completion press the OK softkey.
4. Follow the flow chart below, using the keys to
select values. Use OK to enter selected values and move
on to the next stage. The BACK softkey may be used at any
time to return to the previous screen of the drug library set-
up procedure.
12/24
Enable Units
This option is used to pre-configure the type of units permitted
for use on the pump. Select all possible units which may be
used and disable any that should not be used.
1. Select ENABLE UNITS from the Configured Options menu
using the keys and press the OK softkey.
2. Use the keys to scroll through the list of units,
pressing MODIFY to enable/disable a unit.
3. When all modifications are complete press OK to return to
the Configured Options menu.
Dosing Conversion:
1.0 µg = 1000 ng
1.0 mg/h = 24.0 mg/24 h
1.0 mg/min = 60.0 mg/h
1.0 mg = 1000 µg
The availability of drug
dose units is dependent
on the software version
of the pump.

1000PB00991 Iss. 5.0 13/24
Drug Protocol Record
Asena®CC Drug Protocol Setup
Pressure
Alarm
Bolus
Rate
(ml/hr)
Max
(ml)
Concentration
MaxDefaultMinUnits
Dose Rate
Min
Default
Max
Dose
Units
Drug Name
(12 Chars max*)
No.
(1-50*)
Hospital
Serial Number
Configured by
Date
Ward/Unit
Software Version
Approved by
Date
* - 100 drug names with a maximum of 17 characters are available for V2.2.x software.

1000PB00991 Iss. 5.0
Infusion Specifications -
Maximum infusion rate can be set as part of the configuration.
0.1ml/h - 150ml/h 5ml syringes
0.1ml/h - 300ml/h 10ml syringes
0.1ml/h - 600ml/h 20ml syringes
0.1ml/h - 900ml/h 30ml syringes
0.1ml/h - 1200ml/h 50ml syringes
The Volume Infused range is 0.0ml - 9990ml.
Bolus Specifications -
Maximum Bolus rates can be set as part of the configuration.
Bolus rates are user adjustable.
10 ml/h - 150ml/h 5ml syringes
10 ml/h - 300ml/h 10ml syringes
10 ml/h - 600ml/h 20ml syringes
10 ml/h - 900ml/h 30ml syringes
10 ml/h - 1200ml/h 50ml syringes
The bolus volume limit can be set as part of the configuration.
Minimum: 0.5ml; maximum 25.0ml
Increments of 0.1ml; default 5.0ml
During BOLUS the pressure limit alarms are temporarily
increased to their maximum level.
Critical Volume -
The bolus which can occur in the event of a single internal fault
condition with a 50 ml syringe is :
Maximum Overinfusion - 0.25ml
Purge Specifications -
The purge rate is limited to the maximum rate for the syringe and
can be set as part of the configuration.
100ml/h - 500ml/h.
The purge volume range is 0.5ml - 5ml.
During PURGE the pressure limit alarms are temporarily
increased to their maximum level.
Keep Vein Open (KVO) Rate -
0.1 ml/h - 2.5ml/h.
End Of Syringe Rate -
Stop, KVO (0.1ml/h to 2.5ml/h), or set rate if lower than KVO.
Volume To Be Infused (VTBI) -
0.1ml - 100ml, 1min - 24h
VTBI Complete Rate -
Stop, KVO (0.1ml/h to 2.5ml/h), set rate if lower than KVO or
continue at set rate.
Near End Of Infusion Alarm -
1min - 15min to end of infusion, or 10% of syringe volume,
whichever is smaller.
End Of Infusion (EOI) Alarm -
0.1% - 5% of syringe volume
Electrical Classification -
Class I product. Continuous Mode Operation, Transportable
Maximum Pumping Pressure Limit -
Highest alarm level 1000mmHg (nominal at L-10) Factory Preset,
300mmHg (nominal at L-3).
Occlusion Accuracy without pressure set (% of full scale)* -
Pressure mmHg
L-0 L-3 L-5 L-10
approx. approx. approx. approx.
50 mmHg 300 mmHg 500 mmHg 1000 mmHg
Temp. 23°C ±18% ±21% ±23% ±28%
Occlusion Accuracy with pressure set (% of full scale)* -
Pressure mmHg
0 25 500 1000
Temp. 23°C ±2% ±4% ±5% ±6%
Temp. 5°C-40°C ±4% ±7% ±7% ±10%
* - Using most common 50ml syringes under normal conditions
(95% confidence / 95% of pumps).
Specifications
System Accuracy -
Volumetric Mean +/- 2% (nominal).
Derating -
Temperature +/- 0.5% (5 - 40ºC)
High Rates +/- 2.0% (rates > syringe volume/h eg. > 50ml/h
in a 50ml syringe.)
Important: System accuracy is +/-2% typical by volume as
measured using the trumpet curve test method defined in
IEC60601-2-24 at rates of 1.0ml/h (23ºC) and above when the
instrument is used with the recommended syringes.
Differences in factors such as size and plunger force in
compatible syringes can cause variations in accuracy and
trumpet curves. See also trumpet curves section in this
manual.
Drug Specification -
A maximum of 50 drugs with a maximum of 12 characters are available
with V1.8.x and below software.
A maximum of 100 drugs with a maximum of 17 characters are
available with V2.2.x software.
Battery Specifications -
Rechargeable sealed NiMH. Automatically charges when the pump
is connected to AC power.
Battery life is typically 4h from fully charged @ 5.0ml/h & 20ºC
under normal conditions. Charging takes 2½ hours from discharge
to 90% charge.
Memory Retention -
The electronic memory of the unit will be retained for more than 6
months when not powered up.
Fuse Type -
2 x T 1.25A, slow blowing.
AC Power Supply -
115/230VAC, 50/60Hz, 20VA (nominal).
Case Material -
GE Cycolac S157 (fire retardant to UL94V-2)
Dimensions -
335 mm (w) x 121 mm (h) x 200 mm (d). Weight: 2.5 kg (excluding
power cable).
Alarm Conditions -
Drive Disengaged Occlusion
Check Syringe Battery Low / Battery Empty
Near End Of Infusion End of Infusion
VTBI Done AC Power Failure
Internal Malfunction Attention (Nurse Callback)
Pressure Disc Out Titration not confirmed
Environmental Specifications -
Operating Temperature +5°C - +40°C
Operating Relative Humidity 20% - 90%
Operating Atmospheric Pressure 700mbar - 1060mbar
Transport Temperature -30°C - +50°C
Transport Relative Humidity 10% - 95%
Transport Atmospheric Pressure 500mbar - 1060mbar
Electrical/Mechanical Safety -
Complies with IEC60601-1 (EN60601-1) and IEC60601-2-24
(EN60601-2-24).
EMC -
Complies with EN 60601-1-2:1993 and EN60601-2-24.
Manufacturers Patent Notice -
This instrument is designed and manufactured in the U.K. by
ALARIS Medical UK Ltd. Patents applied for. ALARIS Medical UK
Ltd reserves the right to alter product specifications without notice.
Registered Design Numbers: 2083560, 2083561, 2083563.
14/24

1000PB00991 Iss. 5.0 15/24
Compatible Accessories
5ml 10ml 20ml 30ml 50ml
IVAC®9
AstraZeneca 9
B Braun Omnifix 9 9 9 9 9
B Braun Perfusor 9 9
BD Plastipak 9 9 9 9 9
BD Perfusor 9
BD Precise 9 9
Codan 9 9 9 9
Codan Perfusion 9
Fresenius Injectomat 9 9
Nipro 9 9 9 9
Pentaferte 9 9 9 9
Rapiject* 9
Monoject** 9 9 9 9 9
Terumo 9 9 9 9 9
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.
*- 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.
Recommended Accessory - Asena®Docking Station
Recommended accessory to use in conjunction with the ALARIS®Asena®CC is:
ALARIS®Asena®DS Docking Station

G40215 Opaque Amber PVC Syringe Extension Set (150 cm).
Priming Volume: 1.2ml
G40320 Opaque White PVC Syringe Extension Set (200 cm).
Priming Volume: 3.6ml
G30653M Opaque White PVC Syringe Extension Set with occlusion sensing disc. (200 cm).
Priming Volume: 1.5ml
G40015 Standard PVC Syringe Extension Set (150 cm).
Priming Volume: 2.6ml
G40020B Standard PVC Syringe Extension Set (200 cm).
Priming Volume: 1.5ml
G30402M Standard PVC Syringe Extension Set with occlusion sensing disc. (200 cm).
Priming Volume: 1.5ml
1000PB00991 Iss. 5.0
16/24
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 ALARIS®recommended.
Compatible Accessories - Extension Sets
Please note these drawings are not to scale
Opaque Sets
Low Sorbing Sets
It is recommended that the extension sets are changed according to hospital protocols or as per the extension set
Directions For Use.
Carefully read the Directions For Use supplied with the extension set prior to use.
G40615 Polyethylene Syringe Extension Set (150 cm).
Priming Volume: 1.5ml
G40620 Polyethylene Syringe Extension Set (200 cm).
Priming Volume: 1.6ml
G30303M Polyethylene Syringe Extension Set with occlusion sensing disc. (200 cm).
Priming Volume: 1.5ml
G30453M Opaque White PVC low sorbing Syringe Extension Set with occlusion sensing disc. (200 cm).
Priming Volume: 1.5ml
G30302M Polyethylene Lined Syringe Extension Set with occlusion sensing disc and clamp. (200 cm).
Priming Volume: 1.6ml
G40720 Polyethylene Lined Syringe Extension Set with clamp. (200 cm).
Priming Volume: 1.5ml
Standard Sets

1000PB00991 Iss. 5.0 17/24
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 ALARIS®recommended.
Compatible Accessories - Extension Sets Continued
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
30842 PVC Syringe Extension Set with back check valve, ‘Y’ Site and clamp (32 cm).
Priming Volume: 1.2ml
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
Patient Controlled Analgesia (PCA) Sets
Please note these drawings are not to scale
It is recommended that the extension sets are changed according to hospital protocols or as per the extension set
Directions For Use.
Carefully read the Directions For Use supplied with the extension set prior to use.

1000PB00991 Iss. 5.0
Disposal
The pump 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. Do not send back to the
manufacturer. All other components can be safely disposed of
in the normal manner.
The internal rechargeable battery allows continued operation
when the AC power is unavailable, for example during patient
transfer or AC power failure. A fully charged battery will provide
over 4 hours operation at typical infusion rates. From the
battery low alarm it will take about 2 hours to fully recharge
when reconnected to the AC power supply, whether the unit 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.
Charge retention will eventually degrade. Where retention is
critical the internal battery should be replaced every 3 years.
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.
Battery Operation
To ensure that this instrument remains in good operating
condition, it is important to keep it clean and carry out the
routine maintenance procedures described below. All servicing
should only be performed by a qualified service engineer with
reference to the Technical Service Manual (TSM) for this
product (TSM reference: 1000SM00001).
Refer to the Technical Service Manual for the access code for
technical service features.
Interval Routine Maintenance Procedure
As required Thoroughly clean external surfaces of the pump
before and after prolonged period of storage.
At least once 1. Inspect AC power supply plug and cable for
per year damage.
2. Perform functional tests as outlined in the
Technical Service Manual.
3. Operate the pump on battery power until the
battery low alarm then charge the battery to
confirm battery operation and charging.
Routine Maintenance Procedures
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.
Disinfectants which are known to be corrosive to metals must
not be used. These include disinfectant types
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.
Recommended cleaners are:
Brand Concentration
Hibiscrub™ 20% (v/v)
Virkon™ 1% (w/v)
The syringe and extension line 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.
Important: Before cleaning always switch OFF and
disconnect from the AC power supply. Never allow liquid
to enter the casing 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.
Ensure the pressure transducer is free from residues,
which may prevent correct operation of the disc detector.
Cleaning and Storage
Replacing the AC Fuses
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 plug, or the internal
fuses, have 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 only a qualified service engineer
replaces the AC fuses. For further information regarding the
replacement of internal AC fuses refer to the Technical Service
Manual.
Maintenance
18/24

1000PB00991 Iss. 5.0 19/24
* 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 deduct this volume from the volume infused. Back off will terminate if the pressure reaches the level
recorded by the pump when the infusion was last started, or a maximum back off volume has been withdrawn from the infusion line. It will also
terminate if the volume infused reaches 0.0ml, or a VTBI reaches the value at which it was set.
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.
Use of the dedicated pressure set is recommended. Its use permits the occlusion alarm pressure (mmHg) to be set accurately,
with a small operating margin between the alarm and normal infusion pressures. When using infusion pumps without a pressure
set, line pressures are estimated from pumping force. For this reason the occlusion alarm needs to be set with an operating margin
of at least one level between the alarm and normal infusion levels. The ability to set a small operating margin permits short time
to alarm and small potential bolus volumes to be achieved. Bolus volumes can be minimised as described in the Alarms and
Warnings - Occlusion or by enabling the back off general option.
Without IVAC®Pressure Set fitted -
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.
Occlusion level on Asena®GH or other pumps with occlusion levels: L2
(approx. 200 mmHg).
Auto pressure setting on Asena®CC: (e.g. 55 mmHg).
T1 << T2.
No Pressure Set
Time To Alarm - 1.0 ml/h
No Pressure Set
Bolus Volume without back off
No Pressure Set
Bolus Volume with back off
No Pressure Set
Time To Alarm - 5.0 ml/h
Occlusion Level
hr:min:sec
Occlusion Level
hr:min:sec
Occlusion Level Occlusion Level
ml
typical
typical
typical
typical
ml
With IVAC®Pressure Set fitted, G30402 -
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 G30402 extension set with occlusion sensing disc.
Auto Setting : Asena®CC Asena®CC
Asena®GH

1000PB00991 Iss. 5.0
20/24
IrDA / RS232 / Nursecall Feature
The RS232 / Nursecall feature is an optional feature on
ALARIS®Asena®Syringe Pumps. It allows the pump to be
monitored remotely and/or controlled via a suitable central
monitoring or computer system.
When the pump is started by a command from the serial
interface, communication must take place over the serial
interface, a communication must take place every 15 seconds
or the pump will alarm, display communications failure and stop
infusing. This failure protects against failure of the
communications, including the removal of the RS232 cable.
Important: The nursecall interface provides a remote
backup to the internal audible alarm. It should not be relied
upon to replace monitoring of the internal alarm.
Refer to the Technical Service Manual for further
information regarding the RS232 interface. Since it is
possible to control the syringe pump using the RS232
interface at some distance from the pump and hence
remote from the patient, responsibility for the control of
the pump is vested in the software run on the computer
control system.
The assessment for the suitability of any software used in
the clinical environment to control or receive data from the
pump lies with the user of the equipment. This software
should include detection of the disconnection or other
failure of the RS232 cable. The protocol is detailed in the
Technical Service Manual and is for general information
only.
Any connected analogue and digital components are
required to meet EN60950 for data processing and
EN60601 for medical devices. Anyone connecting
additional devices to the signal input or output is a system
configurator and responsible for meeting the requirements
of the system standard EN60601-1-1.
Test Routines
The test routines are designed to allow confirmation of many of
the pump functions, defaults and calibrations without requiring
internal inspection. They do not represent a full calibration
check.
Important: See the Technical Service Manual for a
complete list of the test procedures, access codes and
calibration procedures.
Nursecall Specification -
Connector D Type - 9 Pin
TXD/RXD EIA RS232-C Standard
TXD Output Voltage Range Minimum: -5V (mark), +5V
(space)
Typical: -7V (mark), +7V (space)
with 3K load to ground
RXD Input Voltage Range -30V - +30V max.
RXD Input Thresholds Low: 0.6V minimum / High: 3.0V
maximum
RXD Input Resistance 3K minimum
Enable Active, Low:-7V to -12V
Active, High:+7V to +12V,
powers up the isolated RS232
circuitry
Inactive: Floating/open circuit,
allows isolated RS232 circuitry
to power down.
Isolation Socket/Pump 1.5kV (dc, or ac peak)
Baud Rate 38.4 kBaud
Start Bits 1 Start Bit
Data Bits 8 Data Bits
Parity Odd Parity / No Parity
Stop Bits 1 stop bit
Nurse Call Relay Contacts Pins 1, 8 + 9, 30V dc, 1A rating
Typical Connection Data -
1 Nursecall (Relay) Normally Closed
2 Transmit Data (TXD) Output
3 Received Data (RXD) Input
4 Power Input (DSR)
5 Ground (GND)
6 Not used
7 Power Input (CTS)
8 Nursecall (Relay) Normally open
9 Nursecall (Relay) Common
RS232 / Nursecall Connection Data
IrDA
Baud Rate 38.4 kBaud