Braun Infusomat Space P User manual

Infusomat® Space P
and Accessories
Instructions for Use
Valid for software 687N
GB
It is recommended that all pumps at
your care unit are equipped with the
same software version or in parallel
use with Software M.
38911866N_Infusomat Space P_GB_060418 LLD Order 3238

2
ONTENTS
Infusomat® Space P Overview...............................................................................................3
Symbols on Product..................................................................................................................5
Patient Safety ........................................................................................................................6
Menu Structure / Navigation...............................................................................................10
hapter 1 Operation .........................................................................................................13
1.1 Start of Infusion.........................................................................................................................13
1.2 Entry With Different ombinations of Rate, VTBI (= Volume To Be Infused)
and Time.......................................................................................................................................16
1.3 Bolus Application.......................................................................................................................17
1.4 Infusion Line hange and New Therapy Start ..................................................................18
1.5 End of Infusion...........................................................................................................................19
1.6 Standby Mode.............................................................................................................................20
hapter 2 Advanced Operations....................................................................................21
2.1 Status Request of Pump when Infusion is Running........................................................21
2.2 Rate, VTBI and Time hange Without Infusion Interruption and Reset
of Status Menu Data ................................................................................................................21
hapter 3 Special Functions* .........................................................................................22
3.1 Dosing Units and Dose Rate alculation (Overview) ......................................................22
3.2 Dose Rate alculation (Operation).......................................................................................22
3.3 Drug Library.................................................................................................................................23
3.4 Patient ontrolled Analgesia (P A)......................................................................................26
3.5 Barcoding .....................................................................................................................................27
3.6 Piggyback Function ...................................................................................................................28
3.7 Ramp and Taper Mode .............................................................................................................30
3.8 Programm Mode.........................................................................................................................33
3.9 Intermittent Mode.....................................................................................................................35
3.10 Dose Over Time...........................................................................................................................37
hapter 4 Autoprogramming .........................................................................................39
hapter 5 Options..............................................................................................................43
5.1 Occlusion Pressure.....................................................................................................................43
5.2 Upstream Occlusion Pressure.................................................................................................44
5.3 Data Lock .....................................................................................................................................44
5.4 Bolus Rate....................................................................................................................................46
5.5 KVO-Mode....................................................................................................................................46
5.6 ontrast / Display Light / Keypad Light ..............................................................................46
5.7 Alarm Volume .............................................................................................................................46
5.8 Date / Time ..................................................................................................................................46
5.9 Macro Mode ................................................................................................................................47
5.10 Language ......................................................................................................................................47
hapter 6 Alarms ...............................................................................................................48
6.1 Device Alarms .............................................................................................................................48
6.2 Pre-Alarms and Operating Alarms........................................................................................48
6.3 Reminder Alarms........................................................................................................................51
6.4 Alarm Hints..................................................................................................................................52
hapter 7 Battery Operation and Maintenance .......................................................53
hapter 8 Start Up Graphs and Trumpet urves......................................................55
hapter 9 Technical Data................................................................................................56
hapter 10 Warranty / Training / TS ** / Service / Disinfecting / Disposal ......63
hapter 11 Instructions for Use Accessory ..................................................................67
Ordering .....................................................................................................................72
*The availability of
the listed features
is depending on
the configuration
of the pump.
**Technical Safety
heck.

Port for drop sensor
INFUSOMAT® SPA E P OVERVIEW
INFUSOMAT® SPACE P OVERVIEW
3
Arrow up and -down
Scroll through menus, change setting of numbers from
0-9, answer Yes/No questions.
Arrow left and -right
Select data from a scale and switch between digits when
numbers are entered. Open a function while pump is
running or stopped with the left arrow key.
Press to reset single values
to zero and switch back to
the previous screen/menu
level.
Press to Start/Stop
infusion.
Press to initiate
auto-programming
orders when prompted.
Open certain functions
and press to confirm
values/settings/alarms.
qc
Port P3 for future options
Cover of Battery Compartment
Before changing the battery, always disconnect the pump from the patient and switch off the device.
To remove the battery cover push the button below the battery compartment with a pointed pen and pull the cover
away from device. Slide green locking mechanism on back of battery up and take out battery pack for exchange.
A crank in order to open the pump door in case of emergency is attached to the inside of the battery compartment
cover (for closer information see 1.4).
Press to turn
pump on/off.
o
Port P2 for power supply, SpaceStation,
connection lead (12V), combi lead and
further accessory leads (staff call, service)
Yellow LED: Pre-alarm, reminder alarm
Green LED: Infusing
Red LED: Operating or device alarm
Blue LED: Initiating connection to wireless
battery or Space Station
Press to
open the
pump door.
x
sf
m
Press to
initiate
bolus.
k
nB

INFUSOMAT® SPA E P OVERVIEW
4
Transport
A maximum of three pumps (Infusomat®
Space P or Perfusor® Space) plus one
Space ontrol may be stacked together (in
ambulance cars and helicopters only one
pump). Avoid external mechanical
influence.
ocking Devices Together
Line up the bar of the lower pump with the
bar of the pump above and slide the lower
pump backwards until the lock clicks and
the green buttons are above each other.
To disconnect, push green locking buttons
of top pump device and slide bottom pump
forward.
aution: Avoid external mechanical action.
Pole Fixation
Push the opening of Pole lamp against the
vertical pole and lock the screw tightly.
Unscrew to release.
For vertical position push lever down and
rotate either way until lever clicks into
notch. Push lever for
rotation.
aution: A maximum of three B. Braun
Space pumps can be stacked together
only in horizontal pump position
when used with the Pole lamp SP.
Pump based free flow
prevention safety clamp
Downstream
pressure sensor
Upstream
pressure sensor
Line guide
cover
Air
sensor
Fixaton of PoleClamp (Universal Clamp)
Line up bar of pump with bar of Pole lamp
and slide Pole lamp forward until locking
mechanism clicks.
To remove, press release button on frame,
push handle down and pull Pole lamp
backwards.
Pole clamp handle
Pole clamp
release button
Pump slots
Yellow
caution light
Opening
lever
Green locking
button

5
SYMBOLS ON PRODU T
SYMBO S ON PRODUCT

PATIENT SAFETY
PATIENT SAFETY
Read Instructions
for Use prior to use.
The infusion device
should only be
used by specially
trained staff.
Intended use
The Infusomat® Space P Volumetric Infusion Pump System includes an external
transportable electronic volumetric infusion pump, dedicated administration
sets, and pump accessories. The system is intended for use on adults, pediatrics,
and neonates for the intermittent or continuous delivery of parenteral and
enteral fluids through clinically accepted routes of administration. These routes
include, but are not limited to intravenous, irrigation/ablation, and enteral. The
system is used for the delivery of medications indicated for infusion therapy
including but not limited to colloids and cristalloids, blood and blood compo-
nents, Total Parenteral Nutrition (TPN), lipids, and enteral fluids. The Infusomat®
Space P Volumetric Infusion Pump System is intended to be used by trained
healthcare professionals in healthcare facilities, home care, outpatient, and
medical transport environments.
Qualified medical staff should decide how the device should be used based on
its features and specifications. For more details, please read the Instructions for
Use.
Operation
• The initial training of the Infusomat® Space P is to be performed by B. Braun
sales personnel or other authorized persons. After each software update, the
user is required to inform himself about the changes to the device and
accessories in the instructions for use.
4waution: Ensure the unit is properly positioned and secured. Do not position
pump unit above patient or in a position where a patient could
come to harm, should the pump fall.
• Prior to administration, visibly inspect the pump for damage, missing parts or
contamination and check audible and visible alarms during selftest.
• Not be used adjacent and stacked with other equipment except B. Braun
Space devices.
• Only connect to patient once the line has been correctly inserted and
completley primed. Interrupt connection during line change to prevent
incorrect dose delivery.
• During priming and bolusing the pressure limits are set to the maximum level.
• Select infusion line/catheter suitable for use with the intended medical
application.
4waution: Position the infusion line free of kinks.
• Recommended change of disposable every 24 h (or as per national hygiene
regulations).
w
6

7
PATIENT SAFETY
• Installation in medically used rooms must comply with the appropriate
regulations (e.g. VDE 0100, VDE 0107 or IE -publications). Observe national
specifications and deviations.
4waution: Operate the pump at least 25 cm from flammable anaesthetics
to prevent explosion.
• ompare the displayed value with the entered value prior to starting
infusion.
• If staff call is used we recommend checking the equipment once after
connecting the pump.
• Protect the device and the power supply against moisture.
• If the pump falls down or is exposed to force, it must be checked by the
service department.
• The displayed data must always be checked by the user prior to making
further medical decisions.
• During mobile use (homecare, patient transport inside and outside the
hospital): Make sure the device is securely fixed and positioned. Positioning
changes and severe shock can lead to minor changes in the delivery accuracy.
• A supplemental patient monitoring must be carried out if life-saving
medication is performed.
• The air detector cannot detect air diffusing in the following components:
three-way stopcocks, infusion adapters and further lines placed between
pump and patient.
• In case high potent drugs are given be sure to have a second infusion pump
for that drug at hand. The therapy documentation should be suitable to
continue the therapy at the second infusion pump.
• Independant of the soft limits the selected values have to be the medically
correct ones for the given patient.
• In case values relevant for the dose rate calculation are changing always the
flow rate will be updated and the dose rate will be fix.
• onsider startup characteristics before using low infusion rates (0.1ml/h)
with critical drugs.
Enteral Nutrition
The Infusomat® Space P may be used for enteral nutrition. Do not use enteral
fluids for intravenous infusion as this may harm your patient. For this reason
only use disposables dedicated and labeled for enteral nutrition.
Transfusion
The Infusomat® Space P may be used for blood transfusion, too. For this therapy
only use disposables dedicated and labelled for transfusion.

8
PATIENT SAFETY
Other components
• Use only pressure-proof and compatible disposable items (min. 2 bar/
1500 mm Hg) to avoid influencing performance data - which would result in
impairing patient safety.
• Where several infusion lines are connected on one single vascular access, the
possibility of the lines exerting a mutual influence over each other cannot be
excluded.
• Refer to respective manufacturer’s information for possible incompatibilities
of equipment with respect to drugs.
• Use only compatible combinations of equipment, accessories, working parts
and disposables with luer lock connectors.
• onnected electrical equipment must comply with the relevant IE /EN-
specifications (e.g. IE /EN 60950 for data-processing equipment). The
user/operator is responsible for the system configuration if additional
equipment is connected. The international standard IE /EN 60601-1-1 has to
be taken into account.
Safety Standards
Infusomat® Space P satisfies all safety standards for medical electrical devices
in compliance with IE /EN 60601-1 and IE /EN 60601-2-24.
• The EM -limits (electro-magnetic compatibility) according to
IE 60601-1-2:2007 and IE 60601-2-24: 2012 are maintained. If the
equipment is operated in the vicinity of other equipment which may cause
high levels of interference (e.g. HF surgical equipment, nuclear spin
tomography units, mobile telephones etc.) may be disturbed. Maintain the
protective distances recommended by the manufacturers of these devices.
• The Infusomat® Space P fulfils the applicable requirements of EN 13718 to
be used in the air, on the water and in difficult terrain. During transport the
Infusomat® Space P needs to be fixed on a suitable restraint system by
means of SpaceStation or Pole lamp SP. When stored under temperature
conditions beyond the defined operating conditions the Infusomat® Space P
needs to remain under room temperature at least one hour before usage.
• As there is no dedicated norm existing for enteral feeding pumps the safety
features of Infusomat® Space P are also for enteral nutrition according to
the a.m. norms.
Safety instructions for using PCA
• In case the demand button is used with SpaceStation the P A pump has to
be placed in the lowest slot of the lowest SpaceStation.
• Access to the pump settings can be prohibited by DataLock 3. The code for
DataLock level 3 should differ from the one for levels 1 and 2 in case the
pump is only allowed to be used by pain management professionals.

• When ending P A and starting it again the therapy data are set to default
values.
• Using the demand button also the patient is a permitted user. With the
demand button only a P A-bolus can be requested. This is limited to pre-
defined doses by drug list and pump settings.
9
PATIENT SAFETY
Safety Instructions for using Pole Clamp
1. Line pump up with the Pole lamp
guide rails.
2. Slide pump fully into place onto the
guide rails.
3. An audible “ lick” should heard.
4. Test the pump is secure.
W
The pump ist now securely attached to
Pole lamp.
• Do not lean on the pump when
attached to the Pole lamp.
• Do not position the pump unit
above the patient.
W
• DO NOT use any Pole lamp that
shows signs of damage.
• DO NOT use Pole lamp with
missing clamp grids.
Underside view
lamp grids

10
At the top of the screen the last therapy is
indicated. Yes/No question can be
answered by pressing ufor yes or d
for no.
Parameters which can be changed (e.g.
rate in ml/h) are opened with lor
k. When editing parameters, switch
digits/levels using l r. White
background indicates current digit/
level. Use uor dto change current
setting. Help text on the bottom/top of
the screen indicates options how to
proceed (e.g. confirm rate with k,
start infusion with sfor clear rate by
pressing c).
Display Meaning
Cutline
MENU STRUCTURE / NAVIGATION
MENU STRU TURE / NAVIGATION
All display screen shots are examples and may be different when related to an
individual patient and individualized therapy.
o On/Off button
x Door open button
sf Start/Stop button
nb Bolus button
C lear button
K OK button
Q Keypad with arrow up, -down,
-left, -right button
m onnection button
Battery
status
onnection to Space om
in SpaceStation
Mains
connection
Unit of drug application
Active VTBI- or time preselection
Scrolling arrows indicate pump is infusing
Set rate can be opened with l
Set pressure limit and current pressure
Therapy profile
Typical display during infusion:
Total volume infused. Alternatively the intermediate volume can be displayed.
Remaining time
Remaining VTBI

11
MENU STRU TURE / NAVIGATION
nb has been pressed while the pump is
infusing. Start manual bolus at
1200 ml/h by pressing k(see top of
display) or proceed to set bolus limit
with l(see bottom of display).
All status information is available in the
bottom line of the display. The desired
information can be selected by using d
u and will be displayed permanently
thereafter (e. g. drug long name, current
system pressure etc.).
Display Meaning
Pre-alarms are indicated by a message on
the display (e.g. “VTBI near end”), an
audible tone andthe yellow LED is con-
stantly on.
To confirm a pre-alarm press k.
This hint pops up if a user tries to edit or
change a parameter by pressing l when
that parameter is unable to be changed.
Press and hold ofor 3 sec to turn pump
off. A white bar stretches from left to
right and counts down the 3 sec.
As long there is an infusion line inserted
the pump will not turn off but will use
standby.
Set pressure level with l or rand
confirm by pressing k.
ancel to edit pressure by using c.
In case of an operating alarm (e.g. "VTBI
infused") the infusion stops, an audible
tone sounds and the red LED flashes.
onfirm alarm by using k.
onfirming does not activate an acoustic
feedback.

MENU STRU TURE / NAVIGATION
12
Prime ?
Start Up
Menu
Main
Menu
Status
Menu
Line
selection
Rate
Special
Functions
Dose Rate
Calculation
VTBI
Time
Use last
therapy ?
Use drug
library ?
Use dose rate
calculation ?
Weight
Concentration
Dose
Drug Library
Change-over
from
continuous
mode to PCA
Intermediate
volume
Intermediate
amount
Intermediate
time
Total
volume
Special
Functions
Options
Status
Options
Menu
Occlusion
Pressure
Total
amount
Total
time
Line
Battery
capacity
WLan
Version
Drug
info
Bolus
Rate
KVO-
Mode
Display
Light
Keypad
Light
Alarm
Volume
Data Lock
Contrast
Date
Time
Macro
Mode
In Dose Mode:
Display of flow
rate in large
scale
Language

13
Chapter 1
OPERATION
OPERATION
1.1 Start of Infusion
• Ensure that the pump is properly installed. heck the equipment for completeness
and damages. Do not attach the infusion bottle below the pump level.
• Put the spike vertically into the infusion bottle. Fill the bottom part of the drop
chamber by max. 2/3.
4waution: lose the roller clamp before inserting the IV line and do not
connect to
patient until properly loaded and primed.
• If the device is connected to the mains, the display indicates the battery status, the
mains connection symbol and the last therapy.
• Press oto switch on the device. Observe the automatic self-test: The message
“Self-test active” and the software version are displayed, two audible tones sound
and all three LEDs (yellow, green/red and blue) flash once. Information about the
power supply (mains or battery operation) and the set pressure level are indicated.
In addition, the line type appears at first (provided that the line is already inserted).
Then, the accumulated air volume and the max. size of air bubbles is indicated
which is triggering the air alarm of the device.
• Press cto start the direct entry of therapy parameters, or press xand uto
open the pump door in order to continue with inserting the line.
4waution: lose the roller clamp before inserting the IV line and do not
connect to patient until properly loaded and primed.
aution: You may only insert the line while the device is switched on and the line
guide element is inserted. Otherwise, there is the danger of freeflow. Pay attention to
keep the roller clamp closed before inserting the infusion line especially at a tempera-
ture scale of 10 - 15 ° . Never leave the pump unattended when inserting the tube.
aution: Inserting different lines into the pump is identical. Please see instructions and
packaging of the different lines (standard, transfusion, opaque, enterel nutrition etc.)
to receive information about preparation and usage of these lines.
The pump offers the possibility to load up to four languages into the pump
(depending on the number of the language specific characters), among which the
user can choose during the operation of the pump. During the first ever start-up of
the device, the user is requested to select the languages and to mark them with
l. After that, the selection has to be confirmed by choosing the last menu item at
the bottom of the list and pressing k. Then the desired language must be selected
with tand confirmed with k. Answer the following question with d in order to
activate the selected language.

14
OPERATION
Chapter 1
aution: Please make sure that the line is straight and not slack to prevent a damage
occurring to the infusion line which leads to an incorrect dosage.
• Firmly press tubing into the air sensor guide to make sure the line is properly
inserted into the sensors. Thread the tubing through the notches on the right and
left side of the pump.
• lose the pump door by firmly placing pressure with both hands on each side of the
pump door, continue to press firmly until you hear and feel the motorized door
latch pull the door shut. Do not open roller clamp until the pump directs you to do
so when self test is completed. Then select the inserted line with tand confirm it
with l. Open the roller clamp.
aution: Before opening door, please close roller clamp and ensure door does not fall
open. If door opens to the horizontal position, please check that the slide clamp (green)
1. Mind flow direction while
inserting the infusion line
(s. pictogramm) to prevent the
danger of backflow.
2. ompletely insert and then gently
press the infusion line into the
guidance and the sensors.
3. Take care that the line is perfectly
engaged with the drive and the
sensors. Especially the air sensor
needs perfect contact to the line!
Press down the opening lever.

15
is properly occluding the IV set and the door extension hook is not broken. If the door
hook is found damaged or broken remove the pump from service.
aution: If a wrong line is selected the time until the pump goes into a pressure alarm
may be prolonged. Also a wrong delivery rate is possible.
• Press uif the prime function is enabled to prime the infusion line with the rate
displayed. ancel priming with k. Repeat the procedure until the line is
completely primed. Then press dto proceed.
Note: During priming, all air and drop alarms are switched off.
• Establish the patient connection.
• Answer the question whether the old therapy is to be used either with uor d
(the question can be deactivated via the service manual). If you select u, the
pump jumps to the Main Menu.
Note: At rates smaller 10 ml/h the detection of a closed roller clamp cannot always be
ensured due to physical reasons. A drop sensor may be used to avoid this risk.
Adjusting the delivey rate:
• In the Main Menu, open the rate with land set it with q.
• Press sfto start the infusion. VTBI is required to start the infusion. Time will
be calculated when rate is entered. When time is entered, rate/doserate will
be calculated. Running arrows on the display and the green LED indicate that
the pump is infusing.
Note: The running infusion can be cancelled at any time by pressing sf. The
pump can be turned off at any time by pressing o for 3 sec (Exception: Data
lock level 2) and as long a disposable is inserted.
Handling with Intrafix® SafeSet
Note: If Intrafix® SafeSet is used, VTBI is not required.
A unique airtight filter membrane acts as a barrier, protecting against air-in-line
situation. As the fluid level reaches the membrane, the upstream alarm will
occur and the pump stops delivery whereas no air will pass the AirStop filter.
For this reason a fast switch over to next container requires no aditionally
workload for priming.
In case of a " heck upstream" alarm, the upstream sensor detects an
underpressure situation in the IV set between the pump and the drip chamber.
Therefore check always if the roller clamp is open, if the line is kinked or if the
bag and/or drip chamber is empty.
Please do not start the pump again by not fixing the " heck upstream" alarm
situation.
If too many times, the pump is started without fixing the situation, the
Chapter 1
OPERATION

16
OPERATION
upstream sensor calibrates on the current existing underpressure in the line and
air might pass the AirStop membrane. In this case please ensure that the the
drip chamber is refilled and then open the door for recalibration of the
upstream sensor.
1.2 Entry With Different Combinations of Rate, VTBI
(= Volume To Be Infused) and Time
The Infusomat® Space P offers the possibility to enter a volume- and time limit in
addition to an infusion rate. When two of these parameters are entered, the third is
calculated by the pump. If a volume and/or time is preselected, an arrow symbol is
placed in front of one of these parameters in the Main Menu. It is called the “target”.
During the infusion of the pump, this target symbol is displayed next to the moving
arrows in the run display (this symbol is not visible in case T I is used). This indicates
that the pump has been programmed, either with a volume- or time limit. The assign-
ment of the target symbol, apparent in the Main Menu, shows the established para-
meter for the application (VTBI or time). When the rate is changed, the so-called target
parameter is principally not adjusted to the new rate but to the parameter which does
not have the target symbol in front. After the infusion has started, the remaining VTBI
and time are displayed in the status menu and the run display (values are counting
down).
1.) Enter VTBI and time: The infusion rate will be calculated and displayed on the
bottom of the display.
Target: Volume
• Select VTBI with t and open with l.
• Enter VTBI with qand confirm with k.
• Select time with t and open with l.
• Enter time with qand confirm with k.
heck calculated rate on plausibility.
Proceed in the same way to calculate 2.) and 3.).
2.) Infusion with volume limit
Enter rate and VTBI: The infusion time will be calculated and displayed on the
bottom of the display.
Target: VTBI
3.) Infusion with time limit
Enter rate and time: The infusion volume will be calculated and displayed on the
bottom of the display.
Target: Time
Changing already entered values of VTBI and time (rate, VTBI and time already exist
at the point of change):
Chapter 1

17
Chapter 1
OPERATION
a) Target symbol is placed in front of VTBI:
• hange of VTBI => Adjustment of time. Old and new target: VTBI
• hange of time => Adjustment of rate. Old and new target: VTBI
b) Target symbol is placed in front of time:
• hange of time => Adjustment of VTBI. Old and new target: Time
• hange of VTBI => Adjustment of time. New target: VTBI
1.3 Bolus Application
After pressing the button nb, the bolus unit can be selected by using d.
Note: The selected unit will not be stored. It is possible to administer a bolus
in ml.
There are three ways to administer a bolus:
1.)Manual Bolus: Press nb. Then press kand hold button. Fluid is
administered for as long as the button is held down.. The infused bolus
volume is displayed.
The max. bolus time is limited to 10 sec.
Reaching this limit is indicated by an acoustic signal.
2.)Bolus with volume preselection: Press nb. Then press l and set bolus dose
limit by using q. Press nbto confirm and start bolus. Depending on the
service tool settings an acoustic signal will sound after finishing the bolus
volume.
3.)Bolus with rate calculation: Press nb. Then press land set bolus dose by
using q. Press kto confirm bolus dose. Set time with qin which a
bolus is to be delivered. alculated bolus rate is shown on top of the display.
Press nbto confirm and start bolus.
You can use the service program to enter a default and a maximum bolus rate.
Once a new therapy is started the device always returns to the default rate
- even if the bolus rate was manually changed beforehand.
Note: If the bolus limit is not entered after pressing nb, the pump switches
back into the run display automatically.
Note: The infused volume during bolus with volume preselection counts up.
In order to purge the line at any time while the pump is stopped press nb.
Answer the following question by pressing uin order to start the purge
process. ancel by pressing kor any other key.
aution: Take care not to overdose! Given a bolus rate of 1200 ml/h, 1 ml will
be administered in just 3 sec. To cancel bolus infusion at any time press k.
At low bolus volumes, under dosages due to the start up characteristic of the
pump and the tolerances in the infusion system cannot be excluded. Disconnect
patient while purging.

18
OPERATION
1.4 Infusion ine Change and New Therapy Start
Note: Always interrupt the patient connection before changing a line to avoid dosing
errors. Never let the pump run unattended when changing the line. heck and clean
the safety clamp regularly.
• Press sfto stop the delivery. The green LED goes out. lose the roller clamp
and interrupt the patient connection.
• Press xand open the pump door with u. Press down the green opening lever
completely until it locks in place, remove the line and insert a new line.
Note: In the unlikely event the pump door cannot be opened remove the allen key
from the inside of the battery compartment cover. Use this key to remove the
emergency aperture cover of the pump. Place the crank in the aperture and turn it
clockwise until the pump door opens.
Push cover opening with pen.
Remove crank from inside of
battery cover.
Turn crank to remove emergency
aperture cover.
Chapter 1

19
Chapter 1
OPERATION
• lose the pump door, confirm the inserted line with kand open the roller clamp.
• If required, prime the pump with u. Then press d to proceed.
• Establish the patient connection and check the parameters with t.
• Start the infusion by pressing sf.
Note: A new therapy can be started at any time during a stopped infusion. If the pump
is in the Main, Status or Options Menu, press C(repeatedly) and follow the
instructions as described.
1.5 End of Infusion
• Press sfto stop the infusion. The green LED goes out. lose the roller clamp
and interrupt the patient connection.
• Press x. Answer the question whether the pump door is to be opened with
u.
• Press down the green opening lever completely until it locks in place.
Remove the line and close the pump door.
• Press ofor 3 sec to switch off the pump.
Note: The settings will be permanently saved by the switched off device.
Note: Pump cannot be powered off with IV line inserted.
Remove emergency aperture cover.
Turn crank inside aperture to open
the door.

20
1.6 Standby Mode
In the case of extended interruption, the user has the option to maintain the set values.
• Press sfto stop the infusion. Then press ofor less than 3 sec.
• onfirm that the pump is supposed to switch to standby by pressing u.
• The pump is now in Standby.
While the pump is in the standby mode, it’s display shows the drug and the
remaining time for this mode. hange of remaining time by pressing l.
Exit standby by pressing c.
As long as a disposable is inserted in the pump will use standby also in case ois
pressed for at least or more than 3 sec.
Chapter 1
SPE IAL FUN TIONS