Nutricia Flocare Infinity User manual

PTIT-CHFR-BE-CH-LUESDE-AT-CH-LUBE-NL UK-IE
INSTRUCTIONS FOR USE
For enteral use onl
Read this manual before using the pump
ZMNL400336_AW.indd 2 3/18/10 3:47:27 PM

BE-NL • INHOUD
Algemene productinformatie 5
Voorbereiding 5
Service en garantie 5
Gebruiksaanwizing 6
Alarmfuncties en
veiligheidsvoorzieningen 10
Onderhoud 10
Problemen en oplossingen 11
Instelmodus 12
Technische specificaties 14
DE-AT-CH-LU • INHALT
Allgemeine Informationen 15
Vorbereitung 16
Service und Gewährleistung 17
Bedienungsanweisung 17
Alarmfunktionen und
Sicherheitstechnik 22
Instandhaltung 22
Fehlersuchtabelle 23
Sstemeinstellungen 24
Technische Daten 25
Bestellinformation 26
ES • ÍNDICE
Introducción 27
Preparación 27
Servicio  garantía 27
Instrucciones de funcionamiento 28
Funciones de alarma  prestaciones
de seguridad 32
Mantenimiento 32
Diagrama de solución de
problemas 33
Modo de configuración 34
Especificaciones técnicas 36
FR-BE-CH-LU • CONTENT
Introduction 37
Précautions d’emploi 37
Service après-vente et garantie 37
Instructions d’utilisation 38
Alarmes et sécurités 42
Entretien 42
Résolutions des problèmes 43
Mode de paramétrage 44
Spécifications techniques 45
IT-CH • CONTENUTI
Introduzione 47
Preparazione 47
Servizio e garanzia 47
Istruzioni per l’uso 48
Allarmi e funzioni di sicurezza 52
Manutenzione 52
Risoluzione dei problemi 53
Funzione di parametrizzazione 54
Specifiche tecniche 55
PT • ÍNDICE
Introdução 57
Preparação 57
Serviço e garantia 57
Instruções de funcionamento 58
Funções do alarme e características
de segurança 62
Manutenção 62
Quadro para soluções e
problemas 63
Modo de configuração - Set up 64
Especificações técnicas 65
UK-IE • CONTENT
Introduction 67
Preparation 67
Service and Warrant 67
Operating instructions 68
Alarm functions and safet features 72
Maintenance 72
Problem solver chart 73
Set up mode 74
Technical specifications 75
Appendix A:
Guidance and manufacturer’s declaration -
Electromagnetic compatibilit 78
ZMNL400336_AW.indd 3 3/18/10 3:47:27 PM

Figure 4
Figure 5c Figure 5d
k
a
Figure 1
d
f c
g
h
e
b
ij
Figure 3
Figure 2
Figure 5a Figure 5b
A
B
ZMNL400336_AW.indd 4 3/18/10 3:47:31 PM

BE-NL
POMPSPECIFICATIES:
Fig. 1:
aPompdeur
bScherm (LCD)
cToetsenbord
dRotor
eStroomopwaartse druksensor
fStroomafwaartse druksensor
gVake voor pompset
hLuchtsensor
Fig. 2:
iGebruiksaanwizing
jBevestigingspunt voor paalklem
kAansluiting voor adapter
Fig. 3: Paalklem
Fig. 4: Adapter
Fig. 5a-5d: De pompset vullen en
inbrengen
DE-AT-CH-LU
KOMPONENTENLISTE:
Fig. 1:
aPumpentüre
bAnzeigefeld (LCD)
cTastatur
dRotor
eVorgeschalteter Drucksensor
fNachgeschalteter Drucksensor
gAnschluss für das Pumpsegment
hLuftsensor
Fig. 2:
iBedienungshinweise
jAnschluss für Schraubhalterung
kBuchse für den Netzanschluss
Fig. 3: Schraubhalterung
Fig. 4: AC/DC Adapter/Ladegerät
Fig. 5a-5d: Einführung des
Pumpsegments
ES
LISTA DE COMPONENTES:
Fig. 1:
aCompuerta de la bomba
bPanel indicador (LCD)
cTeclado
dRotor
eSensor de presión ascendente
fSensor de presión descendente
gReceptáculo para insertar el sis-
tema
hSensor del aire
Fig. 2:
iInstrucciones de uso
jReceptáculo para el fiador del
polo
kToma para la conexión a la uni-
dad cargadora de enchufe
Fig. 3: Fiador del polo
Fig. 4: Cargador
Fig. 5a-5d: Inserción del equipo de
bomba
FR-BE-CH-LU
LISTE DE COMPOSANTS:
Fig. 1:
aPorte
bEcran (LCD)
cClavier
dRotor
eCapteur de pression amont
fCapteur de pression aval
gSite insertion cassette
hDétecteur d’air
Fig. 2:
iInstructions d’utilisation
jSite insertion support
kConnexion de l’adaptateur
Fig. 3: Support
Fig. 4: Chargeur
Fig. 5a-5d: Insertion de la tubulure
IT-CH
ELENCO DEI COMPONENTI:
Fig. 1:
aSportello pompa
bVisualizzatore a cristalli liquidi
(LCD)
cTastiera
dRotore
eSensore della pressione in
ingresso
fSensore della pressione in uscita
gRicettacolo per l’inserto del set
hSensore dell’aria
Fig. 2:
iIstruzioni per l’uso
jRicettacolo per il sistema di fis-
saggio alla piantana
kConnettore per l’alimentatore
Fig. 3: Sistema di fissaggio alla
piantana
Fig. 4: Caricabatterie
Fig. 5a-5d: Inserimento del set
PT
LISTA DE COMPONENTES:
Fig. 1:
aPorta
bEcrã (LCD)
cTeclado
dRotor
eSensor de pressão ascendente
fSensor de pressão descendente
g Receptor para colocação do sistema
hSensor de ar
Fig. 2:
iInstruções de utilização
jReceptor para colocação do
suporte
kConexão para o carregador
Fig. 3: Suporte
Fig. 4: Carregador
Fig. 5a-5d: Colocação do sistema de
alimentação na bomba
UK-IE
LIST OF COMPONENTS:
Fig. 1:
aPump door
bDispla panel (LCD)
cKepad
dRotor
eUpstream pressure sensor
fDownstream pressure sensor
gReceptacle for pump insert
hAir sensor
Fig. 2:
iInstructions for use
jReceptacle for pole clamp
kSocket for connection to the plug
charger unit
Fig. 3: Pole clamp
Fig. 4: Charger
Fig. 5a-5d: Filling and Insertion of the
pump set
ZMNL400336_AW.indd 5 3/18/10 3:47:32 PM

ORDERING INFORMATION
Flocare®Infinit™pump Western Europe corporate code 35676
Flocare®Infinit™Charger
Pole clamp
Instructions for use
Optional accessories
Please refer to our local Nutricia contact for availabilit of Flocare®Infinit™accessories, as
there are: feeding sets, carr bag, PDMS/data cable, nurse call, service suitcase and other.
MANUFACTURER
Nutricia Medical Devices b.v.
Schiphol Boulevard 261
1118 BH Schiphol Airport
The Netherlands
ZMNL400336_AW.indd 6 3/18/10 3:47:32 PM

INTRODUCTION
• The Flocare®Infinit™pump is a small, lightweight pump for both portable and bedside use. The pump is
based on the rotar peristaltic principle and is intended for enteral use onl.
PREPARATION
• Check the integrit of the pump. Do not use the pump if it is damaged. If a technical failure occurs or if
the pump is dropped, the pump should be checked b a qualified technician.
• Do not use the pump in areas where there is a risk of explosions e.g. in the presence of flammable anaesthetics.
• If the pump has been stored for an period of time, it should be plugged into the mains to recharge the bat-
ter before commencing enteral feeding. The batter will be completel charged after approximatel 6 hours.
• The Flocare®Infinit™pump should onl be used in combination with the appropriate Flocare®Infinit™
pump set! (consult our local Nutricia sales representative for information on availbale pump sets).
• This pump operates in an orientation, making it ideal for ambulator use.
• Check the position of the feeding tube, as advised b our healthcare professional, before commencing
tube feeding.
• Pump fed patients should be regularl monitored and supervised. Specific patient groups require consistent
and controlled administration of enteral nutrition as well as simultaneous application of medication (e.g. insu-
lin administration). In these cases, regular and frequent checks, as determined b the attending healthcare
professional, should be carried out to ensure correct administration of nutrition throughout the therap period.
Using the Infinit™pump’s DOSE function is recommended in these cases (see section “To set a Dose”).
• For bedside use, the multi-position pole clamp (figure 3) can be attached to the pump with the screw
provided. The pump can be fixed in an position (rotatable in 360°).
SERVICE AND WARRANTy
The manufacturer recommends an inspection of the pump at an authorised service centre ever 2 ears.
Onl authorised personnel should perform service work on Infinit™pumps. Please contact our local Sales
Organisation / Nutricia Subsidiar for all service and repair of pumps (see address at the back of the booklet).
Limitations of warrant
Solel for the benefit of the original buer/user, Nutricia Medical Devices B.V, warrants all new Flocare® Infinit™ pumps, of
its manufacture to be free from defects in material and workmanship, excluding normal wear and tear, and will replace or
repair, at its service facilit or other location designated b Nutricia Medical Devices B.V, an Flocare® Infinit™ pump returned
to it within thirt-six (36) months of original purchase b the buer/user. Such repair or replacement shall be free of charge.
Nutricia Medical Devices B.V warrants to the original buer/user, all repaired or replaced pumps to be free from defects
in material and workmanship and will replace or repair such products, at its service facilit or other location designa-
ted b Nutricia Medical Devices B.V. Such repair or replacement shall carr a warrant of ninet (90) das from the
date of repair or replacement or the balance of the new pumps warrant as described above, whichever is greater.
THIS WARRANTy APPLIES ONLy TO FLOCARE® INFINITy™ PUMPS MANUFACTURED By NUTRICIA MEDICAL
DEVICES B.V AND IS THE ONLy WARRANTy GIVEN WITH RESPECT TO THE PUMPS. NO WARRANTIES IMPLIED
IN LAW, INCLUDING, BUT NOT LIMITED TO THE IMPLIED WARRANTIES OF MERCHANTABILITy AND FITNESS FOR
PARTICULAR PURPOSE, SHALL APPLy. NUTRICIA MEDICAL DEVICES B.V WILL BE LIABLE, IN ANy EVENT, ONLy
FOR THE PURCHASE PRICE OF THE DEFECTIVE PRODUCT, BUT NOT FOR ANy CONSEQUENTIAL DAMAGES.
This Warrant ma not be modified, amended or otherwise changed, except b a written document properl executed b a cor-
porate officer of Nutricia Medical Devices B.V
THE WARRANTy IS VOID IF THE FLOCARE® INFINITy™ PUMP IS SUBjECT TO ABUSE, ACCIDENT, ALTERATION, MODIFICATION,
TAMPERING, MISUSE OR THE UNAUTHORIZED REPAIR OR SERVICE IN ANy WAy WITHOUT PRIOR AUTHORIZATION FROM
NUTRICIA MEDICAL DEVICES B.V. IN ANy EVENT, NUTRICIA MEDICAL DEVICES B.V.’S LIABILITy SHALL NEVER EXCEED
THE ORIGINAL PURCHASE PRICE OF THE PUMP AND SHALL NOT EXTEND TO ANy CONSEQUENTIAL LOSS OR DAMAGE.
-67-
UK-IE
ZMNL400336_AW.indd 69 3/18/10 3:47:42 PM

-68-
OPERATING INSTRUCTIONS
INSERTION OF THE FLOCARE®INFINITy™PUMP SET
• Connect the set to the feed container as instructed on the packaging of the Flocare®Infinit™pump set.
Remove the dust cap from the step connector.
• The Flocare®Infinit™pump sets are equipped with an “automatic free-flow protection”, as a consequence
the set has no roller clamp.
Fill the pump set completel with feed b gentl pinching on the side of the cassette that is marked with a
drop (point A on figure 5a) or fill the pump set with help of the pump (see paragraph: filling the pump set).
• Open the pump door b pressing up on the lower wall and rotating the door upwards at the same time
(see figure 5b).
• Position the looped section of the silicone tubing around the rotor.
Stretching lightl, (see figure 5c) seat the cassette into the pump (see figure 5d).
• Close the pump door.
SWITCHING “ON”
For proper pump operation, make sure the pump door is closed prior to switching the
pump on. Press the “ON/OFF” ke for 2 seconds.
The pump beeps and carries out a short self test, showing the pump serial number
in 8 digits. Verif that all displa segments and smbols are active as shown in figure
6 (see next page).
The pump displas the total volume delivered since the memor was cleared and
switches in the hold mode read for programming.
SWITCHING “OFF”
Press the “ON/OFF” ke and keep it pressed for 2 seconds. A continuous alarm will be
heard and the pump switches off.
The feeding program (installed parameters) and total volume administered since the
last clearance will be retained in the pump’s memor.
If the pump shuts down due to low batter voltage, the memor will be retained for
24 hours.
“HOLD” MODE
To temporaril pause the pump, or switch into “hold” mode whilst operating, press the
“START/STOP” ke once. Three beeps are heard and the run smbol disappears.
The programmed flow rate (ml/h), volume (DOSE=VOL) and the administered volume
(ml) are retained.
The “hold” mode is used to temporaril stop the flow of feed:
• to change the feeding program (installed parameters),
• to change the feed container,
ON/OFF
ON/OFF
START/STOP
UK-IE
ZMNL400336_AW.indd 70 3/18/10 3:47:42 PM

-69-
• to administer medication without switching the pump off,
• to silence an alarm and correct problems.
After 3 minutes a two tone audible alarm sounds and the message “PUSH STRT” appears in the displa.
Press “START/STOP” to stop the alarm and to extend the hold mode b a further 3 minutes or press “START/
STOP” twice (3 beeps will be heard) to resume programmed settings.
FILLING THE PUMP SET
The FILL SET function offered b the Infinit pump is used to fill a (new) feeding set with
nutrition (or water as the case ma be). When the FILL SET function runs all alarms
are deactivated helping avoid alarms being inadvertentl triggered (e.g. air alarm).
The FILL SET function should onl be used to fill an empt (air-filled) feeding set. Use
of the FILL SET function at an other time ma cause the pump to incorrectl calibrate.
When the FILL SET function is initiated the pump will calibrate to the giving set.
When the pump is in the hold mode:
Press and hold the “FILL SET” ke for 2 seconds to activate the “FILL SET” maneuver. Release the button as
soon as the pump generates a beep and starts pumping at a flow rate of approx. 700ml/h. During this maneu-
ver the message “FILL SET” appears in the displa. The pump will automaticall stop when the Flocare®Pack
Infinit™pump set is completel filled with feed. However this “FILL SET” maneuver can at antime be stopped
b pushing the “FILL SET” ke a second time. The pump will return to the hold mode when the “FILL SET”
maneuver is complete or stopped.
DISPLAy
The pump has a liquid crstal displa (L.C.D.) with large alphanumeric characters, smaller smbols, words
and a back light.
The following information can be found in the displa:
• Flow rate (ml/h), volume (ml), is displaed through the large characters.
Words below describe what the number relates to (rate, dose or volume).
The pump also displas messages, for example “end of dose” will appear when the pump has finished
delivering a single feed dose.
•The arcs around the run smbol rotate when the pump is
running.
•The remaining batter capacit (see paragraph: batter
operation).
•The wall plug smbol indicates that the charger is plugged in.
The back light of the displa turns off 10 seconds after the last ke is pressed.
The back light will switch on for 10 seconds when the charger is connected to the mains.
Figure 6
ON/OFF
FILL SET
d
UK-IE
ZMNL400336_AW.indd 71 3/18/10 3:47:42 PM

-70-
PROGRAMMING THE PUMP
• The Flocare®Infinit™pump can be used for continuous or dose feeding.
• Insert the pump set in the pump, switch the pump on and fill the pump set when necessar (see para-
graph: filling the pump set).
• The displa shows the total volume delivered since the pump was last cleared.
• If necessar clear the volume delivered b pressing the “CLR” ke.
• The last installed flow rate (ml/h) is now displaed.
• The pump is now in the “hold” mode and is read for programming.
CONTINUOUS FEEDING
• Adust the flow rate (ml/h) if required b using the “+” or “-” ke. Hold either ke down to change rapidl.
• If another parameter is indicated in the LCD, it will be necessar to first press the “ml/h” ke followed b the
“+” or “-” ke to set the flow rate.
• The flow rate ranges from 1 - 400 ml/h in 1ml increments.
• The flow rate slows down and stops shortl at 50 - 125 - 250 ml/h.
• Press the “DOSE=VOL” ke and make sure the value is put at 0 ml indicated b the word “CONT”. This
means the pump will run in a continuous mode.
• Start the pump b pressing “START/STOP”.
• The arcs around the word “run” start rotating.
• The flow rate (ml/h) is displaed whilst functioning.
TO SET A DOSE
From the hold mode, with the last flow rate (ml/h) displaed in the LCD:
• Set the flow rate b pressing the “+” or “-” ke.
If another parameter is displaed:
• Press first the “ml/h” ke followed b “+” or “-” ke to adust the flow rate. The flow rate can be set between
1 and 400 ml/h, with increments of 1ml.
• Press the “DOSE=VOL” ke and install the volume to be administered with the “+” and “-” ke. The range
goes from 1 - 4000 ml, with steps from 1ml.
• Start the pump b pressing “START/STOP”.
During functioning the following parameters can be found in the displa:
• B pressing the “ml/h” ke the “flow rate” is displaed.
• B pressing the “INFO” ke the total volume since the memor was cleared will be
visualized.
When the required volume or dose has been delivered, “END OF DOSE” will appear and the pump will beep
(or mute, depending upon the pumps’ configuration (see paragraph: set up mode).
ON/OFF d d d d d
ml/h START/STOP
400 ml/h
+
1 ml/h
-
4000 ml
+
1 ml
-
DOSE=VOL
ON/OFF d d d ml/h 400 ml/h
+
1 ml/h
-START/STOP
INFO
UK-IE
ZMNL400336_AW.indd 72 3/18/10 3:47:43 PM

TO CHANGE THE FEEDING PROGRAM DURING FUNCTIONING
• Press the “START/STOP” ke to pause the pump.
• Change the program b pressing the required ke (ml/h or DOSE=VOL) and adust using the “+” or “-” kes.
• Restart the pump b pressing the “START/STOP” ke again.
CLEARING THE MEMORy
All parameters and values can be cleared one after the other in the following wa:
• Press “START/STOP” to pause the pump.
• Select the parameter that needs to be cleared.
• Press the “CLR” ke to clear the memor. The parameter or value returns to its default value:
ml/h = 0 ml/h
VOL = cont = No dose set. Pump will feed continuousl until feed container is empt or pump
is stopped
INFO = 0 ml = Volume delivered is cleared
In order to keep a clear overview of the dail amount of feed delivered, clear the total volume delivered as
each dail feeding schedule is started, as follows:
• Switch the pump “ON”
• Immediatel after the self-test the pump displas total volume delivered.
• Press the “CLR” ke. The total volume delivered returns to “0 ml”.
• The pump displas the previous programmed flow rate (ml/h).
• The pump is in the “HOLD” mode read for programming.
• When another feeding program needs to be started, or the pump will be used for another patient, all set-
tings (rate and dose) can be returned to default and the volume delivered can be set at zero b simpl
pressing the “CLR” ke and keeping it pressed for 2 seconds.
BATTERy OPERATION
• The Flocare®Infinit™pump is equipped with a Lithium-ion batter.
• The batter smbol in the displa is automaticall replaced b the plug smbol when the adapter is
plugged in. The “fuel gauge” then indicates that the batter is charging b displaing the segments in
an ascending low to high pattern starting with the leftmost segment.
This pattern continuousl repeats while the pump is charging.
• To check the status of the batter, disconnect the charger from the pump and turn the
pump on. The bars between E and F (E=Empt, F=Full) represent the “fuel gauge” of the
batter. Each bar is approximatel 1/4 of a full batter charge. If 2 bars appear the
batter is half full and remaining operating time is approximatel 12 hours at a flow rate
of 125 ml/h.
• In case of power failure the pump automaticall switches to batter powered operation.
• When during functioning the last block is gone, the batter smbol will blink to indicate that there is approxima-
tel 1 hour of charge left. The displa will flash “BATT” ever 3 seconds, alternating with the active displa and
the pump will beep ever 2 seconds to remind the user of the low batter charge condition. Plug in the charger
to continue to run and recharge the batter.
• As the batter level decreases the pump ma not be able to deliver tube feeds at rates greater than 300 ml/h,
even though some batter capacit remains. The pump will alarm and indicate “BATT”. If this happens, either
-71-
START/STOP
CLR
d
UK-IE
ZMNL400336_AW.indd 73 3/18/10 3:47:43 PM

-72-
recharge the batter or select a lower rate to complete the feed ccle.
• In case of batter failure, caused b, for example, an excessive temperature condition (which ma resolve
itself with time) or b a complete batter failure, the E, F and batter smbol will flash. Turn the pump “off” and
contact our healthcare provider or refer the pump to service.
CONNECTION TO AN EXTERNAL ALARM SySTEM
The power connector at the side of the pump offers the option of connecting the pump to an external alarm
sstem or Patient Data Monitoring Sstem (PDMS).
• The Flocare®Infinit™Nurse Call (corporate code 35752) enables connection to an external alarm sstem.
This external alarm sstem ma be with open or closed contact. Follow the instructions for use of the
Flocare®Infinit™Nurse Call to connect the pump.
• The Flocare®Infinit™PDMS Cable (corporate code 35776) enables connection to an external PDMS
sstem. Follow the instructions for use of the Flocare®Infinit™PDMS Cable to connect the pump.
ALARM FUNCTIONS AND SAFETy FEATURES
In case an of the problems listed on the problem solver chart occur, the pump delivers an audible and visual
alarm and stops working. The back light of the LCD automaticall switches on.
Exception to this is the low batter alarm “BATT”, in this situation the pump continues working.
Action in the event of an alarm:
Check the tpe of alarm displaed b the large displa characters.
• Press the “START/STOP” ke to stop the audible and visual alarm.
• Correct the cause of the alarm as described in the table.
• Start the pump again b pressing “START/STOP”.
The problem solver chart on the next page gives a clear explanation of the alarms.
MAINTENANCE
Cleaning:
• Alwas unplug the pump prior to cleaning to avoid electric shock hazard.
• On a regular basis thoroughl clean all surfaces of the pump (including the sensors and rotor) with warm
soap water, a 5% bleach solution in water, or a multipurpose disinfectant cleaner.
• The Flocare®Infinit™pump ma be rinsed b holding under a stream of warm, clean water. Do not sub-
merge the pump!
• Alwas maintain the rollers on the rotor in a clean state to ensure the spin freel.
• The adaptor normall does not require cleaning. When desired, a dr or slightl damp cloth ma be used
to clean the outside surface of the adaptor. Make sure the adaptor is disconnected from the wall outlet.
Safet notes:
• The manufacturer recommends an inspection of the pump at an authorised service centre ever 2 ears.
• If an fault occurs during use, or if the pump is dropped, it should be checked b authorised technical per-
sonnel prior to use.
• Replace the Flocare®Infinit™pump set ever 24 hours to maintain deliver accurac and prevent the
growth of harmful bacteria. Dispose of Flocare®Infinit™disposable sets properl, as required b local law.
• Do not use the Infinit alarm sstems to trigger actions related to secondar (electrical) medical devices
(e.g. a volumetric or sringe pump).
• Do not use pump functions (e.g. the fill set function) for an other purpose than described in this manual,
as this ma cause the pump to incorrectl calibrate.
UK-IE
ZMNL400336_AW.indd 74 3/18/10 3:47:43 PM

-73-
PROBLEM SOLVER CHART
OCC OUT
(repeated)
NO SET
AIR
PUSH STRT
Condition
END OF DOSE
PROG
DOOR
BATT
the pump
remains working
Batter, “E” and “F”
flashing
FILL SET
OCC IN
OCC OUT
• Calibration not et completed
on the current feeding set
• The set is not fitted or wrongl fitted
in the pump.
• The pressure sensor area is dirt
• The air sensor detected an empt
pump set.
• The air sensor area is dirt.
• The feeding set is not inserted cor-
rectl.
• The pump has been untouched in
hold mode for 3 minutes or more.
Cause
• The pump administered the installed
dose = volume.
• No flow rate is installed.
Flow rate = 0 ml/h
• The door is not correctl closed.
• The batter capacit is too low.
The pump is not able to deliver
highl viscous fluids at high flow
rates with the present charge level
of the batter.
• Batter failure.
• The pump is priming the set.
• The pump detected an upstream
occlusion between the pump and
the feeding bag.
• The pressure sensor area is dirt.
• The pump detected a
downstream occlusion between the
pump and the patient.
• The pressure sensor area is dirt.
• Stop the alarm b pressing the “START/STOP” ke.
• Start the pump b pressing the “START/STOP” ke and
let it run onl briefl.
• Stop the pump b pressing the “START/STOP” ke insu-
ring that there has been no occlusion out alarm.
• Remove the feeding set from the pump and reinsert the
feeding set in the pump.
• Restart the pump b pressing the “START/STOP” ke.
• Stop the alarm b pressing “START/STOP”
• Insert the Flocare®Infinit™cassette into the pump as
indicated on the blister packaging and close the door.
• Restart the pump.
• Clean the sensors, reinsert the cassette in the pump and
restart the pump.
• Replace the empt feeding reservoir and continue feeding.
If necessar prime the set.
• Make sure the air sensor is clean.
• Make sure the feeding set is properl inserted
in the pump.
• Stop the alarm and prolong the hold mode with another 3
minutes b pressing “START/STOP” ke.
• Program the pump and start it b pressing the “START/
STOP”.
Correction
• Turn the pump off b pressing the “ON/OFF” ke
and hold it during 2 seconds or
• Clear the memor of the total volume administered (see
paragraph: clearing the memor), reprogram a new fee-
ding schedule and start the pump b pressing “START/
STOP”.
• Make sure the correct flow rate is programmed.
• Make sure the door is properl closed prior to
starting a feeding program.
• Connect the adaptor to the pump and mains and charge
the pump for approx. 6 hours. During charging the pump
can be used.
• Turn the pump “off”, contact our healthcare provider or
refer the pump to service.
• Press the “FILL SET” ke another time to stop the pump
and bring it back in the hold mode.
• Stop the alarm b pressing the “START/STOP” ke.
• Remove the feeding set out of the pump and check the
permeabilit b flushing the line.
• Re-insert the feeding set in the pump and restart.
• Clean the sensors, reinsert the cassette in the pump and
restart the pump.
• Stop the alarm b pressing the “START/STOP” ke.
• Check the permeabilit of the feeding tube b
aspirating liquid via the medication port.
• Clean the sensors, reinsert the cassette in the pump and
restart the pump.
UK-IE
Alwas follow the instructions below in case a problem occurs.
Using methods other than those described ma cause the pump to function incorrectl.
ZMNL400336_AW.indd 75 3/18/10 3:47:43 PM

-74-
SET UP MODE
The set up mode is used • to set the alarm level,
• to lock the kepad,
• to switch the audible alarm off when a dose is administered,
• to switch the light of the LCD permanentl on when connected to the mains,
• to enable connection with a Nurse call or Patient Data
Monitoring Sstem (PDMS).
This set up mode ma onl be entered b healthcare professionals and authorised personnel trained to use
this application of the pump.
The patient or his/her relatives without permission of the phsician, dietician, nurse or other licensed practi-
tioner, ma not change the settings of the set up mode.
TO SET THE ALARM LEVEL
Switch the pump “on” while holding the “+” ke down. The pump enters the set up mode.
First the alarm level can be set:
“BEEP HIGH” (+) or “BEEP LOW” (-)
Use the “+” or “-” ke to change the setting from “high” to “low” or from “low” to “high”.
TO LOCK THE KEyPAD
Press in the set up mode the “FILL SET” ke to switch to the next setting:
“UNLK” the kepad (-) or “LOCK” the kepad (+). In the “LOCK” mode the feeding program of the pump
can no longer be changed.
Use the “+” or “-” ke to change the setting from “lock” to “unlk” or vice versa.
ON/OFF &dBeep high
+Beep low
-
+
2 sec 2 sec
FILL SET dLock
Unlk
-
+
ER01 - ER99
No plug smbol visi-
ble, while the pump
is connected to the
mains.
Condition
LOCK
• The self test detected an electronic
error
• The wall outlet doesn’t work.
• The adaptor is damaged.
Cause
• Onl the current feeding
schedule is allowed for this patient.
Another feeding program is not
allowed b our healthcare profes-
sional.
• Turn the pump “off”, make sure the pump door is closed
and switch the pump back “on”. If the error persists,
contact our healthcare provider or refer the pump to
service.
• Connect the pump to another wall outlet.
• Contact our healthcare professional or
Nutricia subsidiar to replace the adaptor.
Correction
• The programming feature is blocked in the set up mode
of the pump. Ask our healthcare professional to modif
this setting.
UK-IE
ZMNL400336_AW.indd 76 3/18/10 3:47:43 PM

TO MUTE WHEN DOSE DONE
Press in the set up mode the “FILL SET” ke to switch to the next setting:
“BEEP WHEN DONE” (+): the pump will give an alarm when the dose is administered or “MUTE WHEN
DONE” (-): the pump will not give an alarm after administering the dose. Use the “+” or “-” ke to change
the setting from “beep when done” to “mute when done” or vice versa.
TO SWITCH LIGHT ON
Press in the set up mode the “FILL SET” ke to switch to the next setting:
“LITE ON” (+) the light of the LCD remains on when the pump is connected to the mains. “LITE OFF” (-) the
light of the LCD switches off after a few seconds even if connected to the mains. Use the “+” or “-” ke to change
the setting from “lite on” to “lite off” or vice versa.
TO CONNECT WITH NURSE CALL OR PDMS
Press in the set up mode the “FILL SET” ke to switch to the next setting:
“OUTP PDMS” (+) to connect with a Patient Data Monitoring Sstem. “OUTP NRSE” to connect with a NURSE
CALL sstem. Use the “+” or “-” ke to change to setting from “OUTP PDMS”, to “OUTP NRSE” or “OUTP
OFF” and vice versa.
Press the “ON/OFF” ke and hold it down for 2 seconds to exit the SET UP mode. The settings are auto-
maticall saved.
TECHNICAL SPECIFICATIONS
•This Flocare®Infinit™pump in combination with the adapter and the Flocare®Infinit™Nurse Call are designed
to EN 60601-1-2, EN 61000-3-2, EN 61000-3-3, RTCA DO-160D standards for electromagnetic emissions
and immunit and are in compliance with Directive 93/42/EEC.
0344
•IEC 601: Class II Medical Device Directive: Class IIa
•Microprocessor controlled
•BF Equipment
• Charger: input 100-240V AC / 50-60 Hz / 0.4A Max.
output 5 V DC 2.4 A
•Batter: internal rechargeable Lithium ion batter, 3.6 V DC 2000 mAh
• Batter capacit: 24 hours at 125 ml/h
•jet waterproof: IPX 5
•IPX 5: Splash water proof: Water ets from an direction shall have no effect on the pump.
-75-
FILL SET dBeep when done
Mute when done
-
+
FILL SET d d
OUTP PDMS
OUTP NRSE
-
+ON/OFF
2 sec
FILL SET d d
Lite on
Lite off
-
+ON/OFF
2 sec
UK-IE
ZMNL400336_AW.indd 77 3/18/10 3:47:43 PM

-76-
•Dimensions: 140 x 95 x 35 mm
• Weight: approx. 392 g
• Accurac flow rate: ±5,0% with appropriate Flocare®Infinit™pump set
• Humidit: Operation mode: 30% to 75% noncondensing
Storage: 10% to 95 % noncondensing
• Temperature: Operation mode: +5°C to +40°C
Storage and transportation: -20°C to +65°C
• Atmospheric pressure: Operation mode: 70-106 kPa
Storage and transportation: 50-106 kPa
• Occlusion detection pressure: Upstream occlusion: -34 kPa (tolerance 21 kPa)
Downstream occlusion: 83 kPa (tolerane 21 kPa)
• Air bubble detection: The amount of air, that must pass the air sensor before the air alarm is activated, varies
from 0.5 to 1 ml which relates to an air bubble with an approximate length in the silicone pump segment of
6 - 13 cm.
• The Flocare®Infinit™can safel be operated on commercial aircraft.
• The use of other accessories, adaptors and cables than listed within this manual ma result in increased
emissions or decreased immunit of the equipment of the Flocare®Infinit™pump.
• Medical electrical equipment needs special precautions regarding EMC and needs to be installed and put
into service according to the EMC information provided in the accompaning documents.
• Portable and mobile RF communications equipment (cellular telephones) can affect medical electrical equip-
ment. If the Flocare®Infinit™pump is used adacent to or stacked with other equipment, the pump should
be observed to verif normal operation.
• In case of pump scrapping, alwas notif our Nutricia sales unit of the pumps serial number. Pump scrap-
ping should alwas occur according to local legislation.
UK-IE
ZMNL400336_AW.indd 78 3/18/10 3:47:43 PM

-77-
ZMNL400336_AW.indd 79 3/18/10 3:47:43 PM

-78-
Emissions test Compliance Electromagnetic environment – guidance
Guidance and manufacturer’s Declaration – Electromagnetic emissions
Immunit test IEC 60601 test level Electromagnetic environment – guidance
Guidance and manufacturer’s Declaration – Electromagnetic immunit
Compliance level
161 Vac for 0,5 s
95 Vac for 100 ms
0 Vac for 10 ms
0 Vac for 5 s
161 Vac for 0,5 s
95 Vac for 100 ms
0 Vac for 10 ms
0 Vac for 5 s
APPENDIX A: GUIDANCE AND MANUFACTURER’S DECLARATION -
ELECTROMAGNETIC COMPATIBILITy
The Flocare®Infinit™enteral feeding pump is intended for use in the electromagnetic environment specified below.
The customer or the user of the Flocare® Infinit™ enteral feeding pump should assure that it is used in such an
environment.
RF Emissions
CISPR 11
Group 1 The Flocare®Infinit™uses RF energ onl for its internal
function. Therefore, its RF emissions are ver low and are
not likel to cause an interference in nearb electronic
equipment.
RF Emissions
CISPR 11
Class B
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/
Flicker emissions
IEC 61000-3-3
Complies
The Flocare®Infinit™is suitable for use in all
establishments, including domestic establishments and
those directl connected to the public low-voltage power
suppl network that supplies buildings used for domestic
purposes.
The Flocare®Infinit™enteral feeding pump is intended for use in the electromagnetic environment specified below. The
customer or the user of the Flocare®Infinit™enteral feeding pump should assure that it is used in such an environment.
Electrostatic
discharge (ESD)
IEC 61000-4-2
≤ 6 KV contact
≤ 8 KV air
Floors should be wood, concrete or ceramic tile.
If floors are covered with snthetic material, the
relative humidit should be at least 30%.
≤ 6 KV contact
≤ 8 KV air
Electric fast
transient/burst
IEC 61000-4-4
≤ 2 KV for power sup-
pl lines
≤ 1 KV for input/ out-
put lines
Mains power qualit should be that of a tpical
commercial or hospital environment.
≤ 2 KV for power sup-
pl lines
≤ 1 KV for input/ out-
put lines
Surge
IEC 61000-4-5
≤ 1 KV differential
mode
Mains power qualit should be that of a tpical
commercial or hospital environment.
≤ 1 KV differential
mode
Voltage dips, short
interruptions and
voltage variations on
power suppl lines.
IEC 61000-4-6
Mains power qualit should be that of a tpical
commercial or hospital environment. If the user
of the Flocare®Infinit™requires continued
operation during power mains interruptions, it is
recommended that the Flocare®Infinit™enteral
feeding pump be powered from an uninterrupti-
ble power suppl of batter.
ZMNL400336_AW.indd 80 3/18/10 3:47:44 PM

-79-
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres
(m) can be estimated using the equation applicable to the frequenc of the transmitter, where Pis the maximum output
power rating of the transmitter in Watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequenc range applies.
NOTE 2 These guidelines ma not appl in all situations. Electromagnetic propagation is affected b absorption and
reflection from structures, obects and people.
0,01 0,01 0,01 0,02
0,1 0,04 0,04 0,07
10,12 0,12 0,23
10 0,37 0,37 0,74
100 1,17 1,17 2,33
The Flocare®Infinit™enteral feeding pump is intended for use in an electromagnetic environment in which radiated RF dis-
turbances are controlled. The customer or the user of the Flocare®Infinit™can help prevent electromagnetic interference
b maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the
Flocare®Infinit™as recommended below, according to the maximum output power of the communications equipment.
Rated Maximum output
power of transmitter
(W)
Separation distance according to frequenc of transmitter (m)
Recommended separation distances between portable and mobile RF communications euipment and the
Flocare®Infinit™enteral feeding pump
150 KHz to 80 MHz
d = 0,12CD
P
80 MHz to 800 MHz
d = 0,12CD
P
800 MHz to 2,5 GHz
d = 0,23CD
P
Portable and mobile RF communications equi-
pment should be used no closer to an part of
the Flocare®Infinit™, including cables, than the
recommended separation distance calculated
from the equation applicable toe the frequenc
of the transmitter:
Recommended separation distance
Where Pis the maximum output power rating
of the transmitter in watts (W) according to the
transmitter manufacturer and d is the recom-
mended separation distance in metres (m).
Field strengths from fixed RF transmitters, as
determined b an electromagnetic site surve,a
should be less than the compliance level in
each frequenc range.b
Interference ma occur
in the vicinit of equipment
marked with the following
smbol:
Conducted RF
IEC 61000-4-6
3 Vrms
150 KHz to 80 MHz
d= 1,17CD
P
3 Vrms
150 KHz to 80 MHz
Radiated RF
IEC 61000-4-3
3 V/m
80 Mhz to 2,5 GHz
d= 0,12CD
P
d= 0,23CD
P
80 MHz to 800 MHz
800 MHz to 2,5 GHz
30 V/m
80 Mhz to 2,5 GHz
a. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile
radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoreticall with accurac.
To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site surve should be
considered. If the measurement field strength in the location in which the Flocare®Infinit™is used exceeds the appli-
cable RF compliance above, the Flocare®Infinit™should be observed to verif normal operation. If abnormal perfor-
mance is observed, additional measures ma be necessar, such as reorienting or relocating the Flocare®Infinit™.
b. Over the frequenc range 150 KHz to 80 MHz, field strengths should be less than 3 V/m.
NOTE 1 At 80 Mhz and 800 MHz, the higher frequenc range applies.
NOTE 2 These guidelines ma not appl in all situations. Electromagnetic propagation is affected b absorption and
reflection from structures, obects and people.
The Flocare®Infinit™enteral feeding pump is intended for use in the electromagnetic environment specified below. The
customer or the user of the Flocare®Infinit™enteral feeding pump should assure that it is used in such an environment.
Guidance and manufacturer’s Declaration – Electromagnetic immunit
Immunit test IEC 60601 test level Electromagnetic environment – guidanceCompliance level
ZMNL400336_AW.indd 81 3/18/10 3:47:44 PM

-80-
ZMNL400336_AW.indd 82 3/18/10 3:47:44 PM