Perfusor® compact S

Instructions for Use

Software BE

Attention: Consult accompanying documents !

Operation➤ Ensure the unit is properly positioned andsecured.➤ Prior to use check audible and visual alarmsduring self test. Also check the device for possi-ble damage.➤ Connect to patient only after switching onthe device. Interrupt the connection duringsyringe changes to prevent incorrect dosedelivery.➤ Select syringe/catheter suitable for use withthe intended medical application.➤ Position the infusion line free of kinks.➤ Recommended change of disposables after24 h (consider national hygiene regulations).➤ Installation in medically used rooms mustcomply with the appropriate regulations (e.g.VDE 0100, VDE 0107 or IEC-publications).Observe national specifications and deviations.➤ Possible explosion hazard if used inpresence of flammable anaesthetics.➤ Compare displayed value with enteredvalue. Start infusion only if values arecorresponding.➤ Do not use the device when serviceindicator is displayed permanently.➤ If staff call is used we recommend to checkthe equipment once after connecting the pump.➤ Protect the device against moisture.

Other components➤ Variations in pressure (e.g. as caused bychange of level) can affect the accuracy of thedevice.➤ Where several infusion lines are connectedon one single vascular access the possibility oftheir exerting a mutual influence vice-versacannot be excluded.

➤ Refer to respective manufacturer’s informa-tion for possible incompatibilities of equipmentresp. drugs.➤ Use only compatible combinations ofequipment, accessories, working parts anddisposables.➤ The use of not recommended resp. incom-patible disposables may influence the technicalspecifications.➤ Connected electrical equipment must com-ply with the relevant IEC/EN-pecifications (e.g.IEC/EN 60950 for data-processing equipment).The user/operator is responsible for the systemconfiguration if additional equipment is con-nected. The international standard IEC/EN60601-1-1 has to be taken into account.

Safety StandardsPerfusor® compact S satisfies all safety stan-dards for medical electrical devices in compli-ance with IEC/EN 60601-1 and IEC/EN60601-2-24.➤ The EMC-limits (electro-magnetic compati-bility) according to IEC/EN 60601-1-2 andIEC/EN 60601-2-24 are maintained. If theequipment is operated in the vicinity of otherequipment which may cause high levels ofinterference (e.g. HF surgical equipment,nuclear spin tomography units, mobile tele-phones etc.) maintain the recommended pro-tective distances for these devices.

Read Instructions for Use prior to use. Application only under regularly supervision by speciallytrained staff.

Patient Safety

Perfusor® compact S

Contents

Perfusor® compact S / Overview Page 4

Operation Page 6

Special Functions Page 8

Start-up and Trumpet Curves Page 10

Alarms / Displays Page 11

Battery Operation Page 14

Compatible Syringes Page 15

Technical Data Page 19

Warranty / TSC / Service / Cleaning Page 21

Ordering Page 22

The Perfusor® compact S is according toIEC/EN 60601-1 resp. IEC/EN 60601-2-24 atransportbale infusion syringe pump foradministrating fluids in nutritional therapy andinfusion technique as well as for home careapplications. The medical specialist must decideon suitability for application on the basis of thewarranted properties and the technical data.

For further details please refer to theInstructions for Use.

3

Overview

4

HandleAlways use the handle when carrying.

DisplayShows all importantinformation at aglance: rate, syringetype, power source,infusing symbol and alarm symbols(see "Alarms” onpage 11).

Battery CompartmentDisconnect the pump from thepatient while changing thebattery. Switch off the device.Remove screw (1), press in thegreen tab (2) and slidecompartment door down.Always change all batteries.Taking care to observe wastedisposal regulations (see alsopage 21).

Instructions for Useand Syringe TableSlide-out shortinstructions for Useand a syringe table areattached underneaththe pump.

OperationTo access functions, first press the F button

Mains ConnectionConnection for the power supply. In the event of power failure,the pump automatically switches to battery power.

Syringe HolderLocks the syringein place.To remove, pulland turn to theleft.

Syringe Adapter

Locking LeverTo move the driveunit manually, pushthe locking lever upuntil it clicks.

Multi-FunctionConnector (MFC)Connection for staffcall, ambulance (12 V)and interface.

(2)

(1)

5

Special Functions / Function keyFirst press F to access the special functions ofthe pump (= Select / Enter key).

Clear data

Decimal point Alarm indicator

Alarm silence for 2 min.

ON/OFF. Press for 2 sec. to turn off.

Start/Stop Infusion

TransportA maximum of three devices may be connectedtogether. Special care is required here if apatient is already connected. Avoid externalmechanical influence!

Locking Devices TogetherPlace one device on top of the other. Push con-necting rod of top pump down into the slot ofthe pump below until it clicks into place.To lock, turn the "key” until it is vertical.To disconnect, turn the "key” until it ishorizontal. Push the white key in and slide up.

Pole ClampAttach the Perfusor® compact S from above,clicking it into place. To release, press the blackbutton and lift the pump from the clamp. Forsafety purposes attach each device separately tothe IV pole. A rotating pole clamp can be usedfor a vertical fixation of the Perfusor®compact S, as available.

Infusion

1. Insert Syringe➤ Switch on using . Note the automaticself-check: All display elements will appear forapprox. 2 seconds and the audible alarm willsound.- Then the rate display shows:

111.1 222.2 555.5- Then the software version: BE.In addition, the , CC, and decimalpoint will blink.➤ Open the syringe holder, slide the lockinglever up and extend the drive unit.Align the primed syringe so the flange ispositioned in the syringe grip plate, and the topof the plunger is positioned in the syringepressure plate.Press the syringe in. The locking lever shouldsnap back on its own. Close the syringe holder.The syringe code displayed must match that ofthe syringe inserted. (Ref. to the guides attachedunderneath the pump. If the code does notmatch the syringe type inserted, see SyringeTables/-Compatibilities, page 16 ff).

➤ If syringe type code is correct, press F.

➤ Prime the line by using the BOL-key. (Primerate = adjusted bolus rate.) Press F, then BOLonce. The bolus rate will blink. Press and holdBOL key again until the line is primed (max. 1ml respectively for 10 seconds can be delivered).If applicable, repeat priming with BOL key.(During STOP, the infused bolus volume is notadded to TOTAL volume.)

2. Setting the Rate➤ Enter between 0.01 and 200.0 ml/h1)

(e.g. enter 2,56 ml/h press 2 - . – 5 – 6).Check display. To correct:Press C and enter the new rate.

3. Start the Infusion➤ Press START. Rotating infusion symbol isdisplayed.

4. Stop the Infusion➤ Press STOP or for 2 seconds.Disconnect from the patient.

➤ Open the syringe holder. Remove the syringe.

➤ To switch off, press for 2 seconds.

To Change Syringes➤ Press STOP.Disconnect from the patient!

Operation

6

Syringe grip plate 2) Syringe PressurePlate 2)

insert here

Here only insert a 50 ml OriginalPerfusor Syringe (OPS).

Syringe grip plate insert here(all syringes except OPS 50 ml)

Movable DriveMechanism 2)

Locking Lever Syringe Holder

1) See Technical Data2) If syringe is out of alignment at the grip plate and the pressure plate, free flow cannot be excluded. Do not carry the device

during operation by the movable drive mechanism.

➤ Open syringe holder and remove the syringe.Insert a new primed syringe with primed tubing.

➤ Close syringe holder.

➤ Confirm the type of syringe by pressing F.

➤ Connect to patient and press START.

To change the rate

➤ Press STOP.

➤ Press C and enter the new rate.

➤ Press START.

To Change the Rate Without Interrupting theInfusion (Titration)While the infusion is in process: simply press Cand enter new rate, then confirm by pressing F.The new rate now applies. (If F is not pressedafter making the rate change, the display willrevert to the previous rate after 10 seconds.)

7

Syringe SelectionOpen the syringe holder, press thesyringe code blinks. Press C, enter a new syringecode and confirm by pressing F. Close syringeholder and start infusion. Double-check the newsyringe code while infusion is taking place bypressing F and .

BolusTo alter the bolus rate (only when device isstopped):Press F, then BOL. The bolus rate will blink.Press C, set new bolus rate and confirm with F.If bolus rate is set to zero, the bolus and primefunction is switched off.(Bolus and prime rate are identical).

Bolus applications during infusionOption A: Bolus with pre-selected volumePress BOL. The bolus rate will blink. Press C, setvolume (in 0.1 ml steps) and confirm with F.The bolus volume infused will be displayed (max.value corresponds to the syringe size in use).Press any key to stop bolus infusion.

Option B: Bolus on demandPress BOL once, bolus rate is blinking, thenpress and hold BOL again as long as bolusadministration is required (max. bolus allowed is10 % of syringe size or 10 seconds).An audible signal will be given for each mldelivered. Take care not to overdose! Given abolus rate of 800 ml/h, e.g. 0.1 ml will bereached in just 0.45 seconds. During bolus no

syringe pre-/end alarm is given.

StandbyPress F, then STANDBY. and F are displayed,and the infusion is paused indefinitely. Set val-ues are retained. Pressing F again cancels theStandby.

Total Volume InfusedShows the volume already infused. If thisexceeds 999.9 ml this max. value blinks. To clearthe total to 0.0 ml, press C or switch device off.

Volume To Be Delivered (VTBD)Press F, then and enter the volume tobe delivered, confirm value with F. After VTBDhas been set -symbol flashes. Duringinfusion, VTBD counts down. Infusionautomatically stops when VTBD is reached.

Clear VTBD: Press F, then and press C.The display shows: ---.- (for unlimited infusion).Press F to accept or enter new VTBD.

Note: Clearing VTBD also clears the TimeLimitation.

Check remaining VTBD during infusion:Press F and . The remaining amount ofVTBD is displayed.

Note: Bolus infusions influence the VTBD. If arate and VTBD are set, the remaining time ofinfusion is automatically calculated and can be

Special Functions

8

➤ Activate the special functions by pressing the F button (F is shown in the display).➤ During infusion, only statuses can be checked. Excluding rate titration and data lock, changesin values can be made only when the pump is stopped.➤ Use the F button to confirm input values or to exit the function.➤ If a set value is higher than the possible limit, the max. possible value is shown, an alarm willsound. The value can be accepted by pressing the F button. After the device is switched off, allvalues are cleared.

checked during operation (press F andas well as in STOP mode.

Time LimitationPress F, then and enter the requiredtime limitation, confirm value with F. After atime has been set the -symbol flashes.During infusion, the time counts down. Infusionautomatically stops after the time has beenreached.

Clear time: Press F, then and press C.The display shows: --:-- (for unlimitedinfusion). Press F to accept or enter new time.

Note: Clearing the time also clears the VTBD.

Check remaining time during infusion:Press F and The remaining infusion timeis displayed.

Note: If a rate and time are set, the remainingVTBD is automatically calculated and can bechecked during operation (press F and )as well as in STOP mode. Bolus applications andrate changes also will change the time value,based on the remaining VTBD and the set rate.

Volume Over Time (automatic calculation ofthe rate):Set rate to zero. Set VTBD and time values (seedescriptions above). After both values have beenconfirmed by pressing F, the calculated infusionrate is blinking in the display. Start infusionwith START/STOP key.

Note: A change of the rate also will change thetime value, based on the new rate and theremaining VTBD. If the calculated rate is cleared,the time is cleared automatically, but not theremaining VTBD. VTBD only will be cleared after

a new time has been set and the rate has beenset to zero.

Data LockWhen e.g. rate and VTBD or time are set, pressand hold F key; also press data lock key at thesame time. Now all pump data are locked andthe display alternately shows LOC and thecurrent rate. Press START/STOP key to start theinfusion.

Note: When data lock is active, no values canbe changed and the bolus function is switchedoff. It is only possible to stop or to start thedevice.

To deactivate data lock: Press and hold F keyand also press data lock key at the same time.

Note: Data lock may be activated anddeactivated in either STOP Mode or whileinfusion.

Battery CapacityShows the remaining capacity of the battery:

low, medium, high.

The LCD shows: "000b" when using standardbatteries. "xxxA", ” when using rechargeablebatteries. "xxx" = capacity in mAh.

To change Occlusion SensitivityIn case of an occlusion the device goes intoalarm. As lower the pressure setting as fasterthe time to occlusion alarm.

Press F, then Press 1 (low), 2 (medium)or 3 (high), then press F to confirm settings.During an occlusion alarm, the bolus volumebuilt up by the pump is automatically reduced.

9

Start-up and Trumpet Curves

10

The graphs show the accuracy/uniformity of flow in relation totime. Allow for the following:

The delivery behaviour or delivery precision is essentiallyinfluenced by the types of (disposable) syringe used.Significant deviations may be encountered if use is made of(disposable) syringes other than those stated in the order data.

Trumpet CurvesMeasured values for second and last hour in each case.Measurement interval ∆t = 0.5 minObservation interval p x ∆t [min]

Start-up CurvesMeasurement interval ∆t = 0.5 minMeasurement duration T = 120 minFlow Qi (ml/h)

Alarms / Displays

11

Device alarm

➤ During an alarm the -symbol, and one or more of the following symbols will blink.

Symbol / Cause

Display message e.g. "071” andpermanent audible alarm signal. Unit defective,internal device failure.

Symbol / Cause

Battery flat, battery near flat warningbegins 30 min before the battery is dead.

Pressure alarm e.g. because of anocclusion.Fluid is unable to be infused.

Reminder: Data input has not beenentered within 2 min, also pre-alarms areindicated via this symbol.

Correction

Connect to mains and/or replace the alkalinebatteries.

Bolus reduction is automatically initiated by thepump. Check for kinks in tubing, IV patency andfilter patency. Increase occlusion pressure ifnecessary. Check if syringe is empty. Due tovarying syringe tolerances, a pressure alarm mayoccur when the syringe is empty prior to end ofinfusion alarm.

Enter data where indicated.

Prepare to end infusion or to begin nextinfusion. Due to syringe tolerances, some fluidmay be left in the syringe when pump goes into"end of infusion alarm”. At "end of infusionalarm”, the pump goes into an audible alarmdependent on the adjustment in the servicemenue. If some fluid is left in the syringe after"end of infusion alarm” appears, the pumpcontinues to deliver until pressure alarmappears.

Operation alarm

Syringe near empty.Alarm will sound 3 min before syringe is empty(only black syringe field is blinking) resp. end ofinfusion.

Correction

Press and hold ON/OFF key for at least3 seconds until the alarm symbol in the displayis extinguished. Then release the key and switchon the device again. If the unit defective alarmappears again, take the device to service.

Alarms / Displays

12

Symbol / Cause

+ Automatic bolus reduction has beeninterrupted. Bolus has to be reduced manually.

Locking lever at the drive head hasnot clicked into place.

Preset VTBD and/or TIME have beenreached.

Alarm silence: Interrupts the alarmfor a period of 2 min.

Correction

Reduce bolus by disconnecting the infusion linefrom the patient and open the locking lever.

Ensure plunger head is securely positioned inthe syringe pressure plate and the locking leverhas engaged.

Clear VTBD or TIME for unlimited infusion or setnew values.

Operation alarm

Device alarm

Syringe holder not closed.

Set rate required prior to START.Rate has not been set prior to start.

Top of the plunger is improperlypositioned in the syringe pressure plate

Ensure top of syringe plunger is securelypositioned in the syringe pressure plate.

Symbol / Cause Correction

13

Special function is active

Mains / AC power operation

VTBD and/or TIME have been entered.

+ Service indicator blinks when theservice interval has elapsed.

Infusion control:Rotates to show an infusion inprogress.

Displays

General InformationThe Perfusor® compact S is equipped with fourAA non-rechargeable standard batteries (alkali-manganese).

Alternatively, a rechargeable NiCd-battery packfrom B. Braun can be used. This battery pack ischarged by the device during connection tomains.

To ensure safe and reliable battery operation,certain rules of application must be noted:➤ The battery indicator display is a trenddisplay (low, medium, high).➤ The actual battery life available may varydue to

• different battery manufacturers• temperature• varying load (e.g. frequent boluses).

➤ Batteries can explode or leak causingdamage if

• they are opened or burned,• they are inserted incorrectly,• old and new batteries are inserted together or• different brands of batteries are inserted

together.➤ Batteries should be removed from the deviceduring long periods of non-use (storage >3 months).If the batteries are removed from the devicewhile infusing and subsequently a new batteryset is put in, the Perfusor® compact S goes intoalarm (message: "022” is displayed in combina-tion with the alarm symbol). This is a safetyprecaution, as the electric safety systemsuspects a defect in the battery compartment(e.g. loose contact or corroded contacts). Inorder to switch off the alarm, press and holdON/OFF key for at least 3 seconds until thealarm symbol in the display is extinguished.Release the key. Then again switch on the devicein battery mode.

➤ Batteries should be replaced when a "batteryflat” alarm occurs during frequent boluses, orafter 2 years, even if the battery capacitydisplay indicates "full”.➤ During the automatic self-check, the pumpdetermines if the internal energy supply iscapable of sounding a power-failure alarm.If the energy source is exhausted, an alarm isproduced. In this case, the operator may onlyuse the device under constant supervision, sincea power failure would remain undetected by thedevice.➤ Only alkali-manganese batteries may beplaced in the battery compartment because

• Alkali-manganese batteries recommended are free of mercury and cadmium.

• Conventional carbon-cell batteries give an incorrect reading on the capacity display and therefore, cannot guarantee reliable operation.

• NiCd rechargeable batteries must not be connected to the battery contacts as their various physical properties disrupt the alarm.

Attention:After exchange of non-rechargeable batteries,the device has to be switched on once in thebattery mode. The capacity now is detected dur-ing the self-check; the battery symbol in thedisplay displays the actual capacity. If thePerfusor® compact S is switched on after beingconnected to AC power, the symbol "batteryflat” blinks despite having "full” batteries.

14

Battery Operation

Operating Timeswith Standard and Rechargeable Batteries at max. pressure level

15

Compatible Syringes

The syringe types listed in the following tablescan be used with the Perfusor® compact S. Thetables include the Code Number1) of syringebrands which can be selected via the syringeselection key (see page 8).

Please reference the tables below for specificsyringe brand compatibility (e.g. Cat. Nos2)).Note also additional information is providedregarding syringe "near empty” warning foreach syringe size.

The table shows the minimum filling volume(Min. Vol.3)) and the maximum delivery rate(Max. Rate4)) requirements to guarantee3 minute syringe "near empty” warning (presyringe alarm).

The bolus volumes (Bolus Vol.5)) have beenmeasured in the lowest and highest pressuresettings (P1/P3) after the automatic reductionof the post occlusion bolus. The Times toOcclusion6) alarm have been measured at5.0 ml/h. The measured data are typical averagevalues which can vary because of possiblesyringe tolerances.

16

Compatible Syringes

Omnifix2 ml

2461 7029

0.57.0typ.

0.0320.079typ.

00:3801:36

Omnifix5 ml

5461 7053

1.219.2typ.

0.0580.096typ.

01:0102:00

Omnifix10 ml

10461 7100

2.132.0typ.

0.0570.173typ.

01:0303:29

Omnifix20 ml

22461 7207

5.393.4typ.

0.1280.233typ.

02:2605:23

Omnifix30 ml

30461 7304

5.997.9typ.

0.1230.272typ.

02:4908:20

Omnifix50 ml

52461 7509

7.2117.0typ.

0.2250.264typ.

06:2518:13

OPS20 ml

20872 8615

4.478.5typ.

0.1190.218typ.

02:1804:21

OPS50 ml

50872 8810

9.6164.4typ.

0.3050.369typ.

06:2518:13

Proinjekt50 ml

51872 8917

7.1127.0typ.

0.2900.329typ.

04:1817:58

Syringe TypeB. BraunCode No1)

Cat. No.2)

Min. Vol.3) [ml]Max. Rate4) [ml/h]Bolusvolumina5)

P 1 [ml]P 3 [ml]Time to Occl.6)

P 1 [mm:ss]P 3 [mm:ss]

Manufacturer: B. Braun

Manufacturer: B. Braun

Syringe TypeB. BraunCode No1)

Cat. No.2)

Min. Vol.3) [ml]Max. Rate4) [ml/h]Bolusvolumina5)

P 1 [ml]P 3 [ml]Time to Occl.6)

P 1 [mm:ss]P 3 [mm:ss]

17

Manufacturer: TYCO EU

Monoject6 ml5.2

8881-716008

1.216.0typ.

0.0190.068typ.

00:4402:20

Monoject12 ml

158881-

5128782.742.5typ.

0.0290.101typ.

01:5005:20

Monoject20 ml

268881-

5206575.593.0typ.

0.0640.129typ.

02:3007:20

Monoject35 ml

358881-

5357628.5

145.0typ.

0.1230.360typ.

04:3016:00

Monoject50/60 ml

628881-

5601258.6

144.0typ.

0.0780.185typ.

04:2215:56

Syringe TypeTYCO USACode No1)

Cat. No.2)

Min. Vol..3) [ml]Max. Rate4) [ml/h]Bolusvolumina5)

P 1 [ml]P 3 [ml]Time to Occl.6)

P 1 [mm:ss]P 3 [mm:ss]

Manufacturer: TYCO USA

*) To use only with a special syringe adapter (Cat. No. 34506659). This adapter also is usable for all furthersyringe types (exchange via service, see page 4)

Monoject3 ml3.4

1100-603495

1.1013.6typ.

0.0230.050typ.

01:0401:47

Monoject6 ml5.4

1100-606159

1.1616.9typ.

0.0270.053typ.

00:4601:34

Monoject12 ml

161100-

6121732.5140.5typ.

0.1070.199typ.

02:1304:16

Monoject20 ml

291100-

6200363.3651.2typ.

0.2120.332typ.

04:0707:21

Monoject35 ml

391100-

6354308.33144.8typ.

0.3710.465typ.

07:5513:30

Monoject50/60 ml*)

551100-

6500908.54143.2typ.

0.5040.376typ.

10:5714:12

Syringe TypeTYCO EUCode No1)

Cat. No.2)

Min. Vol..3) [ml]Max. Rate4) [ml/h]Bolusvolumina5)

P 1 [ml]P 3 [ml]Time to Occl.6)

P 1 [mm:ss]P 3 [mm:ss]

18

Compatible Syringes

3 ml3.1

SS*03L0.712.1typ.

0.0090.031typ.

00:5201:43

5 ml5.1

SS*05L1.323.3typ.

0.0120.066typ.

00:3502:16

10 ml13

SS*10L1.7

22.0typ.

0.0510.050typ.

01:4403:02

20 ml23

SS*20L3.8

69.7typ.

0.0190.052typ.

01:0404:08

30 ml32

SS*30L4.377.6typ.

0.0810.196typ.

02:5709:48

50 ml54

BS-50LG5.189.6typ.

0.1140.137typ.

05:4415:19

60 ml60

SS*60L5.290.7typ.

0.0380.135typ.

02:1912:55

Syringe TypeTerumoCode No1)

Cat. No.2)

Min. Vol.3) [ml]Max. Rate4) [ml/h]Bolusvolumina5)

P 1 [ml]P 3 [ml]Time to Occl.6)

P 1 [mm:ss]P 3 [mm:ss]

Manufacturer: Terumo

Plastipak3 ml3.3

309585300910

0.710.4typ.

0.0080.038typ.

00:1200:31

Plastipak5 ml5.3

309603300911

1.321.0typ.

0.0380.059typ.

00:5601:26

Plastipak10 ml

11309604300912

2.034.5typ.

0.0280.079typ.

00:2901:26

Plastipak20 ml

24309661300913300134300629

4.772.9typ.

0.0310.134typ.

00:5304:05

Plastipak30 ml

31309662300863309650

6.093.4typ.

0.1080.138typ.

00:3804:51

Plastipak50/60 ml

61309663300865300869

8.0133.2typ.

0.1560.293typ.

04:1912:50

Manufacturer: Becton Dickinson

Syringe TypeB-DCode No1)

Cat. No2)

Min. Vol.3) [ml]Max. Rate4) [ml/h]Bolusvolumina5)

P 1 [ml]P 3 [ml]Time to Occl.6)

P 1 [mm:ss]P 3 [mm:ss]

Type of unit Infusion Syringe Pump

Classification (acc. to IEC/EN 60601-1) defibrillator-proof; CF equipment

Protection class II

Class (acc. to Directive 93/42 EEC) II b

Moisture protection IP 22 (drip protected for horizontal usage)

Power supply integrated:• Rated voltage 220/240 V, 50/60 Hz, AC ~ or

110/120 V, 50/60 Hz, AC ~• Power input 12 VA

External extra-low voltage 12 V DC (e.g. ambulance cars)

Staff call Max. 24 V / 1 A / 24 VAArbitrary connection polarity (VDE 0834)

EMC EN 55011IEC/EN60601-1-2 and IEC/EN 6360601-2-24

Time of operation 100 % (continuous operation)

Operating conditions• Relative humidity 30 % ... 90 % (without condensation)• Temperature + 5 °C ... + 40 °C• Atmospheric pressure 500 mbar ... 1060 mbar

Storage conditions• Relative humidity 30 % ... 90 %• Temperature - 20 °C ... + 55 °C• Atmospheric pressure 500 mbar ... 1060 mbar

Battery type (non-rechargeable) 4 x 1.5 V DC alkali manganese

Operating life of battery > 60 h at ≤ 10 ml/h

Type of Battery pack (rechargeable) NiCd (optional 0.6 Ah)

Operating time of rech. battery > 10 h at ≤ 10 ml/h

Recharging time > 16 h

Weight Approx. 1.6 kg

Dimensions (WxHxD) 190 x 100 x 120 mm

19

Technical Data

20

Technical Data

Volume pre-selecetion / VTBD 0.1 – 999.9 ml

Time pre-selecetion 00:01 – 99:00 h

Techn. Accuracy excl. syringe tolerance ± 0.2 %

Accuracy of set delivery rate: typ. ± 2,5 %(measuring time >1 h and infused volume >2 ml)

Occlusion alarm pressure (occlusion sensitivity) 3 settings: step 1: approx. 0.3 barstep 2: approx. 0.6 barstep 3: approx. 1.2 bar

Alarm in the event of incorrect dosage a) Malfunctions of the deviceFor incorrect dosages of > 0.015 ml due to malfunctions of the device the pumpautomatically switches off.

b) At occlusion typ. 1 ml bolus volume at highest compression phase with 50 ml OPS= max. alarm delay at 5 ml/h = 6:50 min.

Compatible Syringes Customer-specific syringe configuration:list of syringe types see page 16 ff.

Adjustable syringe codes Syringe codes see page 16 ff., enclosed labels have to be attached underneath the pump.

Computer connection RRS 232 in combination with B. Braun interface lead (871 1661) including electrical separation.Interface description on request. Pay attention to safety notices.

Technical inspection (safety check) Every 2 years

Selectable delivery rates Continuous infusion rate range / bolus rates independence on syringe sizes:

Syringe sizes bolus rates cont. rates[ml] [ml/h] [ml/h]50/60 1 – 1.200 0.01 – 99.99

100.00 – 200.0020/30 1 - 700/800 0.01 – 99.99

5/10 1 - 150/200 0.01 – 50.002/3 1 - 70 0.01 – 25.00

21

Responsibility of the ManufacturerThe manufacturer, assembler, installer orimporter considers himself responsible for theeffects on safety, reliability and performance ofthe equipment only if:

• assembly operations, extensions, re-adjust-ments, modifications or repairs are carried out by persons authorised by him,

• the electrical installation of the relevant room complies with the appropriaterequirements (e.g. VDE 0100, 0107 and/or the IEC-publications resp. nationalrequirements),

• the equipment is used in accordance with the Instructions for Use and

• the Technical Safety Checks are carried out regularly.

WarrantyB. Braun provides 24 months warranty, as fromthe date of delivery, for every Perfusor®compact S. This covers repair or replacement ofparts damaged as a result of design/manufacturing errors or material defects.Modifications or repairs to the unit undertakenby the owner or by third parties invalidate thewarranty.

The warranty does not cover the following:Elimination of faults attributable toincorrect/inexpert handling, or to normal wearand tear incl. primary batteries and rechargeablebatteries.

Technical Safety Check*) / ServiceThe Technical Safety Check is recommended tobe carried out every 2 years and should bedocumented.

Service work must be carried out exclusively bypersonnel instructed by B. Braun.

CleaningClean using mild soap suds. Do not use spraydisinfectant at the mains connection.Recommended: disinfectant for wiping availablefrom B. Braun (e.g. Meliseptol®). Before opera-tion the device allow to air for at least 1 min.Do not spray into openings in the device. Besure to observe the instructions provided con-cerning waste disposal and hygiene for batteriesand disposables.

Check regularlyCheck for cleanliness, completeness and dam-age. Use only according to Instructions for Use.Check when switching on: self-check, audiblealarm, process- and alarm control indication.Check battery contacts for corrosion and cleanwith smooth rubber once year.

Warranty / TSC*) / Service / Cleaning

The CE mark confirms that this medical prod-uct complies with the "Council Directive onMedical Devices 93/42/EEC” dated 14th June1993.

B. Braun Melsungen AG

Inspection on DeliveryDespite careful packaging, the risk of transportdamage cannot be entirely prevented. Upondelivery, please check that nothing is missing.Do not use a damaged device! Contact theservice department.

Items includedPerfusor® compact S, Power Cord, Pole Clamp,(Short Instructions for Use and syringe tablesin separate packaging),4 primary batteries.

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Ordering

Art. No.

Perfusor® compact S (230/240 V) 871 4843Perfusor® compact S (110/120 V) 871 4886Recommended accessories for the Perfusor® compact SConnecting lead for staff call 871 1682Connecting lead for ambulance car (12 V) 871 1674Interface lead with electrical insulation 871 1661Rechargeable battery pack 3450 1690Y-lead for central mains power supply for 2 Perfusors 870 0109

Original Perfusor SyringesOriginal Perfusor Syringe 50 ml with draw-off cannula 872 8810FOriginal Perfusor Syringe 50 ml without draw-off cannula 872 8844FOriginal Perfusor Syringe 50 ml with draw-off cannulaand particle filter, with light protection 872 8828FOriginal Perfusor Syringe 50 ml with draw-off cannula and particle filter 872 8852FOriginal Perfusor Syringe 20 ml with draw-off cannula 872 8623Original Perfusor Syringee 20 ml without draw-off cannula 872 8615Original Perfusor Syringe 20 ml with draw-off cannula and particle filter 872 8631Omnifix Syringe 50 ml Luer-Lock 461 7509Omnifix Syringe 30 ml Luer-Lock 461 7304Omnifix Syringe 20 ml Luer-Lock Solo 461 7207Omnifix Syringe 10 ml Luer-Lock Solo 461 7100Omnifix Syringe 5 ml Luer-Lock 461 7053Omnifix Syringe 2 ml Luer-Lock Solo 461 7029

Art. No.

Original Perfusor TubingsOriginal Perfusor Tubing N, made of PVC, with Luer lock connectors; 150 cm 872 2960Original Perfusor Tubing L, made of PVC, with Luer lock connectors; 200 cm 872 2862Original Perfusor Tubing MR, made of PVC, with Luer lock connectors; 75 cm 872 2870Original Perfusor Tubing M, made of PVC,with loose lock nut on patient end, 150 cm 872 2994Original Perfusor Tubing PE, made of PE, with Luer lock connectors, 150 cm 872 2935Original Perfusor Tubing S, made of PVC,light-protected, with Luer lock connectors, 150 cm 872 2919Original Perfusor Tubing PES, made of PE,light-protected, with Luer lock connectors, pressure-resistant, 150 cm 872 3010Original Perfusor Tubing MK, made of PVC,with cannula and Luer lock connectors, 75 cm 872 2889Original Perfusor Tubing, made of PVC,with sterile filter 0.22 µ, with Luer lock connectors, 200 cm(not for use together with 20 ml syringes) 872 3001

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Material-No. 3891 4280, Drawing No. M654010201F04/a3/00 Printed on pulp bleached 100 % chlorine-free

B. Braun Melsungen AGPO box 11 20D-34209 Melsungen

Tel. +49(0)56 61-71 -0Fax +49(0)56 61-71 -20 44

HOSPITAL CARE