B.braun Perfusor Compact S - User Manual

7/21/2019 B.braun Perfusor Compact S - User Manual

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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 on

the 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 of their 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 of equipment, 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 of interference (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, syringe

type, power source,infusing symboland 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 Use

and a syringe table areattached underneaththe pump.

Operation To access functions, first press theFbutton

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, pull

and turn to theleft.

Syringe Adapter

Locking Lever To move the driveunit manually, pushthe locking lever up

until it clicks.

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

(2)

(1)





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 decimal

point 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 of the syringe inserted. (Ref. to the guides attached

underneath the pump. If the code does notmatch the syringe type inserted, see Syringe Tables/-Compatibilities, page 16 ff).

If syringe type code is correct, press F.

Prime the line by using theBOL-key. (Primerate =adjusted bolus rate.) PressF, then BOLonce. The bolus rate will blink. Press and holdBOLkey again until the line is primed (max. 1ml respectively for 10 seconds can be delivered).If applicable, repeat priming with BOLkey.(During STOP, the infused bolus volume is not

added to TOTALvolume.)

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:PressCand enter the new rate.

3. Start the Infusion PressSTART. Rotating infusion symbol isdisplayed.

4. Stop the Infusion PressSTOPor for 2 seconds.Disconnect from the patient.

Open the syringe holder. Remove the syringe. To switch off, press for 2 seconds.

To Change Syringes PressSTOP.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 plateinsert here(all syringes except OPS 50 ml)

Movable DriveMechanism 2)

Locking LeverSyringe 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 pressingF.

Connect to patient and pressSTART.

To change the rate

PressSTOP.

PressCand enter the new rate. PressSTART.

To Change the Rate Without Interrupting theInfusion (Titration)While the infusion is in process: simply pressCand enter new rate, then confirm by pressingF.

The new rate now applies. (If Fis 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. PressC, enter a new syringecode and confirm by pressingF. Close syringeholder and start infusion. Double-check the newsyringe code while infusion is taking place bypressing Fand .

Bolus To alter the bolus rate (only when device isstopped):PressF, then BOL. The bolus rate will blink.

PressC, set new bolus rate and confirm withF.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 volumePressBOL. 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 BOLonce, 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.

StandbyPressF, then STANDBY . andFare displayed,and the infusion is paused indefinitely. Set val-ues are retained. PressingFagain 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, pressCor switch device off.

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

Clear VTBD: PressF, then and pressC. The display shows: ---.- (for unlimited infusion).PressFto accept or enter new VTBD.

Note:Clearing VTBD also clears the TimeLimitation.

Check remaining VTBD during infusion:PressFand . The remaining amount of VTBD is displayed.

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

Special Functions

8

Activate the special functions by pressing theFbutton (Fis 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 Fbutton 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 theFbutton. After the device is switched off, allvalues are cleared.



checked during operation (pressFandas well as in STOP mode.

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

reached.

Clear time: PressF, then and pressC. The display shows: --:-- (for unlimitedinfusion). PressFto accept or enter new time.

Note:Clearing the time also clears the VTBD.

Check remaining time during infusion:PressFand The remaining infusion timeis displayed.

Note: If a rate and time are set, the remainingVTBD is automatically calculated and can bechecked during operation (pressFand )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 of the rate):Set rate to zero. Set VTBD and time values (see

descriptions above). After both values have beenconfirmed by pressing F, the calculated infusionrate is blinking in the display. Start infusionwith START/STOPkey.

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 Lock When e.g. rate and VTBD or time are set, pressand holdFkey; also press data lock key at thesame time. Now all pump data are locked andthe display alternately shows LOC and thecurrent rate. PressSTART/STOPkey 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 holdFkeyand also pressdata 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.

PressF, then Press 1 (low), 2 (medium)or 3 (high), then pressFto 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 Q

i(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 if necessary. Check if syringe is empty. Due tovarying syringe tolerances, a pressure alarm mayoccur when the syringe is empty prior to end of infusion 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 of infusion.

Correction

Press and holdON/OFFkey 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 alarm

appears 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 Information The 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 togetheror•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 into

alarm (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/OFFkey 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, since

a power failure would remain undetected by thedevice. Only alkali-manganese batteries may beplaced in the battery compartment because

•Alkali-manganese batteries recommendedare free of mercury and cadmium.

•Conventional carbon-cell batteries give anincorrect reading on the capacity displayand therefore, cannot guarantee reliableoperation.

•NiCd rechargeable batteries must not beconnected to the battery contacts as their

various physical properties disrupt thealarm.

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 "battery

flat” 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 for

each 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 to

Occlusion6) alarm have been measured at5.0 ml/h. The measured data are typical averagevalues which can vary because of possiblesyringe tolerances.



16

Compatible Syringes

Omnifix

2 ml

2

461 7029

0.5

7.0

typ.

0.032

0.079

typ.

00:38

01:36

Omnifix

5 ml

5

461 7053

1.2

19.2

typ.

0.058

0.096

typ.

01:01

02:00

Omnifix

10 ml

10

461 7100

2.1

32.0

typ.

0.057

0.173

typ.

01:03

03:29

Omnifix

20 ml

22

461 7207

5.3

93.4

typ.

0.128

0.233

typ.

02:26

05:23

Omnifix

30 ml

30

461 7304

5.9

97.9

typ.

0.123

0.272

typ.

02:49

08:20

Omnifix

50 ml

52

461 7509

7.2

117.0

typ.

0.225

0.264

typ.

06:25

18:13

OPS

20 ml

20

872 8615

4.4

78.5

typ.

0.119

0.218

typ.02:18

04:21

OPS

50 ml

50

872 8810

9.6

164.4

typ.

0.305

0.369

typ.06:25

18:13

Proinjekt

50 ml

51

872 8917

7.1

127.0

typ.

0.290

0.329

typ.04:18

17:58

Syringe Type

B. Braun

Code 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 Type

B. Braun

Code 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

Monoject

6 ml

5.2

8881-

716008

1.2

16.0

typ.

0.0190.068

typ.

00:44

02:20

Monoject

12 ml

15

8881-

512878

2.7

42.5

typ.

0.0290.101

typ.

01:50

05:20

Monoject

20 ml

26

8881-

520657

5.5

93.0

typ.

0.0640.129

typ.

02:30

07:20

Monoject

35 ml

35

8881-

535762

8.5

145.0

typ.

0.1230.360

typ.

04:30

16:00

Monoject

50/60 ml

62

8881-

560125

8.6

144.0

typ.

0.0780.185

typ.

04:22

15:56

Syringe Type

TYCO USA

Code 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)

Monoject

3 ml

3.4

1100-

603495

1.10

13.6

typ.

0.023

0.050

typ.

01:04

01:47

Monoject

6 ml

5.4

1100-

606159

1.16

16.9

typ.

0.027

0.053

typ.

00:46

01:34

Monoject

12 ml

16

1100-

612173

2.51

40.5

typ.

0.107

0.199

typ.

02:13

04:16

Monoject

20 ml

29

1100-

620036

3.36

51.2

typ.

0.212

0.332

typ.

04:07

07:21

Monoject

35 ml

39

1100-635430

8.33

144.8

typ.0.371

0.465

typ.

07:55

13:30

Monoject

50/60 ml*)

55

1100-650090

8.54

143.2

typ.0.504

0.376

typ.

10:57

14:12

Syringe Type

TYCO EU

Code 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 ml

3.1

SS*03L

0.7

12.1

typ.

0.009

0.031

typ.

00:52

01:43

5 ml

5.1

SS*05L

1.3

23.3

typ.

0.012

0.066

typ.

00:35

02:16

10 ml

13

SS*10L

1.7

22.0

typ.

0.051

0.050

typ.

01:44

03:02

20 ml

23

SS*20L

3.8

69.7

typ.

0.019

0.052

typ.

01:04

04:08

30 ml

32

SS*30L

4.3

77.6

typ.

0.081

0.196

typ.

02:57

09:48

50 ml

54

BS-50LG

5.1

89.6

typ.

0.114

0.137

typ.

05:44

15:19

60 ml

60

SS*60L

5.2

90.7

typ.

0.038

0.135

typ.

02:19

12:55

Syringe Type

Terumo

Code 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

Plastipak

3 ml

3.3

309585

300910

0.7

10.4

typ.0.008

0.038

typ.

00:12

00:31

Plastipak

5 ml

5.3

309603

300911

1.3

21.0

typ.0.038

0.059

typ.

00:56

01:26

Plastipak

10 ml

11

309604

300912

2.0

34.5

typ.0.028

0.079

typ.

00:29

01:26

Plastipak

20 ml

24

309661

300913

300134

300629

4.7

72.9

typ.0.031

0.134

typ.

00:53

04:05

Plastipak

30 ml

31

309662

300863

309650

6.0

93.4

typ.0.108

0.138

typ.

00:38

04:51

Plastipak

50/60 ml

61

309663

300865

300869

8.0

133.2

typ.0.156

0.293

typ.

04:19

12:50

Manufacturer: Becton Dickinson

Syringe Type

B-D

Code 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 device

For incorrect dosages of >0.015 ml due tomalfunctions of the device the pumpautomatically switches off.

b) At occlusion typ. 1 ml bolus volume athighest 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 labelshave to be attached underneath the pump.

Computer connection RRS 232 in combination with B. Braun interfacelead (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 in

dependence 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 – 99.995/10 1 - 150/200 0.01 – 50.002/3 1 - 70 0.01 – 25.00



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

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

•the electrical installation of the relevant

room complies with the appropriaterequirements (e.g. VDE 0100, 0107 and/orthe IEC-publications resp. nationalrequirements),

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

•the Technical Safety Checks are carried outregularly.

WarrantyB. Braun provides 24 months warranty, as fromthe date of delivery, for every Perfusor®compact S. This covers repair or replacement of

parts 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*) / Service The 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.

Cleaning

Clean 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 regularly

Check 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 transport

damage 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 4843

Perfusor®compact S (110/120 V) 871 4886

Recommended accessories for the Perfusor®compact S

Connecting lead for staff call 871 1682

Connecting lead for ambulance car (12 V) 871 1674

Interface lead with electrical insulation 871 1661

Rechargeable battery pack 3450 1690 Y-lead for central mains power supply for 2 Perfusors 870 0109

Original Perfusor Syringes

Original Perfusor Syringe 50 ml with draw-off cannula 872 8810F

Original Perfusor Syringe 50 ml without draw-off cannula 872 8844F

Original Perfusor Syringe 50 ml with draw-off cannulaand particle filter, with light protection 872 8828F

Original Perfusor Syringe 50 ml with draw-off cannula and particle filter 872 8852F

Original Perfusor Syringe 20 ml with draw-off cannula 872 8623Original Perfusor Syringee 20 ml without draw-off cannula 872 8615

Original Perfusor Syringe 20 ml with draw-off cannula and particle filter 872 8631

Omnifix Syringe 50 ml Luer-Lock 461 7509


Omnifix Syringe 20 ml Luer-Lock Solo 461 7207






Art. No.

Original Perfusor Tubings

Original Perfusor Tubing N, made of PVC, with Luer lock connectors; 150 cm 872 2960

Original Perfusor Tubing L, made of PVC, with Luer lock connectors; 200 cm 872 2862

Original Perfusor Tubing MR, made of PVC, with Luer lock connectors; 75 cm 872 2870

Original Perfusor Tubing M, made of PVC,with loose lock nut on patient end, 150 cm 872 2994

Original 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 2919

Original Perfusor Tubing PES, made of PE,light-protected, with Luer lock connectors, pressure-resistant, 150 cm 872 3010

Original Perfusor Tubing MK, made of PVC,with cannula and Luer lock connectors, 75 cm 872 2889

Original 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)5661-71-0Fax +49(0)5661-71-2044

H OSPI TAL CARE

Documents

B.braun Perfusor Compact S - User Manual