B.braun Perfusor Compact S - User Manual
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Transcript of B.braun Perfusor Compact S - User Manual
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Perfusor®compact S
Instructions for Use
Software BE
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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
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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
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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)
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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.
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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.)
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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.
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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.
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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)
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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.
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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
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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
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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
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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.
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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]
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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]
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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]
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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
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Technical Data
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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 30 ml Luer-Lock 461 7304
Omnifix Syringe 20 ml Luer-Lock Solo 461 7207
Omnifix Syringe 10 ml Luer-Lock Solo 461 7100
Omnifix Syringe 5 ml Luer-Lock 461 7053
Omnifix Syringe 2 ml Luer-Lock Solo 461 7029
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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