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Infusomat
fmS
®
Instructions for Use
Software IFME/IFMe
Related Manuals for B. Braun Infusomat fmS
Summary of Contents for B. Braun Infusomat fmS
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Page 1
Infusomat ® Instructions for Use Software IFME/IFMe… -
Page 2
Patient Safety Attention: Consult accompanying documents! Read Instructions for Use prior to use. Application only under regularly supervision by specially trained staff. ➤ Operation Connected electrical equipment must comply ➤ Ensure the unit is properly positioned and with the relevant IEC/EN-publications secured. -
Page 3: Table Of Contents
Infusomat ® Contents Infusomat® fmS / Overview Page 4 Operation Page 6 Additional Settings Page 7 Special Functions Page 8 Alarm Conditions Page 13 Start-up Graphs and Trumpet Curves Page 15 Technical Data Page 16 Warranty / TSC* / Service / Cleaning Page 18 Ordering Page 19…
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Page 4: Infusomat® Fms / Overview
Overview Handle For easy transport. Display All important information in plain text. Green background illumination only if connected to mains or a key is pushed at battery operation. Keypad for Input Correct Input/CLEAR Display reset to 000.0 Red LED indicates alarm condition Additionally «AAA.A”…
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Page 5
Guide for Short Infusion Pole Multi-Function- Connector (MFC) Mains/Power Connection Connection for staff (protect against ingress of moisture). In case of call, ambulances mains/power failure, the pump switches to (12 V DC) and inter- battery operation. Battery operation time: face for fm anaes- >… -
Page 6: Operation
Operation Infusion upper clip 1. Ensure reliable installation Never position infusion bottle below pump level. ➤ Connect staff call. ➤ Insert spike vertically into infusion bottle. Fill lower part of drop chamber to max. 2/3. ➤ Open roller clamp. Original 2.
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Page 7: Additional Settings
Additional Settings To Change the Delivery Rate volume has to be set. ➤ Press START/STOP. Green operating indicator goes out. ➤ Press C. Target Time (Time Pre-selection) Display reset to 000.0 ➤ Press key below TIME. ➤ Enter new delivery rate. (No setting possible, Enter target time via keypad (50 min = 50;…
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Page 8: Special Functions
Recording the data: In connection with the software “IFME” the The protocol of events only can be transferred Infusomat fmS is equipped with a history func- to a computer via interface (MFC interface tion (memory of events). This permanent lead). For this a terminal programme installed in…
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Page 9
Special Functions Select Special Mode SF Depending on the version, several functions may Interval bolus be deactivated. Contact service. Automatic bolus in set time interval. In case of ➤ To set special functions press key below SF manual bolus administration the interval bolus repeatedly until desired special function is is skipped. -
Page 10
Special Functions ➤ Drug Display Exit from selection: Press key below END. 9 selectable drug names can be stored (input via service program only). Check Battery Capacity Remaining battery life time is displayed, ➤ Select with key below (+). Drug is displayed, e.g. -
Page 11
Dosage Calculation (Overview) values (rate or dosage) are displayed. The dosage calculation automatically calculates ➤ First check rate displayed for plausibility, the delivery rate in ml/h. then confirm RATE. Value is displayed. Setting parameters: ➤ Start infusion. 1. Concentration Note: Dosage value with unit is displayed (down — per ml or on the right). -
Page 12
Special Functions ➤ Check entered or calculated rate for plausi- Secondary infusion bility and confirm with key below RATE. Rate is e.g. 100 ml Primary Infusion bag volume with displayed. e.g. 1000 ml delivery rate 10 ml/h bag volume with ➤… -
Page 13: Alarm Conditions
Alarms Operating alarms — audible alarm every 4 sec., — operating indicator off, — staff call. Remedy failure and restart infusion. ➤ Switch off device. Drop Alarm / Pressure Alarm ➤ Connect to mains/power or 12 V DC power Infusion bottle empty? source.
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Page 14
The delivery rate and a drug can be entered in matically will be switched to integrated the Infusomat® fmS as «proposal” via an rechargeable battery. external computer. Both items of data must be checked on the Infusomat fmS and acknow- Charge Battery ledged. ➤ Charge battery in case of: ➤… -
Page 15: Start-Up Graphs And Trumpet Curves
Start-up Graphs and Trumpet Curves Start-up Graphs Trumpet Curves 2 (ml/h) flow deviation Delivery rate = 1 ml/h Delivery rate = 1 ml/h Epmax Epmin t (min) 120 p∆t (min) 31 50 (ml/h) flow 10 deviation Delivery rate = 25 ml/h Delivery rate = 25 ml/h 37,5 Epmax…
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Page 16: Technical Data
Technical Data Type of unit Volumetric infusion pump Classification (acc. to IEC/EN 60601-1) defibrillator-proof, CF equipment Protection Class I; IP 22 (Moisture protection: drip protected) Class (acc. to Directive 93/42 EEC) II b Rated voltage / current 230 V AC~ (0.06 A), 50/60 Hz Mains fuse T 0.16 A or 200 V/230 V/240 V AC~ (0.06 A), 50/60 Hz…
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Page 17
Air detector Technical sensitivity Air bubbles > 0.01 ml Alarm triggering: With air bubble size of typ. 0.3 ml (limit value 0.4 ml) or 1.5 ml/h (cumulative value of 1 h as of air bubble volume 0.01 ml) Can be set from 0.01 to 0.3 ml via service program only Can be set from 0.5 to 3.5 ml/h via service program only Accuracy of set delivery rate typ. -
Page 18: Warranty / Tsc* ) / Service / Cleaning
Warranty provided concerning waste disposal and hygiene for batteries and disposables. B. Braun provides as from the date of delivery a warranty of 2 years for every Infusomat® fmS. This covers repair or replacement of parts dama- ged as a result of design/manufacturing errors or material defects.
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Page 19: Ordering
Ordering Art.-Nr. Infusomat® fmS 230 V 871 5548 Infusomat® fmS 200 — 240 V 871 5440 Infusomat® fmS 100 – 120 V 871 5416 Recommended accessories for Infusomat® fmS Connecting lead for potential equalisation 870 1628 MFC-Connecting lead for staff call 871 1682 MFC-Connecting lead for ambulance cars (12 V DC) 871 1674…
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Page 20
HOSPITAL CARE B. Braun Melsungen AG P.O.Box 11 20 D-34209 Melsungen Tel. +49 (0) 56 61 – 71-0 Fax + 49 (0) 56 61 – 71-20 44 Material-No. 3891 2341, Drawing No. M671010100F04 05/01 Printed on pulp bleached 100 % chlorine-free…
Infusomat® fmS
Instructions for Use
Software IFME/IFMe
Patient Safety
Attention: Consult accompanying documents!
Read Instructions for Use prior to use. Application only under regularly supervision by specially trained staff.
Operation
Ensure the unit is properly positioned and secured.
Prior to use check audible and visual alarms during self test. Also check the device for possible damage.
If staff call is used we recommend to check the equipment once after connecting the pump.
Connect to patient only after switching on the device. Interrupt the connection during changing administration set(s) to prevent incorrect dose delivery.
Select cannula/catheter suitable for use with the intended medical application.
Position the infusion line free of kinks.
Recommended change of disposables after 24 h (consider national hygiene regulations).
Compare displayed value with entered value. Start infusion only if values are corresponding.
Installation in medically used rooms must comply with the appropriate regulations (e.g. VDE 0100,
VDE 0107 or IEC-publications.
Possible explosion hazard if used in presence of flammable anaesthetics!
Air in line cannot be detected by the air detector at stop-cocks, infusion ports and additional administration set components.
Other components
Variations in pressure (e.g. as caused by change of level) can affect the accuracy of the device.
Where several infusion lines are connected on one single vascular access the possibility of their exerting a mutual influence vice-versa cannot be excluded.
Refer to respective manufacturer’s information for possible incompatibilities of equipment resp. drugs.
Use only compatible combinations of equipment, accessories, working parts and disposables.
It is recommended to use original Infusomat® infusion lines only.
The use of not recommended resp. incompatible disposables may influence the technical specification.
Connected electrical equipment must comply with the relevant IEC/EN-publications
(e.g. IEC/EN 60950 for data-processing equipment). The user/operator is responsible for the system configuration if additional equipment is connected. The international standard IEC/EN 60601-1-1 has to be taken into account.
Safety Standards
The Infusomat® fmS satisfies all safety standards for medical electrical devices in compliance with IEC/EN 60601-1 and IEC/EN 60601-2-24.
The EMC-limits (electro-mangnetic compatibility) according to IEC/EN 60601-1-2 and IEC/EN 60601-2-24 are maintained. If the equipment is operated in the vicinity of other equipment which may cause high levels of interference (e.g. HF surgical equipment, nuclear spin tomography units, mobile telephones etc.) maintain the recommended protective distances for these devices. Under certain conditions malfunctions may occur which lead to a device alarm with permanent alarm tone (see also alarm conditions, page 13). Interferences may occur e.g. at electro-magnetic fields > 10 V/m resp. electro-magnetic discharges > 8 kV.
Special Function «without drip control”, see page 10.
Infusomat® fmS
Contents
|
Infusomat® fmS / Overview |
Page 4 |
|
Operation |
Page 6 |
|
Additional Settings |
Page 7 |
|
Special Functions |
Page 8 |
|
Alarm Conditions |
Page 13 |
|
Start-up Graphs and Trumpet Curves |
Page 15 |
|
Technical Data |
Page 16 |
|
Warranty / TSC*) / Service / Cleaning |
Page 18 |
|
Ordering |
Page 19 |
|
*) Technical Safety Check |
The Infusomat® fmS is according to
IEC/EN 60601-1 resp. IEC/EN 60601-2-24 a volumetric infusion pump for infusion of small and large volumes at highest accuracy and is suitable for intravenous and intra-arterial applications, for blood transfusion and for enteral nutrition.
The medical specialist has to decide on the suitability of the application. The decision has to be made on the basis of the specified properties and technical data.
For further details please refer to the Instructions for Use.
3
Overview
Handle
For easy transport.
Display
All important information in plain text. Green background illumination only if connected to mains or a key is pushed at battery operation.
Keypad for Input
Correct Input/CLEAR
Display reset to 000.0
Red LED indicates alarm condition
Additionally «AAA.A” is flashing in the display. Possible alarms: «drop alarm, air alarm, pressure alarm, pump-door open, battery alarm, standby-alarm”
Operating Indicator
Additional operating control indicator in display.
|
Holder for Drop Chamber |
Adapter for Drop Sensor |
|
|
Prevents unintended |
Replaceable, depending on drop |
|
|
movement (swaying). |
chamber size. Press lateral and pull |
|
|
off. |
||
Universal Pole Clamp
Attach the Infusomat® fmS from above, clicking into its place. To release, press the black button.
4
Guide for Short Infusion Pole
Mains/Power Connection
(protect against ingress of moisture). In case of mains/power failure, the pump switches to battery operation. Battery operation time:
> 3.5 h at highest delivery rate. Automatic overload protection. Mains fuse: directly above the mains/power connector.
Potential Equalisation
To be connected for 
CF-applications.
Mains/Power Supply
For operation with fluid manager system.
Door Opener
Aluminium Housing
Easy-care, drip water protected, resistant to disinfectants.
Special Functions «SF”
Function Keys (Soft keys)
Mains/Power Switch ON/OFF
Suppress alarm tone for 2 min
Infusion START/STOP
Multi-Function- Connector (MFC)
Connection for staff call, ambulances (12 V DC) and interface for fm anaesthesia/fm intensive.
Optical Interface
Infrared Interface for operation on «fluid manager system”.
Flow Inhibitor
Opening door clamps off infusion line automatically.
Peristaltic Pump
For precise and reliable dosage.
Function Keys
VOL Infusion Volume
Press key below VOL. Enter volume
(0.1 … 9999.9 ml). Confirm. Press again key below VOL.
TIME Infusion Time
Press key below TIME. Enter time e.g. 50 min as 5 0 or 2 h 30 min as 2 3 0. Confirm. Press again key below TIME.
RATE Delivery Rate
Only active when rate is calculated automatically. The key below RATE confirms the calculated rate.
SF Special Functions
If activated: dose calculation / bolus function / standby / drug selection / occlusion pressure / drop control / piggyback / battery capacity / data lock / contrast / date, time.
5
Operation
Infusion
1. Ensure reliable installation
Never position infusion bottle below pump level.
Connect staff call.
Insert spike vertically into infusion bottle. Fill lower part of drop chamber to max. 2/3.
Open roller clamp.
2. Filling and Venting
Fill infusion line from bottom to top.
Close roller clamp.
3. Insert Infusion Line
Press door opener.
Insert infusion line: Locate clips first on top, then on bottom.
Keep infusion line in place at air sensor.
Close door. In the area of the peristaltic pump segments and free-flow clamp the infusion line will be positioned self-acting.
Open roller clamp completely. There may not be a continuous drip.
Place drop sensor on drop chamber
(if necessary, use an appropriate adapter).
4. Switch On with
Green mains/power control or yellow battery control, alarm tone and display LED’s are briefly activated.
5.Puncture
6.Setting the Delivery Rate
In the range: 0.1 — 999.9 ml/h and check
(selectable in 0.1 ml/h-increments).
Correction: Press C, then set new rate. Select additional settings, if desired (see page 7).
upper clip 
Original Infusomat® line with silicone-pump element
free flow clamp
lower clip
air sensor 
7. Press START
Operating symbol appears on the display and the green operating indicator lights.
8. Stop the infusion
Press STOP. Green operating indicator goes
out
Close roller clamp.
Press door opener. Infusion line will be clamped off when opening the door.
Remove infusion line. First bottom, then top.- Replacement: Insert new infusion line as described. Then press START again.
To end switch off
Press 
for 2 sec.
6
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texts
B Braun Infusomat fmS Infusion Pump User Manual
B Braun Infusomat fmS Infusion Pump User Manual
- Addeddate
- 2020-05-20 04:27:25
- Classification
- Clinical;Infusion and Syringe Pump;B Braun Infusion and Syringe Pump;B Braun Infusomat fmS
- Identifier
- manual_B_Braun_Infusomat_fmS_Infusion_Pump_User_Manual
- Identifier-ark
- ark:/13960/t1nh3f11k
- Ocr
- ABBYY FineReader 11.0 (Extended OCR)
- Page_number_confidence
- 94.74
- Ppi
- 300
- Scanner
- Internet Archive Python library 1.9.0
comment
Reviews
There are no reviews yet. Be the first one to
write a review.
SIMILAR ITEMS (based on metadata)
Patient Safety
Read Instructions for Use prior to use. Application only under regularly supervision by specially trained staff.
Operation
➤
Ensure the unit is properly positioned and
secured.
➤
Prior to use check audible and visual alarms
during self test. Also check the device for possible
damage.
➤
If staff call is used we recommend to check the
equipment once after connecting the pump.
➤
Connect to patient only after switching on the
device. Interrupt the connection during changing
administration set(s) to prevent incorrect dose
delivery.
➤
Select cannula/catheter suitable for use with the
intended medical application.
➤
Position the infusion line free of kinks.
➤
Recommended change of disposables after 24 h
(consider national hygiene regulations).
➤
Compare displayed value with entered value.
Start infusion only if values are corresponding.
➤
Installation in medically used rooms must comply
with the appropriate regulations (e.g. VDE 0100,
VDE 0107 or IEC-publications.
➤
Possible explosion hazard if used in presence of
flammable anaesthetics!
➤
Air in line cannot be detected by the air detector
at stop-cocks, infusion ports and additional
administration set components.
Other components
➤
Variations in pressure (e.g. as caused by change
of level) can affect the accuracy of the device.
➤
Where several infusion lines are connected on
one single vascular access the possibility of their
exerting a mutual influence vice-versa cannot be
excluded.
➤
Refer to respective manufacturer’s information
for possible incompatibilities of equipment resp.
drugs.
➤
Use only compatible combinations of equipment,
accessories, working parts and disposables.
➤
It is recommended to use original Infusomat®
infusion lines only.
➤
The use of not recommended resp. incompatible
disposables may influence the technical specification.
Attention: Consult accompanying documents!
➤
Connected electrical equipment must comply
with the relevant IEC/EN-publications
(e.g. IEC/EN 60950 for data-processing equipment).
The user/operator is responsible for the system
configuration if additional equipment is connected.
The international standard IEC/EN 60601-1-1 has to
be taken into account.
Safety Standards
The Infusomat® fmS satisfies all safety standards for
medical electrical devices in compliance with
IEC/EN 60601-1 and IEC/EN 60601-2-24.
➤
The EMC-limits (electro-mangnetic compatibility)
according to IEC/EN 60601-1-2 and IEC/EN
60601-2-24 are maintained. If the equipment is
operated in the vicinity of other equipment which
may cause high levels of interference (e.g. HF surgical
equipment, nuclear spin tomography units, mobile
telephones etc.) maintain the recommended protec-
tive distances for these devices. Under certain
conditions malfunctions may occur which lead to a
device alarm with permanent alarm tone (see also
alarm conditions, page 13). Interferences may occur
e.g. at electro-magnetic fields > 10 V/m resp.
electro-magnetic discharges > 8 kV.
Special Function «without drip control»,
see page 10.
Loading…
You can only view or download manuals with
Sign Up and get 5 for free
Upload your files to the site. You get 1 for each file you add
Get 1 for every time someone downloads your manual
Buy as many as you need
- About
- Blog
- Projects
- Help
-
Donate
Donate icon
An illustration of a heart shape - Contact
- Jobs
- Volunteer
- People
Bookreader Item Preview
texts
B Braun Infusomat fmS Infusion Pump User Manual
B Braun Infusomat fmS Infusion Pump User Manual
- Addeddate
- 2020-05-20 04:27:25
- Classification
- Clinical;Infusion and Syringe Pump;B Braun Infusion and Syringe Pump;B Braun Infusomat fmS
- Identifier
- manual_B_Braun_Infusomat_fmS_Infusion_Pump_User_Manual
- Identifier-ark
- ark:/13960/t1nh3f11k
- Ocr
- ABBYY FineReader 11.0 (Extended OCR)
- Page_number_confidence
- 94.74
- Ppi
- 300
- Scanner
- Internet Archive Python library 1.9.0
comment
Reviews
There are no reviews yet. Be the first one to
write a review.
SIMILAR ITEMS (based on metadata)
Patient Safety
Read Instructions for Use prior to use. Application only under regularly supervision by specially trained staff.
Operation
➤
Ensure the unit is properly positioned and
secured.
➤
Prior to use check audible and visual alarms
during self test. Also check the device for possible
damage.
➤
If staff call is used we recommend to check the
equipment once after connecting the pump.
➤
Connect to patient only after switching on the
device. Interrupt the connection during changing
administration set(s) to prevent incorrect dose
delivery.
➤
Select cannula/catheter suitable for use with the
intended medical application.
➤
Position the infusion line free of kinks.
➤
Recommended change of disposables after 24 h
(consider national hygiene regulations).
➤
Compare displayed value with entered value.
Start infusion only if values are corresponding.
➤
Installation in medically used rooms must comply
with the appropriate regulations (e.g. VDE 0100,
VDE 0107 or IEC-publications.
➤
Possible explosion hazard if used in presence of
flammable anaesthetics!
➤
Air in line cannot be detected by the air detector
at stop-cocks, infusion ports and additional
administration set components.
Other components
➤
Variations in pressure (e.g. as caused by change
of level) can affect the accuracy of the device.
➤
Where several infusion lines are connected on
one single vascular access the possibility of their
exerting a mutual influence vice-versa cannot be
excluded.
➤
Refer to respective manufacturer’s information
for possible incompatibilities of equipment resp.
drugs.
➤
Use only compatible combinations of equipment,
accessories, working parts and disposables.
➤
It is recommended to use original Infusomat®
infusion lines only.
➤
The use of not recommended resp. incompatible
disposables may influence the technical specification.
Attention: Consult accompanying documents!
➤
Connected electrical equipment must comply
with the relevant IEC/EN-publications
(e.g. IEC/EN 60950 for data-processing equipment).
The user/operator is responsible for the system
configuration if additional equipment is connected.
The international standard IEC/EN 60601-1-1 has to
be taken into account.
Safety Standards
The Infusomat® fmS satisfies all safety standards for
medical electrical devices in compliance with
IEC/EN 60601-1 and IEC/EN 60601-2-24.
➤
The EMC-limits (electro-mangnetic compatibility)
according to IEC/EN 60601-1-2 and IEC/EN
60601-2-24 are maintained. If the equipment is
operated in the vicinity of other equipment which
may cause high levels of interference (e.g. HF surgical
equipment, nuclear spin tomography units, mobile
telephones etc.) maintain the recommended protec-
tive distances for these devices. Under certain
conditions malfunctions may occur which lead to a
device alarm with permanent alarm tone (see also
alarm conditions, page 13). Interferences may occur
e.g. at electro-magnetic fields > 10 V/m resp.
electro-magnetic discharges > 8 kV.
Special Function «without drip control»,
see page 10.
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