Perfusor® compact S - Frank`s Hospital Workshop
Contents
1. Omnifix Omnifix B Braun 2 ml 5 ml 10 ml 20 ml 30 ml 50 ml Code No 2 5 10 22 30 52 Cat No Min Vol ml 1 2 21 5 3 5 9 7 2 Max Rate ml h 93 4 117 0 Bolusvolumina typ typ P1 ml 0 128 0 225 P3 ml 0 233 0 264 Time to Occl typ typ P1 mm ss 02 26 06 25 P3 mm ss 05 23 18 13 Manufacturer B Braun Syringe Type OPS OPS Proinjekt B Braun 20 ml 50 ml 50 ml Code No Cat No 6 2 8615 872 8810 872 8917 Min Vol ml 4 4 9 6 11 Max Rate ml h Bolusvolumina gt typ typ typ P1 ml 0 119 0 305 0 290 P3 ml 0 218 0 369 0 329 Time to Occl 9 P1 mm ss P3 mm ss 16 Manufacturer TYCO EU Syringe Type Monoject Monoject M onoject Monoject Monoject Monoject TYCO EU 3 ml 6 ml 12 ml 20 ml 35 ml 50 60 mI Code No 34 5 4 16 29 39 55 Cat No 1100 1100 1100 1100 1100 1100 603495 606159 612173 620036 635430 650090 Min Vol ml 1 10 1 16 2 51 3 36 8 33 9 54 Max Rate ml h 13 6 16 9 40 5 51 2 144 8 143 2 Bolusvolumina gt typ typ typ typ typ typ P1 ml 0 023 0 027 0 107 0 212 0 371 0 504 P3 ml 0 050 0 053 0 199 0 332 0 465 0 376 Time to Occl P1 mm ss P3 mm ss Manufacturer TYCO USA Syringe Type Monoject Monoject Monoject Monoject Monoject TYCO USA 6 ml 12 ml 20 ml 35 ml 50 60 ml Code No 5 2 15 26 35 62 Cat No 8881 8881 8881 8881 51282. 3 min before syringe is empty only black syringe field is blinking resp end of infusion infusion Due to syringe tolerances some fluid may be left in the syringe when pump goes into end of infusion alarm At end of infusion alarm the pump goes into an audible alarm dependent on the adjustment in the service menue If some fluid is left in the syringe after end of infusion alarm appears the pump continues to deliver until pressure alarm appears Enter data where Indicated u Reminder Data input has not been entered within 2 min also pre alarms are indicated via this symbol 11 Alarms Displays Device alarm Symbol Cause Top of the plunger is improperly positioned in the syringe pressure plate Operation alarm Symbol Cause mi El Automatic bolus reduction has been interrupted Bolus has to be reduced manually F Locking lever at the drive head has not clicked into place anh Preset VTBD and or TIME have been reached i Alarm silence Interrupts the alarm for a period of 2 min m Syringe holder not closed GHG Rate has not been set prior to start 12 Correction Ensure top of syringe plunger is securely positioned in the syringe pressure plate Correction Reduce bolus by disconnecting the infusion line from the patient and open the locking lever Ensure plunger head is securely positioned in the syringe pressure plate and the locking lever has engaged Clear
3. F and Eales as well as in STOP mode EZECB Time Limitation Press F then ZE 8 and enter the required time limitation confirm value with F After a time has been set the mnl symbol flashes During infusion the time counts down Infusion automatically stops after the time has been reached Clear time Press F then ZE 8 and press C The display shows for unlimited infusion Press F to accept or enter new time Note Clearing the time also clears the VTBD Check remaining time during infusion Press F and EZW 8 The remaining infusion time is displayed Note If a rate and time are set the remaining VTBD is automatically calculated and can be checked during operation press F and EEJ as well as in STOP mode Bolus applications and rate 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 VIBD and time values see descriptions above After both values have been confirmed by pressing F the calculated infusion rate is blinking in the display Start infusion with START STOP key Note A change of the rate also will change the time value based on the new rate and the remaining VTBD If the calculated rate is cleared the time is cleared automatically but not the remaining VIBD VTBD only will be cleared after a new time has been set and the rate has been set to zero EN S Data Lock When
4. Power supply integrated e Rated voltage Power input External extra low voltage Staff call EMC Time of operation Operating conditions e Relative humidity e Temperature e Atmospheric pressure Storage conditions e Relative humidity e Temperature e Atmospheric pressure Battery type non rechargeable Operating life of battery Type of Battery pack rechargeable Operating time of rech battery Recharging time Weight Dimensions WxHxD Infusion Syringe Pump i defibrillator proof CF equipment Protection class Il I b IP 22 drip protected for horizontal usage 220 240 V 50 60 Hz AC or 110 120 V 50 60 Hz AC 12 VA 12 V DC e g ambulance cars Max 24 V 1A 24 VA Arbitrary connection polarity VDE 0834 EN 55011 IEC EN60601 1 2 and IEC EN 6360601 2 24 100 continuous operation 30 96 90 96 without condensation 5 C 40 C 500 mbar 1060 mbar 30 Yo 90 Yo 20 C 55 C 500 mbar 1060 mbar 4 x 1 5 V DC alkali manganese 60 h at x 10 ml h NiCd optional 0 6 Ah gt 10 hat lt 10 ml h gt 16h Approx 1 6 kg 190 x 100 x 120 mm 19 Technical Data Selectable delivery rates Volume pre selecetion VTBD Time pre selecetion Techn Accuracy excl syringe tolerance Accuracy of set delivery rate Occlusion alarm pressure occlusion sensitivity Alarm in the event of incorrect dosage Compatible Syringes Adjustable syring
5. VTBD or TIME for unlimited infusion or set new values Set rate required prior to START Displays F Special function is active JH Mains AC power operation wai VTBD and or TIME have been entered E Service indicator blinks when the service interval has elapsed H Infusion control Rotates to show an infusion in progress 13 Battery Operation General Information The Perfusor amp compact S is equipped with four AA non rechargeable standard batteries alkali manganese Alternatively a rechargeable NiCd battery pack from B Braun can be used This battery pack is charged by the device during connection to mains To ensure safe and reliable battery operation certain rules of application must be noted gt The battery indicator display is a trend display low medium high The actual battery life available may vary due to different battery manufacturers e temperature varying load e g frequent boluses gt Batteries can explode or leak causing damage if e they are opened or burned they are inserted incorrectly old and new batteries are inserted together or different brands of batteries are inserted together gt Batteries should be removed from the device during long periods of non use storage gt 3 months If the batteries are removed from the device while infusing and subsequently a new battery set is put in the Perfusor amp compact S goes into alarm messag
6. cm Original Perfusor Tubing made of PVC with sterile filter 0 22 u with Luer lock connectors 200 cm not for use together with 20 ml syringes Art No 872 2960 872 2862 872 2870 872 2994 872 2935 872 2919 872 3010 8 2 2889 872 3001 23 HOSPITAL CARE in B Braun Melsungen AG PO box 11 20 D 34209 M elsungen Material No 3891 4280 Drawing No M654010201F04 a Tel 49 0 56 61 71 0 3 00 Printed on pulp bleached 100 96 chlorine free Fax 49 0 56 61 71 2044
7. 78 520657 535762 560125 Min Vol Im 271 55 85 86 Max Rate ml h Bolusvolumina Pl ml P 3 ml Time to Occl P1 mm ss P3 mm ss amp To use only with a special syringe adapter Cat No 34506659 This adapter also is usable for all further syringe types exchange via service see page 4 17 Compatible Syringes Manufacturer Terumo Min Vol ml 0 0 7 1 3 1 7 3 8 4 3 5 1 5 2 Syringe Type Terumo 3 ml 5 ml 10 ml 20 ml 30 ml 50 ml 60 ml Code No 31 5 1 13 23 32 54 6 Cat No 2 Max Rate ml h 90 7 Bolusvolumina typ 0 038 0 135 P1 ml P3 ml Time to Occl P1 mm ss P3 mm ss M anufacturer Becton Dickinson typ 02 19 12 55 Bolusvolumina typ typ typ typ P1 ml 0 008 0 038 0 028 0 031 P3 ml 0 038 0 059 0 079 0 134 Time to Occl 9 P1 mmiss P3 mmiss 18 Syringe Type Plastipak Plastipak Plastipak Plastipak Plastipak Plastipak B D 3 ml 5 ml 10 ml 20 ml 30ml 50 60 ml Code No 3 3 5 3 11 24 31 61 Cat No 309585 309603 309604 309661 309662 3090663 300910 300911 300912 300913 300863 300865 300134 309650 300869 300629 Min Vol Im 07 13 20 47 60 80 Max Rate ml typ 0 108 0 138 Technical Data Type of unit Classification acc to IEC EN 60601 1 Class acc to Directive 93 42 EEC Moisture protection
8. Bolus on demand Press BOL once bolus rate is blinking then press and hold BOL again as long as bolus administration is required max bolus allowed is 10 96 of syringe size or 10 seconds An audible signal will be given for each ml delivered Take care not to overdose Given a bolus rate of 800 ml h e g 0 1 ml will be reached in just 0 45 seconds During bolus no 8 syringe pre end alarm is given ET d Standby Press F then STANDBY and F are displayed and the infusion is paused indefinitely Set val ues are retained Pressing F again cancels the Standby BS T Total Volume Infused Shows the volume already infused If this exceeds 999 9 ml this max value blinks To clear the total to 0 0 ml press C or switch device off EE B Volume To Be Delivered VTBD Press F then EEA and enter the volume to be delivered confirm value with F After VTBD has been set symbol flashes During infusion VTBD counts down Infusion automatically stops when VTBD is reached Clear VIBD Press F then wani and press C The display shows for unlimited infusion Press F to accept or enter new VTBD Note Clearing VTBD also clears the Time Limitation Check remainina VTBD during infusion Press F and EEJ The remaining amount of VTBD is displayed Note Bolus infusions influence the VTBD If a rate and VTBD are set the remaining time of infusion is automatically calculated and can be checked during operation press
9. Braun e g M eliseptol amp Before opera tion the device allow to air for at least 1 min Do not spray into openings in the device Be sure to observe the instructions provided con cerning waste disposal and hygiene for batteries and disposables Check regularly Check for cleanliness completeness and dam age Use only according to Instructions for Use Check when switching on self check audible alarm process and alarm control indication Check battery contacts for corrosion and clean with smooth rubber once year Inspection on Delivery Despite careful packaging the risk of transport damage cannot be entirely prevented Upon delivery please check that nothing is missing Do not use a damaged device Contact the service department Items included Perfusor amp compact S Power Cord Pole Clamp Short Instructions for Use and syringe tables in separate packaging 4 primary batteries 21 Ordering Perfusor amp compact S 230 240 V Perfusor compact S 110 120 V Recommended accessories for the Perfusor amp compact S Connecting lead for staff call Connecting lead for ambulance car 12 V Interface lead with electrical insulation Rechargeable battery pack Y lead for central mains power supply for 2 Perfusors Original Perfusor Syringes Original Perfusor Syringe 50 ml with draw off cannula Original Perfusor Syringe 50 ml without draw off cannula Original Perfusor Syringe 50 ml with draw off ca
10. Perfusor compact S Instructions for Use Perfusor compact S Software BE Patient Safety Attention Consult accompanying documents As Read Instructions for Use prior to use Application only under regularly supervision by specially trained staff Operation gt Ensure the unit is properly positioned and secured gt Prior to use check audible and visual alarms during self test Also check the device for possi ble damage Connect to patient only after switching on the device Interrupt the connection during syringe changes to prevent incorrect dose delivery gt Select syringe catheter suitable for use with the intended medical application gt Position the infusion line free of kinks Recommended change of disposables after 24 h consider national hygiene regulations gt Installation in medically used rooms must comply with the appropriate regulations e g VDE 0100 VDE 0107 or IEC publications Observe national specifications and deviations Possible explosion hazard if used in presence of flammable anaesthetics gt Compare displayed value with entered value Start infusion only if values are corresponding gt Do not use the device when service indicator mE is displayed permanently f staff call is used we recommend to check the equipment once after connecting the pump gt Protect the device against moisture Other components gt Variations in pressure e g
11. as caused by change of level can affect the accuracy of the device gt Where several infusion lines are connected on one single vascular access the possibility of their exerting a mutual influence vice versa cannot be excluded gt Refer to respective manufacturer s informa tion for possible incompatibilities of equipment resp drugs gt Use only compatible combinations of equipment accessories working parts and disposables gt The use of not recommended resp incom patible disposables may influence the technical specifications gt 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 system configuration if additional equipment is con nected The international standard IEC EN 60601 1 1 has to be taken into account Safety Standards Perfusor amp compact S satisfies all safety stan dards for medical electrical devices in compli ance with IEC EN 60601 1 and IEC EN 60601 2 24 gt The EMC limits electro magnetic compati bility 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 tele phones etc maintain the recommended pro tective distances for these devices Perfusor compact S Content
12. conds Special Functions 3 gt 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 changes in values can be made only when the pump is stopped gt Use the F button to confirm input values or to exit the function gt f a set value is higher than the possible limit the max possible value is shown an alarm will sound The value can be accepted by pressing the F button After the device is switched off all values are cleared Syringe Selection Open the syringe holder press Exzszi the syringe code blinks Press C enter a new syringe code and confirm by pressing F Close syringe holder and start infusion Double check the new syringe code while infusion is taking place by pressing F and ES X Bolus To alter the bolus rate only when device is stopped 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 prime function is switched off Bolus and prime rate are identical Bolus applications during infusion Option A Bolus with pre selected volume Press BOL The bolus rate will blink Press C set volume 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
13. djust ments modifications or repairs are carried out by persons authorised by him the electrical installation of the relevant room complies with the appropriate requirements e g VDE 0100 0107 and or the IEC publications resp national requirements e the equipment is used in accordance with the Instructions for Use and e the Technical Safety Checks are carried out regularly The CE mark confirms that this medical prod uct complies with the Council Directive on M edical Devices 93 42 EEC dated 14th June 1993 B Braun M elsungen AG Warranty B Braun provides 24 months warranty as from the 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 undertaken by the owner or by third parties invalidate the Warranty The warranty does not cover the following Elimination of faults attributable to incorrect inexpert handling or to normal wear and tear incl primary batteries and rechargeable batteries Technical Safety Check Service The Technical Safety Check is recommended to be carried out every 2 years and should be documented Service work must be carried out exclusively by personnel instructed by B Braun Cleaning Clean using mild soap suds Do not use spray disinfectant at the mains connection Recommended disinfectant for wiping available from B
14. e 022 is displayed in combina tion with the alarm symbol This is a safety precaution as the electric safety system suspects a defect in the battery compartment e g loose contact or corroded contacts In order to switch off the alarm press and hold ON OFF key for at least 3 seconds until the alarm symbol in the display is extinguished Release the key Then again switch on the device in battery mode 14 gt Batteries should be replaced when a battery flat alarm occurs during frequent boluses or after 2 years even if the battery capacity display indicates full gt During the automatic self check the pump determines if the internal energy supply is capable of sounding a power failure alarm If the energy source is exhausted an alarm is produced In this case the operator may only use the device under constant supervision since a power failure would remain undetected by the device Only alkali manganese batteries may be placed in the battery compartment because Alkali manganese batteries recommended are free of mercury and cadmium e 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 th
15. e battery mode The capacity now is detected dur ing the self check the battery symbol in the display displays the actual capacity If the Perfusor amp compact S is switched on after being connected to AC power the symbol battery flat blinks despite having full batteries Operating Times with Standard and Rechargeable Batteries at max pressure level Compatible Syringes The syringe types listed in the following tables can be used with the Perfusor amp compact S The tables include the Code Number of syringe brands which can be selected via the syringe selection key see page 8 Please reference the tables below for specific syringe brand compatibility e g Cat Nos Note also additional information is provided regarding syringe near empty warning for each syringe size The table shows the minimum filling volume Min Vol and the maximum delivery rate M ax Rate requirements to guarantee 3 minute syringe near empty warning pre syringe alarm The bolus volumes Bolus Vol 5 have been measured in the lowest and highest pressure settings P1 P3 after the automatic reduction of the post occlusion bolus The Times to Occlusion alarm have been measured at 5 0 ml h The measured data are typical average values which can vary because of possible syringe tolerances Compatible Syringes M anufacturer B Braun Syringe Type Omnifix Omnifix Omnifix Omnifix
16. e codes Computer connection Technical inspection safety check 20 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 00 99 99 100 00 200 00 20 30 1 700 800 0 01 99 99 5 10 1 150 200 0 01 50 00 213 1 70 0 01 25 00 0 1 999 9 ml 00 01 99 00 h 0 2 Yo typ 2 5 Yo measuring time 1 h and infused volume gt 2 ml 3 settings step 1 approx 0 3 bar step 2 approx 0 6 bar step 3 approx 1 2 bar a Malfunctions of the device For incorrect dosages of 0 015 ml due to malfunctions of the device the pump automatically 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 Customer specific syringe configuration list of syringe types see page 16 ff Syringe codes see page 16 ff enclosed labels have to be attached underneath the pump RRS 232 in combination with B Braun interface lead 871 1661 including electrical separation Interface description on request Pay attention to safety notices Every 2 years Warranty TSC Service Cleaning Responsibility of the Manufacturer The manufacturer assembler installer or importer considers himself responsible for the effects on safety reliability and performance of the equipment only if assembly operations extensions re a
17. e g rate and VTBD or time are set press and hold F key also press data lock key at the same time Now all pump data are locked and the display alternately shows LOC and the current rate Press START STOP key to start the infusion Note When data lock is active no values can be changed and the bolus function is switched off It is only possible to stop or to start the device To deactivate data lock Press and hold F key and also press data lock key at the same time Note Data lock may be activated and deactivated in either STOP M ode or while infusion EN BS Battery Capacity Shows the remaining capacity of the battery 3 low medium high The LCD shows 000b when using standard batteries XXxA when using rechargeable batteries xxx capacity in mAh BST TJ To change Occlusion Sensitivity In case of an occlusion the device goes into alarm As lower the pressure setting as faster the time to occlusion alarm Press F then FTIA Press 1 low 2 medium or 3 high then press F to confirm settings During an occlusion alarm the bolus volume built up by the pump is automatically reduced Start up and Trumpet Curves The graphs show the accuracy uniformity of flow in relation to Trumpet Curves time Allow for the following M easured values for second and last hour in each case Measurement interval At 0 5 min The delivery behaviour or delivery precision is essentially Observation interval p x At
18. min influenced by the types of disposable syringe used Significant deviations may be encountered if use is made of Start up Curves disposable syringes other than those stated in the order data Measurement interval At 0 5 min Measurement duration T 120 min Flow Q ml h 10 Alarms Displays gt During an alarm the A symbol ARAR and one or more of the following symbols will blink Device alarm Symbol Cause d Display message e g 071 and permanent audible alarm signal Unit defective internal device failure Operation alarm Symbol Cause Battery flat battery near flat warning begins 30 min before the battery is dead Fx Pressure alarm e g because of an Correction Press and hold ON OFF key for at least 3 seconds until the alarm symbol in the display Is extinguished Then release the key and switch on the device again If the unit defective alarm appears again take the device to service Correction Connect to mains and or replace the alkaline batteries Bolus reduction is automatically initiated by the occlusion Fluid is unable to be infused JL pump Check for kinks in tubing IV patency and filter patency Increase occlusion pressure if necessary Check if syringe is empty Due to varying syringe tolerances a pressure alarm may occur when the syringe is empty prior to end of infusion alarm Prepare to end infusion or to begin next Syringe near empty Alarm will sound
19. nnula and particle filter with light protection Original Perfusor Syringe 50 ml with draw off cannula and particle filter Original Perfusor Syringe 20 ml with draw off cannula Original Perfusor Syringee 20 ml without draw off cannula Original Perfusor Syringe 20 ml with draw off cannula and particle filter Omnifix Syringe 50 ml Luer Lock Omnifix Syringe 30 ml Luer Lock Omnifix Syringe 20 ml Luer Lock Solo Omnifix Syringe 10 ml Luer Lock Solo Omnifix Syringe 5 ml Luer Lock Omnifix Syringe 2 ml Luer Lock Solo 22 Art No 871 4843 871 4886 8 1 1682 871 1674 8 71 1661 3450 1690 870 0109 872 8810F 872 8844F 072 8828F 872 8852F 872 8623 872 8615 872 8631 461 7509 461 7304 461 7207 461 7100 461 7053 461 7029 Original Perfusor Tubings Original Perfusor Tubing N made of PVC with Luer lock connectors 150 cm Original Perfusor Tubing L made of PVC with Luer lock connectors 200 cm Original Perfusor Tubing MR made of PVC with Luer lock connectors 75 cm Original Perfusor Tubing M made of PVC with loose lock nut on patient end 150 cm Original Perfusor Tubing PE made of PE with Luer lock connectors 150 cm Original Perfusor Tubing S made of PVC light protected with Luer lock connectors 150 cm Original Perfusor Tubing PES made of PE light protected with Luer lock connectors pressure resistant 150 cm Original Perfusor Tubing M K made of PVC with cannula and Luer lock connectors 75
20. rom the patient while changing the battery Switch off the device Remove screw 1 press in the green tab 2 and slide compartment door down Always change all batteries Taking care to observe waste disposal regulations see also page 21 Mains Connection Connection for the power supply In the event of power failure the pump automatically switches to battery power Clear data EN Alarm silence for 2 min BAS ON OFF Press for 2 sec to turn off Eni Start Stop Infusion Special Functions Function key First press F to access the special functions of the pump Select Enter key Decimal point EE Alarm indicator ITE TET Pop rete T mom mom i Pa aan Transport A maximum of three devices may be connected together Special care is required here if a patient is already connected Avoid external mechanical influence Locking Devices Together Place one device on top of the other Push con necting rod of top pump down into the slot of the pump below until it clicks into place To lock turn the key until it is vertical To disconnect turn the key until it is horizontal Push the white key in and slide up Pole Clamp Attach the Perfusor compact S from above clicking it into place To release press the black button and lift the pump from the clamp For safety purposes attach each device separately to the IV pole A rotating pole clamp can be used for a vertical fixation of
21. s Perfusor amp 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 amp compact S is according to IEC EN 60601 1 resp IEC EN 60601 2 24 a transportbale infusion syringe pump for administrating fluids in nutritional therapy and infusion technique as well as for home care applications The medical specialist must decide on suitability for application on the basis of the warranted properties and the technical data For further details please refer to the Instructions for Use Overview Handle Operation Always use the handle when carrying To access functions first press the F button Display Instructions for Use Syringe Holder Locking Lever Shows all important and Syringe Table Locks the syringe To move the drive information at a Slide out short in place unit manually push glance rate syringe instructions for Use To remove pull the locking lever up type power source and a syringe table are and turn to the until it clicks infusing symbol amp amp attached underneath left and alarm symbols the pump see Alarms on page 11 Syringe Adapter Battery Compartment Multi Function Connector MFC Connection for staff call ambulance 12 V and interface Disconnect the pump f
22. the Perfusor compact S as available Operation Infusion 1 Insert Syringe gt Switch on using Ed Note the automatic self check All display elements will appear for approx 2 seconds and the audible alarm will sound Then the rate display shows 111 1 2222 555 5 Then the software version BE In addition the mE CC mnl and decimal point will blink gt Open the syringe holder slide the locking lever up and extend the drive unit Align the primed syringe so the flange is positioned in the syringe grip plate and the top of the plunger is positioned in the syringe pressure plate Press the syringe in The locking lever should snap 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 not match the syringe type inserted see Syringe Tables Compatibilities page 16 ff gt f syringe type code is correct press F gt Prime the line by using the BOL key Prime rate adjusted bolus rate Press F then BOL once The bolus rate will blink Press and hold BOL key again until the line is primed max 1 ml respectively for 10 seconds can be delivered If applicable repeat priming with BOL key During STOP the infused bolus volume is not added to TOTAL volume 2 Setting the Rate gt Enter between 0 01 and 200 0 ml h e g enter 2 56 ml h press 2 5 6 Check displa
23. y To correct Press C and enter the new rate 1 See Technical Data Here only insert a 50 ml Original Perfusor Syringe OPS Syringe grip plate insert here all syringes except OPS 50 ml Movable Drive Mechanism Syringe Holder Locking Lever Syringe grip plate Syringe Pressure Plate insert here 3 Start the Infusion gt Press START Rotating infusion symbol is displayed 4 Stop the Infusion gt Press STOP or Ca for 2 seconds Disconnect from the patient gt Open the syringe holder Remove the syringe gt To switch off press a for 2 seconds To Change Syringes gt Press STOP Disconnect from the patient 2 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 6 gt Open syringe holder and remove the syringe Insert a new primed syringe with primed tubing gt Close syringe holder Confirm the type of syringe by pressing F gt Connect to patient and press START To change the rate gt Press STOP gt Press C and enter the new rate gt Press START To Change the Rate Without Interrupting the Infusion Titration While the infusion is in process simply press C and enter new rate then confirm by pressing F The new rate now applies If F is not pressed after making the rate change the display will revert to the previous rate after 10 se
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