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Page 1
Perfusor® Space and Accessories Instructions for Use It is recommended that all pumps at your care unit are equipped with the same software version. Valid for software 688M… -
Page 2: Table Of Contents
CONTENTS Perfusor® Space Overview………………………3 Symbols on Product ……………………….5 Patient Safety ……………………….6 Menu Structure / Navigation……………………11 Chapter 1 Operation ……………………..14 1.1 Start of Infusion …………………….14 1.2 Entry With Different Combinations of Rate, VTBI (= Volume To Be Infused) and Time……………………….15 1.3 Bolus Application ……………………16 1.4 Syringe Change and New Therapy Start …………….17 1.5 End of Infusion……………………..18 1.6 Standby Mode ……………………..18…
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Page 3: Perfusor® Space Overview
PERFUSOR SPACE® OVERVIEW P E R F U S O R ® S PA C E O V E R V I E W Arrow up and -down Press to reset single values Drive head with Scroll through menus, change setting of numbers from 0-9,…
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Page 4
For vertical fixation of PoleClamp push lever down and rotate either way until lever clicks into notch. Push lever for rotation. Caution: A maximum of three B. Braun Space pumps can be stacked together when used with the PoleClamp SP. -
Page 5: Symbols On Product
SYMBOLS ON PRODUCT S Y M B O L S O N P R O D U C T Symbol Explanation Mandatory action: see instruction for use. See accompanying documents. Type CF unit with defibrillation protection Protection class II device Symbol indicating separate collection for electrical and electronic equipment (2002/96/EC) CE mark compliant to Directive 93/42/EEC…
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Page 6: Patient Safety
Operation • The initial training of the Perfusor® Space is to be performed by B. Braun sales personnel or other authorized persons. After each software update, the user is required to inform himself of the changes to the device and accessories by referring to the Instructions for Use.
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Page 7
PATIENT SAFETY • Only connect to patient once the syringe has been inserted correctly and there is proper fixation of the syringe pressure plate by the claws of the drive head. Interrupt connection during syringe change to prevent incorrect dose delivery. -
Page 8
PATIENT SAFETY Enteral Nutrition The Perfusor® Space may be used for enteral nutrition. Do not use enteral fluids for intravenous infusion as this may harm your patient. For this reason only use disposables dedicated and labeled for enteral nutrition. Other components •… -
Page 9
TCI and properly trained in using the present device. • The use of TCI with B. Braun Space does not limit the responsibility of the anaesthetist for administration of drugs. They need to be fully aware of the available literature for any parameter set used in association with a drug and need to refer to the prescribed information for rate and dosing limits. -
Page 10
PATIENT SAFETY • While using TCI an appropriate patient monitoring is mandatory. • Take care of using the right dilution/concentration of the drug and make sure the right dilution is selected at the pump. • Never administer Propofol or Remifentanil by a second infusion as long as you use TCI. -
Page 11: Menu Structure / Navigation
MENU STRUCTURE / NAVIGATION MENU STRUCTURE / NAVIGATION Cutline On/Off button OK button Start/Stop button Keypad with arrow up, -down, -left, -right button Bolus button Connection button Clear button All display screen shots are examples and may be different when related to an individual patient and individualized therapy.
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Page 12
MENU STRUCTURE / NAVIGATION Display Meaning All status information is available in the bottom line of the dislplay. The desired information can be selected by using and will be displayed permanently thereafter (e. g. drug long name, time until syringe empty, current system pressure etc.). -
Page 13
MENU STRUCTURE / NAVIGATION Start Up Main Special Options Status Menu Menu Functions Menu Menu Syringe Dose Rate Occlusion Intermediate Dose selection Calculation Pressure volume Intermediate Prime ? Concentration Drug Library OccluGuard amount Change-over Use last Pressure Intermediate Weight therapy ? from Leap/Drop time… -
Page 14: Chapter 1 Operation
OPERATION Chapter 1 OPERATION 1.1 Start of Infusion • Ensure correct installation of the pump device. If the pump is connected to mains, the display states information such as the battery status, the mains connection symbol and the last therapy. •…
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Page 15: Entry With Different Combinations Of Rate, Vtbi (= Volume To Be Infused) And Time
OPERATION Chapter 1 • Press to commence infusion. Running arrows on display and green LED above display indicate pump is infusing. Note: Stop the infusion at any time by pressing . The pump can be turned off at any time by pressing for 3 sec (Exception: Data lock level 2) and as long a disposable is inserted.
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Page 16: Bolus Application
OPERATION Chapter 1 a) Target symbol is placed in front of VTBI: • Change of VTBI => Adjustment of time. Old and new target: VTBI • Change of time => Adjustment of rate. Old and new target: VTBI b) Target symbol is placed in front of time: •…
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Page 17: Syringe Change And New Therapy Start
OPERATION Chapter 1 1.4 Syringe Change and New Therapy Start Note: To avoid incorrect dosing, always disconnect the pump from the patient when changing the syringe. Never leave the pump device unattended during syringe change. Before inserting a new syringe check if the axial fixation is properly working. •…
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Page 18: Standby Mode
OPERATION Chapter 1 • Open pump cover. Remove the syringe, move the syringe holder into an upright position and close the front door. • Press for 3 sec. to switch the pump off. The drive moves into parking position. Note: The settings will be permanently saved by the switched off device.
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Page 19: Chapter 2 Advanced Operations
OPERATION Chapter 1 ADVANCED OPERATIONS 2.1 Status Request of Pump when Infusion is Running Press to switch between run display and Main Menu while the device is infusing. Navigate through the menu using to check parameters. In order to check the menu parameters in the Status-/Options Menu, select «Status»…
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Page 20: Chapter 3 Special Functions
ADVANCED OPERATIONS Chapter 2 SPECIAL FUNCTIONS 3.1 Dosing Units and Dose Rate Calculation (Overview) The following list shows the units used in the pump: Gram family: ng, mcg, mg, g Unit family: mIU, IU, kIU, MIU Equivalents family: mEq Mole family: mmol Kilocalorie family: kcal Millitliter family:…
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Page 21: Dose Rate Calculation (Operation)
SPECIAL FUNCTIONS Chapter 3 3.2 Dose Rate Calculation (Operation) a Select dose rate calculation with l. a Select the unit of the active ingredient with and confirm it with l. a Enter the concentration by entering the amount of the active ingredient and the volume.
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Page 22
SPECIAL FUNCTIONS Chapter 3 On the one hand, a drug name including the according therapy data can be taken from the drug library. On the other hand, if a rate, VTBI and/or time were already defined in the Main Menu, the drug name and the adjusted values of the data set will be loaded. -
Page 23
SPECIAL FUNCTIONS Chapter 3 • Select the desired drug with and press l. Before the initial bolus begins, the bolus menu is displayed to allow editing the bolus with q. • Check the parameter and start infusion with Hard Limits: If the set rate/dose/bolus volume and bolus rate exceed the values stored in the drug library (hard limits), the drug will be rejected, a hint will be displayed and the pump will fall back into the drug selection. -
Page 24: Patient Controlled Analgesia (Pca) (Optional)
SPECIAL FUNCTIONS Chapter 3 The Drug Library Upload starts as soon as the pump is in Passive mode. You can cancel the upload by pressing c. Note: Please contact your local sales represantative in case you like to use Remote Drug Library update.
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Page 25
SPECIAL FUNCTIONS Chapter 3 In this state the patient is allowed to demand boli. Depending on the status of the therapy these are either administered or denied. Changing the syringe is also possible by using the code for level 1 or level 2. Altering the settings for PCA or other therapies however is only possible with the code for level 3. -
Page 26: Target Controlled Infusion (Tci) (Optional)
The pharmacokinetic model and its parameters are schematically depicted by the following illustration: B. Braun Space is offering two modes for TCI: • TCI by targeting the plasma concentration In this mode the user selects the desired concentration of a drug in the…
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Page 27
TCI. A pharmacokinetic model modi- fied in such way is schematically depicted by the illustration on the next page. TCI with B. Braun Space is possible with two drugs: Propofol and Remifentanil. For Propofol the user can choose between two parameter sets. The parameter… -
Page 28
SPECIAL FUNCTIONS Chapter 3 Drug / Parameter Propofol Remifentanil [Litre] 0,228 * Weight 4,27 5,1 — 0,0201 * (Age — 40) + 0,072 * (LBM — 55) [min 0,119 0,443 + 0,0107 * (Weight — [2,6 — 0,0162 * (Age — 40) + 77) — 0,0159 * (LBM — 59) + 0,0191 * (LBM — 55)] / [5.1 — 0,0062 * (Height — 177) -
Page 29
Chapter 3 Important note: Before installing an additional drug list please contact your local B. Braun representative! Setting up the pump For TCI a drug list with at least one drug activating the profile TCI is necessary. The drug list in this version is pre-defined. By this the conditions for an effective and safe therapy are defined. -
Page 30
SPECIAL FUNCTIONS Chapter 3 Important notes: • Be sure to enter the data corresponding to the respective patient. • Once the TCI is started patient data can not be altered! Editing a target and starting TCI The editor window for setting the target comes up with the default value from the drug list. -
Page 31
SPECIAL FUNCTIONS Chapter 3 Useful information while pump is running By pressing additional information can be requested. Pressing a second time is offering a graphical overview. The line describes the course of Cp over the time and the area describes the course of Ce over the time. -
Page 32: Barcoding
SPECIAL FUNCTIONS Chapter 3 Barcoding The barcoding functionality is included but initially not activated. Please contact your local sales representative in case you like to use barcoding. Ramp and Taper Mode The Ramp and Taper Mode is designed to deliver infusions with gradual ramp up and taper down rates.
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Page 33
SPECIAL FUNCTIONS Chapter 3 Set Profile Parameters: The therapy can be started directly via the drug library or via the Main Menu/Special functions. Starting Ramp and Taper via Drug Library: Note: Ramp and Taper settings have been configured in the Drug List Manager before and have been uploaded into the pump. -
Page 34: Program Mode
SPECIAL FUNCTIONS Chapter 3 Taper phase The pump linearly decreases the rate in the predefined time until it reaches the KVO rate Note: After starting infusion it is only possible to change rates, time and VTBI in the continuous phase. By editing (increasing/decreasing) the plateau rate, the therapy is recalculated.
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Page 35
SPECIAL FUNCTIONS Chapter 3 Example: Program Mode should only be performed by an experienced user being familiar with the principles of the Program Mode function and properly trained in using the present device. Note: The active Program Mode function always displays this icon in the Display Note: Bolus function is disabled for Program Mode. -
Page 36: Intermittent Mode
SPECIAL FUNCTIONS Chapter 3 The pump can be started now by pressing Starting Program Mode via Special Function Menu: • Switch on pump with and wait until self-check is finished. • Insert disposable. • Go to Special Functions Menu and select Program Mode. •…
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Page 37
SPECIAL FUNCTIONS Chapter 3 Example: Intermittent Mode should only be performed by an experienced user being familiar with the principles of the Intermittent Mode and properly trained in using the present device. Note: The active Multi Dose Mode function always displays this icon in the Display Note: Regular Bolus function is disabled for Intermittent Mode. -
Page 38
SPECIAL FUNCTIONS Chapter 3 Starting Intermittent Mode via Special Function Menu: • Switch on pump with and wait until self-check is finished. • Insert disposable. • Go to Special Functions Menu and select Intermittent Mode. • Press to enter parameters and to confirm. -
Page 39: Dose Over Time
Note: The feature Dose Over Time always requires the usage of dosing units (i.e., mg or mg/kg patient weight). Before using Dose Over Time contact your local B. Braun representative! Starting Dose Over Time via Drug Library: Note: Dose Over Time settings have been configured in the Drug List Manager before and have been uploaded into the pump.
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Page 40
SPECIAL FUNCTIONS Chapter 3 • Insert disposable and use the drug library according to the Instructions for Use. • Select a drug by using and press l. The pump now offers the possible therapy profiles. Select “Dose over Time” with press l. -
Page 41: Take Over Mode (Tom) (Optional)
SPECIAL FUNCTIONS Chapter 3 3.11 Take Over Mode (TOM) Take Over Mode is a feature to support the user during syringe changes by auto- matically starting a second Perfusor® Space pump when the first has run empty. The second pump automatically takes over the infusion rate from the first pump. Activation: •…
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Page 42
SPECIAL FUNCTIONS Chapter 3 • Navigate through the list with and select in alphabetical order (all drugs) or within a category with l. The drug selected in the second pump must be the same as the first. • Navigate through the list with and select a concentration with l. -
Page 43
SPECIAL FUNCTIONS Chapter 3 Note: Start-up behaviour is not influenced by TOM. See Chapter Start Up Graphs and Trumpet Curves. Note: Please use a seperate patient connection for Take Over Mode infusion (e.g. smallbore extension set) or use a back check valve for lines at the same access which are not used for Take Over Mode. -
Page 44
SPECIAL FUNCTIONS Chapter 3 Recommendation Ensure first Perfusor® Space pump is infusing Ensure first Perfusor® Space pump must be running in ‘continuous mode’ (i.e. ml/h or a dose rate; not KVO, PCA etc.) Deactivate Data Lock Data connection must be active between pumps –… -
Page 45
SPECIAL FUNCTIONS Chapter 3 Changes in TOM system: Change Reaction Rate changed in pump No user interaction necessary, will start infusion at new rate when syringe is empty. pump is stopped pump shows “connection lost – TOM aborted” alarm. TOM may be reactivated by pump is put in standby pressing and then… -
Page 46: Chapter 4 Autoprogramming
AUTOPROGRAMMING Chapter 4 A U TO P R O G R A M M I N G Note: All normal pump functions remain in place when orders are received via autoprogramming. The pump can accept drug orders wirelessly from the EHR system or from SpaceStation with SpaceCom.
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Page 47
AUTOPROGRAMMING Chapter 4 Note: Order may be cancelled prior to confirming order. • Once all values are confirmed, the Main Menu is displayed. Note: Soft Limit alert will be issued if value exceeds any soft limits set in drug library, soft limit may be overridden or value re-programmed per institutional policy. -
Page 48
AUTOPROGRAMMNG Chapter 4 • Follow prompt, pressing to accept order or key to cancel and hold order for later. New Primary Infusion: • To accept a new PRIMary order, stop infusion and clear current PRIMary infusion by pressing key and responding “yes” to clear current infusion. PIGGYback Orders: Orders received after PRIMary has been set will be for PIGGYback infusions, follow prompts on screen to stop the PRIMary to accept the PIGGYback order. -
Page 49
AUTOPROGRAMMING Chapter 4 Note: Changing values on any incoming order may only be done after confir- ming all values. Once all values are confirmed you may scroll to any value and open editor with to change value. Alternately, order may be cancelled and request made for revised order to be sent. -
Page 50: Chapter 5 Options
OPTIONS Chapter 5 OPTIONS The options functions may be selected and changed while the pump is infusing or stopped. To edit a menu item, select “Options” in the Main Menu and press l. Then select desired function with and follow the Instructions for Use as described. 5.1 Occlusion Pressure The higher the pressure level is set at, the higher the pressure level must rise before triggering an occlusion pressure alarm.
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Page 51
OPTIONS Chapter 5 OccluGuard activation / deactivation from the Main Menu • Go to Options Menu and press l. • Navigate through the list with and select OccluGuard. • OccluGuard can be activated with and deactivated with d. Pressure Leap/Drop detection The pressure leap/drop software detects sudden increases and decreases in infu- sion pressure respectively which can be caused by problems in IV access, or changes in pump position in the SpaceStation. -
Page 52
OPTIONS Chapter 5 OccluGuard Meaning Recommendation Symbol OccluGuard is active. Infusion is running stably Pending – OccluGuard has not enough data OccluGuard will automatically reactivate as soon as infusion rate OccluGuard Inactive drops below threshold levels – see above. Confirm alarm and check IV access, IV setup and syringe for cause of Occlusion has been occlusion. -
Page 53: Data Lock
OPTIONS Chapter 5 When a change is made to the infusion system (e.g. addition or removal of a pump to a SpaceStation, a change of infusion rate, a bolus application) the OccluGuard and pressure leap/drop are temporarily set to ‘pending’ ( ) to allow the system to reach a hydrostatic balance, and so prevent false alarms.
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Page 54: Bolus Rate
OPTIONS Chapter 5 Activation of the function: • Open data lock in Options Menu with l. • Select between level 1, 2 or 3 (if activated) with and confirm with k. • Enter code with and press in order to activate data lock. Changes to the protected values and the bolus function which are marked withy are only possible after entering the code.
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Page 55: Alarm Volume
OPTIONS Chapter 5 5.7 Alarm Volume Chose between 9 different alarm volume levels. • Open alarm volume in Options Menu with l. • Set volume with and confirm entry with k. 5.8 Date / Time • Open date/time in Options Menu with l. •…
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Page 56: Chapter6 Alarms
ALARMS Chapter 5 ALARMS The Perfusor® Space is equipped with a audible and optical alarm signal. Audible Alarm- Optical signal Staff call User confirmation type signal Red LED Yellow LED Text Device flashes device Press and follow Alarm alarm and the instruction on the alarm code display.
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Page 57
ALARMS Chapter 6 Display message Pre-alarm reason “Syringe nearly empty“ Very little fluid is left in syringe. “VTBI near end“ The preselected volume is nearly infused. “Time near end“ The preselected time is almost over. “Battery nearly empty“ The battery is almost discharged. “KVO mode“… -
Page 58
ALARMS Chapter 6 the alarm message, and the staff call (optional) are all cleared by pressing k. Corrections should be made in accordance with the alarm reason. Display message Alarm reason “Syringe empty“ There is no fluid left in the syringe. Due to varying syringe tolerances of syringes from other manufacturers, some fluid may be left inside the syringe. -
Page 59
ALARMS Chapter 6 “Calibrate device“ Pump calibration data have changed (e.g. after an update). Recalibrate device via the service program. “Claw malfunction“ The emergency release button was pressed and the claws manually opened. Take out syringe and contact technical service department. “Plunger plate not prop. -
Page 60: Reminder Alarms
ALARMS Chapter 6 6.3 Reminder Alarms Reminder alarms only occur in two cases: 1. A syringe is inserted, the pump doesn’t administrate, no value is being edited and the device is not operated for two minutes. An acoustic tone sounds, the yellow LED is constantly on and a staff call is activated.
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Page 61: Battery Operation And Maintenance
BATTERY OPERATION AND MAINTENANCE Chapter 7 BATTERY OPERATION AND MAINTENANCE The battery has an operating lifetime of 8 hours at 25 ml/h when new. For optimal treatment of the battery, the device is equipped with protection against overcharge and deep depletion. The battery pack is charged by the pump during connection to mains.
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Page 62
BATTERY OPERATION AND MAINTENANCE Chapter 7 • If a battery, which is not completely discharged, is charged several times, its capacity can be reduced. • Under normal temperature conditions a battery can be charged and discharged approx. 500 times before its lifetime decreases. •… -
Page 63: Chapter 8 Compatible Syringes
) to ensure specific syringe brand compatibility. The Time to Occlusion alarm has been measured at 5 ml/h. The measured data are typical values which may vary because of possible syringe tolerances. Manufacturer: B. Braun Syringe Type Omnifix Omnifix Omnifix Omnifix Omnifix B.
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Page 64
COMPATIBLE SYRINGES Chapter 8 Manufacturer: TYCO USA Syringe Type Monoject Monoject Monoject Monoject Monoject Monoject 3 ml 6 ml 12 ml 20 ml 35 ml 50/60 ml TYCO USA Mat. No. 8881- 8881- 8881- 8881- 8881- 8881- 513934 516937 512878 520657 535762 560125… -
Page 65
COMPATIBLE SYRINGES Chapter 8 Manufacturer: TERUMO Syringe Type 3 ml 5 ml 10 ml 20 ml 30 ml 50 ml 60 ml TERUMO EU/USA/JAP Mat. No. 3SS*03L 3SS*05L 3SS*10L 3SS*20L 1SS*30LZ1 2BS-50LG 3SS*60L 1SS*05LZ1 1SS*10LZ1 SS*20ES typ. typ. typ. typ. typ. -
Page 66
COMPATIBLE SYRINGES Chapter 8 Manufacturer: Becton-Dickinson Syringe Type BD Precise BD Precise B-D Precise 50 ml A/P 20 ml A/P Mat. No. 300144 300141 Time to Occl. [mm:ss] 03:17 01:11 [mm:ss] 16:36 05:03 Manufacturer: Polfa Syringe Type Polfa 50 ml Mat. -
Page 67
COMPATIBLE SYRINGES Chapter 8 Syringes not specified in IEC/EN 60601-2-24 Nutrition pumps, in contrast to infusion pumps, are not classified as Class IIa according to the infusion pump norm IEC/EN 60601-2-24. There are therefore no direct guide- lines concerning the technical characteristics (accuracy of infusion rate, alarm parameters etc) of the relevant disposables. -
Page 68: Start Up Graphs And Trumpet Curves
START UP GRAPHS AND TRUMPET CURVES Chapter 9 START UP GRAPHS AND TRUMPET CURVES Start Up Curves Trumpet Curves The graphs show the accuracy/uniformity of flow in relation to time. They allow for the following: The delivery behaviour or delivery precision is essentially influenced by the type of (disposable syringe) used.
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Page 69: Is Depending On Chapter10 Technical Data
Moisture protection IP 22 (fluid protected for horizontal usage) External power supply: • Rated voltage Via B. Braun SpaceStation or optional mains adaptor (rated voltage 100 … 240 V AC~, 50/60 Hz) for stand alone operation • External low voltage 11 ……
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Page 70
Delivery rate 1 ml/h: KVO-rate = set rate (default setting 0.1 ml/h) Computer connection USB connection in combination with B. Braun interface lead CAN SP (8713230) including electrical insulation. Please pay attention to safety notices. History protocol < 3000 last history entries. -
Page 71
TECHNICAL DATA Chapter 10 • Only use combined with approved devices/accessories by the manufacturer, otherwise this may lead to higher emission or reduced immunity. • Use only compatible combinations of equipment, accessories, working parts and disposables with luer lock connectors. Essential Performance for Infusion pumps: •… -
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TECHNICAL DATA Chapter 10 EMC (ELECTROMAGNETIC COMPATIBILITY) -
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TECHNICAL DATA Chapter 10… -
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TECHNICAL DATA Chapter 10… -
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TECHNICAL DATA Chapter 10… -
Page 76: Warranty / Tsc* / Service / Training / Cleaning / Disposal
• the Technical Safety Checks are carried out regularly. Warranty The CE mark confirms that this B. Braun provides 24 months warranty, as from the date of delivery, for every medical product Perfusor® Space (12 months for every Battery-Pack SP). This covers repair or complies with the replacement of parts damaged as a result of design/manufacturing errors or «Council Directive…
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Page 77
Note: Do not use Hexaquart® or other alkylamine containing disinfectants. Recommended: disinfectant for wiping available from B. Braun: Meliseptol® Foam pure, Melsitt 10% and Melsept SF 10%. Note: Keep instrument upright and do not allow any part of instrument to become saturated with or submersed in fluid during cleaning operation. -
Page 78
Disposal The pumps as well as battery packs can be returned to B. Braun for further disposal. When taking care of disposing of disposables as well as infusion soluti- ons, please consider the applicable hygiene and disposal regulations. -
Page 79: Instructions For Use Accessory
Comfort additionaly includes a central alarm management and alarm LEDs. PoleClamp SP (8713130) A maximum of three B. Braun Space pumps and one SpaceControl can be stacked together when used with the PoleClamp SP. For detailed instructions on secure fixation of the PoleClamp SP please refer to «Overview Perfusor® Space»…
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Page 80
INSTRUCTIONS FOR USE ACCESSORY Chapter 12 3.) Push plug of Connection Lead SP into 12 V connector. Note: A maximum of three plugs can be stacked upon each other in socket P2. Battery-Pack SP (NiMH) (8713180) Battery-Pack SP (NiMH) incl. Pin (8713180A) For further information on the Battery-Pack SP (NiMH) see “Battery Operation”. -
Page 81
INSTRUCTIONS FOR USE ACCESSORY Chapter 12 Connection Lead SP (12 V) (8713231) Install the Connection Lead SP (12 V) in the following way: 1.) Connect plug to socket P2 on back of pump or F3 on SpaceStation respectively. 2.) Put the connection lead into the car socket. 3.) If necessary, remove red adaptor of motor vehicle connector by slightly turning and simultanously pulling. -
Page 82
INSTRUCTIONS FOR USE ACCESSORY Chapter 12 Caution: The user should always closely observe the local pump alarms as well. Note: A maximum of three plugs can be stacked upon each other in socket P2. Technical Data Connecting Wire white and green white and brown Alarm disconnected… -
Page 83
INSTRUCTIONS FOR USE ACCESSORY Chapter 12 P C A — A c c e s s o r i e s • Space PCA-Kit (REF 8713554) consisting of: : — Demand button — Hook and loop tape for fixation of the demand button at the patient s arm — Line fixation connection between hook and loop tape… -
Page 84: Ordering
ORDERING Art. No. B. Braun Perfusor® Space (100 – 240 V) ……….871 3030 Recommended accessories for the B. Braun Perfusor® Space: SpaceStation ………………..871 3140 SpaceCover Standard ………………871 3147 SpaceCover Comfort ………………871 3145 PoleClamp SP…………………871 3130 Power Supply SP EU III ……………….871 3110D Power Supply SP EU III 3.0m……………..871 3123D…
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Page 85
ORDERING 50ml, yellow inked cylinder and aspiration needle…….87 28801 F 50ml, yellow inked cylinder, aspiration needle and 15 µm particle filter …………….872 8800 F 50ml, black, aspiration needle and particle filter……..872 8828 F Omnifix® syringes Omnifix® 50/60 ml Luer Lock……………461 7509F Omnifix®… -
Page 86
ORDERING Type PCA, PVC tube 1,5 mm, 150 cm, Luer Lock ……..872 6019 with 0.2 µm Sterifix filter, PVC tube 1,5 mm, 200cm, Luer Lock …………………872 3001 with SafeSite valve, PVC tube 1,5 mm, 150 cm, Luer Lock………………..872 2820… -
Page 90
Manufactured by: B. Braun Melsungen AG B. Braun Melsungen AG Sparte Hospital Care 34209 Melsungen 34209 Melsungen Germany Germany Tel +49 (0) 56 61 71-0 Tel.: +49 (0) 56 61 71-0 Fax: +49 (0) 56 61 71-20 44 38916517 • Drawing No. I0688700201 Printed on pulp bleached 100 % chlorine-free www.bbraun.com…
Перфузор Спэйс B/Braun |
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1.0
2
Unit Diagnosis / Calibration
Error Code
1
1100
Timebase too fast
2
1101
Timebase too slow
3
1102
Timebase fail
4
1103
Keyboard High
5
1104
EA_KEY defect 25sec
6
1105
No keydecode
7
1106
ROM Romtest defect Software
8
1107
ROM Program defect
9
1108
CM State without set
K_V_KM_ON
10
1109
MPU_Test failed
11
1110
RAM_Test failed
12
1111
active reset
13
1112 … 1114
Internal Error
14
1115
Drive too fast
15
1116
Drive too slow
16
1117 … 1118
Internal Error
17
1119
lcd backlight on defect
18
1120
lcd backlight off defect
19
1121
red led on defect
20
1122
red led off defect
21
1123
key pressed too long (without EA-
Key) 60sec
22
1124 … 1127
Internal Error
23
1128
Drive motion rightless forward
24
1129
Drive motion rightless backward
25
1130 … 1200
Internal Error
Table 2 — 3 Device alarms of the control microprocessor (Part 1 of 2)
2 — 6
Definition
Quartz of the processor PCB
Quartz of the processor PCB
Quartz of the processor PCB
Keyboard defective
Keyboard defective
Keyboard defective
Software
Software
Software
Software
Voltage supply during operation
interrupted
Motor drive
Recognition of direction of
rotation
Motor drive
Recognition of direction of
rotation
LC display defective
LC display defective
LC display defective
LC display defective
Keyboard defective
Motor drive
Recognition of direction of
rotation
Motor drive
Recognition of direction of
rotation
Possible Cause
Exchange processor PCB
Exchange processor PCB
Exchange processor PCB
Carry out device check
Carry out device check
Carry out device check
Update unit software
Update unit software
Update unit software
Update unit software
Exchange processor PCB
Exchange processor PCB
Exchange operating unit
Exchange operating unit
Exchange operating unit
Exchange operating unit
Carry out device check
Exchange processor PCB
Exchange processor PCB
Fault Clearance
Perfusor® Space, 1.0 gb
Автоматизированная волюметрическая инфузионная система Инфузомат Спэйс B braun состоит из переносного электронного волюметрического насоса, специальных инфузионных систем и принадлежностей к насосу. Система предназначена для проведения терапии у взрослых, детей и новорожденных. Инфузомат Спэйс B braun предназначен для проведения периодического или непрерывного парентерального или энтерального введения растворов через клинически обусловленные доступы. Перечень доступов включает венозный, ирригационный/абляционный и энтеральный, но не ограничивается только ими.
Система Инфузомат Space B braun применяется для введения медикаментов, предназначенных для инфузионной терапии, включая коллоиды и кристаллоиды, кровь и ее компоненты, полное парентеральное питание, липиды, энтеральные смеси, но не ограничивается только ими. Автоматизированная волюметрическая инфузионная система Инфузомат Спэйс B braun предназначена для применения подготовленным медицинским персоналом в стационарных и амбулаторных лечебных учреждениях, на дому и в санитарном транспорте.
Инфузомат Спэйс B braun обзор
Передняя панель
Вид сзади
Установка линии Инфузомат Спэйс B braun
Список лекарств Инфузомат Спэйс B braun
До 720 наименований лекарств, включая параметры инфузии и информацию о лекарстве, могут быть сохранены в 15 категориях. Загрузка списка в насос может быть произведена с помощью отдельной компьютерной программы “Drug List Editor Space” (Редактор Списка Лекарств Спэйс).
Список лекарств доступен из Меню Пуск и Меню Специальные функции. Перед началом применения Списка, Пользователь должен убедиться, что Список лекарств в насосе соответствует данной группе пациентов. Наименование Списка лекарств будет отображен на экране насоса.
Существует несколько способов вызова Списка лекарств из Меню для последующего применения. Это возможно как во время инфузии, так и при остановке насоса. С одной стороны, наименование лекарства со всеми параметрами инфузии может быть выбрано из Списка лекарств. С другой стороны, если скорость, объем и/или время уже были заданы в Главном меню, загружаются наименование лекарства и вновь заданные параметры инфузии. Если расчет дозы уже начат, последующее использование наименования лекарства из списка все равно возможно.
Сигналы и тревоги
Инфузомат Спэйс оснащен звуковой и визуальной сигнализацией тревоги.
Сигналы неисправности прибора
При появлении сигнала неисправности прибора инфузия немедленно прекращается. Нажмите кнопку включения для отключения прибора. Затем включите прибор снова. При повторном сигнале тревоги, закройте роликовый зажим, отсоедините пациента, откройте переднюю дверцу насоса и выньте систему. Прибор необходимо передать в сервисную службу.
Сигналы предупреждения и сигналя оповещения
Сигналы предупреждения:
Предупреждения подаются за несколько минут (в зависимости от сервисных установок) перед сигналами оповещения. Сигнал предупреждения включает звуковой тон, мигающий желтый индикатор и активирует систему вызова персонала (опция). Текстовое сообщение зависит от причины тревоги. Звуковой тон и система вызова персонала отключаются нажатием кнопки «ОК». Экран и индикатор остаются в режиме предупреждения вплоть до отключения сигнала оповещения. Во время подачи сигнала предупреждения инфузия не прерывается.
Объем почти введен
Введение заданного объема близко к завершению.
Время истекает
Заданное время инфузии скоро истечет.
Батарея разряжается
Батарея почти разряжена.
KVO активен
Объем введен/Время истекло и насос продолжает ин-фузию в режиме KVO — Открытая вена.
Ошибка соединения
Насос установлен в систему, хотя бы один из приборов в которой несовместим или неисправен. Применение этого прибора в системе не разрешается. Систему необходимо передать для проверки в сервисную службу.
Сигналы оповещения:
Сигналы оповещения приводят к прерыванию инфузии. Подается звуковой сигнал, мигает красный индикатор и активируется система вызова персонала. На экране появляется сообщения «Тревога» и информация о причине сигнала тревоги. Звуковой сигнал и система вызова персонала могут быть отключены кнопкой «ОК». Коррекция должна быть произведена в соответствие с причиной сигнала тревоги.
Объем введен
Заданный объем введен. Продолжите инфузию или введите новые параметры.
Время истекло
Заданное время инфузии истекло. Продолжите инфузию или введите новые параметры.
Батарея разряжена
Батарея разряжена. Подключите прибор к сети и/или замените батарею. Сигнал о разрядке батареи длится 3 минуты, после этого насос автоматически отключается.
Высокое давление
Обнаружена окклюзия в системе. Достигнут установленный уровень давления. Насос автоматически понижает скорость введения. Проверьте отсутствие петель и перегибов инфузионной системы и проходимость инфузионного фильтра и в/в катетера. Увеличьте уровень окклюзионного давления если необходимо.
KVO остановлен
Время работы в режиме KVO истекло. Продолжите инфузию или введите новые параметры.
Крышка батарейного отсека удалена
Крышка батарейного отсека установлена неправильно. Переустановите крышку до щелчка.
Время паузы истекло
Установленное время паузы истекло. Задайте новое время паузы или возобновите предыдущую инфузию.
Батарея не установлена
Использование насоса без батареи невозможно. Отключите прибор и установите батарею.
Привод блокирован
Шаговый двигатель не работает из-за высокого давления в системе. Отсоедините систему от пациента и переустановите ее.
Откалибруйте прибор
Параметры калибровки насоса были изменены (например, после обновления программного обеспечения). Выполните калибровку через сервисную программу. Выполняется Сервисной службой.
Датчик капель отсоединен
Прерван контакт с датчиком капель во время работы насоса. Проверьте правильность крепления датчика капель на капельной камере инфузионной магистрали. При необходимости переустановите датчик капель или задайте объем и продолжайте инфузию.
Проверьте линию на входе
Сигнал тревоги от входного датчика давления. Убедитесь, что роликовый зажим открыт и отсутствуют перегибы инфузионной линии между флаконом и насосом.
Воздушные пузырьки / Аккумулированный воздух
Воздух в системе. Осмотрите инфузионную систему, отключите ее от пациента и повторите ее заполнение при необходимости.
Нет капель
Датчик капель не обнаруживает капель. Возможные причины: инфузионный флакон пуст, роликовый зажим закрыт, датчик капель не установлен на капельную камеру. Проверьте отсутствие перегибов инфузионной системы, конденсацию на капельной камере (для удаления конденсата, встряхните капельную камеру).
Слишком мало капель
Количество падающих капель меньше заданной скорости инфузии. Возможные причины: отрицательное давление в стеклянном инфузионном флаконе. Для устранения — откройте вентиляционный клапан на капельной камере. Другие причины: инфузионный флакон пуст, роликовый зажим открыт не полностью, перегибы инфузионной линии. При обнаружении – устраните указанные препятствия.
Слишком много капель
Количество падающих капель больше заданной скорости инфузии. Возможные причины: инфузионная система повреждена, неправильно установлена в насос, либо не герметично подсоединена к катетеру.
Свободный поток
Капельная камера заполнена жидкостью или протечка в системе. Проверьте герметичность системы. Проверьте датчик капель.
Данные сброшены
Данные инфузии и насоса не возможно восстановить. Введите данные инфузии и настройки насоса заново.
Данные инфузии сброшены
Параметры инфузии не возможно восстановить. Введите параметры инфузии заново.
Время паузы истекло
Установленное время паузы истекло. Задайте новое время паузы или возобновите предшествующую инфузию.
Блок данных
Была попытка остановить или отключить насос без ввода кода. Введите правильный код для соответствующего продолжения инфузии или выключите насос.
Внимание: Если на экране появляется символ гаечного ключа и/или одновремен-но мигают желтый, красный и синий индикаторы – насос находится в сервисном режиме и его использование для лечения пациентов запрещено. Насос должен быть проверен сервисной службой.
Работа от батареи и обслуживание
Инфузомат Спэйс оснащен современной NiMH-батареей. Время работы насоса с новой батареей составляет 4 часа при скорости инфузии 100 мл/ч. Для оптимальной работы батареи, насос имеет защиту от перегрузки и полной разрядки. Батарея заряжается при включении прибора в сеть. При отключении от сети или в случае падения напряжения, насос автоматически переходит на питание от батареи.
Перед длительным хранением насоса (более 2-х недель без использования), батарея должна быть полностью заряжена, а затем извлечена из насоса. Перед извлечением (сменой) батареи всегда отсоединяйте насос от пациента и отключайте прибор.
Индикатор заряда батареи отображается на экране (низкий, средний, полный заряд). Для получения более детальной информации о состоянии батареи (время работы в часах и минутах) необходимо в меню «Статус» войти в раздел «Батарея».
Важная информация о самотестировании батареи:
Если символ батареи мигает во время работы от сети, батарея либо разряжена, либо быстро разряжается. В этом случае насос не должен отключаться от сети. Если необходимо экстренно отключить насос от сети, убедитесь, что остаточный заряд батареи достаточен для применения. Если символ батареи мигает непрерывно (>1ч), батарея должна быть проверена техническим персоналом и заменена при необходимости.
Обслуживание батареи
Для точной регулировки емкости батареи необходимо ее циклическое обслуживание. Насос запрашивает Пользователя о проведении обслуживания батареи каждые 30 дней. В режиме обслуживания батареи определяется возможная потеря емкости (например, из-за старения батареи) и затем емкость и время работы от батареи пересчитываются заново. После длительного хранения или длительной работы без обслуживания батареи, может случиться так, что время подачи предупредительного сигнала больше не будет поддерживаться. В этом случае необходимо проведение обслуживания батареи.
Для инициализации полной разрядки батареи на экране появляется запрос «Обслуживание батареи» и отображается кнопка «ОК». Для того, чтобы запустить процесс разрядки батареи нажмите кнопку «ОК» и кнопку «ВВЕРХ». При включении насоса процесс прерывается. Если обслуживание батареи необходимо продолжить, необходима повторная активация режима обслуживания. После полной разрядки батареи происходит ее полная зарядка. Полное обслуживание батареи длится приблизительно двенадцать часов.
Инфузомат Спэйс B braun Технические характеристики
Ниже представлены технические характеристики Инфузомата Спэйс B braun.
Гарантия Инфузомат Спэйс B braun
Компания Б. Браун предоставляет 24 месяца гарантии, с момента поставки на каждый Инфузомат Спэйс (12 месяцев на каждый аккумулятор (Battery Pack SP)). Гарантия предусматривает ремонт или замену отдельных частей, вышедших из строя в результате конструкторских или производственных ошибок, а так же дефектов материала. Срок действия гарантии прекращается в случае модернизации или ремонта, проведенных Пользователем или посторонними лицами.
Гарантия не распространяется на устранение дефектов, вызванных неправильным / неумелым обращением или нормальным износом прибора.
Каталожные номера Инфузомат Спэйс B braun и принадлежности
Б. Браун Инфузомат Спэйс (100 — 240 V) …………………………… 871 3050
Рекомендуемые принадлежности для насоса Б. Браун Инфузомат Спэйс:
Инфузионные системы Инфузомат Спэйс:
Скачать инструкцию на Инфузомат Спэйс B braun
Скачать инструкцию и другую документацию на Инфузомат Спэйс B braun можно здесь.
Руководство пользователя ( user manual ) на русском языке Инфузомат Спэйс B braun скачать.
Регистрационное удостоверение Инфузомат Спэйс B braun скачать.
Так же смотрите Модуль Space Control ( Спэйс Контроль ) для SGC терапии.
Service Manual
Perfusor® Space
1.21.0
Version 1.2 English
0
1.2
This Service Manual is valid for: Designation Part No.
Infusion syringe pump Perfusor® Space . . . . . . . . . . . . 0871 3030
This Service Manual is available under the following part number:
Designation Part No.
Service Manual Perfusor® Space, English . . . . . . . . . . . 8713 9020
Languages of this Manual The Service Manual for this unit can be supplied in the followinglanguages:
Designation Part No.
Service Manual Perfusor® Space, German . . . . . . . . . . 8713 9010
Service Manual Perfusor® Space, English (us) . . . . . . 8713 9020U
Service Manual Perfusor® Space, French . . . . . . . . . . . 8713 9030
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1.01.0
0 -Table of Contents
Important Preliminary Remarks Service Work Page 0 — 5
Technical Safety Checks Page 0 — 5Current Versions Page 0 — 5Revision Service Page 0 — 5Responsibility of the Manufacturer Page 0 — 6Quality Management Page 0 — 6Checks and Repair Page 0 — 6Notes on ESD Page 0 — 6Spare Parts and Test Equipment Page 0 — 7Setting Off Page 0 — 7List of Abbreviations Page 0 — 9
Contact Persons Technical Training Page 0 — 11Entry for Technical Training Page 0 — 11Ordering of Spare Parts and Test Equipment Page 0 — 11Service Hotline Page 0 — 11Return of Spare Parts and Test Equipment Page 0 — 11Safety Officer(§ 30 MPG) Page 0 — 11Translation Page 0 — 11
System Overview Description Page 1 — 1System Overview Page 1 — 1Physical Construction Page 1 — 2Function Page 1 — 3Unit Software Page 1 — 6Service Program Page 1 — 7Technical Data Page 1 — 12Options Page 1 — 12Accessories Page 1 — 12
Unit Diagnosis / Calibration General Page 2 — 1Alarms and Error Codes Page 2 — 3The Most Important Error Modes Page 2 — 8Device Check Page 2 — 9Calibration Page 2 — 14Procedural Instructions for Calibration Page 2 — 14Trouble Shooting Page 2 — 29
Disassembly / Assembly General Page 3 — 1Battery Module Page 3 — 9Unit Foot Page 3 — 11Operating Unit Page 3 — 12Upper Part of Housing Page 3 — 17Release Button Page 3 — 19Loudspeaker Page 3 — 19Drive Page 3 — 20Syringe Holder with Piston Brake Page 3 — 27Processor PCB Page 3 — 34Assembly / Installation Page 3 — 35Checks after Repair Page 3 — 47
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Servicing the Unit Cleaning Page 4 — 1Servicing the Battery Page 4 — 1
Technical Safety Check (TSC) Perfusor® Space Page 5 — 1
Technical Safety Check (TSC) Power Supply SP Page 6 — 1
Procedural Instructions on the TSC Visual Inspection Page 7 — 1Electrical Safetyaccording to IEC/EN 60601-1or VDE 0750 and VDE 0751 Page 7 — 2Functional Inspection Perfusor® Space Page 7 — 3Functional Inspection Power Supply SP Page 7 — 5
Test Equipment and Special Tools Test Equipment Page 8 — 1Special Tools Page 8 — 3
Spare Parts List Page 9 — 1
Revision Documentation Description of Version Page 10 — 1Version List of the Individual Pages Page 10 — 1
Index Page 11 — 1
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Service Work The present manual is for your information only. The possession of
this manual does not authorize the performance of service work.Service tasks may only be executed by persons, who
— have received appropriate training on the system fromB. Braun
— are included in the revision service
— possess the necessary test equipment and mechanical aids,and
— fulfill the personal requirements (training and knowledge).
Technical Safety Checks The user is obliged to perform or to have performed the TechnicalSafety Checks on those medial products for which these checkshave been prescribed by the manufacturer and to carry them outaccording to the indications of the manufacturer as well as thegenerally approved technical standards while adhering to theperiods stated (§ 6 MP BetreibV).
B. Braun also recommends training on the Technical SafetyChecks, or to perform at least the steps indicated in the currentversion of the manual, as:
— the TSC requires that the instructions in the manuals areobserved
— the manuals are a reference for measurements
— depending on the unit type, the Service Program must becalled which may lead to a dangerous unit condition in caseof inappropriate operation. Furthermore, a special serviceconnector may be necessary.
Current Versions This manual version corresponds to the state when the manualwas written. B Braun reserves the right to make technicalmodifications. The state of the revision is indicated by the indexnumber in the footer of every page.
Revision Service The possession of this manual does not automatically meaninclusion in the revision service. You will be included in therevision service after:
— technical training by B. Braun Melsungen or
— a written order placed with the sales department of B. Braun(fee required).
Perfusor® Space, 1.2 gb 0 — 5
Important Preliminary Remarks 0
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Responsibility of the Manufacturer The manufacturer, person who assembles, installs or imports thedevice can only be held responsible for safety, reliability andperformance if
— mounting, enhancements, new settings, changes or repairsare carried out by duly authorized persons,
— the electrical installation in the corresponding room meetsthe requirements of the VDE 0107, VDE 0100 part 710 orIEC 60364-7-710 and the national standards,
— the device is used in accordance with the instructions for useand the Service Manual,
— the Technical Safety Checks are performed at regularintervals,
— a current manual which corresponds to the revision state isused when carrying out maintenance, repair and service,
— the service technician takes part in the revision service,
— the technician has participated in a technical training coursefor the specific B. Braun unit.
Quality Management B. Braun is certified in accordance with DIN EN ISO 9001 andISO 13485. This certification also includes maintenance andservice.
The unit has the CE label. The CE label confirms that the devicecorresponds to the “Directive of the Council for Medical Products93/42/EC” of June 14, 1993.
Checks and Repair Training may only be performed by B. Braun. The possession of themanual does not authorize the performance of repairs. Theinstructions on electrostatic sensitive components (ESDstandards) must be observed.
After repair a device check or diagnosis is to be carried out.
Notes on ESD Semiconductors can be destroyed by electrostatic discharge.Especially MOS components can be damaged by interference fromelectrostatic fields, even without discharge via contact. This typeof damage is not immediately recognizable. Unit malfunctionscan even occur after a longer period of operation.
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Important Preliminary Remarks 0
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Each workstation must be equipped according to therecommendations with the necessary static protective measures,if ESD components or boards are handled.
Each workstation must be equipped with a conductive tablesurface. The conductive surface, the soldering iron or thesoldering stations must be grounded via protective resistors.
Chairs must be of antistatic design. The floor or floor mats shouldbe of electrically conductive material.
Personnel must wear conductive wristbands which are connectedto a central ground potential via protective resistors, e.g. theground contact of a wall outlet. Furthermore it is recommendedthat personnel wear cotton clothing and electrically conductiveshoes to prevent electrostatic charge.
Spare Parts and Test Equipment Only use original spare parts from the manufacturer. Do nottamper with assembly groups which can only be exchangedcompletely. The spare parts required are listed in Section 9.
Service personnel are responsible for the calibration of their testequipment. Original test equipment can be calibrated at theworks of B. Braun. Further information is available upon request.
Setting Off Additional notes and warnings are set off as follows:
Note
Is used for additional or special notes concerning information andworking steps.
CAUTION
Is used for working steps which may result in damage to the unit,system or to a connected device.
WARNING
IS USED FOR WORKING STEPS WHICH MAY RESULT IN PERSONALINJURY.
References to chapters are shown as follows(see “Setting Off“ ➨ pg. 0 —
References to figures and tables are shown as followsFig.: 2 — 3 or Table 2 — 1
Fig.: 0 — 1
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Important Preliminary Remarks 0
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References to item numbers in figures are shown as follows(Fig.: 1 — 1 / Item 1)In this case “Fig.: 1 – 1“ is the figure number and “Item 1“ the itemnumber within the figure.
When the Service Manual is stored as pdf-file, these referencesare displayed green. Click with the mouse button on a referenceto jump to the corresponding source.
Menu commands are described as:Menu File.
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List of Abbreviations Abbreviations which are not generally known, but are used in thismanual, are listed below.
CAN Controller Area Network
CE Communauté Européenne
CS Calibration Step
DIN German Industrial Norm
EN European Norm
ESD Electrostatic Discharge
FuP Function Microprocessor
IEC International ElectrotechnicalCommission
ISO International Organization forStandardization
ISP Infusomat® Space
ISPS Infusomat® Space (Silicon)
ISPP Infusomat® Space, (PVC)
CS Calibration Step
KuP Monitoring Microprocessor
LCD Liquid Crystal Display
MOS Shortname of the following company:MOS Technology, Inc.(Commodore Semiconductor Group)
PCA Patient Controlled Analgesia
PSP Perfusor® Space
SP Space (System)
SPC SpaceCover
SPCC SpaceCover comfort
SPCS SpaceCover standard
SPCO SpaceCom
SPCT SpaceControl
SPS SpaceStation
TEMP Temperature
TS Trouble Shooting Step
TSC Technical Safety Check
UTS Unit Test Step
Perfusor® Space, 1.2 gb 0 — 9
Important Preliminary Remarks 0
1.2
VDE Verband der Elektrotechnik, Elektronik und Informationstechnik e.V.(german association of engineers)
0 — 10 Perfusor® Space, 1.2 gb
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0 -Contact Persons
Technical Training Via local representative.
Entry for Technical Training Application for a technical training course must be made via theresponsible representative.
Ordering of Spare Parts and Test Equipment Please contact your local B. Braun subsidary.
International Technicians (Intercompany)Nadja Machal
Fax: +49 5661 / 75 -47 89e-mail: [email protected]
Service Hotline Karl Tippel, Tanja KördelPhone: +49 5661 / 71 — 35 25Fax: +49 5661 / 71 — 35 26e-mail: [email protected]: [email protected]
Return of Spare Parts and Test Equipment B. Braun Melsungen AGSchwarzenberger Weg 73-79Wareneingang Werk C34 212 Melsungen Germany
Safety Officer(§ 30 MPG)
Dr. Ludwig Schütze-mail: [email protected]
Translation Brückner GmbH, Germany
Perfusor® Space, 1.2 gb 0 — 11
Contact Persons 0
1.2
For your notes:
0 — 12 Perfusor® Space, 1.2 gb
11.2
1 -System Overview
Description The Perfusor® Space (PSP) is according to IEC/EN 60601 resp. IEC/
EN 60601-2-24 a transportable infusion syringe pump foradministrating fluids in the nutritional therapy and infusiontechnique as well as for home care applications.
The medical specialist must decide on suitability for applicationon the basis of the warranted properties and the technical data.
System Overview The Space system is a modular design of modern infusiontechnology for stationary, mobile or private use. The key modulesand their connection to the peripheral devices are shown inFig.: 1 — 1.
All the pump types, Perfusor® Space, Infusomat® Space andInfusomat® Space P, as well as the other devices of the system areof modular design. Up to three pumps can be connected togethermechanically using L rails on the bottom of the unit and grooveson the top. They can then be fastened to a drip stand orappropriate rail using the pole clamp.
The SpaceControl module can be used to extend operation. Onesingle pump can be inserted onto this module. The pump is thenconnected via connectors to the module.
The SpaceStation module allows the set-up of a complete pumpsystem with up to 24 pumps. Up to four pumps can be installed inevery SpaceStation. The pumps are supplied with power via theintegrated power supply and the built-in connectors. The pumpsare connected to the optional SpaceCom via these connectors.SpaceControl can also be integrated into the system.
Up to six SpaceStations can be set-up as a column with a total of24 pumps. SpaceStation placed next to each other can beconnected via special connection cables, if the maximum numberof 24 pumps in maximum three columns is not exceeded.
SpaceCover Standard or SpaceCover Comfort forms the top ofeach column. Alarms are signalled by a row of LEDs and aloudspeaker in the SpaceCover Comfort.
Fig.: 1 — 1 Space system
Legend of fig. 1 — 1:ItemDesignation
1 SpaceCover
2 Infusion pump Infusomat® Space
3 Infusion syringe pump Perfusor® Space
4 SpaceControl
5 SpaceStation
1
2
3
4
5
Perfusor® Space, 1.2 gb 1 — 1
System Overview 1
1.0
Physical Construction
Fig.: 1 — 2 Perfusor® Space
Legend of fig. 1 — 2:ItemDesignation
1 Perfusor® Space
2 Drive head
3 Syringe holder with piston brake
4 Operating unit
5 Syringe area
6 Connector “P2“ for SpaceStation module, external 12 V DCand accessories
7 Connector “P3“, connection to SpaceControl module
8 Battery compartment cover
1
4
2
3
6
78
5
1 — 2 Perfusor® Space, 1.0 gb
System Overview 1
1.0
The Perfusor® Space housing mainly consists of the bottom partand the upper part.
The battery module is inserted in the rear of the housing upperpart. The opening is covered by the battery compartment cover.
The operating unit is attached to the front of the bottom part withtwo hinges. This operating unit covers the area for the syringes.The complete drive assembly, consisting of lead screw and drivehead with driving tube is located directly behind the syringe areain the bottom part of the housing. The housing bushing for thedriving tube is located in the side of the housing.
The syringe holder is mounted in the right side of the housingbottom part.
The processor PCB with the external connectors “P2” and “P3” islocated at the bottom of the housing bottom part.
Function There are two power options for the Perfusor® Space:
— via the inserted battery module
— via an external 12 V DC power supply (e.g. SpaceStation, SpaceControl, an external power supply or from an ambulance car) connected to connector “P2”
The voltage supplied is converted to the internal voltages requiredthrough a voltage transforming and monitoring circuit on theprocessor PCB.
An independent circuit in the battery module monitors the batterycells and controls their charge condition.
The Perfusor® Space is connected to a SpaceControl by connector“P3”.
The function processor controls all the functions of the Perfusor®Space. Data is stored in a non-volatile memory which alsocontrols the external data transfer.
The control microprocessor monitors all important responses ofthe function processor to incoming information. If a responsedoes not correspond with that expected by the controlmicroprocessor, an error message is generated and the device isswitched to a safe stop state.
The drive motor is monitored by a detector for speed and directionof rotation. The extended end position of the drive head isdetected by a switch on the processor PCB.
The pressure in the infusion system is measured through a straingauge measuring in the drive head and monitored in the device
Perfusor® Space, 1.0 gb 1 — 3
System Overview 1
1.0
electronics. The data from the strain gauge is continuouslycompared with the limit values which are calculated dependenton the selected syringe type and the pressure settings. When thelimit values are exceeded an alarm is automatically triggered andthe pressure in the infusion system is reduced. In addition themaximum possible pressure is limited via a second independentsystem which monitors motor current.
The syringe holder is connected to a potentiometer. The syringesize is determined from the resistance of the potentiometer.
The syringe is fixed with the syringe holder and the axial fasteningdevice. The syringe piston is fastened with two claws in the drivehead. When a syringe is inserted the syringe piston is held by thepiston brake, until the piston has been caught by the claws.
Keyboard and display as well as the syringe area are illuminated.
1 — 4 Perfusor® Space, 1.0 gb
System Overview 1
1.0
Fig.: 1 — 3 Block diagram Perfusor® Space
Perfusor® Space, 1.0 gb 1 — 5
System Overview 1
1.2
Unit Software Approved Software Versions
688A030032
— Basic software
688A030035
— Improved functions
688A030040
— Improved functions
— Languages French and Swedish added
688B030002
— Improved functions
688B030003
— CAN bus functioning
688C030001
— Dose calculation
— Changed CAN log
688D030001
— — Drug list data base
— — Changed user language
688E030002
— — Improved functions
— — Piggyback
— — Soft limits
Software Update of the Unit
The instructions for updating the software are supplied with thesoftware itself.
CAUTION
If the device is disconnected while the software is being updatedor the device or PC is switched off, a component of the softwaremay be seriously damaged so that repairs are no longer possible.In such a case the software cannot be updated via the PC and thedevice must be returned to B. Braun.
Fig.: 1 — 4
Position 1 2 3 4 5 6 7 8 9 10
Digit 6 8 8 C 0 3 0 0 0 1
Revision level
Hardware
Software group
Device type: Perfusor® Space
1 — 6 Perfusor® Space, 1.2 gb
System Overview 1
1.2
Service Program Approved Version
Note
Please note that text and / or functions of the Service Programmay change depending on the software version. The followingscreen illustrations are only examples and represent the statewhen the manual was printed.
— 0.0.28
— 1.0.0
— 1.1.2
— 1.1.3
— 1.1.4
— 1.2.1
— 1.3.5
— 1.5.0
— 2.0.1
— 3.1.0
Perfusor® Space, 1.2 gb 1 — 7
System Overview 1
1.2
Starting the Service Program
Note
Installation and further operation of the Service Program isdescribed in its separate instructions for use.
1. Start the „HiBaSeD.exe“ program (History, Barcode, Service, Drug list) on the PC. The Service Program is loaded and started and the initial window of the Service Program is displayed.
2. Read the notes carefully.
3. Mark the field “I accept all conditions” and then the field “Yes” to confirm that you have read the notes.
Note
Click the field “English” to switch the language of the notes overto English.
4. Enter the password and confirm it by clicking the field “Start”.
The Service Program checks the PC interfaces for connected devices of the Space system. Units that were found are displayed for a short moment on the screen.
Fig.: 1 — 5
Fig.: 1 — 6
Fig.: 1 — 7
1 — 8 Perfusor® Space, 1.2 gb
System Overview 1
1.2
The work window of the Service Program appears on the screen. All devices recognized are listed in the left column.
5. Activate the desired device from the list on the left in the work window with a double-click. The device data is then displayed below the device name.
Fig.: 1 — 8
Perfusor® Space, 1.2 gb 1 — 9
System Overview 1
1.2
If the unit software version is not compatible with the Service Program version, a window opens prompting the operator to change the Service Program version. This window displays a compatibility list of the Service Program- and unit software versions.
If Service Program- and unit software versions are compatible, all the Service Program functions are activated.
Fig.: 1 — 9
Fig.: 1 — 10
1 — 10 Perfusor® Space, 1.2 gb
System Overview 1
1.2
Service Program Version
1. Open the “HiBaSeD“ window via Help ➨ Info …. The current version of the Service Program is shown in this window.
2. Close the window by clicking “OK”.
Compatibility List
1. Open the “Unit — Compatibility“ window via Help ➨ Compatibility. This window displays the compatibility of the HiBaSeD-version and the unit software version.
2. Close the window by clicking “OK”.
Quit the Service Program
1. Exit the Service Program via File ➨ Exit.
2. Disconnect a power supply which might be connected from the unit.
3. Switch off the unit.
4. Remove the battery module.
5. The device can be restarted after appr. 10 seconds.
Fig.: 1 — 11
Fig.: 1 — 12
Perfusor® Space, 1.2 gb 1 — 11
System Overview 1
1.2
Technical Data All technical data is indicated in the instructions for use.
Options The functions of the individual options are detailed in theinstructions for use.
Perfusor® SpaceDesignation Part No.:
Power supply Euro . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0871 3110A
Power supply UK. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0871 3111A
Power supply USA / Japan . . . . . . . . . . . . . . . . . . . . . . 0871 3112A
Power supply Australia. . . . . . . . . . . . . . . . . . . . . . . . . 0871 3113A
Power supply South Africa. . . . . . . . . . . . . . . . . . . . . . 0871 3115A
Accessories Designation Part No.:
Charger SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0871 3170battery charging station
Connection cable staff call SP. . . . . . . . . . . . . . . . . . . . 0871 3232
Power supply cable 12 V . . . . . . . . . . . . . . . . . . . . . . . . 0871 3231for ambulance cars
CombiLead SP 12 V . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0871 3133connection cable, pump — pump
InterfaceLead SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0871 3234interface cable RS232
InterfaceLead SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0871 3230interface cable CAN SP
SpaceClamp SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0871 3130The SpaceClamp is a holder attached on beds for oneor several Space system pumps.
Short stand SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0871 3135
1 — 12 Perfusor® Space, 1.2 gb
21.1
2 -Unit Diagnosis / Calibration
General
WARNING
WHILE TESTING THE UNIT AND TROUBLE SHOOTING THEOPERATOR/SERVICE TECHNICIAN MUST WORK WITH VOLTAGESUP TO 115 / 230 V AC. THESE VOLTAGES MAY CAUSE INJURIESWHICH ARE DANGEROUS TO LIFE AND LIMB. THE NATIONAL ANDINTERNATIONAL SAFETY REGULATIONS ARE TO BE ADHERED TO.
Before each disassembly and assembly of a unit subsystem checkthe connectors, plug contacts and connections for corrosion andtight fit. These fault types are not described again in the followingtrouble shooting list.
The following equipment and gauges are necessary for testing theunit and/or performing troubleshooting:
— PC
— Service connector SP
— Service Program HiBaSeD
— Interface cable
— Syringe 2 ml / 3 ml
— Syringe 10 ml
— Syringe 30 ml
— Diameter gauge 32.0 mm
— Diameter gauge 23.4 mm
— Diameter gauge 15.7 mm
— Diameter gauge 9.0 mm
— Length gauge PSP
— Syringe gauge “#Lehre OPS 50“with push-button plate and motor power test adapter for Perfusor® Space
There are pictures of the gauges in Chapter „Special Tools“ (➨S. 8 — 3).
CAUTION
Take special care when carrying out measurements on an openand switched-on unit. Short circuits and wrong measuringmethods can cause serious damage to or destroy the subsystemsof the device.
Perfusor® Space, 1.1 gb 2 — 1
Unit Diagnosis / Calibration 2
1.0
The unit check, calibration and trouble shooting are subdividedinto numbered working steps (Unit Test Step UTS, Calibration StepCS, Trouble Shooting TS) and are based on each other.
Beginning with UTS 1 the operation described here has to beexecuted. The consequences of the steps performed are listed inthe “Function“ column. If the result corresponds to theconsequence, the working step must be carried out to whichreference is made in the column “If yes”. If the result does notcorrespond with the function described, the working step incolumn “If no” is to be executed.
One example is given in Fig.: 2 — 1.
Steps for which additional information is required are describedafter the table in detail.
Fig.: 2 — 1 Model tables
UTS Activity Function If yes If no1 UTS 2
2 UTS 3 TS 1
3 UTS 4
4 UTS 5 TS 4
5
Model table 1
TS Activity Function1 UTS 3 TS 2
2 TS 3 TS 4
3 UTS 3
4 UTS 4 TS 4
5 UTS 4
Model table 2
2 — 2 Perfusor® Space, 1.0 gb
Unit Diagnosis / Calibration 2
1.0
Alarms and Error Codes The alarms of the Perfusor® Space are classified in 5 categories.These categories are listed hereafter according to theirimportance.
— Alarm adviceIn case of unacceptable inputs corresponding messages are displayed (e.g. “Caution! Rate out of range“, “The parameter cannot be changed“) and a beep sounds.
— Pre-alarmPre-alarms are triggered several minutes (depending on the service settings) before the operating alarms.
— Reminder alarmA reminder alarm is triggered if the device is not operated for two minutes when input or operation was not finished.
— Operating alarmIn case of an operating alarm the infusion is stopped. An audible signal is released, the red LED flashes and a staff call is triggered. The message “Alarm“ and the cause of the alarm appear on the display.
— Device alarm
The most important alarms and error codes as well as theirmeaning and possible fault clearance are specified in thefollowing lists.
Note
The device should be checked after every repair or service (pleasesee „Device Check“ ➨ pg. 2 — 9).
Perfusor® Space, 1.0 gb 2 — 3
Unit Diagnosis / Calibration 2
1.0
Alarms
Alarm Possible Cause Fault Clearance1 Battery nearly discharged (type: pre-
alarm)The device was not connected to the mains long enough
Operate the device with battery until the message “Battery discharged“ is displayed and the unit is switched off. Then connect the unit to the mains for at least 6 hours.
Battery module defective or too old Replace battery module
2 Battery discharged (type: operating alarm)
The device was not connected to the mains long enough
Connect the unit to the mains for at least 6 hours
Battery module defective Replace battery module
3 Battery cover open (type: operating alarm)
❒ The battery compartment cover is not correctly closed
Insert the battery compartment cover correctly
❒ The magnet in the battery compartment cover is missing
Exchange the battery compartment cover
❒ The battery compartment cover is not recognized by the battery module
Replace battery module
4 Drive blocked (type: operating alarm) ❒ The drive was manually blocked Eliminate blockage
❒ Driving force too low Connect the unit to the mains for at least 6 hours and charge battery
Re-calibrate the device
❒ The drive is physically damaged Replace drive
5 Malfunction of claws (type: operating alarm)
❒ The syringe piston was not recognized
Select or insert correct syringe type
Loosen the syringe via the emergency release button in the drive head and insert again
Re-calibrate the device
❒ The claws or the claw drive are/is damaged
Replace drive head
6 Push-button has no contact (type: operating alarm)
❒ Negative pressure in the syringe system
See instructions for use
❒ Syringe was removed without opening the syringe holder
See instructions for use
❒ Push-button sensor defective Replace drive head
7 Device alarm (type: device alarm) A serious internal fault was detected in the system
Switch device off and on
Carry out a device check (please see „Device Check“ ➨ pg. 2 — 9)
Table 2 — 1 Alarms
2 — 4 Perfusor® Space, 1.0 gb
Unit Diagnosis / Calibration 2
1.0
Device Alarms of the Function Processor
Error Code Definition Possible Cause Fault Clearance1 1001 … 1013 Internal Error
2 1014 Loudspeaker not off Loudspeaker connector Check the loudspeaker connector
Loudspeaker Check the loudspeaker
3 1015 Loudspeaker lost Loudspeaker connector Check the loudspeaker connector
Loudspeaker Check the loudspeaker
4 1016 Loudspeaker shorted Loudspeaker connector Check the loudspeaker connector
Loudspeaker Check the loudspeaker
5 1017 KuP switchoff path defect (K_SM_CLK)
Switch off path
6 1018 ADC pressure out of range Pressure measurement in drive head
Carry out calibration
7 1019 Internal Error
8 1020 FUP Flash Memory Error Software Update unit software
9 1021 FUP different version KuP to FuP Software Update unit software
10 1022 FUP pressure zero test fail Pressure measurement in drive head
Carry out calibration
11 1023 FUP pressure offset test fail Pressure measurement in drive head
Carry out calibration
12 1024 FUP EA key closed to long 20sec Keyboard defective Carry out device check
13 1025 Internal Error
Table 2 — 2 Device alarms of the function processor
Perfusor® Space, 1.0 gb 2 — 5
Unit Diagnosis / Calibration 2
1.2
Device Alarms of the Control Microprocessor
Error Code Definition Possible Cause Fault Clearance1 1100 Timebase too fast Quartz of the processor PCB Exchange processor PCB
2 1101 Timebase too slow Quartz of the processor PCB Exchange processor PCB
3 1102 Timebase fail Quartz of the processor PCB Exchange processor PCB
4 1103 Keyboard High Keyboard defective Carry out device check
5 1104 EA_KEY defect 25sec Keyboard defective Carry out device check
6 1105 No keydecode Keyboard defective Carry out device check
7 1106 ROM Romtest defect Software Update unit software
8 1107 ROM Program defect Software Update unit software
9 1108 CM State without set K_V_KM_ON
10 1109 MPU_Test failed Software Update unit software
11 1110 RAM_Test failed Software Update unit software
12 1111 active reset Voltage supply during operation interrupted
13 1112 … 1114 Internal Error
14 1115 Drive too fast Motor driveRecognition of direction of rotation
Exchange processor PCB
15 1116 Drive too slow Motor driveRecognition of direction of rotation
Exchange processor PCB
16 1117 … 1118 Internal Error
17 1119 lcd backlight on defect LC display defective Exchange operating unit
18 1120 lcd backlight off defect LC display defective Exchange operating unit
19 1121 red led on defect LC display defective Exchange operating unit
20 1122 red led off defect LC display defective Exchange operating unit
21 1123 key pressed too long (without EA-Key) 60sec
Keyboard defective Carry out device check
22 1124 … 1127 Internal Error
23 1128 Drive motion rightless forward Motor driveRecognition of direction of rotation
Exchange processor PCB
24 1129 Drive motion rightless backward Motor driveRecognition of direction of rotation
Exchange processor PCB
25 1130 … 1200 Internal Error
26 1201 different version FuP to KuP Software Update unit software
Table 2 — 3 Device alarms of the control microprocessor (Part 1 of 2)
2 — 6 Perfusor® Space, 1.2 gb
Unit Diagnosis / Calibration 2
1.0
27 1202 E_ERROR_STEPMOTOR_1 Phase not ok
Drive motor, lead screw Exchange processor PCB
28 1203 E_ERROR_STEPMOTOR_2 Current value not 0x55
Motor driveRecognition of direction of rotation
Carry out calibration
29 1204 E_ERROR_STEPMOTOR_3 K_SM_CLK defect
Motor driveRecognition of direction of rotation
Carry out calibration
30 1205 E_ERROR_STEPMOTOR_4 Phase not ok
Motor driveRecognition of direction of rotation
Carry out calibration
31 1206 E_ERROR_STEPMOTOR_5 Current value not 0
Motor driveRecognition of direction of rotation
Carry out calibration
32 1207 E_ERROR_STEPMOTOR_6 Current value not 0x55
Motor driveRecognition of direction of rotation
Carry out calibration
33 1208 E_ERROR_STEPMOTOR_7 Current value not 0xAA
Motor driveRecognition of direction of rotation
Carry out calibration
34 1209 E_ERROR_STEPMOTOR_8 Phases not 0
Motor driveRecognition of direction of rotation
Carry out calibration
35 1210 E_ERROR_DCMOTOR_1 Piston brake drive motor def.Claw drive in drive head defectivePiston brake light barrier def.
36 1211 E_ERROR_DCMOTOR_2
37 1212 E_ERROR_DCMOTOR_3
38 1213 E_ERROR_DCMOTOR_4
39 1214 E_ERROR_DCMOTOR_5
40 1215 no V_MOT Voltage transformer defective Exchange processor PCB
41 1216 overvoltage test fail
42 1217 no V_MOT
43 1218 undervoltage test fail
44 1220 syringeholder defect Syringe holder or potentiometer def.
Replace syringe holderExchange processor PCB45 1221 syringe change timeout
46 1237 … 1238 Internal Error
47 1239 plunger plate sensor defect Pressure measurement in drive head
Replace drive head
48 1240 … 1254 Internal Error
Error Code Definition Possible Cause Fault Clearance
Table 2 — 3 Device alarms of the control microprocessor (Part 2 of 2)
Perfusor® Space, 1.0 gb 2 — 7
Unit Diagnosis / Calibration 2
1.0
The Most Important Error Modes The following list specifies the most important error modes andtheir clearance.
Note
The device must be checked after every repair or service (pleasesee „Device Check“ ➨ pg. 2 — 9).
Error Possible Cause Fault Clearance1 The battery module discharges too fast The device was not used for a longer time.
The battery module was not discharged and charged at regular intervals.
❒ Discharge and charge battery module several times
❒ Replace battery module
Table 2 — 4
2 — 8 Perfusor® Space, 1.0 gb
Unit Diagnosis / Calibration 2
1.2
Device Check
UTS Activity Function If yes If no1 The device is inserted in a SpaceStation or
connected to a SpaceControl.UTS 2 UTS 3
2 Remove the device. UTS 4
3 Loosen all connections from the device. UTS 4
4 Remove syringe and close syringe holder. UTS 5
5 Plug service connector SP on connector “P2”. UTS 6
6 Connect power supply to the device via service connector SP.
All LEDs light up for a short moment. UTS 7 TS 1
7 The battery charge state and the mains connection are displayed at the top left of the LC display (without lighting).
UTS 8 TS 5
8 Switch on unit. All LEDs light up (from left: yellow, green, blue). UTS 9 TS 5
9 A short deep and then a short high beep sound. UTS 10 TS 7
10 The colour of the middle LED changes from green to red, then the LED goes out. The yellow and the blue LED remain on for a short moment.
UTS 11 TS 8
11 The message “Self-test active” and the current software version are displayed.
UTS 12 TS 8
12 Keyboard, LC display as well as the syringe area are illuminated.
UTS 13 TS 9
13 The drive head moves to the extended end position. UTS 14 TS 11
14 The claws in the syringe head close and open. UTS 15 TS 14
15 The message “Drive moves back / Syringe change” appears on the display.
UTS 16 TS 16
16 “Open syringe holder and insert syringe or press “C“ to input parameters“ is displayed.
UTS 17 TS 16
17 Open syringe holder. “Syringe change / Please insert syringe …” is displayed.
UTS 18 TS 17
18 Press the “>“ key. The following service information is displayed:- Brake: stopped by ____- drivetest ok- Size: 35.4 KuP 35.4 FuP
UTS 19 TS 19
19 Insert syringe 30 ml. The syringe piston is fastened with the syringe holder blade.
UTS 20 TS 21
20 “Brake: stopped by current“ is displayed. UTS 21 TS 21
21 Insert syringe 2 ml / 3 ml. “Brake: stopped by holder“ is displayed. UTS 22 TS 21
22 Open syringe holder and remove syringe. “Brake: stopped by light barrier“ is displayed. UTS 23 TS 21
Table 2 — 5 Device check (Part 1 of 5)
Perfusor® Space, 1.2 gb 2 — 9
Unit Diagnosis / Calibration 2
1.2
23 3.54 is shown for FuP on the LC display. The value displayed for FuP may have a maximum tolerance of ± 0.04.
UTS 24 CS 1
24 Close syringe holder. The value for FuP changes to 7.0 ± 0.4. UTS 25 CS 1
25 Insert diameter gauge 9.0 mm. The value for FuP changes to 9.0 ± 0.4. UTS 26 CS 1
26 Insert diameter gauge 15.7mm. The value for FuP changes to 15.7 ± 0.4. UTS 27 CS 1
27 Insert diameter gauge 23.4 mm. The value for FuP changes to 23.4 ± 0.4. UTS 28 CS 1
28 Insert diameter gauge 32.0 mm. The value for FuP changes to 32.0 ± 0.4. UTS 29 CS 1
29 The sum of the tolerances of UTS 23 to UTS 28 must not exceed 1.0.
UTS 30 CS 1
30 Insert syringe 2 ml / 3 ml. UTS 31
31 Press the “>“ key. The syringe selection is displayed. UTS 32
32 Select a syringe. The drive head moves to the syringe piston, the claws in the drive head close and the message “Syringe is caught / Please wait” is displayed.
UTS 33 TS 26
33 Test all buttons on the operating unit during a functional check (carry out infusion).
When the buttons are pressed the desired reaction is carried out.
UTS 34 TS 29
34 Open syringe holder while the infusion is administered.
The red LED on the operating unit flashes and the red LED of the service connector SP lights up. The message “Alarm / Syringe holder” is displayed.
UTS 35 TS 31
35 Close syringe holder and continue infusion. UTS 36
36 Stop infusion. UTS 37
37 Open syringe holder. “Syringe change / Initiate change? Yes / No” is displayed.
UTS 38
38 Confirm with “Yes”. The claws in the drive head open and the drive head moves to the extended end position.
UTS 39
39 Remove syringe. UTS 40
40 Insert syringe gauge for the strain gauge measurement, close syringe holder and select syringe type „#Lehre OPS50“.
WARNING
DURING THE STRAIN GAUGE MEASUREMENT WITHSYRINGE GAUGE THE SYRINGE HOLDER MUST NOTBE OPENED. THE SYRINGE GAUGE IS UNDER VERYHIGH PRESSURE AND MAY CAUSE INJURIES IF THEPRESSURE IS RELIEVED SUDDENLY.
UTS 41
UTS Activity Function If yes If no
Table 2 — 5 Device check (Part 2 of 5)
2 — 10 Perfusor® Space, 1.2 gb
Unit Diagnosis / Calibration 2
1.0
41 Input a delivery rate of 200 ml/h, select pressure stage 1 and start infusion.
When the maximum pressure of this pressure stage is reached, the delivery is stopped, the red LED on the operating unit flashes and the message “Alarm / Pressure too high” is displayed.The value read on the syringe gauge (in N) must match the value indicated for the strain gauge measurement of this pressure stage in the TSC.
UTS 42 CS 1
42 Confirm alarm. UTS 43
43 Select pressure stage 3 and start infusion. When the maximum pressure of this pressure stage is reached, the delivery is stopped, the red LED on the operating unit flashes and the message “Alarm / Pressure too high” is displayed.The value read on the syringe gauge (in N) must match the value indicated for the strain gauge measurement of this pressure stage in the TSC.
UTS 44 CS 1
44 Confirm alarm. UTS 45
45 Select pressure stage 8 and start infusion. When the maximum pressure of this pressure stage is reached, the delivery is stopped, the red LED on the operating unit flashes and the message “Alarm / Pressure too high” is displayed.The value read on the syringe gauge (in N) must match the value indicated for the strain gauge measurement of this pressure stage in the TSC.
UTS 46 CS 1
46 Confirm alarm and pull syringe holder briefly. UTS 47
47 Confirm syringe change, release syringe gauge and remove gauge.
WARNING
WHILE CHECKING THE MOTOR POWER LIMITATIONWITH THE SYRINGE GAUGE THE SYRINGE HOLDERMUST NOT BE OPENED. THE SYRINGE GAUGE ISUNDER VERY HIGH PRESSURE AND MAY CAUSEINJURIES IF THE PRESSURE IS RELIEVED SUDDENLY.
UTS 48
48 Insert the motor power test adapter in the drive head to check the motor power limitation.
UTS 49
49 Dismount the push-button plate from the syringe gauge and insert syringe gauge.
UTS 50
UTS Activity Function If yes If no
Table 2 — 5 Device check (Part 3 of 5)
Perfusor® Space, 1.0 gb 2 — 11
Unit Diagnosis / Calibration 2
1.0
50 Select syringe type “#Lehre OPS 50“. The threaded end of the syringe gauge must be introduced in the opening of the motor power test adapter. To do this, hold on to the syringe gauge, if necessary by hand, in the syringe area.
UTS 51
51 Select pressure stage 1 and start infusion. When the maximum pressure of this pressure stage is reached, the delivery is stopped, the red LED on the operating unit flashes and the message “Alarm / Drive blocked” is displayed.The value read on the syringe gauge (in N) must match the value indicated for the motor power limitation in the TSC.
UTS 52 CS 1
52 Confirm alarm. UTS 53
53 Select pressure stage 3 and start infusion. When the maximum pressure of this pressure stage is reached, the delivery is stopped, the red LED on the operating unit flashes and the message “Alarm / Drive blocked” is displayed.The value read on the syringe gauge (in N) must match the value indicated for the motor power limitation in the TSC.
UTS 54 CS 1
54 Confirm alarm. UTS 55
55 Select pressure stage 6 and start infusion. When the maximum pressure of this pressure stage is reached, the delivery is stopped, the red LED on the operating unit flashes and the message “Alarm / Drive blocked” is displayed.The value read on the syringe gauge (in N) must match the value indicated for the motor power limitation in the TSC.
UTS 56 CS 1
56 Confirm alarm and pull syringe holder briefly. UTS 57
57 Confirm syringe change, release syringe gauge and remove gauge.
WARNING
WHILE CHECKING THE MOTOR POWER LIMITATIONWITH THE SYRINGE GAUGE THE SYRINGE HOLDERMUST NOT BE OPENED. THE SYRINGE GAUGE ISUNDER VERY HIGH PRESSURE AND MAY CAUSEINJURIES IF THE PRESSURE IS RELIEVED SUDDENLY.
UTS 58
58 Insert syringe type 30 ml and lock PCA-lock with PCA-key.
The syringe holder cannot be opened. UTS 59 TS 32
UTS Activity Function If yes If no
Table 2 — 5 Device check (Part 4 of 5)
2 — 12 Perfusor® Space, 1.0 gb
Unit Diagnosis / Calibration 2
1.0
59 Open PCA-lock and remove syringe. UTS 60
60 Insert syringe type 10 ml and lock PCA-lock with PCA-key.
The syringe holder cannot be opened. UTS 61 TS 32
61 Open PCA-lock and remove syringe. UTS 62
62 Switch device off. The message “Pump is switched off in 3 .. 2 .. 1 sec” is displayed.
UTS 63
63 “Drive is parked …/ Please wait …“ is displayed. The drive head moves to the retracted park position.
UTS 64
64 The device switches off. UTS 65 TS 35
65 Pull off the power supply. The blue LED lights up for a short moment. UTS 66 TS 35
66 Switch on unit. UTS 67
67 Open the battery compartment cover when the drive head has moved to the extended end position.
An alarm signal sounds, the red LED flashes and “Alarm / Battery cover open / Confirm with “OK” is displayed.
UTS 68 TS 36
68 Remove battery. A permanent alarm is triggered. UTS 69 TS 38
69 Insert battery, close battery compartment cover and switch on the device.
The message “Devicealarm / 1111” is displayed. UTS 70
70 Switch the device off, remove service connector SP and dismount test structure.
This step terminates the device check.
UTS Activity Function If yes If no
Table 2 — 5 Device check (Part 5 of 5)
Perfusor® Space, 1.0 gb 2 — 13
Unit Diagnosis / Calibration 2
1.2
Calibration
Procedural Instructions for Calibration Starting Calibration
Note
Calibration must be carried out with power supply connected,since the calibration can be interrupted suddenly if the unit isbattery-operated and the battery gets discharged so that thedevice is switched off.
Note
Please note that text and / or functions of the Service Programmay change depending on the software version. The followingscreen illustrations are only examples and represent the statewhen the manual was printed.
1. Start the Service Program (please see „Starting the Service Program“ ➨ pg. 1 — 8).
2. Select the unit to be calibrated in the left column of the window with a double mouse-click. The blue and the yellow LED blinks in opposite with the red LED.
3. Select the register tab “Calibration”.
CS Activity Function If yes If no1 Connect unit to PC with interface cable. CS 2
2 Start Service Program on the PC (please see „Starting the Service Program“ ➨ pg. 1 — 8).
The desired device is found by the Service Program and then displayed.
CS 3
3 Start calibrating the unit (please see „Starting Calibration“ ➨ pg. 2 — 14).
CS 4
4 Carry out calibration of the claws (please see „Claw Calibration“ ➨ pg. 2 — 23).
Calibration of the claws was terminated successfully.
CS 5
5 Carry out calibration of the syringe holder (please see „Syringe Holder Calibration“ ➨ pg. 2 — 23).
Calibration of the syringe holder was terminated successfully.
CS 6
6 Carry out pressure calibration (please see „Pressure Calibration“ ➨ pg. 2 — 26).
Pressure calibration was terminated successfully. CS 7
7 Close the Service Program (please see „Quit the Service Program“ ➨ pg. 1 — 11).
UTS 23
Table 2 — 6 Calibration
2 — 14 Perfusor® Space, 1.2 gb
Unit Diagnosis / Calibration 2
1.2
4. Press the “New device“ button in the frame “Calibration procedure”. The window “Worker ID“ is opened.
Note
If you do not have an allocated worker id, enter “0001”.
Fig.: 2 — 2
Perfusor® Space, 1.2 gb 2 — 15
Unit Diagnosis / Calibration 2
1.2
5. Input your user number in the window “Worker ID” as well as the six-digit serial number of the device, if necessary.
6. Confirm the input with “OK“.
Note
If HiBaSeD could not clearly read the device serial number, thenumber must be entered according to the rating plate.
If the unit is not yet switched on, the window „Unit on/off“ opens and the user is asked to select the desired language.
7. Select the desired language. The respective operating steps are explained in detail in the instructions for use.After the language was confirmed the unit switches on and the window „Unit on/off“ closes.
Fig.: 2 — 3
Fig.: 2 — 4
Fig.: 2 — 5
2 — 16 Perfusor® Space, 1.2 gb
Unit Diagnosis / Calibration 2
1.2
Note
If calibration is interrupted data is written back to the device andmarked as invalid, if this is still possible. When the ServiceProgram is started again the data is marked as faulty andhighlighted red.
Fig.: 2 — 6
Perfusor® Space, 1.2 gb 2 — 17
Unit Diagnosis / Calibration 2
1.2
8. The frame “Data selection” is now activated.
If the “Adjustment …“ button was pressed in the “Calibration process” frame, the desired data for editing and transmission can now be selected in the “Data selection” frame.
Note
The device must not be switched off during calibration even if thismessage is displayed on the LC display (“Turn pump off”, “Switchdevice off”).
Fig.: 2 — 7
2 — 18 Perfusor® Space, 1.2 gb
Unit Diagnosis / Calibration 2
1.2
9. Mark at least the “Calibration data“ field in this frame if you have not selected “New device” and confirm by clicking “OK”. The device switches on and the drive head moves to the extended end position. You are prompted to press the blue connection key on the device.
10. Press the blue connection key on the device after the drive head has moved to the end position.
Fig.: 2 — 8
Perfusor® Space, 1.2 gb 2 — 19
Unit Diagnosis / Calibration 2
1.2
11. In the frame “Calibration mode“ you can choose between a complete or a partial calibration. Select the desired calibration mode with the mouse pointer.
Note
The following description is applicable to a complete and a partialcalibration. All possible calibrations are carried out one after theother if a complete calibration is selected. Interrupting thecalibration may trigger an alarm in the device.
Fig.: 2 — 9
2 — 20 Perfusor® Space, 1.2 gb
Unit Diagnosis / Calibration 2
1.2
12. Press the “OK“ button after you have selected the calibration elements. The necessary device data is read out and stored in the PC.
Fig.: 2 — 10
Fig.: 2 — 11
Fig.: 2 — 12
Fig.: 2 — 13
Perfusor® Space, 1.2 gb 2 — 21
Unit Diagnosis / Calibration 2
1.2
13. The frame “Element selection” is now activated.
If you have selected a complete calibration in the “Calibration mode” frame, the individual calibration elements are already selected and cannot be changed. Actuate the “OK“ button.
If you have chosen a partial calibration in the frame “Calibration mode”, you can click the calibration element “Claw”, “Syringe holder” and “Pressure” with the mouse pointer. A multiple choice is possible. Press the “OK“ button after you have selected the calibration elements.
Fig.: 2 — 14
2 — 22 Perfusor® Space, 1.2 gb
Unit Diagnosis / Calibration 2
1.2
Claw Calibration
1. The frame “Claw calibration“ is activated and calibration is started.
2. The claws in the drive head are closed and the query “Claw closed? Please confirm“ is displayed in the frame “Claw calibration“.
3. Check whether the claws are closed. Then actuate the “Yes” button.
4. The claws in the drive head are opened and the query “Claw open? Please confirm“ is displayed in the frame “Claw calibration“.
5. Check whether the claws are opened. Then actuate the “Yes” button.
Syringe Holder Calibration
1. The frame “Syringe holder calibration“ is activated and calibration is started.
2. Insert diameter gauge 32.0 mm and close the syringe holder.
Note
The diameter gauge must not be held by the axial fastening of thehousing side part. They must be inserted in such a way that thearea of the diameter gauges touches the axial fastening edge.
3. Press the “OK“ button.
Fig.: 2 — 15
Fig.: 2 — 16
Fig.: 2 — 17
Perfusor® Space, 1.2 gb 2 — 23
Unit Diagnosis / Calibration 2
1.2
4. Insert diameter gauge 23.4 mm and close the syringe holder.
5. Press the “OK“ button.
6. Insert diameter gauge 15.7 mm and close the syringe holder.
7. Press the “OK“ button.
Fig.: 2 — 18
Fig.: 2 — 19
2 — 24 Perfusor® Space, 1.2 gb
Unit Diagnosis / Calibration 2
1.2
8. Insert diameter gauge 9.0 mm and close the syringe holder.
9. Press the “OK“ button.
10. Open the syringe holder and remove the diameter gauge. Press the “OK“ button.
Note
The syringe holder must always be completely turned and theaxial fastening completely opened.
Fig.: 2 — 20
Fig.: 2 — 21
Perfusor® Space, 1.2 gb 2 — 25
Unit Diagnosis / Calibration 2
1.2
11. Close the syringe holder and actuate the “OK“ button.
If calibration was not terminated successfully, an error message is displayed on the PC screen.
Pressure Calibration
Note
The term “Power gauge” in the windows of the Service Programcorresponds to the syringe gauge.
1. The frame “Pressure calibration/length/PWM“ is activated and calibration is started.
2. Insert the length gauge and close the syringe holder.
3. Press the “OK“ button.
Fig.: 2 — 22
Fig.: 2 — 23
2 — 26 Perfusor® Space, 1.2 gb
Unit Diagnosis / Calibration 2
1.2
4. If “Insert power gauge and confirm with OK” is displayed in the frame “Pressure calibration/length/PWM”, open the syringe holder and remove the length gauge.
WARNING
DURING PRESSURE CALIBRATION WITH THE SYRINGE GAUGE THESYRINGE HOLDER MUST NOT BE OPENED. THE SYRINGE GAUGE ISUNDER VERY HIGH PRESSURE AND MAY CAUSE INJURIES IF THEPRESSURE IS RELIEVED SUDDENLY.
5. Insert the syringe gauge with the attached push-button plate (small diameter) for the Perfusor® Space and close the syringe holder.
6. Press the “OK“ button.
7. The power calibration is carried out. When calibration is finished the syringe gauge is released.
8. When the drive head has moved to the extended end position, the syringe gauge can be removed.
9. Close the syringe holder. The device can now be switched off.
Note
If the device is switched off before calibration is terminated, thecalibration is invalid and must be repeated.
Evaluation
1. At the end of calibration the result with all the values is displayed in the frame “Calibration process terminated successfully”.
Fig.: 2 — 24
Fig.: 2 — 25
Fig.: 2 — 26
Perfusor® Space, 1.2 gb 2 — 27
Unit Diagnosis / Calibration 2
1.2
This report can be printed out by pressing the “Print” button.
2. Actuate the “OK” button to finish the calibration process and to store the data in the device.
Fig.: 2 — 27
2 — 28 Perfusor® Space, 1.2 gb
Unit Diagnosis / Calibration 2
1.0
Trouble Shooting
Note
The following trouble shooting cannot be carried outindependently. It is based on the precise observance of the stepsfor the device check (please see „Device Check“ ➨ pg. 2 — 9). Fromthere reference is made to the corresponding trouble shootingsteps.
TS Activity Function If yes If no1 Replace power supply. All LEDs light up for a short moment. UTS 7 TS 2
2 At least one LED lights up for a short moment. TS 3 TS 4
3 Replace the LC display. UTS 7
4 A message is displayed on the LC display. TS 6 TS 5
5 Exchange processor PCB. All LEDs light up for a short moment and a message is displayed on the LC display.
UTS 7 TS 6
6 Exchange operating unit. UTS 8
7 Exchange loudspeaker and switch on unit. A short deep and then a short high beep sound. UTS 10 TS 8
8 Exchange processor PCB. UTS 10
9 Exchange operating unit. Keyboard, LC display as well as the syringe area are illuminated.
UTS 13 TS 10
10 Exchange processor PCB. UTS 13
11 Replace drive. TS 12
12 Switch on unit. The drive head moves to the extended end position. UTS 14 TS 13
13 Exchange processor PCB. UTS 14
14 Replace drive head. TS 15
15 Switch on unit. The claws in the syringe head close and open. UTS 15 TS 16
16 Exchange processor PCB. UTS 15
17 Replace syringe holder with piston brake. “Syringe change / Please insert syringe …” is displayed after the syringe holder has been opened.
UTS 18 TS 18
18 Exchange processor PCB. UTS 18
19 Exchange processor PCB and actuate the „>“ button.
The following service information is displayed:- Brake: stopped by ____- drivetest ok- Size: 35.4 KuP 35.4 FuP
UTS 19 TS 20
20 Exchange operating unit. UTS 19
21 Replace syringe holder with piston brake. TS 22
Table 2 — 7 Trouble shooting (Part 1 of 2)
Perfusor® Space, 1.0 gb 2 — 29
Unit Diagnosis / Calibration 2
1.0
22 Switch on unit and insert syringe. The syringe piston is fastened with the syringe holder blade and the default message is displayed on the LC display.
UTS 19 TS 23
23 Exchange processor PCB. TS 24
24 Switch on unit and insert syringe. The syringe piston is fastened with the syringe holder blade and the default message is displayed on the LC display.
UTS 19 TS 25
25 Exchange piston brake ribbon cable. UTS 19
26 Exchange processor PCB. TS 27
27 Switch on unit, insert syringe and select. The drive head moves to the syringe piston, the claws in the drive head close and the message “Syringe change active / Syringe is caught” is displayed.
UTS 33 TS 28
28 Replace drive head. UTS 33
29 Exchange operating unit. TS 30
30 Test all buttons on the operating unit during a functional check.
When the buttons are pressed the desired reaction is carried out.
UTS 34 TS 31
31 Exchange processor PCB. UTS 35
32 Exchange PCA-slide and lock PCA-lock with PCA-key.
The syringe holder cannot be opened. UTS 59 TS 33
33 Exchange PCA eccentric and lock PCA-lock with PCA-key.
The syringe holder cannot be opened. UTS 59 TS 34
34 Replace syringe holder with piston brake. UTS 59
35 Exchange processor PCB. UTS 65
36 Replace battery module. TS 37
37 Switch on unit and open the battery compartment cover when the drive head has moved to the extended end position.
UTS 67 TS 38
38 Exchange processor PCB. UTS 67
39 Disconnect power supply from the device and switch on device.
All LEDs light up for a short moment. UTS 9 TS 41
40 Charge battery module for about 16 hours in the device with power supply connected.
TS 39
41 Replace battery module. UTS 9
TS Activity Function If yes If no
Table 2 — 7 Trouble shooting (Part 2 of 2)
2 — 30 Perfusor® Space, 1.0 gb
31.0
3 -Disassembly / AssemblyPerfusor® Space
3.1 General Remarks on Disassembly / Assembly
Before disassembling the unit, the system must be checked(please see „Device Check“ ➨ pg. 2 — 9) to isolate the part to beexchanged.
The necessary steps to disassemble the complete unit, all itssubsystems and spare parts are detailed in the followingdescription. Steps that are not necessary can be skipped.
Move the drive head to the extended end position before startingdisassembly.
1. Switch the unit on. The drive head moves to the extended end position.
2. Open the syringe holder.
3. Switch the device off when the syringe holder is opened. The drive head stays at the extended end position.
WARNING
PAY ATTENTION TO THE PISTON BRAKE BLADE WHEN WORKINGON THE PISTON BRAKE. THE BLADE IS SHARP AND MAY CAUSEINJURIES.
Note
Special screws for plastic housings are used in this unit. Payattention to the corresponding notes when you fit the screws.
Perfusor® Space, 1.0 gb 3 — 1
Disassembly / Assembly 3
1.2
Preparations for Exchanging the Processor PCB
If the processor PCB is to be replaced a back-up of the pumpsettings is to be carried out, if this is still possible.
1. Start the Service Program (please see „Starting the Service Program“ ➨ pg. 1 — 8).
2. Select the register tab “Modification data”.
3. Press the “From device“ button. The data is read from the pump.
Fig.: 3 — 1
3 — 2 Perfusor® Space, 1.2 gb
Disassembly / Assembly 3
1.2
4. Select the tab “IO”.
5. Press the “To file“ button.
In the window which opens now you are asked for the storage position of the file on the PC hard disk and the file name.
6. Press the “Print” button to transmit the device data to a printer.
Fig.: 3 — 2
Perfusor® Space, 1.2 gb 3 — 3
Disassembly / Assembly 3
1.2
7. Actuate the “Display“ button to display the device data on screen.
With “Close” the window is closed again.
8. Select the storage position in the “Save as” window and input a unique file name.
9. Press the “Save“ button. The data of the pump is saved on the PC hard disk.
Fig.: 3 — 3
Fig.: 3 — 4
3 — 4 Perfusor® Space, 1.2 gb
Disassembly / Assembly 3
1.2
10. Select the tab “Disposable article”.
11. Actuate the “from device“ button. The data is read from the pump.
The data of the disposable articles read out is displayed on screen.
Fig.: 3 — 5
Perfusor® Space, 1.2 gb 3 — 5
Disassembly / Assembly 3
1.2
12. Press the “Save as“ button.
In the window which opens now you are asked for the storage position of the file on the PC hard disk and the file name.
Fig.: 3 — 6
3 — 6 Perfusor® Space, 1.2 gb
Disassembly / Assembly 3
1.2
13. Select the storage position in the “Save as” window and input a unique file name.
14. Press the “Save“ button. The data of the pump is saved on the PC hard disk.
15. Exit the Service Program (please see „Quit the Service Program“ ➨ pg. 1 — 11).
Note
When the new processor PCB has been installed the saved datamust be transferred back to the device (please see „Processor PCB“➨ pg. 3 — 36).
Fig.: 3 — 7
Perfusor® Space, 1.2 gb 3 — 7
Disassembly / Assembly 3
1.2
Service Parts and Screw Kit
All small parts, such as cover caps, are contained in a Perfusor®Space service part kit.
Designation Ord. No.
Service part kit Perfusor® Space . . . . . . . . . . . . . . . . . 3477 4270with:housing cover cap (40 pieces)cover caps for operating unit (10 pieces)cover cap for syringe holder (10 pieces)cover cap for drive head and claw (20 pieces)housing foot (20 pieces)release button SP with leaf spring (5 pieces)wing sensor holder (2 pieces)locking clip for piston brake (10 pieces)PCA key (2 pieces)
Cover caps for housing SP (50 pieces) . . . . . . . . . . . . . 3477 4386
Cover caps for operating unit PSP (50 pieces) . . . . . . 3477 3103
Connector seal P2 (50 pieces) . . . . . . . . . . . . . . . . . . . 3477 3102
All screws used in the device are included in a Perfusor® Spacescrew kit.
Screw kit Perfusor® Space . . . . . . . . . . . . . . . . . . . . . . 3477 4289with:screw EJOT 22×8 WN 5451 TORX 6IP (5 pieces)screw EJOT 25×7 WN 5451 TORX 8IP (5 pieces)screw EJOT 30×6 WN 5451 TORX 10IP (5 pieces)screw EJOT 30×8 WN 5451 TORX 10IP (10 pieces)screw EJOT 20×12 WN 5452 TORX 6IP (5 pieces)screw EJOT 20×14 WN 5452 TORX 6IP (5 pieces)screw EJOT 22×4.5 WN 5452 TORX 6IP (10 pieces)screw EJOT 25×10 WN 5452 TORX 8IP (5 pieces)screw EJOT 30×8 WN 5452 TORX 10IP (10 pieces)screw EJOT 30×12 WN 5452 TORX 10IP (10 pieces)screw EJOT 30×35 WN 5452 TORX 10IP (5 pieces)screw EJOT 22×8 WN 5454 TORX 6IP (5 pieces)locking ring (5 pieces)
3 — 8 Perfusor® Space, 1.2 gb
Disassembly / Assembly 3
1.0
3.2 Battery Module Designation Ord. No.
Battery compartment cover PSP . . . . . . . . . . . . . . . . . 3452 0872
Battery pack SP (NIMH). . . . . . . . . . . . . . . . . . . . . . . . . 0871 3180
Disassembly
Note
Move the drive head to the extended end position before startingdisassembly (please see „General“ ➨ pg. 3 — 1).
1. Press the lock (Fig.: 3 — 8 / Item 2) on the battery compartment cover (Fig.: 3 — 8 / Item 1) and remove the battery compartment cover.
Note
The battery compartment cover of more recent devices is shorterand can only be unlocked using a pointed object.
Fig.: 3 — 8
Legend of fig. 3 — 8:ItemDesignation
1 Battery compartment cover
2 Battery compartment cover lock
2
1
Perfusor® Space, 1.0 gb 3 — 9
Disassembly / Assembly 3
1.0
2. Lift the lock (Fig.: 3 — 9 / Item 3) on the battery pack (Fig.: 3 -9 / Item 1) and remove the battery pack out of the device.
Fig.: 3 — 9
Legend of fig. 3 — 9:ItemDesignation
1 Battery pack
2 Battery compartment cover
3 Battery pack lock
3
1
2
3 — 10 Perfusor® Space, 1.0 gb
Disassembly / Assembly 3
1.0
3.3 Unit Foot Designation Ord. No.
Unit foot(please see „Service Parts and Screw Kit“ ➨ pg. 3 —
Disassembly
1. Pull the unit foot (Fig.: 3 — 10 / Item 1) out of the housing.
Fig.: 3 — 10
Legend of fig. 3 — 10:ItemDesignation
1 Unit foot
1
Perfusor® Space, 1.0 gb 3 — 11
Disassembly / Assembly 3
1.0
3.4 Operating Unit Designation Ord. No.
Operating unit PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 0970
Hinge plate PSP, left . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1011
Hinge plate PSP, right . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1020
PCA-slide PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 0899
PCA-eccentric PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 0902
Rear panel, operating unit PSP . . . . . . . . . . . . . . . . . . . 3452 1003
LC display SP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 0988
Front flap with keyboard PSP . . . . . . . . . . . . . . . . . . . . 3452 0996
Screws and cover caps(please see „Service Parts and Screw Kit“ ➨ pg. 3 —
Note
Please pay attention to the corresponding notes during assemblyand installation (please see „Assembly / Installation“ ➨
pg. 3 — 35).
Disassembly
1. Pierce two cover caps (Fig.: 3 — 11 / Item 1) with a small screwdriver and remove cover caps.
2. Unscrew two screws and remove the right hinge plate (Fig.: 3 — 11 / Item 3) carefully out of the bottom part of the housing and pull it off the (Fig.: 3 — 11 / Item 6) operating unit.
Note
When dismounting the operating unit pay attention to the lengthof the connection cable.
3. Remove the PCA-slide (Fig.: 3 — 11 / Item 5) and the PCA-eccentric (Fig.: 3 — 11 / Item 4) out of the housing bottom part.
Fig.: 3 — 11
Legend of fig. 3 — 11:ItemDesignation
1 Cover cap
2 Screw EJOT 30×8 WN 5452 TORX 10IP A2
3 Hinge plate, right
4 PCA-eccentric
5 PCA-slide
6 Operating unit
6
5
4
3
2
1
3 — 12 Perfusor® Space, 1.0 gb
Disassembly / Assembly 3
1.0
4. Push the right and left connector locks (Fig.: 3 — 12 / Item 2) carefully forward.
5. Disconnect the operating unit connection cable (Fig.: 3 — 12 / Item 1) from the connector.
Fig.: 3 — 12
Legend of fig. 3 — 12:ItemDesignation
1 Operating unit connection cable
2 Connector lock
2
1
Perfusor® Space, 1.0 gb 3 — 13
Disassembly / Assembly 3
1.2
6. Pull the operating unit from the left hinge plate (Fig.: 3 — 13 / Item 3).
7. Pierce two cover caps (Fig.: 3 — 13 / Item 1) with a small screwdriver and remove cover caps.
8. Unscrew two screws and remove the left hinge plate.
Fig.: 3 — 13
Legend of fig. 3 — 13:ItemDesignation
1 Cover cap
2 Screw EJOT 30×8 WN 5452 TORX 10IP A2
3 Hinge plate, left
4 Operating unit
4
3
2
1
3 — 14 Perfusor® Space, 1.2 gb
Disassembly / Assembly 3
1.0
Disassembly
1. Pierce six cover caps (Fig.: 3 — 14 / Item 1) with a small screwdriver and remove cover caps.
2. Unscrew six screws and remove the rear panel (Fig.: 3 — 14 / Item 4).
Note
The three screws of the keyboard must not be loosened. A uniformpressure point of all keys is only guaranteed when a special toolis used for assembly.
Fig.: 3 — 14
Legend of fig. 3 — 14:ItemDesignation
1 Cover cap
2 Screw EJOT 22×4.5 WN 5452 TORX 6IP A2
3 Screws for keyboard: Do not loosen the screws
4 Operating unit rear panel
1 2
4
3
Perfusor® Space, 1.0 gb 3 — 15
Disassembly / Assembly 3
1.0
3. Push the right and left connector locks of the PCB keyboard carefully to the left.
4. Pull the LC display ribbon cable (Fig.: 3 — 16 / Item 1) out of the connector.
5. Lift the LC display out of the operating unit.
Note
The screws of the keyboard must not be loosened. A specialprocedure is required to install the keyboard, so that a uniformpressure point is guaranteed for all keys.
Fig.: 3 — 15
Legend of fig. 3 — 15:ItemDesignation
1 LC display connection cable lock
1
Fig.: 3 — 16
Legend of fig. 3 — 16:ItemDesignation
1 LC display
2 Front flap with keyboard
1
2
3 — 16 Perfusor® Space, 1.0 gb
Disassembly / Assembly 3
1.0
3.5 Upper Part of Housing Designation Ord. No.
Upper part of housing PSP . . . . . . . . . . . . . . . . . . . . . . 3452 0910
Screws and cover caps(please see „Service Parts and Screw Kit“ ➨ pg. 3 —
Note
Please pay attention to the corresponding notes during assemblyand installation (please see „Assembly / Installation“ ➨
pg. 3 — 35).
Disassembly
1. Pierce five cover caps (Fig.: 3 — 17 / Item 4) with a small screwdriver and remove cover caps.
2. Unscrew five screws.
3. Loosen the locking tabs (Fig.: 3 — 17 / Item 1) of the upper part of the housing (Fig.: 3 — 17 / Item 2) carefully by pressing the left and rear outer edge of the housing upwards and remove the housing upper part.
Note
Pay attention to the length of the connection cable and to theconnectors P2 and P3 when dismounting the housing. Do not pullthe connectors together with the upper part out of the bottompart.
Fig.: 3 — 17
Legend of fig. 3 — 17:ItemDesignation
1 Locking tabs
2 Housing upper part
3 Screw EJOT 30×35 WN 5452 TORX 10IP A2
4 Cover cap
5 Screw EJOT 30×12 WN 5452 TORX 10IP A2
2
5 4 3
1
Perfusor® Space, 1.0 gb 3 — 17
Disassembly / Assembly 3
1.0
4. Unscrew two screws and remove the contact strip (Fig.: 3 -18 / Item 3) (Fig.: 3 — 18 / Item 1).
Note
If necessary, the spring-mounted contact pins must be carefullyinserted when the contact strip is dismounted.
Fig.: 3 — 18
Legend of fig. 3 — 18:ItemDesignation
1 Housing upper part
2 Screw EJOT 25×7 WN 5451 TORX 8IP
3 Contact strip
1
23
3 — 18 Perfusor® Space, 1.0 gb
Disassembly / Assembly 3
1.0
3.6 Release Button Designation Ord. No.
Release button PSP with leaf spring(please see „Service Parts and Screw Kit“ ➨ pg. 3 —
Disassembly
1. Pull the release button (Fig.: 3 — 19 / Item 1) out of the housing bottom part.
3.7 Loudspeaker Designation Ord. No.
Loudspeaker SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 0937
Disassembly
1. Pull the loudspeaker connector off (Fig.: 3 — 20 / Item 1) the processor PCB and remove the loudspeaker.
Fig.: 3 — 19
Legend of fig. 3 — 19:ItemDesignation
1 Release button
1
Fig.: 3 — 20
Legend of fig. 3 — 20:ItemDesignation
1 Loudspeaker
1
Perfusor® Space, 1.0 gb 3 — 19
Disassembly / Assembly 3
1.0
3.8 Drive Designation Ord. No.
Drive PSP, cpl. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1046
Drive head PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1038(incl. driving tube)
Claw mechanism PSP . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1550
Drive PCB, PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1569
Side part of housing PSP . . . . . . . . . . . . . . . . . . . . . . . . 3452 1054
Screws(please see „Service Parts and Screw Kit“ ➨ pg. 3 —
Note
Please pay attention to the corresponding notes during assemblyand installation (please see „Assembly / Installation“ ➨
pg. 3 — 35).
Disassembly
1. Tilt the lock (Fig.: 3 — 21 / Item 1) of the drive ribbon cable upwards and pull the cable out of the connector.
2. Loosen one screw (Fig.: 3 — 23 / Item 1) and lift the fastening angle (Fig.: 3 — 23 / Item 2) of the drive ribbon cable.
3. Unscrew one screw (Fig.: 3 — 23 / Item 3) and remove the screw together with the locking washer (Fig.: 3 — 23 / Item 4) from the drive.
4. Pull the left carrier (Fig.: 3 — 22 / Item 1) / (Fig.: 3 — 23 / Item 5) out of the drive slide.
5. Pull out the drive head (Fig.: 3 — 23 / Item 6) together with the driving tube and the guide rail carefully from the drive assembly.
CAUTION
Pay attention to the ribbon cable in the driving tube whendismounting the drive.
Fig.: 3 — 21
Legend of fig. 3 — 21:ItemDesignation
1 Drive connector lock
1
Fig.: 3 — 22
Legend of fig. 3 — 22:ItemDesignation
1 Left carrier
1
3 — 20 Perfusor® Space, 1.0 gb
Disassembly / Assembly 3
1.1
Fig.: 3 — 23
Legend of fig. 3 — 23:ItemDesignation
1 Screw EJOT 22×8 WN 5451 TORX 6IP A2
2 Fastening angle
3 Screw EJOT 22×8 WN 5451 TORX 6IP A2
4 Washer
5 Carrier
6 Drive head
1 2
6
345
Perfusor® Space, 1.1 gb 3 — 21
Disassembly / Assembly 3
1.0
6. Pull the drive motor connector (Fig.: 3 — 24 / Item 2) off the processor PCB.
7. Unscrew one screw (first temporary screw) and remove the processor PCB ground cable (Fig.: 3 — 24 / Item 3).
Fig.: 3 — 24
Legend of fig. 3 — 24:ItemDesignation
1 Screw EJOT 30×8 WN 5451 TORX 10IP
2 Drive motor connector
3 Processor PCB ground cable
1 3 2
3 — 22 Perfusor® Space, 1.0 gb
Disassembly / Assembly 3
1.0
8. Unscrew one screw (second temporary screw) and take the drive assembly (Fig.: 3 — 25 / Item 1) out of the housing.
Note
Please pay attention to the corresponding notes during assemblyand installation (please see „Assembly / Installation“ ➨
pg. 3 — 35).
9. Pull the side part of the housing (Fig.: 3 — 26 / Item 1) out of the bottom part.
Fig.: 3 — 25
Legend of fig. 3 — 25:ItemDesignation
1 Drive assembly
2 Screw EJOT 30×8 WN 5451 TORX 10IP
2
1
Fig.: 3 — 26
Legend of fig. 3 — 26:ItemDesignation
1 Side part of housing
1
Perfusor® Space, 1.0 gb 3 — 23
Disassembly / Assembly 3
1.1
Disassembly of the Drive Head
1. Pierce two cover caps (Fig.: 3 — 27 / Item 4) with a small screwdriver and remove cover caps.
2. Unscrew two screws (Fig.: 3 — 27 / Item 3).
3. Remove claws (Fig.: 3 — 27 / Item 2) carefully out of the drive head.
CAUTION
The membrane plate (Fig.: 3 — 27 / Item 1) of the drive head mustnot be used as thrust bearing when removing the claws. If theforce exerted on the membrane plate is too great the membraneplate and the accessory components are damaged.
4. Pierce three cover caps (Fig.: 3 — 28 / Item 2) with a small screwdriver and remove cover caps.
5. Unscrew three screws (Fig.: 3 — 28 / Item 1).
6. Pull the drive head housing (Fig.: 3 — 28 / Item 3) over the driving tube and off the drive head.
Note
Note cable- or wire layout and sketch if necessary.
Fig.: 3 — 27
Legend of fig. 3 — 27:ItemDesignation
1 Membrane plate
2 Claws
3 Screw EJOT 20×18 WN 5452 TORX 6IP
4 Cover caps
4 3 2
1
Fig.: 3 — 28
Legend of fig. 3 — 28:ItemDesignation
1 Screw EJOT 25×10 WN 5452 A2 TORX 6IP
2 Cover caps
3 Drive head housing
21
3
3 — 24 Perfusor® Space, 1.1 gb
Disassembly / Assembly 3
1.1
7. Pull the claw mechanism (Fig.: 3 — 29 / Item 3) off the drive head cover (Fig.: 3 — 29 / Item 2) until the connection cable connector (Fig.: 3 — 29 / Item 1), (Fig.: 3 — 30 / Item 1) can be easily accessed.
8. Pull the connection cable of the claw mechanism off the drive head PCB and remove the claw mechanism.
9. Tilt the lock (Fig.: 3 — 30 / Item 3) of the drive ribbon cable upwards and pull the cable out of the connector.
Note
Pay attention to the emergency release tappet (Fig.: 3 — 30 /Item 2) during disassembly. The emergency release tappet caneasily drop out of the guide.
Fig.: 3 — 29
Legend of fig. 3 — 29:ItemDesignation
1 Connection cable, claw mechanism
2 Drive head cover
3 Claw mechanism
3
2
1
Fig.: 3 — 30
Legend of fig. 3 — 30:ItemDesignation
1 Connector of claw mechanism connection cable
2 Emergency release tappet
3 Ribbon cable, drive
1
3
2
Perfusor® Space, 1.1 gb 3 — 25
Disassembly / Assembly 3
1.2
10. Unscrew one screw (Fig.: 3 — 31 / Item 2) and remove the ground wire (Fig.: 3 — 31 / Item 1) of the drive PCB (Fig.: 3 -31 / Item 3) from the driving tube.
CAUTION
Pay attention to the strain gauge (Fig.: 3 — 31 / Item 4) whendismantling the drive head PCB. The strain gauge must not bejammed or removed by force out of the drive head cover.
CAUTION
The PCB potentiometer of the drive head must not be turned bymore than approx. 120°.
11. Take the drive PCB with the strain gauge carefully out of the drive head cover. The strain gauge and the PCB should be pulled vertically out of the holder.
Fig.: 3 — 31
Legend of fig. 3 — 31:ItemDesignation
1 Ground wire
2 Screw EJOT-PT Type DG 22×5 WN 1552
3 Drive PCB
4 Strain gauge
21
34
3 — 26 Perfusor® Space, 1.2 gb
Disassembly / Assembly 3
1.0
3.9 Syringe Holder with Piston Brake Designation Ord. No.
Piston brake PSP ribbon cable. . . . . . . . . . . . . . . . . . . . 3452 0864
Syringe holder with piston brake PSP, cpl. . . . . . . . . . . 3452 0945
Syringe holder PSP spring . . . . . . . . . . . . . . . . . . . . . . . 3452 0953
Piston brake PSP guide rail . . . . . . . . . . . . . . . . . . . . . . 3452 0961
Screws and cover caps(please see „Service Parts and Screw Kit“ ➨ pg. 3 —
Disassembly
WARNING
PAY ATTENTION TO THE PISTON BRAKE BLADE WHEN WORKINGON THE PISTON BRAKE. THE BLADE IS SHARP AND MAY CAUSEINJURIES.
1. Push the right and left connector lock (Fig.: 3 — 32 / Item 1) on the processor PCB carefully forward.
2. Pull the ribbon cable (Fig.: 3 — 32 / Item 2) out of the connector.
Fig.: 3 — 32
Legend of fig. 3 — 32:ItemDesignation
1 Processor PCB connector lock
2 Piston brake ribbon cable
1 2
Perfusor® Space, 1.0 gb 3 — 27
Disassembly / Assembly 3
1.0
3. Unscrew one screw and remove the locking clip (Fig.: 3 — 33 / Item 2) from the piston brake PCB.
Fig.: 3 — 33
Legend of fig. 3 — 33:ItemDesignation
1 Screw EJOT 20×14 WN 5452 TORX 6IP
2 Locking clip
1
2
3 — 28 Perfusor® Space, 1.0 gb
Disassembly / Assembly 3
1.0
4. Open the right and left connector lock (Fig.: 3 — 34 / Item 1) on the piston brake PCB carefully.
5. Pull the ribbon cable (Fig.: 3 — 35 / Item 1) out of the connector and remove the cable from the housing.
Fig.: 3 — 34
Legend of fig. 3 — 34:ItemDesignation
1 Piston brake connector lock
1
Fig.: 3 — 35
Legend of fig. 3 — 35:ItemDesignation
1 Piston brake ribbon cable
1
Perfusor® Space, 1.0 gb 3 — 29
Disassembly / Assembly 3
1.0
6. Remove the syringe holder spring (Fig.: 3 — 36 / Item 1) from the post in the bottom part of the housing.
Note
The syringe holder spring can only be removed together with thepiston brake drive.
7. Pull out the syringe holder and turn it clockwise.
8. Pierce two cover caps (Fig.: 3 — 37 / Item 2) in the syringe holder with a small screwdriver and remove cover caps.
9. Unscrew two screws and remove the cover from the syringe holder (Fig.: 3 — 37 / Item 1).
10. Turn and push in the syringe holder housing with piston brake.
Fig.: 3 — 36
Legend of fig. 3 — 36:ItemDesignation
1 Syringe holder spring
1
Fig.: 3 — 37
Legend of fig. 3 — 37:ItemDesignation
1 Syringe holder cover
2 Cover cap
3 Screw EJOT 25×10 WN 5452 TORX 8IP
1
3 2
3 — 30 Perfusor® Space, 1.0 gb
Disassembly / Assembly 3
1.0
11. Drive the piston brake motor with maximum 3 V DC. The blade is moved out of the syringe holder housing.
Note
If the blade moves into the syringe holder housing, then thepolarity on the piston brake motor must be changed.
12. Pull the blade out of the syringe holder housing.
13. Loosen one screw. Remove the piston brake PCB (Fig.: 3 — 39 / Item 2) and put it carefully aside. The connection wires must not be unsoldered.
Note
Pay attention to the light barrier components on the PCBunderside and to the length of the connection wires to the pistonbrake motor when removing the printed circuit board.
Fig.: 3 — 38
Legend of fig. 3 — 38:ItemDesignation
1 Piston brake blade
1
Fig.: 3 — 39
Legend of fig. 3 — 39:ItemDesignation
1 Screw EJOT 20×12 WN 5452 TORX 6IP
2 Piston brake PCB
1
2
Perfusor® Space, 1.0 gb 3 — 31
Disassembly / Assembly 3
1.0
14. Unscrew one screw and remove the bearing cover (Fig.: 3 -40 / Item 2).
15. Take the lock (Fig.: 3 — 40 / Item 3) out of the bearing housing.
16. Open the circlip (Fig.: 3 — 41 / Item 3) and pull it together with the carrier (Fig.: 3 — 41 / Item 2) off the syringe holder housing (Fig.: 3 — 41 / Item 1).
17. Pull the syringe holder housing out of the bottom part of the housing.
Fig.: 3 — 40
Legend of fig. 3 — 40:ItemDesignation
1 Screw EJOT 20×12 WN 5452 TORX 6IP
2 Bearing cover
3 Lock
3
2
1
Fig.: 3 — 41
Legend of fig. 3 — 41:ItemDesignation
1 Syringe holder housing
2 Carrier
3 Circlip
12 3
3 — 32 Perfusor® Space, 1.0 gb
Disassembly / Assembly 3
1.0
18. Unscrew two screws and remove guide rail (Fig.: 3 — 42 / Item 2) out of the bottom part of the housing.
19. Take piston brake motor assembly (Fig.: 3 — 42 / Item 4) out of the housing bottom part.
20. Remove syringe holder spring from the piston brake motor assembly.
Fig.: 3 — 42
Legend of fig. 3 — 42:ItemDesignation
1 Screw EJOT 30×8 WN 5451 TORX 10IP
2 Guide rail
3 Syringe holder spring
4 Piston brake motor assembly
1
2
4
3
Perfusor® Space, 1.0 gb 3 — 33
Disassembly / Assembly 3
1.1
3.10 Processor PCB Designation Ord. No.
Processor PCB PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 0880(incl. connectors andsyringe wing sensor)
Housing bottom part PSP . . . . . . . . . . . . . . . . . . . . . . . 3452 0929
Type plate PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Upon request
Screws and syringe wing sensor holder(please see „Service Parts and Screw Kit“ ➨ pg. 3 —
Note
Please pay attention to the corresponding notes during assemblyand installation (please see „Assembly / Installation“ ➨
pg. 3 — 35).
Disassembly
1. Pull the syringe wing sensor holder (Fig.: 3 — 43 / Item 1) out of the housing.
2. Lift the syringe wing sensor (Fig.: 3 — 43 / Item 6) out of the housing bottom part (Fig.: 3 — 43 / Item 5).
Note
Pay attention to the connection cable to the syringe wing sensorwhen removing the processor PCB. The connection cable is notshown in Fig.: 3 — 43.
3. Unscrew three screws and remove screws together with the processor PCB (Fig.: 3 — 43 / Item 2) and the shielding plate (Fig.: 3 — 43 / Item 4) from the bottom part of the housing.
Fig.: 3 — 43
Legend of fig. 3 — 43:ItemDesignation
1 Syringe wing sensor holder
2 Processor PCB
3 Screw EJOT 30×6 WN 5451 TORX 10IP
4 Shielding plate with earthing wire
5 Housing bottom part
6 Syringe wing sensor
32
6
5
1
4
3 — 34 Perfusor® Space, 1.1 gb
Disassembly / Assembly 3
1.0
3.11 Assembly / Installation Assembly or installation of the modules and subsystems is done inreverse order of disassembly. Special steps to be observed aredescribed hereafter in detail.
Only new cover caps are to be used.
Special Screws
Special screws for plastic housings are used in this unit. Thescrews are not self-cutting but produce a thread in the plastic ofthe housing through deformation when fitted in for the first time.
If the beginning of the thread is not engaged when the screw isfitted, a new thread is produced and the old thread is destroyedso that the security of the fixing can no longer be guaranteed.
Proceed as follows to fit the special screws:
1. Put the screw on the thread.
2. Rotate screw anti-clockwise (loosen) until a faint click can be heard. This click is produced when the screw thread drops into the existing thread.
3. Screw in the screw and tighten with the defined torque.
Zero Force Insertion Connector
Note
Make sure that the ribbon cable is centered between the plugguides when the zero force insertion connector is locked. Checkthe lock and the ribbon cable for correct fit before any furtherinstallation.
Perfusor® Space, 1.0 gb 3 — 35
Disassembly / Assembly 3
1.1
Processor PCB
When the processor PCB is replaced all data of the pump exceptfor the calibration data was probably saved on a PC. (please see„Preparations for Exchanging the Processor PCB“ ➨ pg. 3 — 2)Carry out the following steps to transmit the data back to thedevice.
WARNING
WHEN DATA PREVIOUSLY SAVED IS TRANSFERRED BACK TO THEDEVICE, CALIBRATION DATA IS NOT TRANSFERRED. THEREFORE, ACOMPLETE NEW CALIBRATION OF THE UNIT IS REQUIRED.
1. Start the Service Program (please see „Starting the Service Program“ ➨ pg. 1 — 8).
2. Select the register tab “Modification data”.
3. Press the “from file“ button. The window “Open” is displayed on screen.
3 — 36 Perfusor® Space, 1.1 gb
Disassembly / Assembly 3
1.2
4. Select the desired file with the mouse pointer and press the “Open” button.
Fig.: 3 — 44
Fig.: 3 — 45
Perfusor® Space, 1.2 gb 3 — 37
Disassembly / Assembly 3
1.2
5. Change to the tab „IO“ and actuate the “To device“ button. The data is saved in the Perfusor® Space.
6. Press the “OK“ button when the window “Confirmation“ is displayed.
Fig.: 3 — 46
Fig.: 3 — 47
3 — 38 Perfusor® Space, 1.2 gb
Disassembly / Assembly 3
1.2
7. Enter your worker id in the window “Worker ID“. Press the “OK” button to transmit the data to the device.
A message is displayed that a change of the device data may affect the patients.
Fig.: 3 — 48
Fig.: 3 — 49
Perfusor® Space, 1.2 gb 3 — 39
Disassembly / Assembly 3
1.2
8. Select the tab “Disposable article”.
9. Press the “Load from“ button. The window “Open” is displayed on screen.
Fig.: 3 — 50
3 — 40 Perfusor® Space, 1.2 gb
Disassembly / Assembly 3
1.2
10. Select the desired file with the mouse pointer and press the “Open” button. The data loaded is displayed on screen.
11. Actuate the “To device“ button. The data is saved in the Perfusor® Space.
Fig.: 3 — 51
Fig.: 3 — 52
Perfusor® Space, 1.2 gb 3 — 41
Disassembly / Assembly 3
1.2
12. Press the “OK“ button when the window “Confirmation“ is displayed.
13. Enter your user number in the window “User number“. Press the “OK” button to transmit the data to the device.
A message is displayed that a change of the device data may affect the patients.
14. Exit the Service Program (please see „Quit the Service Program“ ➨ pg. 1 — 11).
Fig.: 3 — 53
Fig.: 3 — 54
Fig.: 3 — 55
3 — 42 Perfusor® Space, 1.2 gb
Disassembly / Assembly 3
1.1
Loudspeaker
1. Route the loudspeaker connection cable between the drive motor and its connection wires, see Fig.: 3 — 56.
Piston Brake
WARNING
PAY ATTENTION TO THE PISTON BRAKE BLADE WHEN WORKINGON THE PISTON BRAKE. THE BLADE IS SHARP AND MAY CAUSEINJURIES.
Note
Pay attention to the light barrier components on the PCBunderside when installing the piston brake PCB.
1. Insert the syringe holder spring on the piston brake drive and fit the drive.
2. Route the ribbon cable to the piston brake drive as shown in Fig.: 3 — 57.
Fig.: 3 — 56
Fig.: 3 — 57
Perfusor® Space, 1.1 gb 3 — 43
Disassembly / Assembly 3
1.2
Drive Head
1. Insert the drive head PCB with the strain gauge vertically in the drive head cover. Please note that the strain gauge must not get jammed in the guide.
Note
The three strain gauge tongues are level with the PCB upper side.
2. The ground wire is to be layed according to the notes or the draft which was prepared before disassembly.
3. Turn the potentiometer (Fig.: 3 — 58) of the drive head PCB before assembly in such a way that the operating square of the upper claw seat can be pushed in.
CAUTION
The PCB potentiometer of the drive head must not be turned bymore than approx. 120°.
4. Position the two claw seats (Fig.: 3 — 58) before assembly in such a way that the marking (dot in material) on the upper claw seat points vertically upwards and the marking on the bottom claw seat points to the right, away from the driving tube.
Note
The motor connection wires and the ground wire must be laidbetween the claw mechanism bearing and the driving tube so thatthey cannot slip in the area of moving parts, e.g. the membranetappet.
Fig.: 3 — 58
Fig.: 3 — 59
3 — 44 Perfusor® Space, 1.2 gb
Disassembly / Assembly 3
1.1
Note
Check the position of the emergency release tappet beforemounting the drive head housing.
5. Push the drive head housing on to the driving tube until the switch flag of the membrane tappet is positioned just before the claw mechanism.
6. Turn the switch flag in such a way that it can be pushed in the switch flag guide.
7. Now mount the drive head housing. The membrane tappet must engage in the claw mechanism when the drive head housing is installed. For this purpose the membrane can be pressed during or after assembly.
Note
Pay attention that the membrane can be moved smoothly.
8. Install both claws and make sure that the sealing lips are not squeezed or damaged.
Drive / Side Part of Housing
Note
Take care not to damage the ribbon cable when inserting thedriving tube into the drive assembly.
Note
Pay attention to the switch on the processor PCB when mountingthe drive. The switch should be operated by the drive assemblyslide.
Fig.: 3 — 60
Fig.: 3 — 61
Perfusor® Space, 1.1 gb 3 — 45
Disassembly / Assembly 3
1.1
Note
Pay attention to the syringe wing sensor when inserting the sidepart of the housing and make sure that the sensor can be operatedcorrectly.
1. Route the ribbon cable through the slide nut before pushing in the driving tube and then through the slide in front of the spindle nut when looking from the rear of the housing.
2. Fold the ribbon cable once through 90° upwards, see Fig.: 3 -62, before mounting the fastening angle.
3. Run the drive motor connector over the loudspeaker connection cable. The loudspeaker connection cable must be positioned between the drive motor housing and the motor connection wires.
Note
Check that the two carriers in the drive slide are protected fromfalling out by the washer and screw.
Housing
Note
Take care that no cables are squeezed, and check that theconnector seals at the back are correctly placed in the housingand that the loudspeaker is correctly located when the housing isfitted.
1. Before mounting check the silicone seals in the housing and grease with silicone high-vacuum grease (part No. 3450 7930).
2. Lower the upper part of the housing vertically and carefully on to the bottom part.
3. Press the upper and bottom parts of the housing carefully together so that the outer edges engage. The locking tabs must click together.
Fig.: 3 — 62
3 — 46 Perfusor® Space, 1.1 gb
Disassembly / Assembly 3
1.0
Operating Unit
Note
Before fitting the rear panel check the screw lengths. The screwsmay only be 4.5 mm long (without head). Longer screws must beexchanged.
Note
Before mounting the operating unit check the plastic foamgaskets in the housing opening for the connection cable to theoperating unit.
1. Attach the left hinge plate to the operating unit, press it into the bottom part of the housing and install the hinge plate.
2. Push the operating unit connection cable into the processor PCB connector. Lock the connector.
3. Insert the PCA-slide and the PCA-eccentric in the bottom part of the housing.
4. Attach the right hinge plate to the operating unit and fit the hinge plate and the operating unit into the bottom part of the housing. Press the PCA-eccentric backwards until it slides into the opening on the right hinge plate.
Checks after Repair Procedure
1. Carry out a calibration after having worked on the drive, the syringe holder with piston brake or the processor PCB while the device was opened (please see „Calibration“ ➨ pg. 2 — 14).
2. Check the device to ensure safe functionality of the unit (please see „Device Check“ ➨ pg. 2 — 9).
3. Depending on the work carried out the specific steps of the TSC must be performed (please see „Technical Safety Check (TSC)“ ➨ pg. 5 — 1).
Perfusor® Space, 1.0 gb 3 — 47
Disassembly / Assembly 3
1.0
Check List for Checks after Repair
Visual Inspection Electrical Safetyaccording to IEC/EN 60601-1or VDE 0750 and VDE 0751
Functional Inspection
❒ Cleanliness❒ Completeness❒ Damage and faults affecting safety❒ Damage to and readability of the label❒ Syringe holder with piston brake❒ Screw covers❒ Connectors “P2” and “P3”
The patient and housing leakage current ofthe Perfusor® Space is caused exclusively bythe operating voltage supply (Power SupplySP or SpaceStation). The Technical Safety Checks of the powersupply SP (drawing No. M001 32 10 05 F04)or of the SpaceStation (drawing No. M69000 00 46 F04) serve to check whether bothlimit values are met.
❒ Locking with second unit❒ Operating unit magnets❒ Battery compartment cover
Switch on unit with power supply❒ Self-test❒ Indicator lamps (LEDs)❒ Audible alarm❒ Status display❒ Lighting of syringe compartment
Operation❒ Syringe fastening❒ Syringe recognition❒ Infusion❒ Staff call❒ Bolus❒ PCA lock
Switch on unit without power supply❒ Self-test❒ Magnetic function of the battery
compartment cover❒ Charge state of the battery module
(Part 1 of 2)
3 — 48 Perfusor® Space, 1.0 gb
Disassembly / Assembly 3
1.1
Pressure cut off according to TSCSyringe type: «#Lehre OPS50“Delivery rate: 200 ml/h
WARNING
REMOVE SYRINGE GAUGE ONLY WHENRELEASED. DANGER OF INJURY!
Strain gauge pressure measurement❒ Pressure stage 1 _______ N❒ Pressure stage 3 _______ N❒ Pressure stage 8 _______ N
Motor power limitation(convert syringe gauge)❒ Pressure stage 1 _______ N❒ Pressure stage 3 _______ N❒ Pressure stage 6 _______ N
Visual Inspection Electrical Safetyaccording to IEC/EN 60601-1or VDE 0750 and VDE 0751
Functional Inspection
(Part 2 of 2)
Perfusor® Space, 1.1 gb 3 — 49
Disassembly / Assembly 3
1.0
For your notes:
3 — 50 Perfusor® Space, 1.0 gb
41.2
4 -Servicing the Unit
Cleaning Clean and disinfect the Perfusor® Space with a humid cloth at
regular intervals. To clean the system we recommend mild soap-suds.
WARNING
WHILE CLEANING AND DISINFECTING THE PERFUSOR® SPACE,DISCONNECT THE UNIT FROM THE MAINS SUPPLY.
CAUTION
Take care that no water or liquid enters the device along thesyringe holder or the driving tube.
For disinfection by wiping, you should use for exampleMeliseptol® from B. Braun. Allow the unit to dry for at least oneminute. When you disinfect the device by spraying, make sure notto spray in the system openings (such as interface sockets andconnectors, loudspeaker opening).
Servicing the Battery The instructions for use contain a detailed description on how toservice the battery.
If a battery module is not discharged completely for more than 28days, a servicing program for the battery module can be startedon the unit.
Perfusor® Space, 1.2 gb 4 — 1
Servicing the Unit 4
1.0
For your notes:
4 — 2 Perfusor® Space, 1.0 gb
1.0
5 -Technical Safety Check (TSC)Perfusor® Space
Index b(Master — to be added to the documentation)
Checklist for Technical Safety Check – Every 24 Months
Unit: Perfusor® SpaceManufacturer: B. Braun Melsungen AG
User
Observe the Service Manual and the instructions for use. All measured values are to be documented. Accessories used should be included in testing. Make exclusive use of calibrated measuring equipment.
Article No. Unit No. Year of Procurement
Visual Inspection Electrical Safetyaccording to IEC/EN 60601-1or VDE 0750 and VDE 0751
Functional Inspection
❒ Perfusor® Space:Cleanliness, completeness, damage and faults affecting safety, damage and readability of the labelParticularly:❒ Syringe holder with blade❒ Syringe fastening❒ Membrane in drive head❒ Axial clearance of drive❒ Screw covers❒ Connectors “P2” and “P3”
❒ Accessories:Cleanliness, completeness, damage and faults affecting safety, damage and readability of the label
❒ Check the unit and the accessories for compatibility
The patient and housing leakage current ofthe Perfusor® Space is caused exclusively bythe operating voltage supply (Power SupplySP or SpaceStation). The Technical Safety Checks of the powersupply SP (drawing No. M001 32 10 05 F04)or of the SpaceStation (drawing No. M69000 00 46 F04) serve to check whether bothlimit values are met.
❒ Locking with second unit❒ Operating unit magnets❒ Battery compartment cover
Switch on unit with power supply❒ Self-test❒ Indicator lamps (LEDs)❒ Audible alarm❒ Visual alarm❒ Status display❒ Lighting
Operation❒ Syringe fastening❒ Syringe recognition❒ Infusion❒ Buttons on the operating unit❒ Staff call❒ Bolus❒ PCA lock
Switch on unit without power supply❒ Self-test❒ Magnetic function of the battery
compartment cover
(Part 1 of 2)
Perfusor® Space, 1.0 gb 5 — 1Sheet 1 of 2
M688 70 01 05 F04 / 3891 7319 (GB)
Technical Safety Check (TSC)
Index b(Master — to be added to the documentation)
1.1
Pressure cut-offSyringe type: «#Lehre OPS50″Delivery rate: 200 ml/h
— Strain gauge pressure measurement❒ Pressure stage 1 (11 … 16 N) ______ N❒ Pressure stage 3 (27 … 33 N) ______ N❒ Pressure stage 8 (68 … 76 N) ______ N❒ Error message “Alarm / pressure too
high” at every pressure stage
— Motor power limitation❒ Pressure stage 1 (12 … 27 N) ______ N❒ Pressure stage 3 (32 … 48 N) ______ N❒ Pressure stage 6 (61 … 79 N) ______ N❒ Error message “Alarm / drive blocked”
at every pressure stage
Mechanical Aids and Measuring Equipment Used
Accessories Used
❒ Syringe gauge, serial No.___________Calibrated on____________________
❒ Service connector SP❒ ____________________________❒ ____________________________
❒ Power Supply SP _______________❒ Battery module__________________❒ Staff call lead _______________❒ ____________________________❒ ____________________________
Test result:
Defects found which could endanger patients, users or third parties: Yes No
Inspection performed by:
Measures to be taken: Repair ___________________
Unit handed over on:
Special features / documentation:To:
Date / Signature:
Next deadline for TSC:
Visual Inspection Electrical Safetyaccording to IEC/EN 60601-1or VDE 0750 and VDE 0751
Functional Inspection
(Part 2 of 2)
5 — 2 Perfusor® Space, 1.1 gbSheet 2 of 2
M688 70 01 05 F04 / 3891 7319 (GB)
1.2
6 -Technical Safety Check (TSC)Power Supply SP
Index c(Master — to be added to the documentation)
Checklist for Technical Safety Check – Every 24 Months
Unit: Power Supply SPManufacturer: B. Braun Melsungen AG
User
Observe the Service Manual and the instructions for use of the respective device. All measured values are to be documented. Make exclusive use of calibrated measuring equipment.
Article No. Unit No. Year of Procurement
Visual Inspection Electrical Safetyaccording to IEC/EN 60601-1or VDE 0750 and VDE 0751
Functional Inspection
❒ Power Supply SP:Cleanliness, completeness, damage and faults affecting safety, damage and readability of the label
❒ Connecting lineCleanliness, damage and faults affecting safety
❒ Mains voltage ____ V~ (AC)❒ Leakage current ≤ 7 µA ____ µA
Measurement is to be carried out with service adapter SP between primary and secondary circuit.
Note
This measurement ensures that theadmissible limit values regarding thepatient and housing leakage current of thePerfusor® Space or the Infusomat® Spaceare met.
❒ Connector locking❒ After connecting the power supply the
respective unit displays that it is operated in mains operation
❒ Check of power supply, ord. — no. 3310 2708:Check lock of primary adapter with power supply. The adapter must engage on both sides.
Mechanical Aids and Measuring Equipment Used
❒ Perfusor® Space, serial No. _________❒ Infusomat® Space, serial No.:________❒ _____________________________
Test result:
Defects found which could endanger patients, users or third parties: Yes No
Inspection performed by:
Measures to be taken: none Dispose of power supply SP
Unit handed over on:
Special features / documentation:To:
Date / Signature:
Next deadline for TSC:
Perfusor® Space, 1.2 gb 6 — 1Sheet 1 of 2
M001 32 10 05 F04 / 3891 6142 (GB)
Technical Safety Check (TSC)
Index c(Master — to be added to the documentation)
1.0
For your notes:
6 — 2 Perfusor® Space, 1.0 gbSheet 2 of 2
M001 32 10 05 F04 / 3891 6142 (GB)
71.0
7 -Procedural Instructions on the TSC
Visual Inspection Perfusor® Space
1. Check the Perfusor® Space and accessories for cleanliness.
2. Check the Perfusor® Space and accessories for completeness and check configuration.
3. Check the Perfusor® Space and its accessories for damage and the labels for readability. Pay special attention to the following parts:
a) Syringe holder with piston brake
b) Piston brake blade in syringe holder
c) Membrane in drive head(cracks, porous)
d) Axial play of drive
e) Screw covers
f) Connectors “P2” and “P3”
Power Supply SP
1. Check the Power Supply SP and connecting line for cleanliness.
2. Check the Power Supply SP incl. connecting line for damage and the labels for readability.
Perfusor® Space, 1.0 gb 7 — 1
Procedural Instructions on the TSC 7
1.1
Electrical Safetyaccording to IEC/EN 60601-1or VDE 0750 and VDE 0751
Perfusor® Space
The patient and housing leakage current of the Perfusor® Space iscaused exclusively by the operating voltage supply (Power SupplySP or SpaceStation).
The Technical Safety Checks of the power supply SP (drawing No.M001 32 10 05 F04) or of the SpaceStation (drawing No. M69000 00 46 F04) serve to check whether both limit values are met.
Power Supply – Leakage Current
Note
The values to be measured are indicated in the TSC (please see„Technical Safety Check (TSC)“ ➨ pg. 5 — 1).
The leakage current is to be measured between primary andsecondary circuit using the service adapter SP.
Designation Ord. No.
Service adapter SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0770 5174
Check
1. Select leakage current on the testing equipment.
2. Bridge pins 6, 7 12 and 13 with service adapter SP at the connector to the unit.
3. Measure value.
4. Measure value with reverse polarity of the mains connection.
5. Document the largest value.
Fig.: 7 — 1
Legend of fig. 7 — 1:ItemDesignation
1 Mains connection
2 Primary of the power supply
3 Secondary of the power supply
4 Service adapter SP with probe
5 Leakage current measuring device
1 2 43
5
7 — 2 Perfusor® Space, 1.1 gb
Procedural Instructions on the TSC 7
1.0
Functional Inspection Perfusor® Space Mechanical Inspection
1. Fit the unit to be tested on top of another Space device and check the proper functioning of the lock.
2. Fit the unit to be tested under another Space device and check the proper functioning of the lock.
3. Hold the device with the operating unit downwards. The operating unit must not open.
4. Check the battery compartment cover lock for proper operation.
Functional Check
Note
Carry out the check with power supply connected.
1. Switch on unit and check the following details:
— Self-testDisplay on the LC display
— Indicator lampsLEDs (yellow, green, blue) light up for a short moment
— Visual alarmRed LED lights up for a short moment
— Audible alarmA deep and a high sound
— Staff callDepending on the device settings, the red LED on service connector SP lights up permanently or for one second after an alarm was triggered
— Status displayBattery capacity, mains operation (service connector SP)
— LightingIllumination of syringe compartment, LC display and buttons
2. Syringe fastening
a) Axial fastening holds syringe wing
b) Syringe holder blade fixes syringe piston
c) Both claws in drive head catch the syringe piston plate
Perfusor® Space, 1.0 gb 7 — 3
Procedural Instructions on the TSC 7
1.0
3. Check syringe recognition.
a) Insert approved 2 ml / 3 ml syringe.The syringe size is recognized.
b) Insert approved 50 ml syringe.The syringe size is recognized.
4. Carry out infusion and bolus with any syringe and press all buttons at least once.Infusion and bolus are performed and all buttons trigger the function desired.
5. Staff call
a) Plug service connector SP on connector “P2”.
b) Open syringe holder while the infusion is administered.The red LED on the service connector SP lights up.
6. PCA lock
a) Check the PCA lock with an approved 30 ml syringe.
Battery Check
1. Switch device off.
2. Pull off the power supply.
3. Switch on unit.Self-test is carried out.
4. Open battery compartment cover during operation.An alarm is activated.
Pressure Cut-Off (Strain Gauge Pressure Measurement)
WARNING
DURING THE STRAIN GAUGE MEASUREMENT WITH SYRINGEGAUGE THE SYRINGE HOLDER MUST NOT BE OPENED. THESYRINGE GAUGE IS UNDER VERY HIGH PRESSURE AND MAYCAUSE INJURIES IF THE PRESSURE IS RELIEVED SUDDENLY.
1. Plug service connector SP on connector “P2”.
2. Insert syringe gauge and select syringe type “#Lehre OPS 50“.
3. Input a delivery rate of 200 ml/h.
4. Select pressure stage according to the TSC and start infusion.Read off value on the syringe gauge upon an alarm and compare with the specifications in the TSC.
7 — 4 Perfusor® Space, 1.0 gb
Procedural Instructions on the TSC 7
1.0
Pressure Cut-Off (Motor Power Limitation)
WARNING
WHILE CHECKING THE MOTOR POWER LIMITATION WITH THESYRINGE GAUGE THE SYRINGE HOLDER MUST NOT BE OPENED.THE SYRINGE GAUGE IS UNDER VERY HIGH PRESSURE AND MAYCAUSE INJURIES IF THE PRESSURE IS RELIEVED SUDDENLY.
1. Plug service connector SP on connector “P2”.
2. Insert motor power test adapter at drive head.
3. Disassemble push-button plate for Perfusor® Space from syringe gauge, insert syringe gauge and select syringe type “#Lehre OPS50“.
Note
The threaded end of the syringe gauge must be introduced in theopening of the motor power test adapter. Hold on to syringegauge – if necessary by hand – in the syringe area, until thethreaded end of the syringe gauge is inserted in the opening ofthe motor power test adapter.
4. Input a delivery rate of 200 ml/h.
5. Select pressure stage according to the TSC and start infusion.Read off value on the syringe gauge upon an alarm and compare with the specifications in the TSC.
Functional Inspection Power Supply SP Mechanical Inspection
1. Connect power supply to a Space system device and check the lock for proper function.
Functional Check
1. The device connected operates correctly after being switched on.
Perfusor® Space, 1.0 gb 7 — 5
Procedural Instructions on the TSC 7
1.0
For your notes:
7 — 6 Perfusor® Space, 1.0 gb
81.2
8 -Test Equipment and Special Tools
Test Equipment Designation Ord. No.
For Device Check
Syringe 2 ml / 3 ml
Syringe 10 ml
Syringe 30 ml
Service connector SP . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1062
HiBaSeD Service-CD . . . . . . . . . . . . . . . . . . . . . . . . . . . 0871 3301
Diameter gauge kit PSP . . . . . . . . . . . . . . . . . . . . . . . . . 0770 5166Diameter gauge 32.0 mmDiameter gauge 23.4 mmDiameter gauge 15.5 mmDiameter gauge 9.0 mm
Length gauge PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0770 5190
Fig.: 8 — 1 Diameter gauges
Fig.: 8 — 2 Length gauge
Perfusor® Space, 1.2 gb 8 — 1
Test Equipment and Special Tools 8
1.1
Syringe gauge PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0770 5204Syringe gauge “#Lehre OPS 50“with push-button plate andmotor power test adapter for Perfusor® Space
For the TSC
Syringe 2 ml / 3 ml
Syringe 30 ml
Measuring instrument for electrical safety
Service adapter SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0770 5174for electrical safety
Service connector SP . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1062
Syringe gauge PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0770 5204Syringe gauge “#Lehre OPS 50“with push-button plate andmotor power test adapter for Perfusor® Space
Fig.: 8 — 3 Syringe gauge
Fig.: 8 — 4 Motor power test adapter
8 — 2 Perfusor® Space, 1.1 gb
Test Equipment and Special Tools 8
1.2
Special Tools Designation Ord. No.
For Repairs
TORX screwdriver kit5 — 10, 25
TORX plus screwdriver kit5 — 10, 25
Screwdriver 6IPx60 TORX plus . . . . . . . . . . . . . . . . . . . 4002 4806
Screwdriver 8IPx60 TORX plus . . . . . . . . . . . . . . . . . . . 4002 4814
Screwdriver 10IPx60 TORX plus . . . . . . . . . . . . . . . . . . 4002 4822
Perfusor® Space, 1.2 gb 8 — 3
Test Equipment and Special Tools 8
1.0
For your notes:
8 — 4 Perfusor® Space, 1.0 gb
91.2
9 -Spare Parts List
Item Designation Ord. No.
Perfusor® Space Service part kit Perfusor® Space . . . . . . . . . . . . . 3477 4270with:housing cover cap (40 pieces)cover caps for operating unit (10 pieces)cover cap for syringe holder (10 pieces)cover cap for drive head and claw (20 pieces)housing foot (20 pieces)release button SP with leaf spring (5 pieces)wing sensor holder (2 pieces)locking clip for piston brake (10 pieces)PCA key (2 pieces)
Cover caps for housing SP (50 pieces) . . . . . . . . 3477 4386
Cover caps for operating unit PSP (50 pieces) . 3477 3103
Connector seal P2 (50 pieces) . . . . . . . . . . . . . . . 3477 3102
Screw kit Perfusor® Space . . . . . . . . . . . . . . . . . . 3477 4289with:screw EJOT 22×8 WN 5451 TORX 6IP (5 pieces)screw EJOT 25×7 WN 5451 TORX 8IP (5 pieces)screw EJOT 30×6 WN 5451 TORX 10IP (5 pieces)screw EJOT 30×8 WN 5451 TORX 10IP (10 pieces)screw EJOT 20×12 WN 5452 TORX 6IP (5 pieces)screw EJOT 20×14 WN 5452 TORX 6IP (5 pieces)screw EJOT 22×4.5 WN 5452 TORX 6IP (10 pieces)screw EJOT 25×10 WN 5452 TORX 8IP (5 pieces)screw EJOT 30×8 WN 5452 TORX 10IP (10 pieces)screw EJOT 30×12 WN 5452 TORX 10IP (10 pieces)screw EJOT 30×35 WN 5452 TORX 10IP (5 pieces)screw EJOT 22×8 WN 5454 TORX 6IP (5 pieces)locking ring (5 pieces)
Perfusor® Space, 1.2 gb 9 — 1
Spare Parts List 9
1.1
Fig.: 9 — 1 Exploded drawing Perfusor® Space
1
2
3
4 5 67
8
10
9
11
12
13
14
17
18
1819
21
22
23
15
16
9 — 2 Perfusor® Space, 1.1 gb
Spare Parts List 9
1.1
1 Battery compartment cover PSP . . . . . . . . . . . . . 3452 0872
2 Battery pack SP (NIMH) . . . . . . . . . . . . . . . . . . . . 0871 3180
3 Operating unit PSP . . . . . . . . . . . . . . . . . . . . . . . 3452 0970
4 Hinge plate PSP, left . . . . . . . . . . . . . . . . . . . . . . 3452 1011
5 Hinge plate PSP, right . . . . . . . . . . . . . . . . . . . . . 3452 1020
6 PCA-slide PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 0899
7 PCA-eccentric PSP . . . . . . . . . . . . . . . . . . . . . . . . 3452 0902
8 Rear panel, operating unit PSP . . . . . . . . . . . . . . 3452 1003
9 LC display SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 0988
10 Front flap with keyboard PSP. . . . . . . . . . . . . . . . 3452 0996
11 Upper part of housing PSP . . . . . . . . . . . . . . . . . 3452 0910
12 Loudspeaker SP . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 0937
13 Drive PSP, cpl. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1046
14 Drive head PSP . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1038(incl. driving tube)
15 Claw mechanism PSP . . . . . . . . . . . . . . . . . . . . . 3452 1550
16 Drive PCB, PSP. . . . . . . . . . . . . . . . . . . . . . . . . . . . 3452 1569
17 Side part of housing PSP . . . . . . . . . . . . . . . . . . . 3452 1054
18 Piston brake PSP ribbon cable . . . . . . . . . . . . . . . 3452 0864
19 Syringe holder with piston brake PSP, cpl. . . . . . 3452 0945
20 Syringe holder PSP spring. . . . . . . . . . . . . . . . . . . 3452 0953
21 Piston brake PSP guide rail . . . . . . . . . . . . . . . . . 3452 0961
22 Processor PCB PSP . . . . . . . . . . . . . . . . . . . . . . . . 3452 0880(incl. connectors andsyringe wing sensor)
23 Housing bottom part PSP . . . . . . . . . . . . . . . . . . 3452 0929
Type plate PSP . . . . . . . . . . . . . . . . . . . . . . . . . Upon request
Perfusor® Space, 1.1 gb 9 — 3
Spare Parts List 9
1.0
9 — 4 Perfusor® Space, 1.0 gb
101.2
10 -Revision Documentation
Description of Version Version 1.0 (Base Version)
— First version of this Service Manual
— Release date: 07.01.05.
Version 1.1
— Description for disassembly of the drive head added.
— Claw mechanism and drive head PCB added as new spare parts.
— Description of the Service Program HiBaSeD changed to new version 1.5.0.
— Release date: 20.03.06
Version 1.2
— New kinds of power supplies.
— Changed TSC of the power supply.
— Changed service part kit and screw kit.
— Release date: 02.04.07
Version List of the Individual Pages
Perfusor® Space, 1.2 gb 10 — 1
Revision Documentation 10
1.0
10 — 2 Perfusor® Space, 1.0 gb
10
1.2
Title and Leading Pages
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Chapter 1 «System Overview»
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Chapter 2 «Unit Diagnosis / Calibration»
Page 2 — 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
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Chapter 3 «Disassembly / Assembly»
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Page 3 — 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 7 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 10 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 11 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 12 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Perfusor® Space, 1.2 gb 10 — 3
10
1.2
Page 3 — 13 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 14 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 15 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 16 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 17 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 18 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 19 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 20 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 21 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 3 — 22 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 23 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 24 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 3 — 25 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 3 — 26 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 27 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 28 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 29 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 30 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 31 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 32 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 33 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 34 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 3 — 35 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 36 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 3 — 37 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 38 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 39 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 40 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 41 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 42 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 43 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 3 — 44 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 3 — 45 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 3 — 46 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 3 — 47 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 48 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 3 — 49 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 3 — 50 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Chapter 4 «Servicing the Unit»
Page 4 — 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 4 — 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Chapter 5 «Technical Safety Check (TSC)»
Page 5 — 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 5 — 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Chapter 6 «Technical Safety Check (TSC)»
Page 6 — 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 6 — 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Chapter 7 «Procedural Instructions on the TSC»
Page 7 — 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 7 — 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 7 — 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 7 — 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 7 — 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Page 7 — 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Chapter 8 «Test Equipment and Special Tools»
Page 8 — 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 8 — 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 8 — 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 8 — 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Chapter 9 «Spare Parts List»
Page 9 — 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 9 — 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 9 — 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.1
Page 9 — 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Chapter 10 «Revision Documentation»
Page 10 — 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 10 — 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
10 — 4 Perfusor® Space, 1.2 gb
10
1.2
Page 10 — 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 10 — 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 10 — 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 10 — 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.0
Chapter 11 «Index»
Page 11 — 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Page 11 — 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Version 1.2
Perfusor® Space, 1.2 gb 10 — 5
10
1.0
10 — 6 Perfusor® Space, 1.0 gb
111.2
11 -Index
A
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 12
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 — 3
Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 1, 3 — 35
B
Battery compartment cover . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 9
Battery module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 9
Servicing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 — 1
Block diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 5
C
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 — 14
Procedural instructions . . . . . . . . . . . . . . . . . . . . . . . . . 2 — 14
Checks after repair . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 47
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 — 1
Compatibility list . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 11
Current versions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 — 5
D
Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 1
Device check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 — 9
Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 1
Drive
Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 45
Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 20
Drive head . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 21
Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 44
Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 24
E
Error codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 — 3
Error modes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 — 8
F
Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 3
H
Housing
Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 46
Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 17
Housing upper part . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 17
I
Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 1
L
List of abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 — 9
Loudspeaker
Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 43
Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 19
O
Operating unit
Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 47
Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 12, 3 — 15
Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 12
P
Physical construction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 2
Piston brake
Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 43
Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 27
Processor PCB
Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 36
Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 34
R
Release button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 19
Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 — 6
Revision service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 — 5
S
Service Program . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 7
Servicing the unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 — 1
Side part of housing . . . . . . . . . . . . . . . . . . . . . . . . 3 — 23, 3 — 45
Perfusor® Space, 1.2 gb 11 — 1
Index 11
1.2
Software update . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 6
Spare parts list . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 — 1
Special tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 — 1
Syringe holder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 27
System overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 1
T
Technical data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 12
Technical Safety Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 — 5
Perfusor® Space . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 — 1
Power supply SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 — 1
Test equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 — 1
Trouble shooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 — 29
TSC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 — 5
Perfusor® Space . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 — 1
Power supply SP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 — 1
Procedural instructions . . . . . . . . . . . . . . . . . . . . . . . . . 7 — 1
Test equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 — 2
U
Unit foot . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 — 11
Unit software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 — 6
11 — 2 Perfusor® Space, 1.2 gb