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AV-S Service Manual:AV-S Service Manual.qxd.qxd

1. Bellows Assembly aaa ie Pre use Checklists Daily Checklist uci enema e RR C ee a Function TeSt uiae ded cue TR uama ak mb aac S edd dnce ee ih Weekly Checklist 2 2 0 2 224444 44d sent khen d Rd oaa Oxygen Monitor Set up eee Installation 14 Lud sus waked de ke RR RC RE eae Gua RR hok Calibration 4 2 da diese dae Rr eod ha ae ate a ss Sensor Low Indication llle Setting the High and Low O2Alarms SERVICE PROCEDURES Service Intervals Control Unit Patient Block Removal Valve Calibration 2 222 2slxu edo a a EETesa SERVICE SCHEDULE Service Scheduled ee PARTS LISTS Preventive Maintenance Kits Assemblies ees APPENDIX Back up Battery iussus ss eek eR YO X X e Ree S SR Men System cirsrsrrT irk hR A Ara Ventilator Spirometry System _ sss Cleaning Sterilisation Oxygen sensor replacement Software Upgrade Installation Procedure Calibration and Output Checks for a New Ventilator Menu structure amendments v1 86 01 02 04 DoocBRomz iv USER RESPONSIBILITY This anaesthesia ventilator has been bu
2. 3 End of Expiratory Phase With the bellows at the top of its housing fresh gas continues to flow To prevent a high pressure build up the exhalation diaphragm 6 lifts and allows gas to exit through the exhaust valve 4 4 PEEP Positive End Expiratory Pressure user selectable The patient proportional valve 3 applies PEEP pressure plus 20 cmH20 to the exhaust valve which remains closed at this stage As fresh gas flows in the patient circuit any pressure increase above PEEP pressure in the bellows 5 will cause gas to bleed past the exhaust valve 4 If there is a fall in pressure in the breathing circuit the continuous flow from the drive gas proportional valve 1 helps maintain the set PEEP pressure DESCRIPTION A Pneumatic Flow Diagram 0 90 cmH2O DESCRIPTION 3 3 Pneumatic System 3 3 1 System Operation Refer to the pneumatic system diagram on the previous page A Gas inlet manifold block The AV S Ventilator is designed to operate on a 310 689 kPa 45 100 psi drive gas supply oxygen or air to customer s requirement 1 DISS Connector The gas source is connected to the DRIVE GAS SUPPLY fitting on the rear of the ventilator control unit The gas supply should be capable of a flow rate of 80 L min while maintaining a minimum pressure in excess of 310 kPa 45 psi 2 Filter The drive gas is filtered with a 40 micro
3. Check serial number to determine service required Check general condition of ventilator Check configuration of attachments tubing cables and connectors Note or replace as necessary Power On and Display Checks every 6 months Mains indicator illuminates amber when unit is switched off and connected to the mains Turn ventilator on Check audible alarm activates Default selection screen appears and automatically defaults to adult mode in Standby after approximately eight seconds Mains indicator illuminates green Check screen is undamaged display is clear and that the touch sensitive screen functions are operating correctly Check operation of On screen Indicator control using navigator wheel Menu Selection Tests every 6 months Press Menu button and check menu screen appears Rotate Navigator wheel and check menu scrolls Check sub menus can be selected by pressing the Navigator wheel Note some menu selections will time out after approximately 8 seconds of inactivity Restore any changed settings during above tests Engineers Mode Available in Standby only every 6 months Press Menu button and select Service Menu Select Clock Menu check date and time are correct Year 2005 2099 Month 1 12 Jan Dec Date 1 31 Hour 1 23 Minute 1 59 Select Upgrade Menu check software revisions I O Firmware for the main board Main Firmware for CPU core Select Ambient Pressure check read
4. AV S Ventilator Remote Display Module and Interface for use with A200SP Absorber Service Manual Partnership for Life THE IMPORTANCE OF PATIENT MONITORING WARNING Anaesthetic systems have the capability to deliver mixtures of gases and vapours to the patient which could cause injury or death unless controlled by a qualified anaesthetist There can be considerable variation in the effect of anaesthetic drugs on individual patients so that the setting and observation of control levels on the anaesthesia systems does not in itself ensure total patient safety Anaesthesia system monitors and patient monitors are very desirable aids for the anaesthetist but are not true clinical monitors as the condition of the patient is also dependent on his respiration and the functioning of his cardio vascular system IT IS ESSENTIAL THAT THESE ELEMENTS ARE MONITORED FREQUENTLY AND REGULARLY AND THAT ANY OBSERVATIONS ARE GIVEN PRECEDENCE OVER MACHINE CONTROL PARAMETERS IN JUDGING THE STATE OF A CLINICAL PROCEDURE IMPORTANT Servicing and Repairs In order to ensure the full operational life of this ventilator servicing by a Penlon trained engineer should be undertaken periodically The ventilator must be serviced to the following schedule a Six monthly service inspection and function testing b Annual two year four year services inspection and function testing and component replacement Details of
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6. PRE OPERATION PROCEDURES 5 2 Pre use Checklist 5 2 1 Daily Checklist The following tests must be carried out at the beginning of every working day Alarm System WARNING The operation of each alarm function should be verified daily If the audible alarm or the visual display for any alarm function fails to activate during any alarm condition or fails to reset after the alarm has been cleared refer the unit to an authorised service technician Back up Battery WARNING If the internal battery is fully discharged the ventilator will not function Recharge the battery before the ventilator is used Clinically Charging the battery for 14 hours from a discharged state will allow a minimum of 30 minutes of continuous operation Connect the ventilator to a mains power supply The mains power indicator will illuminate to show that the battery is being charged it is not necessary to turn on the ventilator Ventilator internal test Press the ON OFF switch 1 A three second internal test is initiated d The power up screen is displayed 2 The audible alarm sounds 3 The ventilator reverts to STANDBY mode if no selection is made NOTE special operating system on ventilators interfaced with Prima SP2 see section 3 5 2 a Turn the anaesthetic machine Gas Delivery Switch to ON the ventilator will power up b While machine power is ON the Ventilator can be turned OFF and ON using the ventilator On O
7. cmH20 Reconnect test lung and ensure alarm clears Disconnect test lung and open patient connector Ensure Low Airway Pressure alarm occurs Reconnect test lung refill bellows and ensure alarm clears Volume cycle the ventilator adjust Vt Set to achieve a peak airway pressure of greater than 30 cmH20 of water At peak pressure clamp the pressure sensing tube The displayed waveform should show pressure greater than 30 cmH20O continuously Check that High Continuous Pressure alarm is activated Unclamp pressure sensing tube and allow the ventilator to cycle Reset ventilator to default settings Disconnect mains power supply Verify that the ventilator continues to operate on battery Check that the AC Power Fail alarm is displayed Reconnect mains power supply to ventilator Remove drive gas line from gas supply outlet Check that the Low Supply Pressure alarm activates Reconnect drive gas line and ensure alarm clears Pressure Ventilation every 6 months Switch Ventilator to Pressure The ventilator will automatically set Target Pressure to 10 cmH20 Verify pressure is held at this setting 64 SERVICE SCHEDULE 16 2 16 3 17 1 4 17 2 17 3 17 4 18 18 1 18 2 18 3 18 4 18 5 NOTE Carry out leak test Set Rate to 5 BPM EE to 1 1 and Pressure Target to 50 cmH20 Ensure flowmeter on anaesthesia machine is set to minimum Fill bellows using O2 flush allow bellows to cyc
8. interference The driving gas supply must be clean and dry fo prevent ventilator malfunction This ventilator is designed to be driven by oxygen or medical air only The drive gas is set during manufacture and the ventilator is calibrated for that gas Before the ventilator is used clinically for the first time the commissioning engineer must confirm that the air oxygen selection is set correctly for the drive gas that is to be used The use of any other gas will cause inaccurate operation and may damage the ventilator resulting in potential injury to the patient 10 The driving gas is discharged through the opening in the back of the ventilator control unit The discharged gas may contaminate the environment and should therefore be extracted using a gas scavenging system The bellows can only support approximately 1 kPa 10 cmH20 differential positive pressure above which it may be dislodged from the mounting ring resulting in dangerous malfunction of the ventilator Do not connect a positive end expiratory pressure PEEP valve or other restrictive device to the exhaust port on the bellows base This would increase the pressure inside the bellows and the bellows could detach from the base causing serious malfunction Breathing System The breathing system which conveys gases from the anaesthetic machine to the patient and disposes of expired gases must conform to the requirements of ISO 8835 2 B
9. 1 Switch Ventilator to Volume Mode 2 Set Vt to 600 ml BPM to 10 1 E to 1 2 and Pressure Limit to 80 Set the flow on the anaesthetic machine to basal flow 3 From the main menu select FRESH GAS Main menu COMPENSATION OFF EXIT MENUS The bellows delivers 600 ml 50 ml but the ERE ee ean measured volume may be reduced to as low as SPECIAL MODES i WAVEFORM 500 ml with a standard test lung due to the ALARM SETTINGS compliance losses of the circuit GAS MIXTURE O2 AIR USER SETTINGS 4 Note If bellows delivery is out of specification SERVICE MENU repeat the Valve Calibration procedure 5 Apply a flow of 8 L min Oxygen from the Anaesthetic Machine Check that the displayed Vt Meas value rises 6 From menu select FRESH GAS COMPENSATION ON Allow 2 minutes for the reading to stabilise Observe that the bellows delivers less gas than before Check displayed Vt Meas 600 ml 50 ml Using a Wrights Respirometer check the expiratory volume value is within 50 ml of the displayed value 7 Note If Vt Meas is out of specification repeat zero spirometry calibration and 10 I min spirometry calibration it may be necessary to set a flow slightly above or below the 10 l min graduation on the flowmeter due to tolerance mismatch between the flow sensor and the flow tube 93 APPENDIX 6 Main Menu Amendments v1 86 01 02 04 On screen Menu Structure Additional sub menu Leak
10. 7 5 2 3 7 5 3 3 7 5 4 3 8 3 9 3 10 3 11 3 12 3 13 1 3 12 2 3 12 3 3 12 4 3 12 5 3 12 6 USER RESPONSIBILITY WARNINGS AND CAUTIONS PURPOSE ciar ara DEGREE AR DESCRIPTION General ota Sb o d cere e ee Ventilation Cycle en Pneumatic System System Operation iile ko db Re EROR eee eee eee W Electrical System 22 be eee eee in Control Panel 222c2 sdbe040586 42444645 000 meu ode a we caw edd Touchscreen Operation and Navigator wheel push button User Adjustable Parameters eee Operational capability 6 ee Output Compensation Functions Interface with Prima SP and A200SP Ventilation Modes slandby Mod6 escocia aa Saeed Gee baa aa Volume Mode used a A QR EY PES ead ee Pressure Mod ua suasana RREXX ew ERES ERR den ii Spontaneous Mode Advanced Spontaneous Breathing Modes SIMV Synchronised Intermittent Mandatory Ventilation SMMV Synchronised Mandatory Minute Ventilation i PSV Pressure Supported Ventilation PEEP Positive End Expiratory Pressure On screen Menus Spirometry 22 ssh cee eee eee ee ee Display Waveforms 00 0 Al
11. O2 AIR Enter PIN 123 USER SETTINGS Select ENGINEER MENU SERVICE MENU Select PENLON OPTIONS MENU Select CAL PRESSURE Service menu This will zero all pressure transducers ESCAPE FROM MENU LANGUAGE ENGLISH Check that the Barometric Pressure PRINT PAENT DATA reading is correct if necessary adjust and CLOCE MENU confirm AEN UPGRADE MENU AMBIENT PRESSURE 988 mBar DISPLAY HISTORY 2 Disconnect the fresh gas hose from the SERVICE PIN 0 Common Gas Oullet E ENGINEER MENU Switch the Bag Vent switch D to Bag and remove the bag from the arm E Remove the patient circuit 90 APPENDIX 6 Calibrate the drive gas flow transducer Select O2 MONITOR amp SPIROMETRY O2 Monitor amp Spirometry menu Select CAL SPIRO ESCAPE FROM MENU If menu shows calibration at 10 L min O2 MONITOR on O rotate the wheel to set at 0 L min CALIBRATION 100 I HIGH ALARM SET 105 Press to confirm note that display will LOW ALARM SET 18 flash a message SPIROMETER on This will zero the Drive Flow Transducer SPIRO CALIBRATION 0 L min 3 Use a safety bung to occlude the Driving Gas Output A Select ENGINEER MENU Select CAL VALVE MENU Select VALVE CAL TYPE Select zero dv Wait for display message zero dv cal complete a 4 Remove the bung Reconnect hoses to Driving Gas Output A and Patient Pressure Connector B Reconnect the fresh gas hose to the Common Gas Outlet Connect the
12. Prima SP2 with A200SP absorber connect to absorber see section 5 1 5 Outlet Exhaust Valve connect to scavenge system Electrical Connection 4 Electrical mains input and fuse unit 42 Interface and Parameter inputs 5 A200SP Absorber Bag Vent switch interface and Spirometer connector 6 Prima SP2 Interface connector SP2 primary on off switch 7 Pressure Monitor Port 8 Input socket Oxygen monitor sensor Data and Printer Ports 9 Data Output 10 Output to remote screen 11 Ethernet 12 USB 13 VGA 14 Printer port 15 RS232 manufacturer s use only NOTE USB port is for access only by engineers trained by the manufacturer All other data ports are read only For further information please contact your distributor s service department or the manufacturer PRE OPERATION PROCEDURES 5 1 5 Bellows drive gas hose 1 Prima SP2 with A200SP absorber Connect a 16 mm diameter corrugated hose between the ventilator control unit drive gas outlet labelled DRIVE GAS and the outlet 1 at the rear of the A200SP absorber 2 All other AV S configurations Connect a 16 mm diameter corrugated hose between the control unit drive gas outlet labelled DRIVE GAS and the bellows base DRIVE GAS inlet port 5 1 6 Anaesthetic Gas Scavenging System 1 Connect the EXHAUST valve port on the control unit to a properly functioning scavenging system Use a 19 mm hose 2 Fit a 10 cmH20 p
13. Test Main Menu EXIT MENUS O2 MONITOR amp SPIROMETRY LEAK TEST MENU r FRESH GAS COMPENSATION ON SPECIAL MODES WAVEFORM ALARM SETTINGS GAS MIXTURE O2 AIR USER SETTINGS SERVICE MENU Leak Test ESCAPE FROM MENU lt START STOP LEAK TEST gt LEAK STATUS unknown LEAK LEVEL 0 mL min BSYS COMP 7 0 mL cmH2O 94 0473 Cat No 52968 Doc No AV S 0208 SM June 2008 Manufactured by Penlon Limited Abingdon Science Park Barton Lane Abingdon OX14 3PH UK Technical Support Tel 44 0 1235 547076 Fax 44 0 1235 547062 E mail technicalsupport penlon co uk International Sales Tel 44 1235 547001 Fax 44 1235 547021 E mail export penlon co uk UK Sales Tel 01235 547036 Fax 01235 547023 E mail uksales penlon co uk
14. Use a breathing system bacterial filter in the expiratory limb of the breathing circuit to protect the oxygen sensor b Use a heat and moisture exchanger HME at the patient Y piece a combined HME bacterial filter can also be used but note that the expiratory limb bacterial filter is still required CAUTION Replacement Disposal always follow the instructions supplied with the filter or HME Fit new components at the recommended interval 3 Connect a 2 litre breathing bag to the patient connection as a test lung 4 Close the anaesthetic machine APL valve 5 1 10 Spirometer 5 1 10 1 Flow sensors fitted to an A200SP Absorber mounted on a PrimaSP2 1 Use a breathing system bacterial filter see section 5 1 9 operation 2 CAUTION Replacement Disposal always follow the instructions supplied with the filter Always renew components at the recommended interval 2 The two spirometry flow sensors are mounted within the A200SP Absorber in the inspiratory and expiratory airways 3 Connect the cable assembly between the connector at the rear of the A200SP Absorber A and the the socket B at the rear of the Ventilator control unit 4 Check that the cable connections are secure NOTE A If the connections are incorrectly made the ventilator will alarm LOW TIDAL VOLUME or HIGH TIDAL VOLUME B To allow the ventilator to be used in the event of damage or non functioning of the spirom
15. as well as flow rate Laser trimmed thick film and thin film resistors provide consistent interchangeability from one device to the next The microbridge mass airflow sensor uses temperature sensitive resistors deposited within a thin film of silicon nitride They are suspended in the form of two bridges over an etched cavity in the silicon The chip is located in a precisely dimensioned airflow channel to provide a repeatable flow response Highly effective thermal isolation for the heater and sensing resistors is attained by etching the cavity space beneath the flow sensor bridges The small size and thermal isolation of the microbridge mass airflow sensor are responsible for the extremely fast response and high sensitivity to flows Dual Wheatstone bridges control airflow measurement one provides closed loop heater control the other contains the dual sensing elements APPENDIX The heater circuit minimizes shift due to ambient temperature changes by providing an output proportional to mass flow The circuit keeps the heater temperature at a constant differential 160 C above ambient air temperature which is sensed by a heat sunk resistor on the chip The ratiometric voltage output of the device corresponds to the differential voltage across the Wheatstone bridge circuit Sensor flow characteristics The graph shown below is a typical flow versus resistance graph for the Honeywell spirometer head units for the f
16. automatically upgraded when connected to an auto upgrade disc with a USB floppy drive 1 connected into the ventilator USB port 2 IMPORTANT NOTES 1 The ventilator must be connected only to a USB floppy disk drive as illustrated Use an industry standard drive for this application to avoid data transfer errors It is not necessary to remove the cover from the ventilator for the software to be upgraded automatically Do notinstall the upgrade from a PC or USB Memory Stick device Automatic Software Upgrade de Connect the AV S to a mains power source but do not power the ventilator on Connect a floppy disk drive to the USB port on the rear of the ventilator Ensure the upgrade installation disk is inserted in the drive Switch the AV S on After a self testing sequence the floppy disk drive should power up and display on screen the upgrade status followed by the success or failure of upgrade When instructed switch off the ventilator by pressing and holding the on off button for about six seconds Disconnect the the floppy disk drive cable from the ventilator USB connector 2 and switch the ventilator on 89 Check on the AV S start up screen that the software version matches the installation disk Carry out the valve calibration procedure detailed in section 6 3 Read the notes on the datasheet issued with the upgrade Ensure that any User Datasheet that accompanies the upgrade
17. battery is allowed to remain in a discharged state Never discharge the battery to below 10 2 volts A Battery installed in ventilator The battery must be charged before the machine is released for use with an 14 hour charge from the ventilator s internal power supply ventilator connected to the mains supply but not running Note that the mains power indicator on the front panel will show a yellow light during charging Subsequently the recharge periods for a battery on a ventilator in store are similar to those in B below Batteries in machines in normal use will be kept charged by the internal power supply Note that the Low Battery Alarm indicator may be displayed if automatic recharging is taking place as the ventilator is in use B Battery care storage requirements During storage batteries will require a periodic recharge the frequency of which is determined by the storage temperature which must not exceed 50 C 120 F Storage Recharge temperature period 38 to 50 C 100 to 122 F 1 month 21 to 38 C 70 to 1009F 3 months 7 to 21 F 45 to 70 F 6 months 0 to 79C 32 to 45 F 9 months 5 to 09C 23 to 32 F 12 months Duration recharge for a minimum of 12 hours typically overnight It is recommended that at each charge an updated label is affixed to the unit to indicate date of the last charge C Disposal of used batteries Follow all hospital local state and federal regulations Note
18. breathing circuit and test lung Select Vent on absorber Bag Vent switch B Set a fresh gas flow of 5 L min Wait for the bellows to fully inflate Select ENGINEER MENU Select CAL VALVE MENU Select VALVE CAL TYPE Select zero pv Wait for display message Patient valve calibrated Reduce gas flow to minimum 5 Disconnect the drive gas hose from the rear of the absorber F Connect a flow measurement device Select ENGINEER MENU Select CAL VALVE MENU Select VALVE CAL TYPE Select dv meas Check measured value is approximately 20 L min If not adjust using Trim Valve Flow on Menu After each trim valve flow adjustment press the navigator wheel to confirm change Wait for the displayed value to adjust and settle to 20 L min Select none from Menu to end calibration Remove the flow measurement device but leave the hose disconnected 91 APPENDIX 6 7 Select ENGINEER MENU Select CAL VALVE MENU Select VALVE CAL TYPE Select dv curve Observe valve oscillation and increasing flow delivery up to maximum flow Valve calibration is now complete Spirometer Calibration 1 Check the condition of the external Spirometer cables and connections Disconnect the fresh gas hose from the anaesthesia machine Common Gas Oullet Switch the Bag Vent D switch to Bag Remove the bag from bag arm E Remove the test lung from the patient connector if fitted
19. cmH20 Inspiratory Flow 2 70 L min Spontaneous Mode Active Volume and Pressure Alarms Advanced Breathing Modes selectable see section 4 6 Electronic PEEP 4 20 cmH20 Oxygen Monitor Fuel Cell type For full specification see section 4 15 Spirometry Resolution 10 ml Ventilator Performance accuracy of delivered volumes 2300 ml 2096 2100 ml 300 ml 2096 100 ml 50 NOTE The ventilator is designed for use with Spirometry ON Accuracy of delivered volumes with Spirometry OFF may vary from the figures given above 35 SPECIFICATION 4 6 Advanced Spontaneous Breathing Modes SIMV SMMV PSV Trigger PEEP Referenced 0 7 to 4 L min Trigger Window Set 60 of Expiratory Time Vt and Vm As Volume Mode Insp Time Ti 0 5 to 5 secs Support Pressure 3 to 20 cmH2O Default settings Volume Adult Paediatric Pressure Adult Paediatric SIMV Adult Paediatric SMMV Adult Paediatric PSV Adult Paediatric 4 7 4 8 4 9 4 10 4 11 4 12 4 13 4 14 Vt BPM E Pmax 600ml 10 1 2 38 cmH2O 150ml 15 1 2 38 cmH2O Vt BPM LE P target 600ml 10 1 2 10 cmH20 150ml 15 1 2 10 cmH20 Vt BPM Insp time Trigger 600ml 6 2 sec 1 L min 200ml 10 1 sec 1 L min Vm BPM Insp time Trigger 3 6L 6 2 sec 1 L min 2L 10 1 sec 1 L min Support Pressure Insp time 10 cmH2O 1 L min 10 cmH20 1 L min Disinfection and Sterilisation Patient Block assembly can be sterilised if necessary section 6 NOTE The bellows
20. d Quantity 4 X A gt PARTS LIST Display Screen Assembly Item 1 Part No 300540 300541 300575 300573 01253 300550 019122 300516 01013 300547 300524 01059 025606 15056 15446 Description Front Moulding Rear Cover Spinner 038 mm Gasket M4 X 25 SKT HD Cap Membrane Switch LED s M3 X 6 LG Button HD LVDS Encoder Assembly M4 X 10 SKT HD Cap O Ring Cord TFT Sub Assembly M2 5 X 6 CH HD M3 Fibre Washer Product Label Warranty Label 68 Quantity 1 1 1 2 4 1 4 1 4 1 1 2 6 1 1 PARTS LIST Screen Assembly 300524 Item 1 0 Do WwW N Part No 300565 300531 300567 300599 5000544 300536 300537 300566 Description 8 4 TFT Screen NEC TFT Mounting Plate Inverter 5V M2 5 X 16 Butt HD SS M2 5 Nyloc Nut ST STL Tape Touch Screen To TFT Tape TFT To Plate 8 4 Touch Screen 69 Quantity mk A A A X X e PARTS LIST Control Unit Assembly 5000453 Item 1 2 3 4 al 10 11 12 Part No 01056 300534 019171 300564 019049 5000489 5000499 15446 15056 034072 5000460 Description M5 x 12 SKT HD Cap Screw SP Mounting Plate M4 x 10 But Flanged HD Short Form Instructions M3 X 10 LG Pan HD Chassis Assembly Tray Assembly Remote Warranty Label Product Label M5 Cover Plug Cover AVS 70 Quantity 4 1 10 mk P X PARTS LIST PARTS LIST Control Unit Cha
21. displayed at bottom right of touch screen SIMV checks 13 5 Switch ventilator to Standby From the Special Modes menu select SIMV 13 6 Re select Spont Mode Select SIMV Message on screen will read Switch absorber to vent position Change absorber position to Vent Ventilator now displays SIMV message in white 13 7 Note If absorber switch is not enabled in service menu the message will read Switch absorber to vent position Press SIMV once again 13 8 Operate Test Lung very gently by hand Check that occasional ventilator assistance is given 13 9 Stop operation of test lung Ensure test lung is ventilated at the default settings 600ml 6 bpm 3 3 sec Ti SMMV checks 13 10 Switch ventilator to Standby From the Special Modes menu select SMMV 13 11 Re select Spont Mode Select SMMV The message on screen will read Switch absorber to vent position Change absorber position to Vent Ventilator now displays SMMV message in white 13 12 Note If absorber switch is not enabled in service menu the message will read Switch absorber to vent position Press SMMV once again 13 13 Operate Test Lung very gently by hand Check that occasional ventilator assistance is given and that the measured Minute Volume is 3 6 litres Stop operation of test lung Ensure test lung is ventilated at the default settings 3 6 litres 6 bpm 3 3 sec Ti PSV checks 13 14 Switch ventilator to Standby From the Special Modes
22. low priority alarm single note will sound The sensor must be replaced as the output will fall very quickly to zero within two to three weeks of normal usage See section 6 5 for sensor replacement 3 12 6 Oxygen Monitor Alarm Mute In an alarm condition pressing the ALARM MUTE button will deactivate the audible alarm but the alarm message display will remain on Screen The switch will illuminate and a single note will sound The alarm mute can not be operated a Until the mute time is over or the alarm condition has been rectified b When 02 concentration drops below 18 4 SPECIFICATION 4 1 Application 4 2 Internal Compliance Adult bellows Paediatric bellows 4 3 Physical Size mm control unit only with adult bellows Screen Size Weight control unit only with adult bellows Bellows Adult Latex free Paediatric Ventilation for use in anaesthesia 3 ml cmH2O nominal 2 ml cmH2O nominal 290 wide x 300 deep x 185 high 290 wide x 300 deep x 385 high 210 mm 8 4 TFT 7 6 kg 9 kg 20 ml 1600 ml 20 350 ml Note latex free paediatric available as option Power Battery Back up Drive Gas 4 4 Alarms Alarm Mute Apnoea Low Drive Gas Pressure High Continuous Airway Pressure Low Pressure Incorrect Rate or Ratio Mains Failure Low Battery Ventilator Inoperative Outlet Blocked Alarms User Adjustable Low Tidal Volume High Tidal Volume Low Minute Volum
23. oxygen 10 Scroll to ESCAPE FROM MENUS and press the button 6 to exit 11 Turn off the flow of oxygen 12 Refit the absorbent canister 1 52 02 Monitor amp Spiro ESCAPE FROM MENU 02 MONITOR on CALIBRATION 100 HIGH ALARM SET 105 LOW ALARM SET 18 SPIROMETER on SPIRO CALIBRATION 0 L min PRE OPERATION PROCEDURES O2 Monitor 5 3 3 Sensor Low Indication The unit automatically detects when sensor life is low The message OXYGEN SENSOR LOW OUTPUT will appear on screen to indicate that the sensor must be replaced The sensor output will fall very quickly to zero over a period of two to three weeks from the first time that the alarm is activated Sensor replacement see Appendix 4 5 3 4 Setting the O2 Alarms 5 3 4 1 Set High Alarm The high alarm value cannot be set below 19 or above 105 Note that in certain conditions of excess pressure the readout may show a value above 100 1 Touch the O2 concentration display or Press the menu switch on the ventilator front panel and select the O2 monitor sub menu 2 Scroll to HIGH ALARM SET and press the navigator wheel 3 Rotate the wheel to change the displayed alarm figure to the desired value 4 Press the wheel to confirm 5 Scroll to ESCAPE FROM MENUS and press the wheel to exit 5 3 4 2 Set Low Alarm The low alarm value cannot be set lower than 18 or above 99 1 Touch the O2 concentration display or P
24. ventilator to Volume Mode Connect test gauge to primary regulator test point and check regulator set to 262 kPa 21 kPa 38 psi 3 psi during inspiratory phase If adjustment is necessary the cover must be removed Connect manometer to output of patient proportional valve small probe and check for 90 cmH20 10 during the inspiratory phase and zero during the expiratory phase Adjust secondary regulator as necessary During expiratory phase ensure that there is no gas flow from the Drive Gas connector If necessary carry out Drive Gas Valve Offset calibration Control Unit every 6 months From Diagnosis Menu check flow transducer zero offset levels Drive flow Inspiratory Flow and Expiratory Flow should all read approximately 80 mV Check all electrical connections and components for security every 12 months Replace back up battery every 2 years NOTE Check battery type 30 minutes back up or 1 hour back up Replace Real Time battery every 4 years Set Up every 6 months 59 SERVICE SCHEDULE 9 1 9 2 9 3 9 4 9 5 9 6 9 7 10 10 1 10 2 10 3 10 4 10 5 10 6 11 5 11 6 Select drive hose O2 or Air Attach to the Driving Gas Input connection to the rear panel Connect the long corrugated hose to the Drive Gas Output connector of vent and the vent drive gas connector at rear of absorber Connect the pressure tube to Patient Pressure connection on the rear panel
25. volume User adjustable option If the maximum pressure limit is achieved the ventilator cycles to the expiratory phase 3 7 2 3 Volume Type Selection Use the menu to switch between Tidal Volume and Minute Volume NOTE Minute Volume is derived from a rolling average during a 30 second period 21 DESCRIPTION 3 7 3 Pressure Mode 3 7 3 1 Parameters In pressure mode the ventilator delivers a flow of gas to achieve a set pressure at fixed breath intervals The Patient is making no respiratory effort This is a common mode for the ventilation of small paediatric patients Inspiratory pressure 10 70 cmH20 Rate 4 100 bpm LE ratio 1 0 3 1 8 PEEP Off or adjustable 4 20 cmH20 Inspiratory decelerating flow is controlled by the ventilator according to the pressure setting There is no Inspiratory Pause function in pressure mode 3 7 3 2 Pressure Mode Operating Functions Pressure mode defaults to a target pressure of 10 cmH20 at switch on A high Inspiratory Flow is used to achieve and maintain the target pressure The exhaust valve operates to prevent excess pressure 22 DESCRIPTION 3 7 4 Spontaneous Mode 3 7 4 1 Parameters The ventilator monitors the following patient parameters Rate E ratio Pressure Tidal volume In spontaneous mode the waveform displays are active and inspiratory oxygen levels are measured 3 7 4 2 Spontaneous Mode Operating Functions Selection during Venti
26. which is small enough to exclude microbial contamination All wrapping materials must comply with EN 868 Packaging Materials for Sterilization of Wrapped Goods Processing Equipment The sterilizer must comply with the stated performance class BS 3970 and HTM 2010 and with additional requirements stated in Section D If a Porous load sterilizer is used it must conform to the specifications in EN 285 and the safety specifications in EN 61010 Part 2 041 Sterilization must be achieved by direct contact with good quality saturated steam Post processing Following reprocessing the patient block must be kept in a sterile plastic pouch to avoid being re contaminated prior to being fitted to the ventilator Refit in accordance with section 6 2 5 5 Function test the ventilator before clinical use see section 5 2 1 Bellows Assembly Components Item Method Bellows Gas liquid autoclave 20 cycles maximum Hoses Gas liquid autoclave O rings Gas liquid autoclave Bellows base Gas liquid autoclave Exhalation valve Gas liquid pasteurise low temperature autoclave assembly Bellows canister Liquid autoclave 87 APPENDIX 4 Oxygen Monitor Sensor Cleaning Disinfection Sterilisation In case of contamination the sensor 1 may be cleaned with distilled water and allowed to dry naturally CAUTION The sensor is not suitable for sterilisation by steam or exposure to chemicals such as ethylene oxide or hydrogen
27. 17 DESCRIPTION 3 5 4 Output Compensation Functions WARNING The AV S automatically compensates for fresh gas spirometry On fresh gas mixture spirometry and oxygen monitor On and altitude However the actual tidal volume delivered to the patient may be different to the ventilation parameters set by the user due to A an extreme compliance condition B a substantial system leak C patient circuit pressure effects or D extreme fresh gas flows In addition high fresh gas flows will lead to an increased Vt being delivered to the patient The patient must be monitored independently from the ventilator It is the responsibility of the user to monitor the patient for adequate ventilation Fresh Gas Compensation Adjusts delivered volume up to 60 An alarm is triggered if the measured volume varies by 50 from the set volume This function is user adjustable NOTE Fresh gas compensation is disabled if a The spirometry system is turned OFF through the menu system or b The spirometry system is not functioning correctly Fresh Gas Mixture Compensation models with Spirometry The spirometry system compensates for fresh gas mixture the user must access the menu system and select the gas mixture that will be used for each clinical procedure NOTE Fresh gas mixture compensation is disabled if a The spirometry system is turned OFF through the menu system or b The spirometry system is not fun
28. GS 1 We recommend calibration of the oxygen monitor every time the system is turned on as a safety precaution Do not attempt to open the fuel cell The sensor contains small quantities of a electrolyte classified as a harmful irritant which is potentially hazardous and b lead Used or defective cells must be disposed of according to hospital local state and federal regulations ALWAYS check the integrity of the sensor assembly before use Once exhausted the sensor must be disposed of according to hospital local state and federal regulations The sensor measures oxygen partial pressure and its output will rise and fall due to pressure change An increase in pressure of 10 at the sensor inlet will produce a 10 increase in sensor output The oxygen sensor is not suitable for sterilisation If contamination is suspected fit a new sensor see section 6 4 and dispose of the contaminated unit according to hospital local state and federal regulations CAUTIONS 1 Do not sterilise any oxygen monitor component Do not autoclave or expose the sensor to high temperatures Ifthe sensor shows signs of being affected by condensation dry the sensor with soft tissue Do not use heat to dry the sensor NOTES f The O2 SENSOR FAULT alarm indicates that one of the following conditions has occurred a Internal electrical fault b Software electronics fault c Oxygen sensor fault Th
29. O PORT 4 USING SILICON TUBE 011092 CONNECT PORT 1 TO PORT 5 USING 4mm O D TUBE 300638 CONNECT PORT 2 TO PORT 6 USING 5mm O D TUBE 300637 74 PARTS LIST Regulator Assembly and Control Block Assembly Item Part No Description Quantity 1 300526 Regulator Assembly 1 2 5000482 Control Block Assembly 1 3 019037 M3 X 35 Cap HD 4 4 041221 O Ring 8 1 X 1 6 1 75 PARTS LIST Patient Block Assembly Item OMAN O Oi ON _ o 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 Part No 300580 300581 300583 5000478 300593 300594 5000448 5000450 5000451 5000452 5000453 0501 01014 011169 019028 019087 019128 019153 041214 041217 041250 300561 5000444 5000445 5000475 5000476 Description Diaphragm One way valve Inline Relief Valve Check Valve Cap Taper Adaptor Tapered Conn Spring Guide Valve Body Seat Insert Drive Gas Block Valve Base O Ring M4 X 16 SKT HD Cap Screw Ss M4 Skiffy Cap M3 X 6 Grub Ss Cup M3 X 16 Cap HD Screw M4 X 8 Butt HD CHEM BLK M4 X 50 Cap Head SS O Ring RM 0221 16 Viton O Ring O Ring 227 6 X 2 4 Compression Spring M4 Tappex Trisert M3 Tappex Trisert Mounting Plate Mounting Plate Label 76 Quantity gt gt gt e P o PARTS LIST TT 9 APPENDIX APPENDIX 1 Care of Back up Battery CAUTION Damage may occur if the
30. RE OPERATION PROCEDURES 1 Bellows 2 Ventilator Control Unit 3 Outlets to Anaesthetic Gas Scavenging System AGSS 4 Bacterial Filter 5 Absorber valve block 6 Heat and moisture exchanger a combined unit with a bacterial filter can be used see 5 1 9 7 Patient 8 CGO Block on anaesthetic machine Fresh Gas Supply 9 Auxiliary Outlet on anaesthetic machine Drive Gas Supply 10 Flow sensor expiratory 11 Flow sensor inspiratory 12 Connectors sensor pressure monitor 13 Expiratory Valve Absorber 14 Inspiratory Valve Absorber 15 Inlet from Ventilator Bellows 16 Connector Reservoir Bag 17 Inlet Absorber Fresh Gas Supply 18 Drive Gas Inlet Ventilator 19 Drive gas Outlet ventilator control unit to bellows 20 Outlet Exhaust Valve 21 Inlet Bellows Drive Gas 22 Outlet to breathing system 23 Input socket Oxygen monitor sensor 24 Input socket Prima SP interface SP on off switch 25 Input socket i A200SP Absorber Bag Vent control position ii Spirometer sensor signal 26 Interface connections on Prima SP2 and A200SP 27 APL Valve 28 Outlet from APL Valve to AGSS 29 Oxygen sensor 30 Remote screen unit 31 Cable control unit to screen 41 PRE OPERATION PROCEDURES Control Unit Rear Panel Gas Connections 1 Ventilator drive gas inlet connect to anaesthetic machine auxiliary gas outlet Bellows Drive Gas Output connect to bellows on
31. Removal replacement of battery must only be undertaken by a trained technician 78 APPENDIX 2 APPENDIX 2 On screen Menus NOTE 1 All selection or changes in the menu are followed by a CONFIRM message prompt on the screen and accompanied by a BEEP user volume set The selected text or option will invert in colour User settings menus only activate in Standby mode Clock menu Upgrade menu Diagnostic menu only activate in Standby mode Special Modes on screen tab only activates in Spontaneous mode Adult default settings VT 600 mL RATE 10 bpm IE RATIO 1 2 Plimit 38 cmH2O Ptarget 10 cmH20 Paediatric default settings VT 150 ml RATE 15 BPM IE RATIO 1 2 Plimit 38 cmH2O Ptarget 10 cmH20 79 Menu Structure Main Menu EXIT MENUS O2 MONITOR amp SPIROMETRY FRESH GAS COMPENSATION ON 4 SPECIAL MODES WAVEFORM ALARM SETTINGS GAS MIXTURE O2 AIR USER SETTINGS SERVICE MENU O2 Monitor amp Spirometry ESCAPE FROM MENU O2 MONITOR on if CALIBRATION 100 HIGH ALARM SET 105 LOW ALARM SET 18 SPIROMETER on SPIRO CALIBRATION 0 L min off on Toggle option 21 100 Toggle option 19 105 Integer 18 99 Integer off on Toggle option 0 L min 10 L min Fresh Gas Compensation ON OFF off on Special Modes ESCAPE FROM MENU SUPPORT MODE none TRIGGER 5 L min SIGH TO BREATH RATIO 1 50 Support Mode pick list Trigge
32. aMMS 26H 254406 eee ESS Eee AG pad da Oxygen Monitor System Operation aia arar ARE ARA ERG The MOX 3 Oxygen Sensor Menus seacdadGeeesuededde bere et enetdade eeu Display u cues RR RR DRE uu eee ho Alarms u su s usss sa as ended uhu wa Q 2 0 Q 6 Qipa Q S Alarm MUS us eaten rtu ein Ei Ord wawa rabat E RR EBORE SPECIFICATION oscar ewes gd we daa Ventilator ess doe OE ey YS q utat cioe ence Oxygen Monitor o iii Page No 13 13 14 15 15 16 17 18 19 20 20 21 22 23 24 24 25 26 27 28 29 29 30 31 31 31 32 33 33 33 34 37 CONTENTS 5 1 5 1 1 5 1 2 5 1 3 5 1 4 5 1 5 5 1 6 5 1 7 5 1 8 5 1 9 5 1 10 5 1 11 5 1 12 5 2 5 2 1 5 22 5 2 3 5 3 5 3 1 5 3 2 5 3 3 5 3 4 6 1 6 2 PRE OPERATION PROCEDURES Ventilator Set up soo 5 44h4 res t SE a ERR RA Mounting the Ventilator lu ee Electrical Power Connections Ventilator Gas Supply id ee Breathing System Schematic ee Bellows Drive GaS sanidad dara Odea aad ee RR RS Anaesthetic Gas Scavenging System Remote Screen suisse ER aa d AA da huacas ch Printer dixe eee de eC dead hdd dh ae Nei ek a a RC E Breathing Systemi lp LU RERGRRARREERAGU EGO NR RA RR E Rd Spirometer Connections Pressure Monitor Connections
33. airway pressure limit and should agree with the setting Open the patient Y piece to ambient pressure At the second cycle the LOW AIRWAY PRESSURE alarm should be activated Select STANDBY mode Before using the ventilator clinically check that all connections are correct and verify that there are no leaks If there is any malfunction the ventilator must NOT be used If the problem cannot be rectified the ventilator must be checked by an engineer trained by the manufacturer PRE OPERATION PROCEDURES 5 2 3 Weekly Checklist At least every week in addition to the daily function test the following checks must be carried out Alarms 1 Select STANDBY MODE 2 Unplug the mains power cable from the AC outlet The MAINS FAILURE alarm should activate 3 Reconnect the mains power cable to the AC outlet The alarm should turn off 4 Disconnect the drive gas supply hose The LOW SUPPLY PRESSURE alarm should activate NOTE If there is any malfunction the ventilator must NOT be used If the problem cannot be rectified the ventilator must be checked by an engineer trained by the manufacturer Bellows Check the condition of the bellows and exhalation diaphragm valve Note that the bellows assembly is built into the A200SP Absorber please refer to the user manual for this product 50 PRE OPERATION PROCEDURES O2 Monitor 5 3 O2 Monitor System Set up 5 3 4 Installation Fit the p
34. assembly oxygen monitor sensor and spirometer sensors are built into the A200SP Absorber for information please refer to the User Manual for A200SP Bacterial Filter None always use a bacterial filter in the breathing system to protect the oxygen sensor see section 5 1 4 Fail Safe Mechanism Battery back up in case of mains electricity failure Gas shut off in the event of electronic failure Reliability MTBF 5x106 to 50x10 cycles Waveform Tests Not applicable Volume Tests Not applicable Mobility and Mounting A Mobility Secure mounting required B Mounting Control unit and remote screen are mounted on anaesthetic machine The bellows assembly is built into the A200SP Absorber Fuse mains supply Two fuses Type T 2AH 2A 250 V rating 20 mm anti surge ceramic 36 SPECIFICATION O2 Monitor 4 15 Oxygen Monitor Measurement Range Resolution Accuracy and Linearity Response Time Operating Temperature Storage Temperature Relative Humidity Range Battery Back up High Priority Alarm Medium Priority Alarm Low Priority Alarm Alarm Mute Low Alarm Set Range High Alarm Set Range Cable length Sensor Type Life 0 100 11 12 of full scale at constant temperature and pressure 90 of final value in approximately 10 seconds air to 100 O2 50 F to 100 F 10 C to 38 C 23 F to 122 F 5 C to 50 C 5 95 non condensing As per ventilator Flashing 5 audio pulse
35. continuously If the drive gas supply pressure drops below a nominal 241 kPa 35 psi the LOW DRIVE GAS SUPPLY alarm will activate both audibly and visually Patient minute volume may be reduced due to lowered flow rates An audible alarm indicates an anomalous condition and should never go unheeded The characteristics of the breathing circuit connected between the ventilator and the patient can modify or change patient ventilation To assist the maintenance of the delivered patient tidal volume the ventilator control system software includes A a compliance compensation algorithm B a fresh gas compensation algorithm However patient ventilation must be monitored independently from the ventilator It is the responsibility of the user to monitor patient ventilation Care must be taken to ensure that the flow sensors are connected correctly to the inspiratory and expiratory ports of the absorber The Vent Inop ventilator inoperative alarm indicates that one of the following conditions has occurred a The drive gas solenoid has failed b The flow control valve has failed c Internal electronic fault d Internal electrical fault e Software error WARNINGS AND CAUTIONS 25 26 Note that if a ventilator error is detected Ventilator Inoperative will be displayed on the front control panel display The High and Low Airway Pressure Alarms are important for patient care It is importan
36. ctioning correctly If the O2 monitor is switched OFF a 40 60 mixture of O2 N2O is assumed Altitude Compensation This function monitors ambient pressure and adjusts the delivered volume accordingly NOTE Altitude compensation is automatically applied during calibration of the oxygen monitor see section 5 3 2 18 DESCRIPTION 3 6 Interface to Prima SP2 3 and A200SP The AV S is designed to interface with the Prima SP2 Anaesthetic Machine and the A200SP Absorber 3 6 1 Prima SP2 Interface The interface cable links the socket A on the control panel to a socket on the rear panel of the anaesthetic machine a Turn the anaesthetic machine Gas Delivery Switch to ON The ventilator will power up b While the anaesthetic machine power is ON the Ventilator can be turned OFF and ON using the ventilator On Off switch as described in section 3 5 1 c Turn the anaesthetic machine Gas Delivery Switch to OFF The ventilator will power down 3 6 2 A200SP Absorber Interface The interface cable links the socket B on the control panel to a socket C at the rear of the absorber a The A200SP is fitted with a sensor that detects the position of the absorber bag vent control D The sensor signal cabling is routed internally to connector C and a second cable runs to the the rear of the AV S control unit b Operation of the Bag Vent control will trigger automatic Mode switching on the AV S ventilato
37. cts Water vapour volumes in the breathing gas are not detectable in normal breathing system dynamics Additional Features Additional spirometry features available for selection by the user are the ability to turn off the automatic compliance and fresh gas compensation and also the feedback provided by the oxygen monitor In this event the ventilator relies on the basic delivery look up table and the internal flow sensor to confirm delivery volumes as near as possible under the circumstances Accuracies for spirometry measurement are gt 300 ml 20 gt 100 ml lt 300 ml 20 lt 100 ml 50 83 Flow sensor description The microbridge mass airflow sensor operates on the theory of heat transfer Mass airflow is directed across the surface of the sensing elements Output voltage varies in proportion to the mass air or other gas flow through the inlet and outlet ports of the package The specially designed housing precisely directs and controls the airflow across the microstructure sense element The microbridge mass airflow sensor has a unique silicon chip based on advanced microstructure technology It consists of a thin film thermally isolated bridge structure containing heater and temperature sensing elements The bridge structure provides a sensitive and fast response to the flow of air or other gas over the chip Dual sensing elements positioned on both sides of a central heating element indicate flow direction
38. d volume is adjusted by up to 60 f This delivered volume will consist of the volume id SUPE bci 4320 emhi2O delivered from the ventilator bellows plus the fresh Inspiratory pressure limit 10 to 100 cmH20 gas flow from the anaesthetic machine fresh gas Inspiratory pause 2596 supply minus any compliance loss and minus any does not affect I E ratio leak Sigh Approximately 1 5 x This gives a total actual inspired tidal volume Set Vt is delivered An alarm is triggered if the measured volume is 50 above or below the set volume This function is user adjustable once twice three times or four times every 50 breaths user Altitude Compensation selects frequency This function monitors ambient pressure and adjusts the delivered volume accordingly 3 7 2 2 Operating Functions Inspiratory Pause function This function creates a plateau that equates to 2596 of the inspiratory time Sigh function When the ventilator is in Volume Cycle mode the Sigh option is available When selected this option provides extra volume for 1 to 4 breaths in 50 the user can select 1 2 3 or 4 breaths The extra volume will be approximately 50 above the tidal volume set by the user Note that the High Volume Alarm is not triggered when sigh is selected Volume measurement Volumes are measured if the Spirometry function is selected Automatic High or Low volume alarms are triggered if the measured volume is 50 above or below the set
39. e High Minute Volume Low and High O2 Concentration High Airway Pressure 100 240 VAC 50 60 Hz 30 minutes assumes fully charged battery Note Optional 1 hour back up battery is fitted to some models Oxygen or Air dry and oil free at 45 to 100 psi 310 to 689 kPa 30 or 120 seconds see 3 11 Flow referenced no breath detected within 15 seconds Less than 235 kPa 35 psi Above 30 cmH20 at start of cycle 4 14 cmH20 PEEP referenced Fully charged standard battery provides 30 mins nominal backup Fully charged high power battery option provides one hour nominal backup 5 minutes use Internal or Battery Failure Exhaust valve outlet blocked Measured value is below 5096 of volume set Range 0 1600 ml Measured value exceeds 15096 of volume set Range 20 1600 ml Calculated value is 50 below volume set Range 0 10L Calculated value exceeds 150 of volume set Range 0 30L 1896 10596 10 80 cmH20 adjustable 34 SPECIFICATION 4 5 Functional Tidal Volume Adult bellows 20 to 1600 ml 10 Paediatric bellows 20 to 350 ml 10 At ambient temperature of 20 C 10 and ambient atmosphere of 101 3 kPa 10 Minute Volume 0 to 30L Rate 4 100 bpm LE Ratio 1 0 3 1 8 Pressure Limit 10 100 cmH20 Fresh Gas Compensation Automatic Tidal Volume adjustment Modes Off Standby Volume Cycle Pressure Controlled Spontaneous includes advanced breathing modes Pressure Control 10 70
40. e concentration read out may in certain conditions of excess pressure show a value above 100 To accommodate these conditions it is possible to set the high alarm value up to 105 see section 5 To maintain maximum sensor life i always switch off the anaesthetic machine after use to ensure that the basal flow ceases ii disconnect the breathing circuit after use The accuracy of flow and volume measurements may be reduced if the oxygen monitor is not in use Fresh gas mixture compensation is disabled if the oxygen monitor is switched OFF 2 PURPOSE The AV S Ventilator is a software controlled multi mode ventilator designed for mechanical ventilation of adult and paediatric patients under general anaesthesia In addition in spontaneous mode it can be used to monitor spontaneously breathing patients It is designed for use in closed circuit anaesthesia Indications for use of the device The AV S Ventilator is intended to provide continuous mechanical ventilatory support during anaesthesia The ventilator is a restricted medical device intended for use by qualified trained personnel under the direction of a physician Specifically the ventilator is applicable for adult and paediatric patients The ventilator is intended for use by health care providers i e Physicians Nurses and Technicians with patients during general anaesthesia The AV S ventilator is not intended for use in intensive care applicat
41. eat two year service plus Replace PCB battery and bellows diaphragm valve Details of these service operations are given in section 7 of this manual Always ensure that a record is kept of any service or repair work 54 SERVICE PROCEDURES 6 2 Control Unit Patient Block Assembly Removal On a regular basis in line with hospital procedures for infection control the patient block 1 must be removed cleaned and sterilised see Appendix 4 1 Detach the hoses from the outlets 2 Note different diameters for correct refitment 2 Undo the securing knobs 3 3 Carefully detach the assembly 1 from the control unit Note that resistance will be felt until the metal tubes 4 disengage 4 Wash thoroughly then sterilise as recommended in Appendix 4 Do not disassemble Refitting 5 Position the patient block and push fully into the control unit ensuring that the metal tubes 4 are engaged in their unions 6 Fit the securing knobs 3 7 Function test the ventilator eese 55 SERVICE PROCEDURES 6 3 Valve Calibration 1 Disconnect the hoses from the Drive Connector Airway Pressure Connector and Exhaust Connector on rear of ventilator Carry out an Ambient Pressure calibration This will zero all pressure transducers 2 Disconnect the fresh gas hose from the anaesthesia machine Common Gas Outlet Switch the Bag Vent switch t
42. ecause breathing systems require frequent cleaning and disinfection they are not a permanent part of the anaesthetic ventilator and therefore cannot be directly under the control of the anaesthetic ventilator manufacturer However we strongly recommend that only breathing systems which have been approved and authorised by the manufacturer for use with AV S should be employed Do not use conductive breathing system hoses When mechanical ventilation is employed the patient breathing system must be connected directly to a pressure relief valve to prevent the possibility of barotrauma The spirometer sensors are mounted within the A200SP absorber Do not fit a spirometer sensor to any other location The device will not measure exhaled volumes in any other position WARNINGS AND CAUTIONS 11 12 13 The operation of each alarm function should be verified daily Periodically check the alarms at clinically suitable intervals If the audible alarm or the visual indicator of any alarm function fails to activate during any alarm condition or fails to reset after the alarm has been cleared refer the unit to an authorised service technician Before using the ventilator check that all connections are correct and verify that there are no leaks Patient circuit disconnects are a hazard to the patient Extreme care should be taken to prevent such occurrences It is recommended that Safelock fittings are used througho
43. entilator has a a gas composition setting whereby the user is able to select the gasses being delivered i e oxygen air oxygen nitrous oxide etc b an oxygen monitor Thus the ventilator knows the overall oxygen concentration and the majority of the remaining gas composition APPENDIX Altitude Effects Gas flow measurements are also affected by atmospheric pressure in a linear relationship To compensate for altitude effects an ambient pressure sensor is available When the spirometers are calibrated for zero flow the ambient pressure is recorded so that the measured volume may be adjusted The measured volume is multiplied by the ratio of Pamb to Pcal where Pamb is the latest ambient pressure and Pcal is the ambient pressure recorded when the spirometers were calibrated at zero flow Carrier Gas Effects The effect of air as the dilutent gas is different to that of nitrous oxide and as the ventilator includes only an oxygen monitor the additional information of gas being ventilated is included to increase available accuracy Anaesthetic Agent Effects The addition of anaesthetic agent is known also to increase the spirometry readings depending on the agent and its concentration by up to approximately 2 Again this minor volume measurement variation is of no known clinical disadvantage and is therefore not compensated for other than that due to oxygen variation due to the percentage change Water Vapour Effe
44. eral Law restricts the sale and use of this device to or on the order of a licensed practitioner Statements in this manual preceded by the following words are of special significance WARNING means there is a possibility of injury to the user or others CAUTION means there is a possibility of damage to the apparatus or other property NOTE indicates points of particular interest for more efficient and convenient operation Always take particular notice of the warnings cautions and notes provided throughout this manual 1 WARNINGS AND CAUTIONS The following WARNINGS and CAUTIONS must be read and understood before using this ventilator WARNINGS General Information 1 Personnel must make themselves familiar with the contents of this manual and the machine s function before using the ventilator Before Using the Ventilator 2 Before the ventilator is used clinically for the first time verify that the hospital engineering department has carried out an earth continuity test Excessive electronic noise caused by other poorly regulated devices such as an electrocautery unit may adversely interfere with the proper functioning of the ventilator To avoid this problem do not connect the ventilator s power cord into the same electrical wall outlet or adaptor strip into which an electrocautery unit is connected If used with a mains extension cord the unit may be subject to electro magnetic
45. eter heads turn off the spirometry function see MENU function section 3 5 If the spirometer is switched OFF a Fresh gas compensation is disabled b Fresh gas mixture compensation is disabled c Patient support function is disabled 44 PRE OPERATION PROCEDURES 5 1 10 2 Spirometer Calibration Flow sensors fitted to an A200SP Absorber mounted on a Prima SP The Spirometry sensor heads must be calibrated with zero flow going through them 1 10 11 12 13 Turn the anaesthetic machine gas flow off at the Gas Delivery on off switch This will stop all gas flows including the AHD basal flow This will also turn the AV S off Turn the AV S on at the ventilator Do not use the Prima SP Gas Delivery switch or Disconnect the fresh gas hose from the CGO block on the anaesthetic machine Remove the breathing circuit hoses from the inspiratory and expiratory connectors 1 on the absorber Disconnect the hose that connects the APL valve outlet 2 at the rear of the manifold block to the AGSS receiver or disconnect at receiver a Remove the bag and set the Bag Vent control 3 to Bag position or b Ensure that the ventilator bellows is empty Calibrate the spirometer via the ventilator menu procedure Press the menu switch on the front panel Scroll down the main menu and select O2 MONITOR amp SPIROMETRY Select SPIRO CALIBRATION Press the wheel to ini
46. ff switch c Turn the machine Gas Delivery Switch to OFF The ventilator will power down Calibrate the Spirometer 5 1 10 2 Calibrate the O2 Monitor 5 3 2 48 Function Test Set the AIRWAY PRESSURE LIMIT to 50 cmH20 PRESSURE TRANSDUCER connection Check that the port on the rear of the control unit is correctly connected to the port on the rear of the absorber assembly see section 5 1 10 Connect a 2 litre breathing bag to the patient connection as a test lung Adult bellows only Set the tidal VOLUME to 600 ml RATE to 10 bpm and E RATIO to 1 2 0 Use the O2 flush button on the anaesthetic machine to fill the bellows Select VOLUME CYCLE mode The delivered tidal volume indicated on the scale printed on the bellows housing should be approximately 600 ml If the delivered tidal volume is less than 500 ml or greater than 700 ml refer the ventilator to an engineer trained by the manufacturer Set a basal flow only on the anaesthetic machine Check the bellows after 10 breaths the bellows should return to the top of the housing Failure to return to the top of the housing indicates a leak in the breathing circuit Rectify the leak before clinical use 49 10 11 NOTE PRE OPERATION PROCEDURES Occlude the patient Y piece The HIGH AIRWAY PRESSURE alarm should be activated The peak pressure read on the breathing system pressure gauge is the maximum working
47. flow generated by the patient s spontaneous breath results in synchronised pressure support PSV must be pre selected in Standby mode Select Standby Mode Select Menu Select Special Modes Select Support Mode Select PSV Escape Menu PSV will be displayed on the main screen when Spontaneous mode is selected or triggered Activate PSV during Ventilation NOTE PSV will not function unless already pre selected in Standby Mode 1 Select Special Mode on the display If the absorber Bag Vent switch is not detected a message will appear SET ABSORBER TO VENT Press the navigator wheel push button to confirm 2 Move the absorber Bag vent switch to Ventilator 3 Check that PSV is functioning correctly NOTE 1 The trigger window is pre set to 60 of the BPM cycle time 2 The trigger pressure is PEEP referenced 3 If the Spirometry system is disabled then PSV is not available 4 If the pressure limit and alarm are activated the inspiratory phase is terminated PSV Default Settings The ventilator will default to pre set values for Support Pressure Inspiratory Time and Trigger Level after selecting PSV Note 1 Support Pressure can be adjusted before PSV is confirmed 2 The trigger setting is adjustable between 0 7 and 4 0 L min PSV Pressure Supported Ventilation A Set Inspiratory Time B Pressure Support Level C Spontaneous Breath results in a synchronised pressu
48. g calibration We recommend calibration with a 10096 oxygen standard source at a pressure and flow similar to your application 51 PRE OPERATION PROCEDURES O2 Monitor 5 3 2 1 Calibration Using 100 Oxygen AV S ventilator mounted on a Prima SP2 anaesthetic machine fitted with a A200SP absorber Calibrate with the sensor in position within the absorber 1 Detach the absorbent canister 1 2 Remove the breathing circuit hoses from the inspiratory and expiratory connectors 2 on the absorber This will give a free flow of oxygen through the sensor 3 Switch on the ventilator 3 and the anaesthetic machine gas delivery switch The oxygen monitor automatically switches ON when the ventilator is switched on Ensure that all vaporizers are OFF 4 Apply 10096 oxygen only at 5 L min from the anaesthetic machine flowmeter 5 Allow the oxygen to flow until the oxygen monitor readout 4 stabilises 6 Calibrate the sensor using the AV S ventilator menu procedure as follows de Press the menu switch 5 and select the O2 monitor sub menu 8 Scroll to CALIBRATION If the menu shows 21 which indicates calibration using air press the navigator wheel button 6 to switch to 100 calibration using oxygen 9 A message will flash on the screen O2 AT 100 Press the button 5 to confirm NOTE The message OXYGEN SENSOR LOW OUTPUT will appear on screen if the user attempts to calibrate at 21 in 100
49. gain to change the displayed value see section 5 3 4 for full procedure 19 to 105 18 to 99 High Alarm range Low Alarm range The displayed figure will flash on and off Press to confirm Scroll to EXIT MENUS and press the wheel to exit O2 Monitor sub menu O2 Monitor amp Spiro ESCAPE FROM MENU O2 MONITOR on CALIBRATION 10096 HIGH ALARM SET 105 LOW ALARM SET 18 SPIROMETER on SPIRO CALIBRATION 0 L min O2 Monitor sub menu calibration O2 Monitor amp Spiro ESCAPE FROM MENU O2 MONITOR on CALIBRATION 10096 HIGH ALARM SET 105 LOW ALARM SET 18 SPIROMETER on SPIRO CALIBRATION 0 L min O2 Monitor sub menu alarms O2 Monitor amp Spiro ESCAPE FROM MENU O2 MONITOR on CALIBRATION 10096 HIGH ALARM SET 105 LOW ALARM SET 18 SPIROMETER on SPIRO CALIBRATION 0 L min DESCRIPTION O2 Monitor 3 12 4 Display High set low set and oxygen concentration percentage readings are displayed on screen Touch the tab to activate O2 menu Oxygen Concentration The display provides a direct readout of measured oxygen concentrations in the range 0 100 Low Alarm Set limited within 18 99 The oxygen percentage set by the user at which the low alarm will be activated To set the low oxygen alarm see section 5 3 4 High Alarm Set limited within 19 105 The oxygen percentage set by the user which the high alarm will be activated Note that in certain conditio
50. gnificant output loss is only shown at the very end of its life Typical sensor drift rates are less than 1 per month when the sensor is exposed to gas in typical applications Sensor life approximately 1500000 02 hours at 20 C minimum one year in most normal applications Sensor lifetime is governed by the mass of lead available to react with the oxygen and its rate of consumption High oxygen partial pressure and high temperature will increase the sensor output current thus shortening the operation life At the point where all lead has been consumed the output will fall very quickly to zero over a period of two to three weeks 31 O2 Sensor Location Prima SP with A200SP Absorber DESCRIPTION 3 12 3 O2 Monitor sub menu ON OFF Turn the navigator wheel to switch between ON and OFF Press to confirm Scroll to EXIT MENUS and press the wheel to exit NOTE The oxygen monitor automatically switches ON and defaults to the previous values for high and low alarm settings when the ventilator is switched on Fresh gas mixture compensation is disabled if the O2 monitor is switched OFF CALIBRATION Press the navigator wheel to initiate the calibration procedure see section 5 3 2 for full procedure To exit the menu scroll to EXIT MENUS and press the wheel HIGH ALARM SET LOW ALARM SET Scroll to the required parameter and press the navigator wheel to activate Rotate the navigator wheel a
51. h no flow from anaesthesia machine bellows should not drop Move hand from Inspiratory connector and occlude drive gas hose at rear of absorber Bellows will fall momentarily but then should stop falling Note Failure of either 6 11 or 6 12 indicates a bellows leak diaphragm valve leak drive gas hose leak or canister leak 58 SERVICE SCHEDULE 7 2 7 3 7 4 7 5 7 6 7 7 7 8 7 9 8 2 8 3 8 4 Pneumatic System Tests every six months With unit switched off disconnect mains supply Unscrew thumbscrews at rear of unit and withdraw Patient Valve Block Remove Diaphragm valve spring and spring cap Remove the Non return Valve Clean and examine for damage or discolouration Replace as necessary Refit the Non return Valve With the spring spring cap and the diaphragm still removed use a suitable bung to occlude the spring orifice Use an inflation bulb to apply pressure to the drive gas connector Pressure should relieve at 100 cmH20 10 Replace diaphragm valve and non return valve every 12 months Replace 5 mm 7mm and 12 mm O rings probe every 12 months Reassemble the patient valve block Leak test gas inlet to unit On Off valve Ensure less than 7 kPa min With patient valve still removed connect ventilator to power supply reconnect gas supply and switch on the unit In Standby Mode set inspiratory flow of 5 L min using front panel settings 500 5 1 1 OFF 38 Switch
52. ilt to conform with the specification and operating procedures stated in this manual and or accompanying labels and notices when checked assembled operated maintained and serviced in accordance with these instructions To ensure the safety of this device it must be checked and serviced to at least the minimum standards laid out in this manual A defective or suspected defective product must not under any circumstances be used The user must accept responsibility for any malfunction which results from non compliance with the servicing requirements detailed in this manual Additionally the user must accept responsibility for any malfunction which may result from misuse of any kind or non compliance with other requirements detailed in this manual Worn broken distorted contaminated or missing components must be replaced immediately Should such a repair become necessary it is recommended that a request for service advice be made to the nearest Penlon accredited agent This device and any of its constituent parts must be repaired only in accordance with written instructions issued by Penlon Limited and must not be altered or modified in any way without the written approval of Penlon Limited The user of this equipment shall have the sole responsibility for any malfunction which results from improper use maintenance repair damage or alteration by anyone other than Penlon or its appointed agents USA and Canadian Fed
53. ing is correct 10 mbar Adjust as necessary by selecting Engineer Menu Penlon Options Menu Cal Pressure Adjust to correct value 57 SERVICE SCHEDULE 5 1 5 2 5 3 6 1 6 2 6 3 6 4 6 5 6 6 6 7 6 8 Engineer Error Codes every six months Select Service Menu Engineer Menu Diagnosis Menu Display Error Log Check and investigate errors Up to 30 Error Codes can be stored Format is Date Time Fault Example 08 05 01 09 12 40 Cut Valve Reset Error log Bellows Assembly every six months Remove and clean canister Remove bellows from base and inspect bellows Discard old bellows and replace with new every 12 months Remove diaphragm valve 3 x thumbscrew Inspect valve seat for damage Check valve disc hangs level Replace diaphragm valve every four years If necessary clean valve seat and valve disc using alcohol wipe Do not attempt to dismantle diaphragm assembly Replace large orange O ring on bellows base every 12 months If AV S is used with an A200SP Absorber this O ring is replaced as part of the absorber service procedure Replace small O ring from diaphragm valve every 12 months Apply oxygen approved grease Refit diaphragm valve and secure 3 x thumb screws Refit bellows and canister With hand occlude the Inspiratory connector of the absorber Inflate bellows assembly using flush button until bellows is at top of housing Wit
54. ions Oxygen Monitor The Oxygen Monitor is intended to continuously measure and display the concentration of oxygen in breathing gas mixtures used in anaesthesia and is intended for adult and paediatric patients The oxygen monitor is an integral part of the ventilator The oxygen monitor is intended for use by health care providers i e Physicians Nurses and Technicians for use with patients during general anaesthesia 3 DESCRIPTION 3 1 General Description The AV S Ventilator is a pneumatically driven software controlled multi mode ventilator The ventilator is a time cycled volume pressure controlled and pressure limited The ventilator has compliance compensation and a user selectable option of an inspiratory pause fixed at 25 of the inspiratory time In addition fresh gas compensation and user selectable gas mixture compensation is a standard feature Ventilation Modes Volume Mode continuous mandatory ventilation Pressure Mode pressure controlled ventilation Spontaneous with advanced patient support SIMV SMMV PSV PEEP Patient Monitoring Airway pressure measured from the expiratory limb of the breathing circuit Tidal Volume and Minute Volume measurement is provided by a dual spirometry system An integral oxygen monitor system measures oxygen concentration in the breathing circuit inspiratory limb The print function provides a permanent record of function activity for up to eight hour
55. is read and understood by the clinicians that will use the ventilator APPENDIX 6 Calibration and Output Checks for a New Ventilator Applicable to Software version v1 81 11 On Screen Menus Menu Switch To Access Press the menu switch on the front panel EXIT MENUS 1 O2 MONITOR amp SPIROMETRY Navigator Wheel and FRESH GAS COMPENSATION ON Press Button SPECIAL MODES WAVEFORM Turn the wheel to scroll ALARM SETTINGS through the menus GAS MIXTURE O2 AIR Press the wheel to enter the USER SETTINGS required sub menu SERVICE MENU HA Rotate the wheel to change the value of displayed parameters Press the wheel to confirm the required value To Exit Press the menu switch on the front panel or select EXIT MENUS and press the navigator wheel Before clinical use for the first time the following Valve Calibration Spirometry Calibration and Volume Delivery Checks must be carried out Drive Valve and Patient Valve Calibration 1 Disconnect the hoses from the Driving Gas Output A Patient Pressure Connector B and Exhaust outlet C on the rear of the ventilator oo das ae Main menu EXIT MENUS O2 MONITOR amp SPIROMETRY FRESH GAS COMPENSATION ON SPECIAL MODES Calibrate the pressure transducers Press the menu switch Scroll down select SERVICE MENU B WAVEFORM Scroll down select SERVICE PIN C ALARM SETTINGS GAS MIXTURE
56. lation Move the absorber Bag vent switch to Bag the ventilator will switch from Pressure Mode or Volume Mode to Spontaneous Mode see 3 6 2 Absorber Interface Functions No mechanical ventilation No Inspiratory Pause function Patient Monitoring Bag mode and Ventilator mode Airway pressures FiO2 Tidal volume Rate E ratio Supply pressures Advanced Ventilation Modes Patient support modes are selectable from this mode see below and section 3 7 5 3 7 4 3 Patient Support Modes The following support modes are selectable from the Special Modes menu and must be pre select from the main menu whilst in Standby SIMV Synchronised Intermittent Mandatory Ventilation SMMV Synchronised Mandatory Minute Ventilation PSV Pressure Supported Ventilation CAUTION The required patient support mode must be pre selected in Standby Mode select from main menu before it can be activated during the ventilation of a patient Please refer to sections 3 7 5 1 3 7 5 2 3 7 5 3 Note that if the system fails to detect an absorber bag vent switch a confirm message will be displayed 23 DESCRIPTION 3 7 5 Advanced Spontaneous Breathing Modes 3 7 5 1 SIMV Synchronised Intermittent Mandatory Ventilation SIMV provides a minimum level of tidal volume SIMV allows spontaneous breaths and a set mandatory breath synchronised with the start of a patient breath SIMV must be pre selected in Standby M
57. le adjusts as Vt is changed 0 to 0 5 L 1 0 L 2 0 L X axis a The scale adjusts as Rate is changed 0 to 15 sec 5 sec 3 sec b In Vol v Pres mode the scale adjusts as Plimit is changed 20 to 40 60 80 cmH20 29 DESCRIPTION Alarms 3 11 NOTE User Adjustable Alarms use the menu system to set the required limits press the menu switch on the front panel see 3 8 and select ALARM SETTINGS pajeadas uo e Buig Kjuoug MOT onewoiny onewoiny onewoiny onewoiny onewoiny jnejeq Jesn jnejeq 4esf ynejeg sN ynejeg iesn oneuloiny yneyag Jes ynejeg Jasn onewoiny onewoiny jnejeq SN ony opewony opewony opewony opewony opewony onewoiny Aq 38S OJOZ S 0 L OJez S 0 L OJoZ S 0 L S 0 L OJez S 0 L S 0 L S 0 L S 0 L S 0 L S 0 L S 0 L S 0 L S 0 L s 0 S 0 L S 0 S 0 OJez OJoZ 019Z 01 Z un SINN pejeedai seuoj Buipueose say Kjuoug winipayy Jaded ou sey Jo jewod ou sey 10 pejoeuuoosip Jejuld N3119 JIOYS JO uonoeuuoosiq Z LL oJeq peddoup seu beyon Aueneg peBueuosip Ajje o 40 Buissiu Jo pejoeuuoosip Aueyeg Auepmeq Jamod ufiu yym suitu 09 esn su pe s n AJayeq peBueuo ApnJ sje Jamod sule uluu 1 GZ apisino sBumes pejoeuuoosip Josuas pejsneuxe i Josues an ea jos ULY Jewo ZO Pases anjea Jes speeoxe ZO peunsee y aNJEA 18S JO OG speeoxe enjeA paje noJeg
58. le and verify bellows remain full If necessary adjust flow from anaesthesia machine to maintain full bellows Maximum permissible flow leak 200 ml Check waveform holds the airway pressure values Level display A falling display indicates a leak either in the driving circuit the patient circuit or the absorber system Electrical Safety Checks every 6 months Earth Continuity Max 0 2 ohms at 1 Amp or less Insulation Resistance not less than 20 Meg Ohms at 340 500 Vdc Earth Leakage Max 500 micro amps Enclosure Leakage Max 100 micro amps Paperwork every 6 months Restore user settings Sign and date service card indicate service 6 12 24 or 48 month Attach label This Equipment Has Been Serviced in prominent position THINK carry out visual checks Remove all tools and test equipment Fill out appropriate service report This checklist is prepared for use by Penlon Service Engineers It is not a maintenance manual and should not be used as such Other parts may be replaced if signs of wear are apparent If a replacement is necessary the hospital must be informed 65 8 PARTS LIST Preventive Maintenance Kits One year Kit Part No 57298 Patient Block Assembly Exhaust diaphragm 300580 One way valve 300581 O ring 5 mm 041204 O ring 7 mm 041245 O ring 12 mm 041222 Bellows Assembly O ring 5 mm 041204 Bellows 57550 O ring bellows base 041226 Fit this O ring only if the AV S is not used
59. livery control system and secondly in the patient breathing system During use of the ventilator the user will set a required tidal volume and at the first breath the ventilator will use its pre calibrated delivery flow rate valve settings to set the proportional delivery valve position to deliver the requested tidal volume To confirm that the correct flow rate tidal volume is being delivered by the ventilator delivery system an internal flow sensor a Honeywell AWM43300V mass flow sensor monitors the delivered flow rate and makes adjustments every 30 ms using proportional regulation As this sensor is always measuring the known drive gas rather than breathing system gas the volumes measured will always be independent of breathing system gas composition This system ensures accurate delivery volume from the ventilator control unit To monitor for correct delivery volumes in the breathing system there are two breathing system mass flow sensors Honeywell AWM 720P1 spirometers One sensor is located in the inspiratory limb and one in the expiratory limb Measurements are taken from these sensors to determine the actual delivered and exhaled gas volumes in the breathing system This enable measurements to be made to compensate for fresh gas flow compliance losses and possible breathing system leaks During the inspiratory cycle the inspiratory flow sensor measures the gas volume delivered to the patient 82 The flow se
60. low range showing typical hysteresis between up and down flow measurements and repeatability 4 5 3 5 Resistance 3 cmH20 T 1 5 0 5 Flow L min 84 APPENDIX 4 APPENDIX 4 Cleaning Outside surfaces and bellows housing CAUTION Care must be taken not to allow liquids to run into the control unit serious damage may result Check that the unit is disconnected from the electrical supply before cleaning Do not use cleaning solutions containing alcohol the bellows housing may be damaged To clean the outside surface of the ventilator use a damp cloth If necessary use a warm mild detergent solution to remove resistant grime Make sure that all detergent residues are fully removed after cleaning Never use any harsh abrasive cleaning agent The transparent acrylic bellows housing and in general the surfaces of the control unit are not scratch resistant The inside of the bellows housing under normal conditions is not in contact with the breathing gas and therefore only needs cleaning as described above Remove the bellows housing A by slightly twisting it counter clockwise until the tabs at the bottom clear the bayonet locks then lift it straight up from the base Touchscreen Use a soft cloth only Never use any harsh abrasive cleaning agent Bellows and exhalation diaphragm valve Each time the bellows assemblies are opened for cleaning all visible components must be carefully inspec
61. ly applied during calibration 38 5 PRE OPERATION PROCEDURES 5 1 5 1 1 Ventilator Set up Mounting the Ventilator The remote screen is mounted on an adjustable arm with the control unit mounted at the rear or side of the anaesthetic machine Option control unit location Preferably mount the control unit permanently on the shelf of the anaesthesia machine or on a strong bracket This will protect the unit from accidental fall and disconnection of hoses and cables To fit the ventilator control unit permanently on a mounting bracket 1 Align the four mounting feet over the mating holes in the bracket 2 Use the four M4 screws supplied with the mounting bracket kit inserted through the bracket and rubber feet and screwed into the threaded inserts in the base of the ventilator Only use the screws supplied with the kit Pole mount type mounting brackets and side frame brackets are available from the manufacturer Bellows unit The bellows unit is built into the A200SP absorber 5 1 2 Electrical Power Connection Before connecting the ventilator to the mains supply check that the power supply is within the correct rating as stated on the label on the rear of the control unit WARNING Excessive electronic noise caused by other poorly regulated devices such as electrocautery may adversely interfere with the proper functioning of the ventilator To avoid this problem do not connect the ventilat
62. menu select PSV 62 SERVICE SCHEDULE 13 15 13 16 13 17 13 18 14 14 1 14 2 14 3 14 4 14 5 14 6 14 7 14 8 14 9 Re select Spont Mode Select PSV Message on screen will read Switch absorber to vent position Change absorber position to Vent Ventilator now displays PSV message in white Note If absorber switch is not enabled in service menu the message will read Switch absorber to vent position Press PSV once again Operate Test Lung by hand and check that ventilator assistance is given with a pressure of 4 cmH20 Stop operation of test lung Ensure pressure reading falls to zero and after 15 sec delay check that the Apnoea alarm is triggered and that Vt meas shows Volume Cycle amp Flow Compensation Tests every 6 months Switch Ventilator to Volume Mode Set Vt to 600 ml BPM to 10 I E to 1 2 and Pressure Limit to 80 From Menu select Fresh Gas compensation OFF The bellows delivers 600 ml 50 ml but the measured volume may be reduced to approximately 500 ml with a standard test lung due to the compliance losses of the circuit Note If bellows delivery is out of specification carry out valve calibrations section 6 3 Apply a flow of Oxygen from anaesthetic machine of 8 L min Check displayed Vt Meas rises From Menu select Fresh Gas compensation ON Allow 2 minutes for reading to stabilise Observe that the bellows delivers less gas
63. n Input Gas Filter which protects the pneumatic components from incoming particulate matter 3 The Low Supply Pressure Detector The pressure switch is set at a predetermined level to detect a loss or reduction of the input gas source pressure When the pressure falls below 235 kPa 35 psi 1 psi the LOW SUPPLY PRESSURE indicator will be displayed and the high priority audible alarm will activate 4 Input Pressure Regulator Regulates the input drive gas to 260 kPa 21 kPa 38 psi 3 psi 5 Cut off Valve The valve isolates the the gas supply a when the ventilator is switched off b when a fault condition occurs 6 Airway Pressure Sensor Connected to expiratory limb of breathing circuit B Pneumatic Control Manifold Block 7 Drive Gas Proportional Valve 8 Drive Gas Flow Sensor 9 Drive Gas Pressure Sensor 10 Low Pressure Regulator 11 Patient Proportional Valve 12 PEEP pressure sensor 13 Restrictor The restrictor allows a flow of up to 2 L min lt 2 L min bleeding C Exhaust Manifold Block 14 Check Valve 15 Diaphragm Valve 16 Pressure Relief valve Set to 100 cmH20 17 Exhaust Port to AGSS 18 Bellows drive gas outlet to bellows assembly 13 DESCRIPTION 3 4 Electrical System Mains Supply The mains supply inlet is designed for connection to any mains voltage from 100 to 240 VAC and a frequency of 50 to 60 Hz without any adjustment The connector is a standard IEC type Back u
64. n if the O ring is missing See next page for information on sterilisation procedures Refitting Refit the diaphragm valve assembly to the bellows base and reassemble the bellows assembly If a paediatric bellows is fitted press the adaptor C into the ventilator bellows assembly base then fit the bellows CAUTION Always check for correct fitment of the bellows see illustration and function test the ventilator before clinical use Spirometer Sensors The sensors are built into the A200SP absorber and cleaning and sterilisation can only be carried out when the absorber assembly is removed for cleaning For further information please refer to the user instructions supplied with the A200SP 86 Exhalation Diaphragm Valve Assembly APPENDIX 4 Sterilisation CAUTION To prevent possible damage to components peak sterilisation temperatures must not exceed 134 C 275 F for steam autoclave Do not sterilise the ventilator control unit Apart from the patient block assembly the internal components are not compatible with sterilisation techniques and may be damaged Recommended Sterilisation Parameters Control Unit Patient Block Assembly 1 Clean as described in section 6 2 5 3 2 Autoclave at 134 C for a holding time of 3 5 minutes using packaging and equipment as listed below Packaging Pack the control unit with material which is permeable to air and steam but has an effective maximum pore size
65. ng Functions and Parameters The functions parameters shown on the screen can be activated as follows a touch the screen at the appropriate tab area b rotate the navigator wheel and press it when the indicator arrow is on the required parameter tab Note that parameters default to factory set values when the ventilator is switched on and no further user selection is made 3 5 2 User Adjustable Parameters Variable parameters can be altered by rotating the navigator wheel When the required value is displayed press the active tab or the wheel to confirm the setting Tidal Volume Range 20 1600 ml Rate 4 100 bpm I E Ratio 1 0 3 to 1 8 PEEP 4 20 cmH20 Can be set to OFF Pressure Limit Volume mode 10 80 cmH2O Pressure mode 10 50 cmH2O Alarm limits user adjustable alarms only see 3 11 16 DESCRIPTION 3 5 3 Operational Capability Tidal Volume Rate and E ratio settings are all limited by a maximum inspiratory flow of 75 L min LE Ratio 16 15 1 4 13 1 2 1 1 1 0 3 Tidal 10 Volume 9 litres 0 8 Vt 0 7 0 6 0 5 0 4 0 3 0 2 0 1 0 10 20 30 40 50 60 70 80 Rate bpm The ventilator is capable of operating at the volumes and rates below each I E ratio curve Example f Select required volume Vt e g 0 8 L 2 Select rate e g 10 bpm 3 Select I E ratio of 1 2 The point X on the graph lies beneath the 1 2 ratio curve and is therefore within the ventilator s capability
66. none CLOCK MENU UPGRADE MENU AMBIENT PRESSURE 988 mBar DISPLAY HISTORY SERVICE PIN 0 ENGINEER MENU Language pick list ENGLISH ITALIANO TURKCE POLSKI ESPANOL Serial mode pick list NONE Philips SPACELABS Clock ESCAPE FROM MENU YEAR 2005 MONTH 3 DATE 16 DOW 3 HOUR 9 MINUTE 57 UPDATE CLOCK DAYLIGHT SAVING off Upgrade ESCAPE FROM MENU I O HARDWARE 2 1 0 FIRMWARE v0 47 Build 68 Clock pick list 2005 2099 1 12 1 31 1 7 1 Monday 0 23 0 59 off on MAIN FIRMWARE v0 92 Build 32 REGISTRATION KEY unknown UPGRADE FIRMWARE unavailable ADD NEW FEATURE unavailable History Display ESCAPE FROM MENU MANUFACTURER DATE 03 03 05 TOTAL HOURS RUN 100 LAST SERVICE DATE 13 08 04 HOURS SINCE SERVICE 100 DRIVE VALVE CYCLES 1253 PATIENT VALVE CYCLES 822 CUTOFF VALVE CYCLES 72 integer integer integer integer integer integer integer toggle option NOTE Service PIN Engineer Menu Sub menus are not accessible by users 81 APPENDIX 3 APPENDIX 3 AV S Ventilator Spirometry System Ventilator Spirometry Measurement The AV S ventilator drive gas and spirometry system uses a total of three mass flow gas sensors to monitor and then independently measure the gas flows within the ventilator and breathing system This ensures that correct volumes are delivered to the patient These monitors are measuring firstly in the ventilator de
67. ns of excess pressure the readout may show a value above 100 To set the high alarm see section 5 3 4 3 12 5 Oxygen Monitor Alarms HIGH O2 ALARM The high O2 alarm is triggered when the oxygen concentration is 1 above the set value a The High O2 Alarm visual indicator will illuminate b Ahigh priority audible alarm will sound To cancel this alarm the high alarm setting must be equal to or above the oxygen concentration The alarm can be muted for 120 seconds LOW O2 ALARM The low alarm is triggered when the oxygen concentration is 196 below the set value a The Low O2 Alarm visual indicator will illuminate b Ahigh priority audible alarm will sound To cancel this alarm the low alarm setting must be equal to or below the oxygen concentration The alarm can be muted for 120 seconds O2 SENSOR FAULT The alarm is triggered i when either the oxygen sensor is disconnected or approaching the end of its life ii if the O2 concentration exceeds 110 a The message O2 SENSOR FAULT will be displayed 33 Measured O2 concentration High Alarm Set Value 02 100 A Low Alarm Set Value b A high priority audible alarm will sound To cancel this alarm check the sensor connection or replace the sensor The alarm can be muted for 120 seconds O2 SENSOR LOW This alarm indicates the sensor has approached the end of its life The legend O2 SENSOR LOW will be displayed and a
68. nsor output is read at least every 2 msec and then five sets of readings are averaged and the averaged value is sent every 10 ms to the processor for calculation of the volume delivered to the patient This delivered volume will consist of the volume delivered from the ventilator bellows plus the fresh gas flow from the anaesthetic machine fresh gas supply minus any compliance loss and minus any leak This gives a total actual inspired tidal volume A similar measurement method is used for the exhaled volume During the exhalation period the measured exhaled volume is subtracted from the inspired volume and at the end of exhalation A negative more gas coming out volume indicates that fresh gas has increased the delivered volume A positive volume less gas coming out indicates a leak in the circuit The ventilator control system will then adjust the next delivered tidal volume up to a maximum of 100 ml This will bring the delivered volume to exactly as set If the variation between set and delivered is greater than the maximum rate of change allowed the adjustment will occur gradually over several breaths The displayed volume is the average of the inspiratory and expiratory volumes If this value is less or more than 50 of set volume a low or high volume alarm is given Breathing System Gas Composition Gas flow measurements are affected by the breathing system gas composition To compensate for these effects the v
69. ny displayed values and press to confirm 4 To exit the menu display A Press the menu switch on the front panel B Scroll to EXIT MENUS and press the navigator wheel NOTE A If confirmation does not take place within 8 seconds the parameter reverts to its previous value B If another parameter is selected using the touchscreen the menu is de selected C While any menu is selected the alarms are active the ventilator can be switched off See Appendix 2 for a further information on the Menu system 28 DESCRIPTION 39 Spirometry Spirometry can be enabled or disabled via the on screen menu system NOTE If the spirometry system is turned OFF a Fresh gas fresh gas mixture compensation is disabled b Special Modes are disabled See Appendix 3 for a detailed description of the spirometry system 3 10 Display Waveforms NOTE 1 The default waveform is always Pressure v Time cmH20 v seconds 2 Wave Freeze is available when ventilation is in progress Second waveform The second waveform can be displayed by using the menu control or by touching the waveform on screen Select from Volume v Time litres v seconds Volume v Pressure litres v cmH20 Compliance loop waveform First loop can be frozen Subsequent loops overlaid Display Functions Automatic Scale adjustment Y axis a The scale adjusts as Plimit is changed 20 to 40 60 80 cmH20 b In Vol v Time mode the sca
70. o Bag and remove bag from bag arm Remove the patient circuit Carry out Spirometry Zero calibration This will zero the Drive Flow transducer 3 Using a safety bung occlude the Drive Connector on rear of ventilator From Cal Valve menu select ZeroDV Wait for ZeroDV cal complete message 4 Remove the bung and connect the breathing circuit as for normal use With Absorber in Vent position set the Fresh Gas flow from anaesthesia machine to 5 L min From Cal Valve menu select ZeroPV Wait for ZeroPV cal complete message Reduce fresh gas flow to minimum 5 Disconnect the hose from Drive Connector and connect a flow measurement device From Cal Valve menu select DV Meas Check that the measured value is the same as the measurement device approximately 20 Lmin If not adjust using Trim Drive Flow control After each adjustment press wheel to confirm change and wait for displayed value to adjust and settle back at 20 L min Adjust again as necessary until the displayed value is the same as the measured value Select None to end calibration 6 From Cal Valve menu select DV Curve The valve will oscillate several times then generate an increasing flow delivery to its maximum flow 7 Valve calibration procedure is now completed 56 7 SERVICE SCHEDULE 1 2 1 3 2 2 2 3 2 4 2 5 2 6 2 7 3 2 3 3 4 1 4 2 4 3 Initial Checks every six months
71. ode Select Standby Select Menu Select Special Modes Select Support Mode Select SIMV Escape Menu SIMV will be displayed on the main screen when Spontaneous mode is selected or triggered NOTE 1 The trigger window is pre set to 6096 of the BPM cycle time 2 The trigger is flow activated 3 If Spirometry is disabled then SIMV is not available 4 If the pressure limit and alarm are activated the inspiratory phase is terminated Activate SIMV during Ventilation NOTE SIMV will not function unless already pre selected in Standby Mode 1 Select Special Mode on the display If the absorber Bag Vent switch is not detected a message will appear SET ABSORBER TO VENT Press the navigator wheel push button to confirm 2 Move the absorber Bag vent switch to Ventilator 3 Check that SIMV is functioning correctly SIMV Default Settings The ventilator will default to pre set values for Tidal volume Vt Rate Inspiratory Time and Trigger Level after selecting SIMV Note 1 Vt can be adjusted before SIMV is confirmed 2 The trigger setting is adjustable between 0 7 and 4 0 L min PEEP J 0 cmH2O SIMV Spontaneously Breathing Patient A Cycle Time set from BPM B Trigger Window C Spontaneous Breath D Trigger E Mandatory breath at the set tidal volume Vt Inspiratory flow in the Trigger Window generated by the patients spontaneous breath results in a synchroni
72. of the control module to the Pressure Sensing port on the rear of the absorber Connect the cable from the Interface connector on the rear panel of the control module and to the Interface connection on the rear of the absorber Connect the cable from the Prima Master connector on the rear panel of the control module and the rear of the Prima SP anaesthesia Attach the Fresh Gas Supply hose from the absorber to the CGO of the PrimaSP Connect a patient breathing circuit to the CO2 absorber and attach the patient connector to a test lung Connect the Gas Scavenging System to the Exhaust connector on the rear of the vent If no scavenge system is attached to the rear of the ventilator a continuous bleed during the inspiratory phase will be audible Standby every 6 months Power On the Anaesthesia machine Ventilator should switch ON Power Off the Anaesthesia machine Ventilator should switch OFF Press the Power button on the ventilator Default selection screen appears and automatically defaults to adult mode after approximately eight seconds Note Standby mode is highlighted white in the bottom right of screen Set incorrect rate i e increase Vt and or Rate controls Check Incorrect Rate Or Ratio displayed on screen and three alarm tones sound Do not confirm settings wait for default values to return Oxygen Analyser Function and Calibration Tests every 6 months Connect a calibrated O2 Analyser into inspi
73. onnected Check Spirometer is enabled in menu From menu select Oxygen Monitor amp Spirometry Spiro Calibration Rotate dial until 0 L min is displayed Press Navigator wheel to calibrate Spiro Display will flash Calibrating Zero If successful Calibration complete will be displayed Connect short hose between CGO and absorber Expiratory connection Connect the absorber Fresh Gas connector to the Bag arm connector to ensure a closed system Adjust oxygen flowmeter on anaesthetic machine to achieve accurate 10 L min flow Re enter Oxygen Monitor amp Spirometry Spiro Calibration in menu system Rotate Navigator wheel until Calibrate 10 L min is displayed Press Navigator wheel to calibrate Spiro Display will flash Calibrating 10 litres If successful Calibration complete will be displayed Reconnect fresh gas hose patient circuit and manual bag Reset bag vent switch to Vent position Spontaneous and Special Modes every 6 months Switch absorber to Bag Select Spont Mode on touchscreen 61 SERVICE SCHEDULE 13 2 Operate Test Lung by hand Check Vt meas BPM and I E at bottom of display indicate readings Observe waveform displayed 13 3 Stop operation of test lung Ensure pressure reading falls to zero and after 15 sec delay check Apnoea alarm triggered and Vt meas shows 13 4 Press Mute Verify audible alarm is muted for 120 seconds Note alarm mute countdown
74. or power cord into the same electrical wall outlet or strip into which an electrocautery unit is connected 39 5 1 3 Ventilator Gas Supply 1 Verify the drive gas specified for the ventilator oxygen or air Always use the correct drive gas 2 Connect the drive gas inlet port on the rear of the control unit to a dry oil free supply Supply pressure range 45 to 100 psi 3 1 6 9 bar 310 689 kPa OXYGEN SUPPLY a O2 cylinder b Anaesthetic machine O2 auxiliary gas outlet c O2 pipeline supply from a wall outlet AIR SUPPLY a Air cylinder b Anaesthetic machine Air auxiliary gas outlet c Air pipeline supply from a wall outlet Supply pressure should be monitored by a separate means e g pressure gauge on anaesthetic machine or supply line NOTE It is possible to reconfigure the ventilator for use with a different drive gas to the gas originally specified This work must be carried out by an engineer trained by the manufacturer 5 1 4 Breathing System Schematic The following page contains a schematic diagram showing the cables and tubing for an AV S ventilator mounted on a Prima SP2 anaesthetic machine with an integral A200SP Absorber PRE OPERATION PROCEDURES Hoses and Cables Schematic AV S and A200SP Absorber Note 1 AV S has spirometry and oxygen monitor 2 Interface cabling is shown for connection to Prima SP2 On Off switch and A200SP Bag Vent switch 40 P
75. or remove patient circuit Ensure the gas scavenging circuit is not connected O2 Monitor amp Spirometry menu Check Spirometer is enabled in menu ESCAPE FROM MENU O2 MONITOR on From main menu select O2 MONITOR amp CALIBRATION 100 SPIROMETRY HIGH ALARM SET 105 LOW ALARM SET 18 Select SPIRO CALIBRATION SPIROMETER on gt SPIRO CALIBRATION 0 L min Rotate the navigator wheel until 0 L min is displayed Press Navigator wheel to confirm setting This will calibrate the spirometry system The display will flash Calibrating Zero If successful Calibration complete will be displayed Connect a short hose between the CGO and the absorber Expiratory connection G Connect the absorber Fresh Gas connector to the Bag arm connector H to ensure a closed system Connect a short hose from the Inspiratory connector J open to atmosphere This will reduce vale oscillation Adjust oxygen flowmeter on anaesthetic machine to achieve an accurate 10 L min flow Re enter O2 MONITOR amp SPIROMETRY Select SPIRO CALIBRATION 92 APPENDIX 6 10 Rotate Navigator wheel until Calibrate 10 L min is displayed Press Navigator wheel to confirm Display will flash Calibrating 10 litres 11 If successful Calibration complete will be displayed 12 Reconnect fresh gas hose patient circuit and manual bag Reset the Bag Vent switch to Vent position Volume Cycle and Flow Compensation Tests
76. p Battery In the event of mains electrical failure the back up battery cuts in automatically Standard battery A fully charged battery will power the ventilator for approximately 30 minutes High power battery option A fully charged battery will power the ventilator for approximately one hour See Appendix for battery care procedures 14 DESCRIPTION Freeze Waveform Pmax Pmean cmH20 cmH2O 24 10 Vm SET Vp MEAS SET InspTime PEEP LIMIT BPM Sec cmH20 cmH2O Standby I I 6 2 5 38 A Touchscreen control 3 5 Control Panel 3 5 1 Touchscreen and Navigator Wheel Push Button 3 5 1 1 Control Panel 1 On Off control Switch On Short internal test sequence Switch Off Power down sequence with progress indicator Status indicators for electrical power mains battery supply Yellow indicator illuminated whenever power is applied to the unit and internal battery is being charged Green indicator illuminates when the unit is switched on Menu switch The menu function provides access to user and service pages including alarm settings Alarm mute switch 30 second or 120 second alarm silence depending on alarm status Note also that some alarms are not mutable see 3 11 Navigator Wheel and Press Button Turn the wheel to select a function or parameter or to alter the value of an active parameter Press to confirm the setting 15 DESCRIPTION 3 5 1 2 Selecti
77. peroxide Do not immerse the sensor in any cleaning solution Do not autoclave or expose the sensor to high temperatures Bacterial Filter Use a breathing system bacterial filter in the expiratory limb of the breathing circuit to protect the oxygen sensor see section 5 1 8 CAUTION Replacement Disposal always follow the instructions supplied with the filter and always replace at the recommended interval Oxygen Sensor Replacement WARNING The sensor contains A A small quantity of electrolyte classified as a harmful irritant which is potentially hazardous B Lead Do not attempt to open a cell ALWAYS check the integrity of the sensor assembly before use Once exhausted the sensor must be disposed of according to hospital local state and federal regulations Remove and Refit Replacement parts 102714 Sensor 1 Detach the cable connector 2 from the sensor 1 2 Unscrew the sensor from the A200SP Absorber and discard 3 Discard the expired sensor 4 Screw the new sensor 1 into the absorber 5 Attach the cable connector 2 6 Fit the assembly into the absorber 7 Calibrate the new sensor see Appendix 6 check software version 8 Dispose of the used components according to hospital local state and federal regulations 88 APPENDIX 5 APPENDIX 5 Software Upgrade Installation Procedure Automatic Software Upgrade Installation The AV S software is designed to be
78. pressure 3 Switch the A200SP Absorber Bag Vent control A to the Bag position The ventilator automatically switches to Spontaneous Mode PEEP is automatically switched off does not function in Spontaneous Mode PEEP display is blank 4 Reset the Bag Vent control Vent position The ventilator automatically switches to the mode previously set by the user PEEP is Off PEEP display indicates Off 5 Set the ventilator to Volume Ventilation Mode PEEP remains Off Select PEEP if required 27 DESCRIPTION 3 8 On Screen Menus To Access Press the menu switch on the front panel to access the following functions and parameters via drop down menus EXIT MENUS O2 MONITOR amp SPIROMETRY FRESH GAS COMPENSATION ON SPECIAL MODES WAVEFORM ALARM SETTINGS GAS MIXTURE O2 AIR USER SETTINGS SERVICE MENU Menu Switch Turn the wheel To Exit i to scroll through Press the menu switch on the front panel or select the menus EXIT MENUS and press the wheel Press to enter sub menu NOTE The menu window will not be displayed if A Control parameters VT MEAS BPM I E PEEP or LIMIT are enabled but not confirmed B A display window is active To Operate 1 Rotate the navigator wheel clockwise to scroll through the menu options the cursor gt aligns with each parameter in turn 2 Press the wheel to enter the required sub menu 3 Rotate the navigator wheel to change a
79. r as follows i Ventilator in Volume or Pressure mode Switching the absorber Bag Vent control from Vent to Bag the ventilator will change from Volume Mode or Pressure Mode into Spontaneous Mode ii Ventilator in Spontaneous Mode Switching the absorber Bag Vent control from Bag to Vent A Ifthe ventilator was previously in Volume or Pressure or Special Mode and Spontaneous Mode was automatically selected by the 19 dEz 3O oles operation of the bag vent control from Vent to Bag as described above the ventilator will revert to that previous mode B Ifthe ventilator was in Standby Mode and Spontaneous Mode selected on screen the ventilator will default to Volume Mode C If the ventilator was put into Standby Mode after automatic mode switching to Spontaneous the ventilator will default to Volume Mode DESCRIPTION 37 Ventilation Modes 3 7 1 Standby Mode Allows parameters to be set Some patient alarms are active High airway pressure at 80 cmH20 High Low Oxygen Negative pressure Incorrect Rate Ratio 20 DESCRIPTION 3 7 2 Volume Mode The ventilator delivers a mandatory set volume of Volume Mode Parameters gas at preset fixed breath intervals The Patient is making no respiratory effort Tidal volume 20 1600 mL Rate 4 100 bpm 3 7 2 1 Fresh Gas Compensation LE ratio 1 0 3 1 8 The delivere
80. r pick list none pressure simv smmv 0 7 L min 0 7 L min Sigh to Breath 0 7 Limin Ratio pick list 0 5 L min 1 50 1 0 L min 2 50 1 5 L min 3 50 2 0 L min 4 50 2 5 L min 3 0 L min 4 0 L min Waveform ESCAPE FROM MENU SECOND WAVEFORM off Second waveform pick list off vol vs time vol vs press Alarm settings ALARM MENU ESCAPE FROM MENU ALARM MODE default HIGH TIDAL VOLUME off VM MIN 0 3 L VM MAX 0 9 L VT MIN 300 mL VT MAX 900 mL APNOEA ALARM LIMIT 0 3 cmH20 ALARM VOLUME 50 default user Toggle option off on Toggle option 0 0 7 4 Integer 0 1 7 5 Integer 10 1600 Integer 20 2400 Integer 0 3 3 5 Integer 50 100 Integer Gas mixture O2 Air O2 AIR O2 N2O O2 Xe O2 He User Settings ESCAPE FROM MENU SELECT SETTINGS SAVE SETTINGS BACK LIGHT LEVEL 50 VOLUME TYPE tidal Select settings ESCAPE FROM MENU USER1 CCT1 USER2 CCT2 USER3 CCT3 USER4 CCT4 USER5 CCT5 ADULT DEFAULT PAEDIATRIC DEFAULT Save settings ESCAPE FROM MENU USER1 CCT1 CONFIRM CCT1 USER2 CCT2 CONFIRM CCT2 USER3 CCT3 CONFIRM CCT3 USER4 CCT4 CONFIRM CCT4 USERS CCT5 CONFIRM CCT5 Backlight level 0 100 integer Volume type tidal minute toggle Service See next page 80 Toggle option Toggle option Service ESCAPE FROM MENU LANGUAGE ENGLISH PRINT PATIENT DATA SERIAL MODE
81. ratory connector Check Vent O2 sensor is inserted into the absorber O2 sampling point For A200SP absorber remove absorbent canister For A100SP absorber set absorber On Off switch to Off Attach a short hose to Inspiratory limb Use O2 flush for 20 seconds then set a 5 L min flow of oxygen and allow reading to stabilise Ensure 100 indicated on test device and ventilator display is stable Calibrate Vent in 100 Oxygen From menu select Oxygen Monitor amp Spirometry Calibration Adjust until 100 is indicated 60 SERVICE SCHEDULE 11 10 12 12 1 12 2 12 9 12 4 12 5 12 6 12 7 12 8 12 9 12 10 12 11 12 12 13 13 1 Press navigator wheel to confirm Exit menu and set fresh gas flow to minimum Expose both sensors to air and check reading is 21 2 On ventilator adjust high and low O2 alarms Check alarms trigger when values are lower or higher than the reading on the ventilator O2 display respectively Return alarm levels to original settings Restore ventilator O2 sensor to correct location Remove test O2 analyser Spirometer Calibration every 6 months Check condition of external Spirometer cables and connections Disconnect fresh gas hose from anaesthesia machine Common Gas Outlet Switch the Bag Vent switch to Bag and remove bag from bag arm Remove test lung from patient connector if fitted or remove patient circuit Ensure scavenging circuit is not c
82. re supported breath PSV is used to support spontaneously breathing patients ONLY If the patient makes no attempt to breathe the ventilator will not provide support and the apnoea alarm will be activated 26 DESCRIPTION 3 7 5 4 PEEP Positive End Expiratory Pressure The AV S ventilator includes a microprocessor controlled electronically integrated PEEP system regulated by the secondary pressure on the exhaust diaphragm see 3 2 The ventilator controls PEEP by allowing flow from or delivering flow into the bellows drive circuit thereby maintaining the set pressure NOTE 1 PEEP is electronically controlled 2 PEEP is variable from 4 20 cmH20 in increments of 1 cmH20 3 The display shows OFF when PEEP is not in use 4 PEEP is switched off when the ventilator is switched off 5 PEEP is switched off during Spont mode to minimise patient s breathing effort Selecting PEEP 1 Select by touching the screen tab PEEP or using the navigator wheel The setting will flash 2 Rotate the navigator wheel to set the required PEEP pressure A confirm message will be displayed 3 Press the Screen Tab or Wheel to confirm Note that Electronic PEEP does not function in Spontaneous Mode PEEP on off sequence Using the A200SP Absorber Interface Ventilator Mode Selection 1 Switch the ventilator to Volume Ventilation Mode 2 Select PEEP and set pressure to the required level The PEEP display indicates
83. ress the menu switch on the ventilator front panel and select the O2 monitor sub menu 2 Scroll to LOW ALARM SET and press the navigator wheel 3 Rotate the wheel to change the displayed alarm figure to the desired value 4 Press the wheel to confirm 5 Scroll to ESCAPE FROM MENUS and press the wheel to exit 53 High Alarm Set Value Low Alarm Set Value O2 Monitor amp Spiro ESCAPE FROM MENU O2 MONITOR on CALIBRATION 100 HIGH ALARM SET 105 LOW ALARM SET 18 SPIROMETER on SPIRO CALIBRATION 0 L min On Off Switch Alarm Mute Menu Switch Navigator Wheel and Press Button 6 SERVICE PROCEDURES 6 1 Service Intervals At 6 months 12 months 2 years and 4 years the ventilator must be serviced by a Penlon trained engineer following the schedule given below and the procedures given in section 7 in this Service Manual Every day Pre use function check Every week Check the condition of the diaphragm valve and clean as required Test the Mains Failure Alarm and the Low Supply Pressure Alarm Every 6 months Inspection and Function Check Remove patient block assembly and clean Check condition of bellows Every 12 months Repeat six month procedure plus Replace components including O seals exhaust diaphragm one way valve Preventive maintenance kit available Every 2 years Repeat 12 month service plus Replace battery Every 4 years Rep
84. ressure relief valve between the exhaust valve port and the inlet port of the AGSS receiver Note that the diaphragm valve under the bellows is connected internally to the EXHAUST port to facilitate the discharge of excess breathing gas at the end the expiratory phase WARNING Do not use a scavenging system that restricts drive gas flow when negative pressure is exerted on it Applying negative or positive pressure to the bellows exhaust port results in positive pressure in the patient breathing system Therefore the scavenging system must not generate more than 0 5 cmH20 positive or negative pressure when connected to the ventilator Any problem arising from an improperly functioning scavenging system is solely the user s responsibility 5 1 7 Remote Screen Attach the DVI cable supplied with the screen between the interface connectors 1 on the rear of the control unit and screen WARNING Check that the cable between the control unit and remote display screen unit is securely connected before use Always use a cable type recommended by the manufacturer 5 1 8 Printer Attach a printer to the printer port 2 if a printed output of the ventilator function is required 43 865002000559 EEE ESO 8928889 Br PRE OPERATION PROCEDURES 5 1 9 Breathing System 1 Connect the ventilator bellows base BREATHING SYSTEM port to the breathing system 2 a
85. robe A to the A200SP absorber Connect the cable to the input socket B on the back of the AV S ventilator control unit NOTE The anaesthetic machine gas control switch must be in the ON position for gas delivery WARNING The sensor contains a small quantity of electrolyte classified as a harmful irritant which is potentially hazardous Do not attempt to open a cell ALWAYS check the integrity of the sensor assembly before use Once exhausted the sensor must be disposed of according to hospital local state and federal regulations NOTE To maintain maximum sensor life i always disconnect the breathing circuit after use ii Switch off the anaesthetic machine to cut off the basal flow through the system Bacterial Filter Use a breathing system bacterial filter in the expiratory limb of the breathing circuit to protect the oxygen sensor see section 5 1 9 CAUTION Replacement Disposal always follow the instructions supplied with the filter and always replace at the recommended interval 5 3 2 Calibration The new unit must be calibrated before clinical use Thereafter as a safety precaution we recommend calibration of the unit every time the system is switched on Calibration must also be performed A when the sensor is replaced B when point of use elevation changes by more than 160 m 500 ft NOTE Altitude compensation is automatically applied durin
86. s during a procedure or can be used to record waveforms Screen Remote arm mounted 210 mm 8 4 inch high definition colour TFT screen with single dual waveform display Bellows unit The bellows unit 1 is built into the A200SP absorber A paediatric bellows assembly is available as an option Drive gas supply The drive gas supply can be oxygen or air The supply must be at 310 to 689 kPa 45 to 100 psi Note that the drive gas is specified by the customer and set during manufacture Conversion from one drive gas to another must only be carried out by an authorised service engineer trained by the manufacturer AV S Ventilator Spontaneous Mode Patient Support SIMV Synchronised Intermittent Mandatory Ventilation SMMV Synchronised Mandatory Minute Ventilation PSV Pressure Supported Ventilation PEEP Positive End Expiratory Pressure DESCRIPTION Control Unit Rear Panel Gas Connections 1 Ventilator drive gas inlet connect to anaesthetic machine auxiliary gas outlet 2 Bellows Drive Gas Output connect to bellows via A200SP absorber see section 5 1 5 3 Outlet Exhaust Valve connect to scavenge system see section 5 1 6 Electrical Connection 4 Electrical mains input and fuse unit Interface and Parameter inputs 5 A200SP Absorber Bag Vent switch interface and Spirometer connector Prima SP2 Interface connector SP2 primary on off switch Press
87. s with 6 seconds repeat time Flashing 3 audio pulses with 24 seconds repeat time Static with single beep sound 30 seconds for high priority alarm 120 seconds for medium priority alarm 1896 9996 x 196 19976 10596 x 196 2 m 6 ft fully extended Galvanic fuel cell sensor 0 100946 1500000 O2 hours One year minimum in typical applications Interference Gases and Vapours in 30 Oxygen 70 Nitrous Oxide Interference Nitrous Oxide Carbon Dioxide Halothane Enflurane Isoflurane Sevoflurane Volume Dry Interference in O2 80 lt 1 5 lt 1 5 lt 1 5 lt 1 5 lt 1 5 lt 1 37 SPECIFICATION O2 Monitor Oxygen Monitor continued Humidity Effects Sensor output is relatively unaffected by prolonged operation in either high or very low relative humidity If the sensor shows signs of being affected by condensation dry the sensor with soft tissue CAUTION DO NOT use heat to dry the sensor Temperature Effects The sensor has a built in temperature compensation circuit and is relatively unaffected by temperature changes within the operating temperature range given above Pressure Effects The sensor measures O2 partial pressure and its output will rise and fall due to pressure change e g changes in barometric pressure or breathing system pressure An increase in pressure of 10 at the sensor inlet will produce a 10 increase in sensor output NOTE Altitude compensation is automatical
88. sed mandatory breath at a preset volume and rate SIMV No breathing effort by Patient A Cycle Time set from BPM B Trigger Window C Flat Pressure Trace no breathing effort D Mandatory breath at the end of the Trigger Window at the set Vt If the patient makes no effort to breathe during a cycle a mandatory breath at the end of the trigger window will still be delivered at the preset volume and rate DESCRIPTION 3 7 5 2 SMMV Synchronised Mandatory Minute Ventilation SMMV provides a set level of minute volume ventilation SMMV allows spontaneous breaths combined with a synchronised mandatory breath to achieve the set minute volume SMMV must be pre selected in Standby Mode Select Standby Select Menu Select Special Modes Select Support Mode Select SMMV Escape Menu SMMV will now be displayed on the main screen when Spontaneous mode is selected or triggered NOTE J The trigger window is pre set to 60 of the BPM cycle time 2 The trigger is flow activated 3 If the Spirometry is disabled then SMMV is not available 4 If the pressure limit and alarm are activated the inspiratory phase is terminated Activate SMMV during Ventilation NOTE SMMV will not function unless already pre selected in Standby Mode 1 Select Special Mode on the display If the absorber Bag Vent switch is not detected a message will appear SET ABSORBER TO VENT Press the navigator wheel pu
89. sh button to confirm 2 Move the absorber Bag vent switch to Ventilator 3 Check that SMMV is functioning correctly SMMV Default Settings The ventilator will default to pre set values for minute volume Vm Rate Inspiratory Time and Trigger Level after selecting SMMV Note 1 Vm can be adjusted before SMMV is confirmed 2 The trigger setting is adjustable between 0 7 and 4 0 L min PEEP 0 cmH20 SMMV Spontaneously Breathing Patient A Cycle Time set from BPM B Trigger Window C Spontaneous Breath D Trigger E Mandatory Breath tidal volume This is equal to Vm BPM minus the volume spontaneously breathed during the cycle this maintains the set Vm Inspiratory flow in the Trigger Window generated by the patient s spontaneous breath results in a synchronised mandatory breath ensuring that the set minute volume is achieved SMMV No breathing effort by Patient A Cycle Time set from BPM B Trigger Window C Flat Pressure Trace no breathing effort D Mandatory breath at the end of the Trigger Window at the set Vm If the patient makes no effort to breathe during a cycle a mandatory breath at the end of the trigger window will still be delivered at the preset volume and rate DESCRIPTION 3 7 5 3 PSV Pressure Supported Ventilation PSV assists each spontaneous breath to achieve a preset pressure thus reducing the effort required to breathe Inspiratory
90. ssis Assembly 5000489 Item O Q N 11 12 13 14 15 16 1 18 19 20 21 22 23 24 26 27 29 30 31 32 33 34 36 37 38 39 40 Part No 5000459 5000156 300595 011240 01235 01149 103996 5003058 104715 2220 099 5000449 35150 019122 5000505 5000498 5000504 5000472 300569 300634 5000540 5000488 041204 500506 5000487 054541 041245 300609 019067 011241 019087 057002 011169 019121 300638 300637 011092 104038 Description Chassis AVS Regulator amp Control Assembly DISS Con Nut Rubber Foot M8 Internal Star M8 Locknut Battery 30 minutes backup Battery 1 hour backup LEC Mains Connector Filter LEC Mains Plug Retainer Assembly Patient Valve Block Assembly Hose Hose Panel Connector M3 X 6 LG Button HD External Circlip 10 mm Shaft Power Supply Bracket External Circlip 8 mm Shaft Chassis Label AVS Power Supply Straight Connector 5 O D Tube M5 Bostik Silicone Sealant Pressure Connector 5 1 I D X 1 6 CS Viton Tray Gasket Bleed Adaptor Tube Conn O Seal Q7 0 X 1 5 Sensor Assembly M4 X 12 SKT HD Cap D S Tape 3M s X 105 mm Long M3 X 16 Cap HD Screw Loctite 222 M4 Skiffy Cap M4 X 8 Button HD Tube 4 0 O D Tube 5 0 O D Silicon Tube O D 6 mm X I D 3 mm Fuse 2 Amp T HRC 20 mm UL 72 Quantity wA cA P X X Nhaa 73 PARTS LIST PNEUMATIC CONNECTIONS CONNECT PORT 3 T
91. such panels missing There is a possible electric shock hazard Bellows Assembly 32 The valve seat on the patient gas exhalation diaphragm valve in the base of the bellows assembly must be cleaned regularly Note that the bellows assembly is built into the A200SP Absorber please refer to User Manual for this product Failure to keep the valve seat clean could result in the diaphragm sticking thus preventing exhalation Great care must be taken not to damage the precision surface of the valve seat on the patient gas exhalation diaphragm valve in the base of the bellows assembly Never use any hard object or abrasive detergent to clean it use only a soft cloth If the valve seat is damaged the valve will leak and may cause serious ventilator malfunction WARNINGS AND CAUTIONS CAUTIONS NOTES 1 Do not sterilise the ventilator control unit The patient block assembly must be 1 The term cycle is used to designate the removed from the control unit before transition to the exhalation phase sterilisation see section 6 2 5 E All other internal components are not 2 The term trigger is used to indicate the compatible with sterilisation techniques transition to the inhalation phase and damage may result Ze For ventilator components which require sterilisation peak sterilisation temperatures should not exceed 134 C 2759F to prevent possible damage See section 6 3 Care must be taken not
92. t that the sensor is properly located in the expiratory limb of the circuit refer to section 5 1 10 The patient must be continuously attended and monitored when Advanced Breathing Modes are in use User Maintenance Control Unit 27 28 29 30 Opening the control unit by unauthorised personnel automatically voids all warranties and specifications Prevention of tampering with the control unit is exclusively the user s responsibility If the control unit seal is broken the manufacturer assumes no liability for any malfunction or failure of the ventilator For continued protection against fire hazards replace the two fuses only with the identical type and rating of fuse See section 4 for fuse rating If the internal battery is fully discharged the ventilator will not function in the event of mains power failure The battery must be recharged before the ventilator is used clinically otherwise backup cannot be guaranteed See Appendix for battery maintenance See also CAUTION No 7 Used or defective batteries must be disposed of according to hospital local state and federal regulations No oil grease or other flammable lubricant or sealant must be used on any part of the ventilator in close proximity to medical gas distribution components There is a risk of fire or explosion 31 Exterior panels must not be removed by unauthorised personnel and the apparatus must not be operated with
93. ted and damaged parts must be replaced Bellows As with all elastomers the bellows material deteriorates with aging and should be inspected at least every six months or after 1200 hours of use whichever comes first The bellows must be replaced if it shows signs of aging The bellows B can be removed by carefully pulling it off the base If a paediatric bellows is fitted the bellows adaptor C must also be removed Do not dismantle the bellows 85 Paediatric Bellows Assembly APPENDIX 4 Exhalation Diaphragm Valve The exhalation diaphragm valve is under the bellows and can be removed by loosening the three thumbscrews The valve seat is now visible WARNING Great care must be taken Do not damage the precision surface of the valve seat D Never use any hard object or abrasive agent to clean it use only a soft cloth If the valve seat is damaged the diaphragm valve will leak and may cause serious malfunction Clean the seat and the metal disk E attached to the base of the diaphragm valve thoroughly and remove all contamination from the surfaces of both components NOTE If excessive contamination is discovered check that a bacterial filter is used in the expiratory limb of the breathing circuit or an HME at the patient tee piece After cleaning check that the small O ring F located in the bellows base under the diaphragm valve is in place The ventilator will not functio
94. than before Check displayed Vt Meas 600ml 50 ml Using a Wrights Respirometer check the expiratory volume is 50 ml of the displayed value Note If Vt Meas is out of specification repeat spirometery calibrations at zero and 10 l min Press Insp Pause Check for 25 pause during the inspiratory phase Switch Off Inspiratory pause Reduce fresh gas flow to basal Press Wave Freeze and check waveform freezes Press again to clear Set PEEP to 10 cmH20 Check waveform to see that it displays 10 cmH2O of PEEP Straight line is good Decline of line indicates leak Turn off PEEP 63 SERVICE SCHEDULE 14 10 14 11 14 12 15 15 1 15 2 15 3 15 4 15 5 15 6 15 7 15 8 16 16 1 Adjust Airway Pressure Observe changing scale on waveform Reset to 38 cmH20 Touch waveform screen Check that the following second waveforms are selectable and waveform is displayed 1 Volume v Time 2 Pressure v Volume Compliance Loop Reset back to None Check the ventilator is operating smoothly and that the test lung is inflating Check that the absorber manometer indicates 5 cmH20 of the system pressure displayed on the ventilator screen Airway Alarm Tests every 6 months Set ventilator to default settings and ventilate test lung in Volume mode Disconnect test lung and occlude patient connector Ensure High Airway Pressure alarm occurs and circuit pressure is limited to 38
95. the A200SP Absorber For additional information please refer to the user manual for that product CAUTION Always ensure correct fitment of bellows see illustration above and carry out a full function test before clinical use if a bellows is removed and refitted 1 Remove the bellows housing 1 Twist carefully counterclockwise until the bayonet tabs become free then lift up from the base 2 2 Remove the bellows 3 3 Refit the bellows and check for correct assembly as illustrated 4 4 Fit the bellows housing by pushing down then twisting clockwise until the bayonet tabs completely engage 5 Function test the ventilator section 5 3 1 NOTE If there is any malfunction the ventilator must NOT be used If the problem cannot be rectified the ventilator must be checked by an engineer trained by the manufacturer Paediatric Bellows Assembly 1 47 Remove the adult bellows housing 1 twist carefully counterclockwise until the bayonet tabs become free then lift up from the base 2 Remove the bellows 3 Fit the paediatric adaptor 5 press the adaptor into the ventilator bellows assembly base 2 Fit the paediatric bellows 6 to the adaptor Check for correct assembly as illustrated 4 Fit the paediatric bellows housing 7 to the base by pushing down then twisting clockwise until the bayonet tabs completely engage Function test the ventilator section 5 3 1
96. these operations are given in this Manual for the AV S available only for Penlon trained engineers For any enquiry regarding the servicing or repair of this product contact the nearest accredited Penlon agent or communicate directly with Technical Support Penlon Limited Abingdon Science Park Barton Lane Abingdon OX14 3PH UK Tel 44 0 1235 547076 Fax 44 0 1235 547062 E mail technicalsupport penlon co uk Always give as much of the following information as possible Type of equipment Product name Serial number Approximate date of purchase Apparent fault O9 Row FOREWORD This manual has been produced to provide authorised personnel with information on the function routine performance service and maintenance applicable to the AV S Anaesthesia Ventilator Information contained in this manual is correct at the date of publication The policy of Penlon Limited is one of continued improvement to its products Because of this policy Penlon Limited reserves the right to make any changes which may affect instructions in this manual without giving prior notice Personnel must make themselves familiar with the contents of this manual and the machine s function before servicing the apparatus Copyright Penlon Limited 2008 All rights reserved ii CONTENTS 3 1 3 2 3 3 3 3 1 3 4 3 5 3 5 1 3 5 2 3 5 3 3 5 4 3 6 3 7 3 7 1 3 7 2 3 7 3 3 7 4 3 7 5 3 7 5 1 3
97. tiate calibration Calibration is completed Scroll to ESCAPE FROM MENUS Press the wheel to confirm 45 On Off Switch Alarm Mute Menu Switch Navigator Wheel and Press Button O2 Monitor amp Spiro ESCAPE FROM MENU O2 MONITOR on CALIBRATION 100 HIGH ALARM SET 105 LOW ALARM SET 18 SPIROMETER on gt SPIRO CALIBRATION 0 L min PRE OPERATION PROCEDURES 5 1 11 Pressure Monitor Connections WARNING The High and Low Airway Pressure Alarms are important for patient care The connection point must be properly located in the expiratory limb of the breathing system 1 PATIENT PRESSURE port A on the rear panel of the control unit Use the tubing assembly supplied by the manufacturer to connect to the expiratory limb of the breathing system close to the circle system expiratory valve Push fit self sealing connectors B Push in the tube as far as possible Do not use excessive force The connector end piece X will also move inwards Pull the tube carefully outwards The end piece X will be pulled outwards to the locked position Connect the tubing with adaptor Part No 053049 to the push fit self sealing connector C at the rear of the A200SP Absorber EDO Sk vu So 46 PRE OPERATION PROCEDURES 5 1 12 Bellows Assemblies Note that the bellows assembly is built into
98. to let any liquid run into the control unit serious damage may result 4 The exhalation valve located in the bellows base assembly and the paediatric bellows adaptor must be cleaned and sterilised separately Note that the bellows assembly is built into the A200SP Absorber please refer to User Manual for this product 5 Always check for correct fitment and carry out a full function test before clinical use if the bellows has been removed and refitted for any reason See section 6 Note that the bellows assembly is built into the A200SP Absorber please refer to User Manual for this product 6 Damage may occur to the battery if it is allowed to remain in a discharged state Check the battery frequently if the ventilator is in storage see Appendix 1 7 Fresh gas compensation is disabled if a The spirometry system is turned OFF through the menu system or b The spirometry system is not functioning correctly 8 Fresh gas mixture compensation is disabled if a The spirometry system is turned OFF through the menu system or b The spirometry system is not functioning correctly c The O2 monitor is switched OFF 9 Circuit compliance is not activated until Fresh Gas Compensation is switched OFF WARNINGS AND CAUTIONS Oxygen Monitor Oxygen Monitor Note that the sensor for the oxygen monitor is built into the A200SP Absorber for additional information please refer to the A200SP User Manual WARNIN
99. ure Monitor Port Input socket Oxygen monitor sensor Data and Printer Ports 9 Data Output 10 Output to remote display 11 Ethernet 12 USB 13 VGA 14 Printer port 15 RS232 manufacturer s use only NOTE USB port is for access only by engineers trained by the manufacturer All other data ports are read only For further information please contact your distributor s service department or the manufacturer DESCRIPTION 32 Ventilation Cycle This section provides a simplified description of the ventilation cycle ib 1 Inspiratory Phase The drive gas proportional i valve 1 in the control unit i opens 4 Drive gas is delivered to the bellows housing 2 The patient proportional nl gt valve 3 opens and gas 3 5 flows through the bleed A valve The back pressure ensures that the exhaust k valve 4 is kept closed Hu Drive gas pressure builds 2248 up above the bellows 5 which starts to move down The diaphragm 6 in the bellows assembly base is held closed and patient gas is forced out of the bellows base 7 into the breathing system 2 Beginning of Expiratory Phase The drive gas proportional valve 1 closes The patient proportional valve 3 closes The exhaust valve 4 opens Patient gas returns to the bellows 5 As the bellows rises redundant drive gas is pushed out through the exhaust valve 10 DESCRIPTION
100. ut the breathing circuit Check that the cable between the control unit and remote display screen unit is connected before use Always use a cable type recommended by the manufacturer Using the Ventilator 14 15 16 The AV S ventilator is not intended for use in intensive care applications This apparatus must not be used with or in close proximity to flammable anaesthetic agents There is a possible fire or explosion hazard Anaesthesia apparatus must be connected to an anaesthetic gas scavenging system AGSS to dispose of waste gas and prevent possible health hazards to operating room staff This requirement must be observed during test procedures as well as during use with a patient The scavenging transfer and receiver system must conform to ISO 8835 3 Any problem arising from an improperly functioning scavenging system is solely the user s responsibility Do not use a scavenging system that restricts drive gas flow when negative pressure is exerted on it 17 18 19 20 21 22 23 24 When the ventilator is connected to a patient it is recommended that a qualified practitioner is in attendance at all times to react to an alarm or other indication of a problem In compliance with good anaesthesia practice an alternative means of ventilation must be available whenever the ventilator is in use It is recommended that the patient oxygen concentration should be monitored
101. v snonunuo uBiH eJnsseJg sec SAG swoljleg UBIH eJnssaeJg sec AUA SMO SG MOT eunsseJg Ajddng ses eAug o1 1184 0 noqy Jamod pexoolq jenno doul juan AlJB1 dou 40je nueA wuejy 30 DESCRIPTION O2 Monitor 3 42 Oxygen Monitor The oxygen monitor continuously measures and indicates the concentration of oxygen in the breathing system and triggers an alarm when the concentration varies from the set levels 3 12 1 System Description The Oxygen Monitor uses a fast responding oxygen specific self powered sensor that achieves 90 of final value in less than 10 seconds An external probe 1 is supplied with a 2 m 6 ft extendable cable The system has user adjustable high level and low level alarms with visual and audible indication of alarm conditions Bacterial Filter Always use a breathing system bacterial filter in the expiratory limb of the breathing circuit to protect the oxygen sensor and breathing system components from contamination see section 5 CAUTION Replacement Disposal always follow the instructions supplied with the filter and always replace at the recommended interval 3 12 2 The Oxygen Sensor The oxygen sensor offers quick response linear output over the entire 0 100 oxygen range and long service life The sensor is a self powered galvanic cell that generates a current proportional to oxygen concentration The cell has a highly stable output over its operating life Si
102. with an A200SP Absorber Two year Kit Part No 57299 with standard battery As One year kit plus 12v battery 30 minutes backup 103996 Two year Kit Part No 57302 with high power battery As One year kit plus 12v battery 5003058 1 hour backup 041204 041245 O ring O ring 041222 Four year Kit Part No 57300 with standard battery As Two year kit 57299 plus 3v PCB battery Bellows diaphragm valve 104019 406020 Four year Kit Part No 57301 with high power battery As Two year kit 57302 plus 3v PCB battery Bellows diaphragm valve 104019 406020 Note If a paediatric bellows assembly is used with the AV S the O ring on the bellows adaptor must be renewed annually Order O ring Part No 041225 57550 Bellows 041204 041226 O ring O ring adi See Note above IMPORTANT Discard clear plastic slotted spacer if fitted Always reassemble with solid opaque spacer Diaphragm 300581 One way Valve Patient Block 66 PARTS LIST 5000492 Arm Assembly Control Unit and Remote Display Screen Assemblies Item 1 a WwW N Part No 01056 300529 5000543 01130 300549 5000599 Description M5 x 12 SKT HD Cap Screw Screen Display Assembly Remote Chassis Assembly Remote M5 X 16 SKT Cap Head Screw ST STL Interface Cable screen to control unit not shown Interface Cable A200 Absorber to control unit not shown 67 SR

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