Home

IVAC®P7000 Syringe Pump

Contents

1. 24 e Maintenance eme 26 e Occlusion Pressure Limits ees ep Oe ieoi epo sepe eene tapete nee en eee 28 e RS232 and Nurse call 5 1 29 Trumpet Curves 8 Start up Curves 30 e Service CORPER 31 e Document History RR H sss isss 31 e Tr 32 e Spare Parts 32 e T 33 1000DF00136 Iss 2 1 36 ntroduction The IVAC P7000 Syringe Pump herein after referred to as pump is a fully featured high end variable pressure syringe pump suitable for critical care applications Intended Use The pump is designed to meet the infusion requirements within the operating environment specified in this Directions For Use DFU including general wards critical and intensive care neonatal operating rooms and accident and emergency rooms This pump is suitable for use by appropriately trained clinicians or nurses The syringe pump is suitable to d
2. Volume Infused VI is not added BOLUS fluid or drug delivered at an accelerated rate Pump is infusing Extension set is connected to the patient Vlis added OPTION button Press to access optional features see Basic Features PRESSURE button Use this button to display the pumping pressure display and alarm level CHEVRON keys Double or single for faster slower increase or decrease of values shown on display BLANK SOFTKEYS Use in conjunction with the prompts shown on the display Indicators Symbol BATTERY indicator When illuminated the pump is running on the internal battery When flashing the battery power is low with less than 30 minutes of use remaining AC POWER indicator When illuminated the pump is connected to an AC power supply and the battery is being charged 1000DF00136 Iss 2 4 36 Symbol Definitions Labelling Symbols nid Attention Consult accompanying documents Potential Equalisation PE Connector RS232 Nurse call Connector Optional Type CF applied part Degree of protection against electrical shock IP X 4 Protected against vertically falling drops of vvater Device complies vvith the requirements of the EC Directive 93 42 EEC Registered vvith the CE Mark Date of Manufacture Manufacturer Not for Municipal VVaste mportant information Class II Equipment Functional Earth 1000DF00136 Iss 2 5 36 Operating Precautions Luer Lo
3. Dosing Conversion 1 0 ug 1000 ng 1 0 mg h 24 0 mg 24 h 1 0 mg min 60 0 mg h 1 0 mg 1000 ug Review the drug set up data on the display then press the OK softkey to confirm 1000DF00136 Iss 2 DOSE UNITS DEFAULT DOSERATE MIN DOSERATE MAX DOSERATE DEFAULT CONC BOLUS RATE MAX BOLUS PRESSURE ALARM 20 36 Drug Protocol Record Aq UOISA A 1 u lun uuely anss lq uoneuo uo 9jey esoq 3uf p4bM REESE STE RE nig duq abulsAs 000Zd eo J Aq paaosddy 4aquinyw 101 95 xew saeu 2 awey 11450 21 36 1000DF00136 Iss 2 Specifications Infusion Specifications Maximum infusion rate can be set as part of the configuration 0 1ml h 150ml h 5ml syringes 0 1ml h 300ml h 0 1ml h 600ml h 0 1ml h 900ml h 0 1ml h 1200ml h The Volume Infused range is 0 0ml 9990ml 10ml syringes 20ml syringes 30ml syringes 50ml amp 100ml syringes Bolus Specifications Maximum Bolus rates can be set as part of the configuration Bolus rates are user adjustable 10ml h 150ml h 10ml h 300ml h 10ml h 600ml h 10ml h 900ml h 10ml h 1200ml h Bolus volume limit 25 0ml During BOLUS the pressure limit alarms are temporarily increased to their maximum level 5ml syringes 10ml syringes 20ml syringes 30ml syringes 50ml amp 100ml syringes Critical Volume
4. Fax 31 30 225 86 58 www cardinalhealth com nl support alaris nl cardinal com NO Cardinal Health Solbraveien 10 A 1383 ASKER Norge Tel 47 66 98 76 00 Fax 47 66 98 76 01 www cardinalhealth com no A technical supportNO cardinal com NZ Cardinal Health 14B George Bourke Drive Mt Wellington 1060 PO Box 14 518 Panmure 1741 Auckland New Zealand Tel 09 270 2420 Freephone 0508 422734 Fax 09 270 6285 www cardinalhealth com nz Q l techservice nz cardinal com SE Cardinal Health Hammarbacken 4B 191 46 Sollentuna Sverige Tel 46 8 544 43 200 Fax 46 8 544 43 225 www cardinalhealth com se A SE technical supportSE cardinal com Us Cardinal Health 10020 Pacific Mesa Blvd San Diego CA 92121 USA Tel 1 800 854 7128 Fax 1 858 458 6179 www cardinalhealth com alaris ZA Cardinal Health Unit 2 Oude Molen Business Park Oude Molen Road Ndabeni Cape Town 7405 South Africa Tel 27 0 860 597 572 Tel 27 21 510 7562 Fax 27 21 5107567 www cardinalhealth com za e SA Technical Support cardinal com Document History Revision CO Number 1 6934 2 8701 Date September 06 July 08 1000DF00136 Iss 2 31 36 Cardinal Health Alaris Products Cardinal Health warrants that A Each new infusion instrument pump controller or peripheral instrument is free from defects in material and workmanship under n
5. The bolus which can occur in the event of a single internal fault condition with a 50ml syringe is Maximum Overinfusion 0 5ml Purge Specifications The purge rate is limited to the maximum rate for the syringe 100ml h 500ml h The purge volume limit is 2ml During PURGE the pressure limit alarms are temporarily increased to their maximum level VTBI Complete Keep Vein Open KVO Rate Stop 1ml h 2ml h or continue at set rate End Of Syringe KVO Rate Stop 1ml h or set rate if lower than 1ml h Volume To Be Infused VTBI 0 1ml 100ml 1min 24h Near End Of Infusion Alarm 1min 15min to end of infusion End Of Infusion EOI Alarm 0 596 596 of syringe volume Maximum Pumping Pressure Limit Highest alarm level 650mmHg nominal at L 7 1000DF00136 Iss 2 Electrical Classification Class Il product with functional earth Continuous Mode Operation Transportable System Accuracy Volumetric Mean 2 nominal Important System accuracy is 2 typical by volume as measured using the trumpet curve test method defined in IEC EN60601 2 24 at rates of 1 0ml h 23 C and above when the pump is used with the recommended syringes Differences in factors such as size and plunger force in compatible syringes can cause variations in accuracy and trumpet curves See also trumpet curves section in this manual Battery Specifications Rechargeable Sealed Lead Acid Automatically charges when
6. This warranty shall apply solely to the original purchaser This warranty shall not apply to any subsequent owner or holder of the product Furthermore this warranty shall not apply to and Cardinal Health shall not be responsible for any loss or damage arising in connection with the purchase or use of any Cardinal Health product which has been A repaired by anyone other than an authorised Cardinal Health service representative B altered in any way so as to affect in Cardinal Health s judgement the stability or reliability of the product or has had the product s serial or lot number altered effaced or removed C subjected to misuse or negligence or accident or D improperly maintained or used in any manner other than in accordance with the written instructions furnished by Cardinal Health This warranty is in lieu of all other warranties express or implied and of all other obligations or liabilities of Cardinal Health and Cardinal Health neither assumes nor authorises any representative or other person to assume for it any other liability in connection with the sale of Cardinal Health products CARDINAL HEALTH DISCLAIMS ALL OTHER WARRANTIES EXPRESS OR IMPLIED INCLUDING ANY WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE Spare Parts A comprehensive list of spare parts for this pump is included within the Technical Service Manual The Technical Service Manual 1000SM00012 is now available in electronic format
7. on the World Wide Web at www cardinalhealth co uk alaris A username and password are required to access our manuals Please contact local customer services representative to obtain login details 0000EL00004 Internal Battery Pack 1000DF00136 Iss 2 32 36 Symbols 24 Hour Log 15 A About This Manual 2 Alarms 16 Battery See also Battery Operation Battery Operation 26 Bolus 3 4 11 15 22 C Cleaning 27 Clock Set 19 Concentration 27 Controls CHEVRON 4 HOLD 10 ON OFF 4 OPTION 3 4 PRESSURE 3 4 10 16 PURGE BOLUS 3 4 SOFTKEYS 4 D Dedicated 12 Display 3 16 Disposal 27 Docking Station 31 Dosing 13 20 Drug 3 13 14 20 21 Drug library 20 Enable Syringes 19 Enable Units 19 Event Log 15 Extension Sets 6 24 25 F Fuses 26 G General Options 17 H Hands On 11 Hospital Name 19 l Indicators AC POWER 4 BATTERY 4 Installation 8 Introduction 2 L Labelling Symbols 5 1000DF00136 Iss 2 Language 19 Loading a Syringe 9 M Maintenance 26 27 Mount 6 8 N Nurse Call 7 29 o Occlusion 22 28 Operating Precautions 6 P Pole Clamp 3 8 Pressure 3 12 22 28 Pressure transducer 3 Purge 3 4 10 11 22 Q Quick Start Guide 2 See also Starting the Pump Rate Lock 15 RS232 5 7 29 31 S Service Contacts 32 Spare Parts 31 Specifications 22 Start up Curves 30 Starting the Pump 10 Storage 27 Syringe 2 3 8 9 18 21 22 24 25 31 See also Loadi
8. the MODIFY softkey When all the desired modifications have been carried out press the OK softkey r 0 nee Fither select the next configuration option from the menu or turn the pump OFF returning it to operation as required FASTSTART8 BACKOFF SET VTBI OVER TIME VTBI Enablesdriveslackfaststartandthe motortoreverse torelievelinepressurevvhenanocclusion occurs Enables or disables the VTBI function Sets a specific volume to be infused over a fixed period of time INDUCTION Enables or disables the induction option MULTIDOSE Enables or disables the multidose option RATE LOCK When enabled the rate can be locked to prevent unwanted changes of the set infusion rate QUIET MODE When enabled the low priority alarms and the button beeps are muted PRESSURE ALARM Sets the default pressure alarm level MAXPRESSUREALARM Sets the maximum pressure alarm level AUTOPRESSUREALARM Enables disables the automatic pressure alarm level option AC FAIL When enabled the AC Power Failure Alarm will sound if the AC power is disconnected RATE TITRATION When enabled the rate can be changed whilst the pump is infusing NEOI WARNING Sets the Near End Of Infusion warning time as time left to End Of Infusion EOI POINT Sets the End Of Infusion point KVO AT EOI When enabled the pump will switch to running at the KVO rate when EOI is reached BEAM ALARM Sets the default beam alarm level PATIENT WEIGHT Sets the default patient weight in kg PURGE R
9. 2 RXD PIN 2 TXD PIN 2 RXD PIN3 TXD PIN3 RXD PIN5 GND PIN5 GND PIN7 GND PIN 7 RTS PIN 8 CTS PIN 4 RTS PIN 8 CTS L PIN 7 RTS L PIN 5 CTS PIN 4 DTR PIN 20 DTR PIN 6 DSR L PIN 6 DSR The IBM connector pins grouped in pairs above should be linked at the connector 29 36 Trumpet Curves 6 Start up Curves n this pump as vvith all infusion systems the action of the pumping mechanism and variations in individual syringes cause short term fluctuations in rate accuracy The following curves show typical performance of the system in two ways 1 the delay in onset of fluid flow when infusion commences start up curves and 2 the accuracy of fluid delivery over various time periods is measured trumpet curves The start up curves represent continuous flow versus operating time from the start of the infusion They exhibit the delay in onset of delivery due to mechanical compliance and provide a visual representation of uniformity Trumpet curves are derived from the second hour of this data Tests performed per IEC EN60601 2 24 standard Trumpet curves are named for their characteristic shape They display discrete data averaged over particular time periods or observation windows not continuous data versus operating time Over long observation windows short term fluctuations have little effect on accuracy as represented by the flat part of the curve As the observation window is reduc
10. 25 DE Cardinal Health Pascalstr 2 52499 Baesweiler Deutschland Tel 49 2401 604 0 Fax 49 2401 604 121 www cardinalhealth com de DK Cardinal Health Firskovvej 25 B 2800 Lyngby Danmark TIL 45 70 20 30 74 Fax 45 70 20 30 98 ES Cardinal Health Edificio Veganova Avenida de La Vega n 1 Bloque 1 Planta 1 28108 Alcobendas Madrid Espana Tel 34 902 555 660 Fax 34 902 555 661 www cardinalhealth com es servicio tecnico cardinal com FR Cardinal Health mmeuble Antares Technoparc 2 rue Charles Edouard Jeanneret 78300 POISSY France Tel 33 1 30 06 74 60 Fax 33 1 39 11 48 34 www cardinalhealth com fr FR Assistance Technique cardinal com GB Cardinal Health The Crescent Jays Close Basingstoke Hampshire RG22 4BS United Kingdom Tel 44 0800 917 8776 Fax 44 1256 330860 www cardinalhealth com alaris A UK Technical Supportocardinal com HU Cardinal Health D brentei ter 1 H 1013 Budapest Magyarorszag Tel 36 14 88 0232 Tel 36 14 88 0233 Fax 36 12 01 5987 i AlarisCE cardinalhealth com IT Cardinal Health Via Ticino 4 50019 Sesto Fiorentino Firenze Italia T l 39 055 30 33 93 00 Fax 39 055 34 00 24 www cardinalhealth com it assistenza tecnica cardinal com NL Cardinal Health De Molen 8 10 3994 DB Houten Nederland Tel 31 30 228 97 11
11. ATE Sets the purge rate BOLUS Enables disables the bolus feature DEFAULT BOLUS Sets the default bolus rate CAP BOLUS RATE Sets the maximum value for bolus rate CAP RATE Sets the maximum value for the infusion rate EVENT LOG DISPLAY LOGLASTPATIENTONLY Enables disables the event log to be accessed via the options menu If enabled the event log shows only the last patient since new patient selected If disabled the complete log can be viewed NURSE CALL Enables disables the Nurse Call feature NURSECALLINVERTED When enabled the nurse call output is inverted COMMSPUMPADDRESS Sets the Pump Communications Address COMMSMONITORONLY When disabled allows remote control ofthe pump from the communications link Monitor is always COMMS ODD PARITY COMMS ASCII possible If enabled communications parity is odd If enabled communications protocol is in ASCII 1000DF00136 Iss 2 17 36 IVAC P7000 Syringe Pump Configured Options Record Enter the pump specific information for your records on a copy of this page Software Version V3R2 FAST START amp BACKOFF Enabled SET VTBI OVER TIME Disabled INDUCTION Disabled MULTIDOSE Disabled RATE LOCK Disabled QUIET MODE Disabled PRESSURE ALARM 300mmHg MAXIMUM PRESSURE ALARM 750mmHg AUTO PRESSURE ALARM Disabled RATE TITRATION Disabled NEO WARNING 5 minutes KVO AT EO Enabled BEAM Occlusion L3 PATIENT WEIGHT 70kg PURGE RATE 500ml h DEFAULT BOLUS 200ml h CAP BOLUS
12. CONNECT TO PATIENT Connect the extension set to the patient access device 9 START Press to commence operation INFUSING will be displayed The AMBER STOP light will be replaced by the flashing GREEN START light to indicate that the pump is in operation 10 STOP Press EJ to halt the operation ON HOLD will be displayed The AMBER STOP light will replace the GREEN START light to indicate that the pump is on hold 1000DF00136 Iss 2 10 36 Basic Features The ai button allows the delivery of a limited volume of fluid in order to purge the extension set prior to being connected to the patient access device or after changing a syringe 1 Press the 144 button when the pump is not infusing Ensure that the extension set is not connected to the PURE patient VOLUME i T 500 ml h 0 0 ml 2 Press and hold the PURGE softkeys until fluid flows PURGE PURGE and the purging of the extension set is complete The volume used during purging will be displayed but it is not added to the volume infused 3 When purging is complete release the PURGE softkeys Press the QUIT softkey to exit back to the main display The pump will not purge if the rate lock has been enabled During PURGE the pressure limit alarms are temporarily increased to their maximum level 1 Bolus Infusion Bolus Administering a controlled volume of fluid or drug at an increased rate for diagnostic or therapeutic purposes The pump
13. IVAC P7000 Syringe Pump Directions For Use English CardinalHealth Page e bo TIRE 2 e About This Manual escsceisccccccssstnssesocsccsseoussesseuscocecsepstsusseusscusesctsesuussudescessousedussdeasesussctonsensdeusescaveestenss 2 e Quick Start Guide wessiscdicscscssvccsscscicccc esdeacusasnnssiecssevsdvcoscsvescesscseesccscdssnusedscendeuseseceseskevesses desecccssssenevane 2 o Features of the PUMP M 3 e Controls amp Indicators 4 e Symbol pini r 5 e Operating Precautions cccssccscssessscssssssscsscesssssssssscsssesssssssssssssssssssscesscsssscssocsssssssssssssssecsosees 6 e Getting Started 8 e EEEIMIQUIIB 11 e Alarms and warnings ceres eene eere eere ee enne tn seen seno setenta senos 16 e 17 Drugs Protocol 21 MISI A 22 e Compat ble Syringes ee 23 e Compatible Extension Sets s sss s sss ss s sss s ss s ss ss ea
14. RATE 1200ml h CAP RATE 1200ml h EVENT LOG DISPLAY Enabled LOG LAST PATIENT ONLY Enabled NURSE CALL Disabled NURSE CALL INVERTED Disabled COMMS PUMP ADDRESS 1 COMMS MONITOR ONLY Enabled COMMS ODD PARITY Disabled COMMS ASCII Enabled Syringes Enabled Hospital Name Serial No Software Version Approved by Configured by Date Date 1000DF00136 Iss 2 18 36 Configured Options Continued Clock Set This option allows the user to set the pump s internal clock 1 Select CLOCK SET from the Configured Options menu using the keys and press the OK softkey 2 Use the keys to adjust the date displayed pressing the NEXT softkey to access the next field 3 When the correct time and date are displayed press the OK softkey to return to the Configured Options menu Hospital Name This option allows the user to programme in the name of the hospital ward or department This will appear during the power up display sequence 1 Select HOSPITAL NAME from the Configured Options menu using the keys and press the OK softkey 2 Use the keys to adjust the character displayed pressing NEXT to access the next field 3 When the correct name is displayed press OK to return to the Configured Options menu Enable Syringes This option is used to pre configure the type and size of syringe permitted for use on the pump Select all possible syringes which may be used and disable any that should not be used 1 Select ENABLE SYRINGES from the Con
15. afe mode the pump will duly stop the infusion and alert the user by generating a combination of visual and audible alarms Should any encountered alarm condition persist even after user intervention it is recommended to replace that particular pump and quarantine the pump for the attention of appropriately trained technical personnel Consult Technical Service Manual for further information An explosion hazard exists if the pump is used in the presence of flammable anaesthetics Exercise care to locate the pump away from any such hazardous sources Dangerous Voltage An electrical shock hazard exists if the pump s casing is opened or removed Refer all servicing to qualified service personnel When connected to an external power source a three wire Live Neutral Earth supply must be used If the integrity of the external protective conductor in the installation or its arrangement is in doubt the pump should be operated from the battery Do not open the RS232 Nurse Call protective covering when not in use Electrostatic discharge ESD precautions are required when connecting RS232 Nurse Call Touching the pins of the connectors may result in ESD protection failure It is recommended that all actions must be taken by appropriately trained personnel If this pump is dropped subjected to excessive moisture fluid spillage humidity or high temperature or otherwise suspected to have been damaged remove it from service for
16. but disconnected from patient Insert pressure disc into pressure transducer 6 INFUSION RATE Change rate if necessary using the keys 7 PURGE Press the button followed by the PURGE softkey 8 Connect extension set to the patient access device 9 Press the button to start the infusion 1000DF00136 Iss 2 2 36 Features of the IVAC P7000 Syringe Pump Potential Equalisation v Pole Clam PE connector p PURGE BOLUS START OPTION Pressure transducer PRESSURE ON OFF Carrying Handle Chevron keys Softkeys Main Display Features Pump Syringe type fitted Pressure Status Drug name Information PUMP STATUS SyaNGE TYPE y 10 46 3 0 VOLUME PRESSURE Un 10 0mi L 3 ADJUST Volume Infusion Review Infused Rate Data 1000DF00136 Iss 2 3 36 Controls 8 Indicators Controls ON OFF button Press once to switch the pump ON Press and hold down for approximately 3 seconds to switch the pump OFF START button Press to start the infusion The green LED will flash during infusion STOP button Press to put the infusion on hold The amber LED will be lit while on hold Also Press to silence alarm for 2 minutes The alarm will resound after this PURGE BOLUS button Press to access PURGE or BOLUS softkeys Press and hold down softkeys to operate PURGE the extension set during set up Pump is on hold Extension set is not connected to the patient
17. ces Anyone connecting additional devices to the signal input or output is a system configurator and responsible for meeting the requirements of the system standard IEC EN60601 1 1 RS232 Nurse call Connection Data Nurse call Specification Connector TXD RXD TXD Output Voltage Range RXD Input Voltage Range RXD Input Thresholds RXD Input Resistance Enable Isolation Socket Pump Baud Rate Start Bits Data Bits Parity Stop Bits Nurse Call Relay Contacts D Type 9 Pin EIA RS232 C Standard Minimum 5V mark 5V space Typical 7V mark 7V space with 3K load to ground 30V 30V max Low 0 6V minimum High 3 0V maximum 3K minimum Active Low 7V to 12V Active High 7V to 12V powers up the isolated RS232 circuitry Inactive Floating open circuit allows isolated RS232 circuitry to power down 4kV dc or ac peak 9600 Baud 1 Start Bit 8 Data Bits Odd Parity No Parity 1 stop bit Pins 1 6 9 30V dc 1A rating 1000DF00136 Iss 2 Typical Connection Data 1 Nurse call Relay Normally Closed NC C 2 Received Data RXD Input 3 Transmit Data TXD Output 4 Not used 5 Ground GND 6 Nurse call Relay Normally open NC O 7 Request To Send RTS Input 8 Clear To Send CTS Output 9 Nurse call Relay Common NC COM GND TXD RXD NCC 5 4 3 2 1 6 7 8 NCO RTS 5 com IBM IBM COMPATIBLE COMPATIBLE 9 PIN PUMP 25 PIN PIN 3 TXD PIN
18. ck y m Disposable Syringes and Extension Sets This IVAC P7000 Syringe Pump has been calibrated for use with single use disposable syringes To ensure correct and accurate operation only use 3 piece Luer Lock versions of the syringe make specified on the pump or described in this manual Use of non specified syringes or extension sets may impair the operation of the pump and the accuracy of the infusion Uncontrolled flow or syphoning may result if the syringe is located incorrectly in the pump or if it is removed from the pump before the extension set is properly isolated from the patient Isolation may include closing a tap in the patient line or activating a flow stop clamp When combining several apparatus and or instruments with extension sets and other tubing for example via a 3 way tap the performance of the pump may be impacted and should be monitored closely Mounting the Pump The pump must be mounted within 1 0m above or below the patients heart The most accurate pressure monitoring in the extension set is achieved when the pump is positioned close to the patients heart level Do not mount the pump in a vertical position vvith the syringe pointing upvvards as this could lead to an infusion of air vvhich may be in the syringe To protect against the introduction of air the user should regularly monitor the progress of the infusion syringe extension set and patient connections and follow
19. d I V poles of a diameter of up to 40mm The pole clamp can also be fitted in a choice of 4 fixing positions allowing the pump to be mounted to vertical and horizontal poles equipment rails and hospital furniture in a variety of convenient operating orientations The pole clamp may be adjusted for use with horizontal fittings by using the existing fixings screws with the alternative fixing holes in the pole clamp The pole clamp may also be secured to the base of the pump in a choice of four positions The multi position pole clamp hinge will support the unit at a range of angles on an I V pole To adjust the angle the unit needs to be secured to a pole using a hand at either end of the instrument change the screen viewing and syringe access angle of the instrument Do not mount the pump with the AC power inlet or the syringe pointing upwards This could affect the electrical safety in the event of a fluid spill or lead to the infusion of air which may be in the syringe 1000DF00136 Iss 2 8 36 Getting Started continued Loading a Syringe Syringe Clam V slot Plunger holder Finger grips Only use a syringe of the type stated on the pump or in this manual Using an incorrect syringe could adversely affect the accuracy of the infusion and the performance of the pump When initially loading the syringe allow for the volume of fluid contained in the extension set and retained in the syringe at the end of infusion as
20. d it should be first cleaned and the internal battery fully charged Store in a clean dry atmosphere at room temperature and if available employ the original packaging for protection Once every 3 months during storage carry out functional tests as described in the Technical Service Manual and ensure that the internal battery is fully charged Before cleaning always switch OFF and disconnect from the AC power supply Never allow liquid to enter the casing and avoid excess fluid build up on the pump Do not use aggressive cleaning agents as these may damage the exterior surface of the pump Do not steam autoclave ethylene oxide sterilise or immerse this pump in any fluid Ensure the pressure transducer is free from residues which may prevent correct operation of the disc detector Disposal Information on Disposal for Users of Waste Electrical amp Electronic Equipment This symbol on the product and or accompanying documents means that used electrical and electronic products should not be mixed with municipal waste If you wish to discard electrical and electronic equipment please contact your Cardinal Health affiliate office or distributor for further information Disposing of this product correctly will help to save valuable resources and prevent any potential negative effects on human health and the environment which could otherwise arise from inappropriate waste handling Information on Disposal in Countries outside the Europ
21. e and type of syringe specified on the pump display um Ek c ee e EES Astrazeneca v v z Yazd on ai BBraunPerfusor v v j kit gs SUE ae Sei BDPlastipak ov vi uv d ov d irae See eS Fresenius injectomat_ Meet v v v TT 2 M A oooi i a a REST TYCO Healthcare KENDALL MONOJECT 1000DF00136 Iss 2 23 36 Compatible Extension Sets The pump uses standard single use disposable extension sets and syringes vvith Luer lock connectors The user is responsible for verifying the suitability of a product used if it is not recommended by Cardinal Health Standard Sets G40015 G40020B G402EP G30402M G302EP Standard PVC Syringe Extension Set 150 cm Priming Volume 2 6ml Standard PVC Syringe Extension Set 200 cm Priming Volume 1 5ml Extension set luer lock connectors Kink resistant DEHP free PVC yellow striped tubing Bore 1mm Length 200cm Priming volume 1 6ml g LET LTB l Lp Standard PVC Syringe Extension Set vvith occlusion sensing disc 200 cm Priming Volume 1 5ml Extension set vvith pressure sensing disc luer lock connectors Kink resistant DEHP free PVC yellovv striped tubing Bore 0 9mm Length 200cm Priming volume 1 5ml Low Sorbing Sets G40615 G40620 G30303M G30453M G30302M G40720 Polyethylene Syringe Extension Set 150 cm Priming Volume 1 5ml Polyethylene Syringe Extension S
22. e infusion Excessive pressure measured in the extension set at the pressure sensing disc exceeding the alarm limit Identify and remove the cause of the blockage in the drive syringe patient access site or administration system before restarting the infusion Incorrect size of syringe has been fitted the syringe has not been positioned correctly or has been disturbed during operation Check the syringe location and the position The syringe plunger is not correctly fitted in the plunger holder Check the syringe plunger location The pressure disc has been removed from the pressure transducer during the infusion The infusion will stop Replace the pressure disc then restart the infusion Battery charge low with 30 minutes operation remaining Battery indicator will flash and after 30 minutes a continuous audible alarm will indicate that the battery is exhausted Reconnect to the AC power supply to continue operation and charge the internal battery Battery may be low empty When the pump was last turned off the battery was low If the pump has not been charged since then operate on AC power only The internal battery is exhausted Connect the pump to the AC power supply The pump is nearing the end of the infusion This value can be configured The pump has reached the end of the infusion A pre set volume will remain in the syringe to minimise the risk of the infusion of air bubbles into the set This value can be configured The p
23. ean Union This symbol is only valid in the European Union The product should be disposed of taking environmental factors into consideration To ensure no risk or hazard remove the internal rechargeable battery and the battery from the control board and dispose of as outlined by the local country regulations All other components can be safely disposed of as per local regulations 1000DF00136 Iss 2 27 36 Occlusion Pressure Limits Occlusion Pressure Limits for IVAC 50ml Syringes The following tables show the worst case values for line pressure time to alarm and bolus volume that can be expected in the event of an occlusion when the IVAC 50ml syringe is selected G40020B administration set Alarm level Rate ml h Maximum time Nominal occlusion Maximum bolus to occlusion alarm alarm pressure volume ml h min mmHg o 1 0 0 02 0 50 50 0 1 18 1 0 0 09 90 50 90 0 2 27 1 0 0 22 190 50 150 0 3 3 1 0 0 34 280 100 100 0 5 4 1 0 0 56 370 4100 100 0 7 5 1 0 1 10 460 100 100 0 9 6 1 0 1 30 560 100 100 1 0 7 1 0 1 45 650 100 100 1 3 07 5 0 0 01 0 50 50 0 1 12 5 0 0 02 90 50 90 0 2 2 5 0 0 06 190 50 150 0 4 3 5 0 0 08 280 100 100 0 6 4 5 0 0 12 370 4100 100 0 8 5 5 0 0 14 460 100 100 1 0 6 5 0 0 17 560 100 100 1 2 7 5 0 0 19 650 100 100 1 4 Tests at these levels may alarm immediately the force at these levels is commonly less than the friction in the syringe w
24. ed 1 Press the 7 button to access the options menu 2 Select the UNLOCK RATE option using the keys and press the OK softkey To enable the rate lock if not selected 1 Press the 7 button to access the options menu 2 Select the RATE LOCK option using the keys and press the OK softkey 1000DF00136 Iss 2 15 36 Alarms and VVarnings Alarms and vvarnings are indicated by a combination of an audible alarm flashing amber STOP light and a descriptive message in the display First press the MUTE softkey to silence the alarm for a maximum of 2 minutes then check the display for a message Press CANCEL 1 to cancel the message 2 If the infusion has stopped rectify the cause of the alarm warning then press the 23 button to resume the infusion Display DRIVE DECLUTCHED OCCLUSION LINE OCCLUSION CHECK SYRINGE LOCATION CHECK PLUNGER LOCATION PRESSURE SET NOT FITTED BATTERY LOW BATTERY WAS LOW AT LAST POWER OFF HAS PUMP BEEN RECHARGED BATTERY EMPTY NEAR END OF SYRINGE SYRINGE EMPTY VTBI DONE AC POWER FAIL ERROR Code and Message ATTENTION with 3 Beeps Description and Troubleshooting Guide The drive system has been disengaged during operation Check the finger grips and the position of the syringe Excessive pressure measured at the syringe plunger exceeding the alarm limit Identify and remove the cause of the blockage in the drive syringe or administration system before restarting th
25. ed short term fluctuations have greater effects as represented by the mouth of the trumpet Knowledge of system accuracy over various observation windows may be of interest when certain drugs are being administered Short term fluctuations in rate accuracy may have clinical impact depending on the half life of the drug being infused therefore the clinical effect cannot be determined from the trumpet curves alone Start up and trumpet curves may not be indicative of operation under negative pressure Differences in factors such as size and plunger force in compatible syringes produced by other manufacturers can cause variations in accuracy and trumpet curves as compared to those represented Additional curves for compatible syringes are available upon written request For applications where flow uniformity is a concern rates of 1 0ml h or above are recommended Start up Trend BD Plastipak 50ml 0 1ml h Trumpet Curve BD Plastipak 50ml 0 1ml h 90 0 0 5 70 0 0 3 50 0 30 0 g 01 g 100 E x 10 0 01 e 8 E 30 0 a 0 3 50 0 70 0 i 10 20 30 40 50 60 70 80 90 100 110 120 9 0 5 10 15 20 25 30 35 Time mins Observation Window mins Start up Trend BD Plastipak 50ml e 1 0ml h Trumpet Curve BD Plastipak 50ml e 1 0ml h 5 0 30 0 25 0 4 0 20 0 ikas 15 0 3 0 10 0 E 5 0 20 S E 5 5 0 E 10 nai 10 0 15 0 y 14 42 oN 20 0 40 25 0 0 10 20 30 40 50 60 70 80 90 100 110 120 Time m
26. eliver fluids and medications via intravenous and epidural routes Supporting fluid therapy blood transfusions and parenteral feeding The pump functions with a wide range of standard single use disposable Luer lock syringes It accepts syringe sizes from 5ml to 100ml See the Compatible Syringes section for a full list of compatible syringes Simple to set up and easy to operate X Large graphics format display including pressure trending Rate Range from 0 1 to 1200ml h e In pressure monitoring from 0 to 1000 mmHg Event logging records operation of pump Configurable drug protocols for simplified drug dosing About This Manual The user must be thoroughly familiar with the IVAC P7000 Syringe Pump described in this manual prior to use All illustrations used in this manual show typical settings and values which may be used in setting up the functions of the pump These settings and values are for illustrative use only Where stated a minimum infusion rate refers to a nominal rate of 1 0ml h and an intermediate infusion rate refers to a nominal rate of 5 0ml h The complete range of infusion rates settings and values are shown in the Specifications section Quick Start Guide 1 Press the amp button to turn the pump on 2 NEW PATIENT NO retains previous data YES clears previous data 3 Load syringe 4 Confirm correct size and brand of syringe 5 Ensure extension set is attached to syringe
27. et 200 cm Priming Volume 1 6ml Polyethylene Syringe Extension Set vvith occlusion sensing disc 200 cm Priming Volume 1 5ml El MB IE Opaque VVhite PVC lovv sorbing Syringe Extension Set vvith occlusion sensing disc 200 cm Priming Volume 1 5ml El IE O p Polyethylene Lined Syringe Extension Set with occlusion sensing disc and clamp 200 cm Priming Volume 1 6ml Polyethylene Lined Syringe Extension Set with clamp 200 cm Priming Volume 1 5ml It is recommended that extension sets are changed in accordance with the Directions for Use Carefully read the Directions For Use supplied with the extension set prior to use Please note these drawings are not to scale 1000DF00136 Iss 2 24 36 Compatible Extension Sets Continued The pump uses standard single use disposable extension sets and syringes vvith Luer lock connectors The user is responsible for verifying the suitability of a product used if it is not recommended by Cardinal Health Light Protected Sets G40215 Amber PVC Syringe Extension Set 150 cm Priming Volume 1 2ml G40320 White PVC Syringe Extension Set 200 cm Priming Volume 3 6ml B Yess _ G30653M Opaque White PVC Syringe Extension Set with occlusion sensing disc 200 cm Priming Volume 1 5ml Patient Controlled Analgesia PCA Sets 30822 PVC Syringe Extension Set with clamp 152 cm Priming V
28. figured Options menu using the keys and press the OK softkey 2 Use the keys to scroll through the list of syringes pressing MODIFY to enable disable a syringe brand and individual models within the brand 3 When all modifications are complete press OK to return to the Configured Options menu This option is used to pre configure the type of units permitted for use on the pump Select all possible units which may be used and disable any that should not be used 1 Select ENABLE UNITS from the Configured Options menu using the keys and press the OK softkey 2 Use the keys to scroll through the list of units pressing MODIFY to enable disable a unit 3 When all modifications are complete press OK to return to the Configured Options menu 1000DF00136 Iss 2 19 36 N Configured Options Continued Drug Set up Select the DRUG SETUP option from the Configured Options menu and press the OK softkey Select the required drug with the keys and press the OK softkey To use a drug it must be enabled Press the YES softkey to enable the selected drug To add or change a drug name use the keys to scroll through the alphabet To select a letter press the NEXT softkey On completion press the OK softkey Follow the flow chart using the keys to select values Use OK to enter selected values and move on to the next stage The BACK softkey may be used at any time to return to the previous screen of the drug set up procedure
29. he battery For further information regarding the replacement of batteries refer to the Technical Service Manual Test Routines The test routines are designed to allow confirmation of many of the pump functions defaults and calibrations without requiring internal inspection They do not represent a full calibration check See the Technical Service Manual for a complete list of the test procedures access codes and calibration procedures 1000DF00136 Iss 2 26 36 Maintenance continued Cleaning and Storage Before the transfer of the pump to a nevv patient and periodically during the use clean the pump by vviping over vvith a lint free cloth lightly dampened with warm water and a standard disinfectant detergent solution Recommended cleaners are Brand Concentration Hibiscrub 20 v v Virkon 1 w v Do not use the following disinfectant types Disinfectants which are known to be corrosive to metals must not be used which include NaDcc such as Presept Hypochlorites such as Chlorasol Aldehydes such as Cidex Cationic Surfactants such as Benzalkonium Chloride Use of lodine such as Betadine will cause surface discoloration Concentrated Isopropyl alcohol based cleaners will degrade plastic parts The syringe and extension sets are disposable single use items and should be discarded after use according to their manufacturers instructions If the pump is to be stored for an extended perio
30. he induction RATE using the keys then press the OK softkey Ev wm Select the induction VOLUME using the keys then press the OK softkey If an incorrect value has been entered press the BACK softkey to return to the previous stage Enter the MAINTENANCE infusion rate using the keys then press the OK softkey 7 Review the induction data on screen then press CONFIRM If necessary use the BACK softkey to return to the data Once confirmed the pump will return to the main display po The induction can be cleared Stop the infusion then press the button Select CLEAR INDUCTION with the keys and press the OK softkey to confirm 1000DF00136 Iss 2 14 36 Basic Features Continued This option allovvs a Multidose to be set if enabled in configured options Press the 7 button to access the options menu Select the MULTIDOSE option using the keys Press the OK softkey indicated on the screen to confirm the selection Adjust the multidose RATE using the keys then press the OK softkey Ur de Mw Select the multidose VOLUME using the keys then press the OK softkey If an incorrect value has been entered press the BACK softkey to return to the previous stage Enter the MAINTENANCE infusion rate using the keys then press the OK softkey 7 Select the FREQUENCY hr mins of each multidose using the keys then press the OK softkey 8 Review the multidose data on screen then press CONFIRM If nece
31. he rate adjust options SET BY DOSERATE and SET BY ml h An arrow to the left of the rate display indicates the rate that will change when the keys are used to increase decrease the infusion rate To set a doserate precisely the arrow must be pointing to the doserate mg kg h the flowrate will be calculated from the doserate To accurately set a flowrate the arrow must be pointing to flowrate ml h the doserate will be calculated from the flowrate Selecting the Set By Doserate Option 1 Stop the infusion Press the 7 button to access the options menu 2 Select the SET BY DOSERATE option using the keys and press the OK softkey 3 This will select the set by doserate option and an arrow will automatically point to the doserate on the display If necessary the doserate can be increased or decreased using the keys Selecting the Set By Doserate Option 1 Stop the infusion Press the 7 button to access the options menu 2 Select the SET BY ml h option using the keys and press the OK softkey 3 This will select the set by flowrate option and an arrow will automatically point to the flowrate on the display If necessary the flowrate can be increased or decreased using the keys This option allows an Induction to be set if enabled in configured options Press the 7 button to access the options menu Select the INDUCTION option using the keys Press the OK softkey indicated on the screen to confirm the selection Adjust t
32. ice for examination by a qualified service engineer All preventative and corrective maintenance and all such activities shall be performed at a compliant work place in accordance with the information supplied Cardinal Health will not be responsible should any of these actions be performed outside the instructions or information supplied by Cardinal Health Refer to the Technical Service Manual for the access code for technical service features Interval Routine Maintenance Procedure As per Hospital Policy Thoroughly clean external surfaces of the pump before and after prolonged period of storage At least once per year 1 Inspect AC power supply plug and cable for damage Refer to TSM for 2 Perform functional tests as outlined in the Technical Service Manual identification of parts 3 Operate the pump on battery power until the battery low alarm then charge the battery to confirm battery operation and charging Please refer to Technical Service Manual for calibration procedures The units of measurement used in the calibration procedure are standard SI The International System of Units units Replacing the AC Fuses If the pump continually illuminates the battery symbol and the AC power indicator light does not illuminate when the pump is connected to the AC power supply and switched ON either the power supply fuse in the AC plug if fitted or the internal fuses have blown First check the power supply fuse in the AC
33. ins 0 5 10 15 20 25 30 35 Observation Window mins Start up Trend BD Plastipak 50ml 5 0ml h Trumpet Curve BD Plastipak 50ml 5 0ml h 11 0 10 0 9 0 8 0 7 0 L5 g 9 40 5 30 ui 2 0 1 0 0 0 1 0 10 0 58rkv Gu n mx sm mi 10 20 30 40 50 60 70 80 90 100 110 120 0 5 40 15 20 25 30 35 Time mins Observation Window mins 1000DF00136 Iss 2 30 36 Service Contacts For service contact your local Affiliate Office or Distributor AE Cardinal Health PO Box 5527 Dubai United Arab Emirates Tel 971 4 28 22 842 Fax 971 4 28 22 914 www cardinalhealth com international distributors alaris AU Cardinal Health 3 167 Prospect Highway PO Box 355 Seven Hills NSW 2147 Australia Tel 61 2 9838 0255 Fax 61 2 9674 4444 www cardinalhealth com au A Q l techservice au cardinal com BE Cardinal Health Leuvensesteenweg 248 D 1800 Vilvoorde Belgium Tel 32 2 267 38 99 Fax 32 2 267 99 21 VVVVVV Cardinalhealth com be al tech belux cardinal com CA Cardinal Health 235 Shields Court Markham Ontario L3R 8V2 Canada Tel 1 905 752 3333 Fax 1 905 752 3343 www cardinalhealth com ca CN Cardinal Health Shanghai Representative Office Suite 9B Century Ba Shi Building 398 Huai Hai Rd M Shanghai 200020 China Tel 56 8621 63844603 Tel 56 8621 63844493 Fax 56 8621 6384 40
34. inspection by a qualified service engineer When transporting or storing the pump use original packaging where possible and adhere to temperature humidity and pressure ranges stated in the Specifications section and on the outer packaging Latex Content ThelVAC P7000 Syringe Pump does not contain any Latex 1000DF00136 Iss 2 7 36 Getting Started Initial Set up Before operating the pump read this Directions For Use manual carefully 1 Check that the pump is complete undamaged and that the voltage rating specified on the label is compatible with your AC power supply 2 Items supplied are VAC P7000 Syringe Pump User Support CD Directions For Use AC Power Cable as requested 6 Protective Packaging 3 Connect the pump to the AC power supply for 24 hours to ensure that the internal battery is fully charged verify that the AC Power indicator is lit The pump will automatically operate from its internal battery if the pump is switched on without being connected to the AC power supply Prior to use on battery power verify the pump continues to function on battery power once disconnected from the AC power supply Should the pump fail to perform correctly replace in its original protective packaging where possible and contact a qualified service engineer for investigation Pole Clamp Installation The pole clamp is supplied fitted to the rear of the pump and will provide secure fixing to standar
35. ith no additional fluid pressure The result is that the pressure relating to the lovv forces vvill be less than the nominal quoted occlusion pressure Bolus volume following occlusion will be minimised by the back off feature if enabled The back off will reduce the line pressure by removing the volume stored in the occluded extension set and deducting this volume from volume infused The following tables show the worst case values for line pressure time to alarm and bolus volume that can be expected in the event of an occlusion when the IVAC 50ml syringe is selected G30402M administration set Alarm Pressure Rate ml h Maximum time Nominal occlusion Maximum bolus mmHg to occlusion alarm alarm pressure volume ml h min mmHg 50 1 0 0 06 50 25 25 0 2 100 1 0 0 12 100 25 25 0 3 200 1 0 0 26 200 25 25 0 4 300 1 0 0 36 300 25 25 0 6 400 1 0 0 54 400 25 25 0 8 500 1 0 1 10 500 28 28 1 0 600 1 0 1 20 600 31 31 1 2 750 1 0 1 40 750 35 35 1 4 50 5 0 0 03 50 25 25 0 2 100 5 0 0 04 100 25 25 0 3 200 5 0 0 06 200 25 25 0 4 300 5 0 0 09 300 25 25 0 6 400 5 0 0 12 400 25 25 0 8 500 5 0 0 14 500 28 28 1 0 600 5 0 0 16 600 31 31 12 750 5 0 0 20 750 35 35 1 4 1000DF00136 Iss 2 28 36 RS232 and Nurse call Specification RS232 Nurse call Feature The RS232 Nursecall feature fitted to this IVAC P7000 Syringe Pump allows the pump to be monitored remotely and or contr
36. mains plug if fitted If the AC power indicator light does not illuminate remove the pump from service It is recommended that only a qualified service engineer replaces the AC fuses For further information regarding the replacement of internal AC fuses refer to the Technical Service Manual If the fuses continue to blow suspect an electrical fault and have the pump and power supply checked out by a qualified service engineer Battery Operation The internal rechargeable battery allows continued operation when the AC power is unavailable for example during patient transfer or AC power failure A fully charged battery will provide over 4 hours of operation at typical infusion rates From the battery low alarm it will take about 24 hours to fully charge when reconnected to the AC power supply whether the pump is in use or not The battery is maintenance free Sealed Lead Acid and requires no routine servicing However to achieve optimum operation ensure that the battery is fully recharged after full discharge before storage and at regular 3 month intervals during storage Cardinal Health recommend verification that the pump operates on battery power once the pump has been removed from the AC power supply refer to Starting the Pump section Charge retention will eventually degrade Where retention is critical the internal battery should be replaced every 3 years It is recommended that only a qualified service engineer replaces t
37. nect the pump to the AC power source 2 NEW PATIENT Answering NO will retain all previous rate and volume settings YES will automatically clear patient information including resetting the rate and volume settings to zero 3 LOAD SYRINGE Load the syringe according to the procedure in this manual 4 Insert the pressure disc into the pressure transducer PRESSURE TRANSDUCER Detects if an extension set with a pressure disc is fitted The pressure transducer will measure positive extension set pressures Warning To remove or insert pressure disc from or into pressure transducer assembly insert finger into the recess in the pressure disc and pull forward or push back with care DO NOT PULL THE EXTENSION SET TO REMOVE OR TO INSERT THE PRESSURE DISC 5 CONFIRM SYRINGE Check that the syringe type and size being used matches the display If required the make of syringe can be changed by pressing the TYPE button Press CONFIRM when the correct type and size are shown 6 INFUSION RATE Check the rate shown if old patient data has been retained and change the rate if necessary using the keys 7 PURGE if required Press the 16 button and then press and hold the PURGE softkeys until fluid flows and the purging of the syringe extension set is complete Release the softkeys The volume used during purging will be displayed Purge extension set massaging pressure disc to prevent ballooning and ensuring all air removal 8
38. ng a Syringe T Technical Service Manual 31 Test 26 Titration 22 Transducer 2 3 10 16 27 See also Pressure transducer Trumpet Curves 30 V Volume Infused 3 22 Volume to be Infused See VTBI VTBI 13 14 15 16 22 W Warnings 16 Warranty 33 VVeight 22 VVorkstation 31 33 36 Page Intentionally Left Blank 1000DF00136 Iss 2 34 36 Page Intentionally Left Blank 1000DF00136 Iss 2 35 36 Page Intentionally Left Blank 1000DF00136 Iss 2 36 36 CardinalHealth IVAC is a registered trademark of Cardinal Health Inc or one of its subsidiaries All other trademarks belong to their respective owners 2000 2008 Cardinal Health Inc or one of its subsidiaries All rights reserved 1000DF00136 Issue 2 This document contains proprietary information of Cardinal Health Inc or one of its subsidiaries and its receipt or possession does not convey any rights to reproduce its contents or to manufacture or sell any product described Reproduction disclosure or use other than for the intended purpose without specific written authorization of Cardinal Health Inc or one of its subsidiaries is strictly forbidden Cardinal Health 1180 Rolle Svvitzerland www cardinalhealth co uk alaris
39. olled via a suitable central monitoring or computer system When the pump is started by a command from the serial interface communication must take place over the serial interface a communication must take place every 15 seconds or the pump will alarm display communications failure and stop infusing This failure protects against failure of the communications including the removal of the RS232 cable The nurse call interface provides a remote backup to the internal audible alarm It should not be relied upon to replace monitoring of the internal alarm Refer to the Technical Service Manual for further information regarding the RS232 interface Since it is possible to control the syringe pump using the RS232 interface at some distance from the pump and hence remote from the patient responsibility for the control of the pump is vested in the software run on the computer control system The assessment for the suitability of any software used in the clinical environment to control or receive data from the pump lies with the user of the equipment This software should include detection of the disconnection or other failure of the RS232 cable The protocol is detailed in the Technical Service Manual and is for general information only This relates to IVAC P7000 Syringe Pumps fitted with the RS232 communication interface Any connected analogue and digital components are required to meet IEC EN60950 for data processing and IEC EN60601 for medical devi
40. olume 0 5ml PVC Y Syringe Extension Set with back check valve and 2 clamps 178 cm Priming Volume 1 5ml rm b D 30842E PVC Syringe Extension Set with back check valve Y Site and clamp 32 cm Priming Volume 1 2ml ez MR x PVC Y Syringe Extension Set with anti siphon valve back check valve and 2 clamps 183 cm Priming Volume 1 8ml D d 7 2 eee PVC Syringe Extension Set vvith anti siphon valve and clamp 156 cm Priming Volume 0 6ml t is recommended that extension sets are changed in accordance vvith the Directions for Use Carefully read the Directions For Use supplied vvith the extension set prior to use Please note these dravvings are not to scale 1000DF00136 Iss 2 25 36 Routine Maintenance Procedures To ensure that this pump remains in good operating condition it is important to keep it clean and carry out the routine maintenance procedures described below All servicing should only be performed by a qualified service engineer with reference to the Technical Service Manual TSM Circuit diagrams and components parts lists and all other servicing information which will assist the qualified service engineer in performing repair of the parts designated as repairable are available upon request from Cardinal Health If the pump is dropped damaged subjected to excessive moisture or high temperature immediately take it out of serv
41. ormal use and service for a period of two 2 years from the date of delivery by Cardinal Health to the original purchaser B Each new accessory is free from defects in material and workmanship under normal use and service for a period of ninety 90 days from the date of delivery by Cardinal Health to the original purchaser C Each Mains Cable Battery Flow Sensor ECD and non disposable probe is free from defects in material and workmanship under normal use and service for a period of ninety 90 days from the date of delivery by Cardinal Health to the original purchaser D Each new Thermometer is free from defects in material and workmanship under normal use and service for a period of one 1 year from the date of delivery by Cardinal Health to the original purchaser If any product requires repair during the applicable warranty period the purchaser should communicate directly with its local Cardinal Health service centre to determine the appropriate service facility Except as provided otherwise in this warranty repair or replacement will be carried out at Cardinal Health s expense The product requiring service should be returned promptly properly packaged and postage prepaid by purchaser Loss or damage in return shipment to Cardinal Health shall be at purchaser s risk In no event shall Cardinal Health be liable for any incidental indirect or consequential damages in connection with the purchase or use of any Cardinal Health product
42. re set Volume To Be Infused is complete AC Power has been disconnected and the pump is operating on battery power Reconnect AC power supply or press the button to silence the alarm and continue with battery operation The alarm will automatically cancel if the AC power supply is reconnected The alarm system has detected an internal malfunction Note the malfunction code Remove pump from service for examination by a qualified service engineer Three beeps will sound if the pump has been left on for more than 2 minutes without starting the operation Press the J button to silence the alarm for a further 2 minutes Alternatively press and hold down the button and wait for 3 beeps in succession this will put the warning alarm on standby for 15 minutes 1000DF00136 Iss 2 16 36 Configured Options This menu comprises a list of options vvhich are configurable by the user 1 Turn the pump OFF 2 Whilst holding down the EJ button turn the pump ON 3 The main display will show 000 Enter the access code for Configured Options using the keys pressing NEXT to move through the digits A full list of access codes can be found in the Technical Service Manual 4 When the complete code shows on screen press OK to enter The Configured Options menu will be displayed General Options Select GENERAL OPTIONS from the menu using the keys and press the OK softkey Select the option required to be enabled disabled or adjust and press
43. s UR ADJUST REVIEW DATA 1000DF00136 Iss 2 12 36 Basic Features Continued Drugs and Dosing The follovving options enable the pump to be set up for use vvith a specific drug and or dosing protocol Drugs are pre configured in a drug library see Configured Options to enable rapid selection of the drug name dosing units and default rate For increased security using a configured drug maximum and minimum safety limits are programmable for concentration and dose rates To access the Drugs and Dosing menu 1 Press the 7 button to first access the options menu 2 Select DRUGS AND DOSING from the list using the keys 3 Press the OK softkey to confirm the selection The mass infused display is a sum of all drug masses infused which may be of different concentrations and even drug type Therefore it should be noted that the relationship between currently displayed volume infused and mass infused may not directly relate to the current concentration Drug Name Only 1 Select a drug name from the list and press the YES softkey 2 If no protocol is required press the NO softkey 3 If no dosing is required press the NO softkey Pre configured drug dosing protocol Select the drug name from the list displayed using the keys Press the YES softkey to confirm the selection Press the YES softkey indicated on the screen to select DOSING Press the YES softkey to select PROTOCOL This will select the pre defined pro
44. should always be infusing and always attached to the patient Drugs given by an IV bolus could achieve immediate and high drug concentration levels Bolus can be used at the start of an infusion or during an infusion If the volume of the bolus reaches the bolus volume limit the bolus will stop and the pump will automatically revert to infuse at the set rate If the volume to be infused is reached during a bolus the volume to be infused complete alarm will operate and the pump will revert to its previous state Press MUTE to stop the alarm or CANCEL to acknowledge the alarm A Bolus cannot be administered if the RATE LOCK is active or if a multidose set up is in use During BOLUS the pressure limit alarm is temporarily increased to the maximum level 1 During infusion press the 168 button once to display 1 the bolus screen 2 Use the keys to adjust the bolus rate if required 3 To deliver the bolus press and hold the BOLUS softkeys During the bolus the volume being infused BOLUS is displayed When the desired bolus volume has been S 1200 delivered or the bolus volume limit is reached release V 9 the softkeys The bolus volume is added to the total volume infused Press the QUIT softkey to exit back to the main display 1000DF00136 Iss 2 11 36 Basic Features Continued Pressure Level vvith pressure set fitted 1 To check and adjust the pressure level press the button Bar graph will be displayed showing the pre
45. ssary use the BACK softkey to return to the data Once confirmed the pump will return to the main display The review section of the display will show either multidose volume remaining or time between multidoses remaining The multidose can be cleared Stop the infusion then press the 7 button Select CLEAR MULTIDOSE with the keys and press the OK softkey to confirm so 24 Hour Log This option allows the 24 hour log of volume infused to be reviewed Press the button to access the options menu Select the 24H LOG option using the keys and press the OK softkey Press the NEXT softkey to access the hourly volume infused log Press the QUIT softkey to exit the log PWN Event Log This option allows the event log to be reviewed 1 Press the button to access the options menu 2 Select the EVENT LOG option using the keys and press the OK softkey 3 Scroll through the log using the keys Press the QUIT softkey to exit the log Rate Lock If Rate Lock is enabled when the infusion rate has been set and the infusion started or following a bolus infusion the rate lock prompt will appear on the main display To select the rate lock function press the YES softkey Press the NO softkey if the rate lock is not required When rate lock is enabled the following are unavailable Changing the infusion rate Bolus purge Switching the pump off VTBI over time infusions To disable the rate lock if select
46. ssure alarm level and current pressure level LINE PRESSURE g ADJUST 2 Press the keys to increase or decrease the pressure alarm level The new level will be indicated on the display 3 The AUTO Pressure feature may be used when a stable pressure has been achieved over a short period of infusion If AUTO Pressure has been enabled the automatic pressure alarm level is calculated and set by pressing the AUTO softkey 4 Press the QUIT softkey to exit the pressure screen LINE PRESSURE a 89 us ADJUST Pressure Level without pressure set fitted not applicable when FULLY DEDICATED 1 To check and adjust the pressure level press the 4 button A bar graph will be displayed showing the pressure alarm level and the current pressure level 2 Press the keys to increase or decrease the alarm level The new level will be indicated on the display 3 Press QUIT to exit the screen The interpretation of pressure readings and occlusion alarms are the responsibility of the clinician depending on the specific application PUMPING PRESSURE 7 gt ADJUST To review the protocol data press the REVIEW softkey The protocol data will be displayed in the main display Press the REVIEW softkey to toggle between the pressure setting and the VTBI status Je CES Repeat until the protocol data required is displayed in the main display INFUSING SYRINGE NAMEZ VOLUME PRESSURE 10 0 O
47. the pump is connected to AC power Battery life is typically 4h from fully charged 5 0ml h and 20 C under normal conditions Charging takes 10 hours from discharge to 80 charge and 24 hours to 100 charge Memory Retention The electronic memory of the pump will be retained for more than 6 months when not powered up AC Power Supply 115 230VAC 50 60Hz 20VA nominal Dimensions 400mm w x 115mm h x 180mm d Weight 3 5 kg excluding pole clamp and power cable Protection against fluid ingress IPX4 Protected against splashing fluid Alarm Conditions Drive Declutched Occlusion Check Syringe Location Battery Low Battery Empty Near End Of Syringe VTBI Done Internal Malfunction Pressure Set Not Fitted Syringe Empty AC Power Fail Attention Nurse Callback Check Plunger Location Line Occlusion Environmental Specifications 5 C 40 C 30 90 700hPa 1060hPa 20 C 50 C Transport amp Strorage Relative Humidity 5 95 Transport amp Strorage Atmospheric Pressure 600hPa 1060hPa Electrical Mechanical Safety Complies with IEC EN60601 1 and IEC EN60601 2 24 EMC Complies with IEC EN60601 1 2 and IEC EN60601 2 24 Operating Temperature Operating Relative Humidity Operating Atmospheric Pressure Transport amp Strorage Temperature 22 36 Compatible Syringes The pump is calibrated and labelled for use vvith single use disposable Luer lock syringes Only use the siz
48. the infusion and generate visual and audible alarms Users must perform regular checks to ensure that the infusion is progressing correctly and no alarms are operating 1000DF00136 Iss 2 6 36 Operating Precautions continued Electromagnetic Compatibility amp Interference This pump is protected against the effects of external interference including high energy radio frequency emissions magnetic fields and electrostatic discharge for example as generated by electrosurgical and cauterising equipment large motors portable radios cellular telephones etc and is designed to remain safe when unreasonable levels of interference are encountered This pump is a CISPR 11 Group 1 Class A device and uses RF energy only for its internal function in the normal product offering Therefore its RF emissions are very low and are not likely to cause any interference with the nearby electronic equipment However this pump emits a certain level of electromagnetic radiation which is within the levels specified by IEC EN60601 1 2 and IEC EN60601 2 24 If the pump interacts with other equipment measures should be taken to minimise the effects for instance by repositioning or relocation n some circumstances the pump may be affected by an electrostatic discharge through air at levels close to or above 8kv or by radio frequency radiation close to or above 10v m If the pump is affected by this external interference the pump will remain in a s
49. the priming procedure specified herein Operating Environment When using any infusion pump in conjunction with other pumps or devices requiring vascular access extra care is advised Adverse delivery of medication or fluids can be caused by the substantial variation in pressures created within the local vascular system by such pumps Typical examples of those pumps are used during dialysis bypass or cardiac assist applications This pump is suitable for use in Hospital and clinical environments other than domestic establishments and those directly connected to the public single phase AC mains power supply network that supplies buildings used for domestic purposes However it may be used in domestic establishments under the supervision of Medical professionals with additional necessary appropriate measures Consult Technical Service Manual appropriately trained technical personnel or Cardinal Health for further information This pump is not intended to be used in the presence of a flammable anaesthetic mixture with air or oxygen or nitrous oxide Operating Pressure This is a positive pressure pump designed to achieve very accurate fluid administration by automatically compensating for resistance encountered in the infusion system The pumping pressure alarm system is not designed to provide protection against or detection of IV complications which can occur Alarm Conditions Several alarm conditions detected by this pump will stop
50. the pump has delivered the set volume it vvill alarm Press the CANCEL softkey to clear the alarm Press the CLEAR softkey to turn the VTBI function off or set a new VTBI using the keys Clear Volume This option enables the volume infused to be cleared Oy Oy VERS M 1 Press the 7 button to access the options menu 2 Select the CLEAR VOLUME option using the keys and press the OK softkey indicated on the screen 3 Press the YES softkey to clear the volume Press the NO softkey to retain the volume 1000DF00136 Iss 2 13 36 Basic Features Continued 7 Set VTBI over Time This option allows a specific VTBI and delivery time to be set if enabled in configured options The rate necessary to deliver the required volume within the specified time is calculated and displayed Stop the infusion Press the Z button to access the options menu 2 Select the SET VTBI OVER TIME option using the keys and press the OK softkey 3 Adjust the volume to be infused using the keys When the desired volume has been reached press the OK softkey 4 Enter the time over which the volume is to be infused The infusion rate will automatically be calculated Press the OK softkey to enter the value 5 Select the rate at VTBI end from the list using the keys and press the OK softkey The default is STOP Set by Doserate Set by ml h To set rates accurately in doserate or flowrate increments it may be necessary to switch between t
51. this dead space will not be infused Place the pump on a stable horizontal surface or secure as described above Prepare load and prime the single use disposable syringe and extension set using standard aseptic techniques 1 Squeeze the finger grips on the plunger holder and slide the mechanism to the left Lift the syringe clamp and rotate clockvvise 2 Insert the syringe into the slots on the plunger holder 3 Squeeze the finger grips on the plunger holder and slide the mechanism to the right until the syringe finger flanges locates in the V slot Gently advance the syringe until the finger flanges touch the front of the V slot closest to the syringe clamp This is important to prevent delay at the start of the infusion 4 Rotate the syringe clamp anticlockwise until it locks onto the syringe barrel to secure the syringe 5 Check that the syringe plunger and finger flanges are correctly located in their slots aint S ID 1000DF00136 Iss 2 9 36 Getting Started Continued Starting the Pump Connect the pump to an AC power supply using the AC power cable Press the button e The pump will run a short self test Ensure that two beeps are activated during this test Check the display test pattern and ensure that rovvs are missing Prior to beginning an infusion disconnect the pump from the AC power supply confirm the pump continues to function on battery power Then recon
52. tocol for the selected drug Enter the dosing information prompted on the display for the selected drug using the OK softkey Press the CONFIRM softkey to enter the drug name dosing information and the protocol selected UY de M c When a protocol is used the drug name will be followed by an The set by ml h set by doserate option is now available User programmed drug dosing Select the drug name from the list displayed using the keys Press the YES softkey to confirm the selection Press the YES softkey to select DOSING This now enables user programmed information to be entered Press the NO softkey to avoid selecting PROTOCOL Enter the required dosing information as prompted on the display using the keys and the OK softkey Press the CONFIRM softkey to enter the drug name dosing information and the protocol selected o Us dro Volume to be infused VTBI This option allovvs a specific volume to be infused to be set The rate at the end of this VTBI can also be set selecting from stop 1ml h 2ml h or continuous infusion at the set rate Press the 7 button to access the options menu Select the SET VTBI option using the keys and press the OK softkey indicated on the screen Enter the volume to be infused using the keys and press the OK softkey Select the rate at the end of the VTBI using the keys to scroll through the on screen choices The default is STOP Press the OK softkey to exit the VTBI menu VVhen

Download Pdf Manuals

Related Search

Related Contents

GIS Platforms for WINCE\374  広報621号  KOHLER K-14461-BN Installation Guide  

Copyright © All rights reserved. Failed to retrieve file