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Graseby Instruction Manuals This publication has been compiled and approved by Graseby Medical Ltd for use with their respective products. It is supplied in this format to permit users to access the text and illustrations for their own use e.g. training and educational purposes. Users of the equipment must ensure that they have read and understood the contents of the complete manual including the warnings and cautions and have been trained in the correct use of the product. Graseby Medical Ltd cannot be held responsible for the accuracy and any resulting incident arising from information that has been extracted from this manual and compiled into the users documentation. These manuals are subject to revision and it is the users responsibility to ensure that the correct version of manual/ text/illustration is used in conjunction with the equipment.

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Page 1: Graseby Instruction Manuals

Graseby Instruction Manuals

This publication has been compiled and approved by Graseby Medical Ltd for use with their respective products. It is supplied in this format to permit users to access the text and illustrations for their own use e.g. training and educational purposes.

Users of the equipment must ensure that they have read and understood the contents of the complete manual including the warnings and cautions and have been trained in the correct use of the product.

Graseby Medical Ltd cannot be held responsible for the accuracy and any resulting incident arising from information that has been extracted from this manual and compiled into the users documentation.

These manuals are subject to revision and it is the users responsibility to ensure that the correct version of manual/text/illustration is used in conjunction with the equipment.

Page 2: Graseby Instruction Manuals

I n s t r u c t i o nM a n u a l

M o d e l 5 0 0a n d M i c ro 5 0 5Vo l u m e t r i cI n f u s i o nP u m p

Page 3: Graseby Instruction Manuals

Published by Graseby Medical Limited.

All possible care has been taken in the preparation of this publication, but GrasebyMedical Limited accepts no liability for any inaccuracies that may be found.

Graseby Medical reserves the right to make changes without notice both to thispublication and to the product which it describes.

Copyright © 2002 Graseby Medical Limited

No part of this publication may be reproduced, transmitted, transcribed, or stored ina retrieval system or translated into any human or computer language in any form orby any means without the prior permission of Graseby Medical Limited.

GRASEBY MEDICAL LIMITEDColonial Way,Watford,Hertfordshire,United Kingdom,WD24 4LG

Telephone: +44 (0)1923 246434Facsimile: +44 (0)1923 231595

http://www.graseby.co.uk

Registered in England. Company number 995550

Trademarks and acknowledgements:Graseby and Smiths are registered trademarks of the Smiths Group plc.All other trademarks are acknowledged as the property of their respective owners.

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V o l u m e t r i c I n f u s i o n P u m p s

G r a s e b y M e d i c a l L t d . W a r n i n g s a n d C a u t i o n s

Warnings tell you about dangerousconditions, that could lead to death orserious injury to the user or patient, thatcan occur if you do not obey all of theinstructions in this manual.1. WARNING: You should ensure that the

performance offered by the pump is fit for theintended purpose. Failure to do so may resultin compromised function of the product,patient injury or user injury.

2. WARNING: Do not use a faulty pump. If thepump detects a fault when it is first turned on,or if it develops a fault during operation then acontinuous system alarm sounds. The pumpmust be referred to a suitably qualifiedtechnician or returned to Graseby Medical inorder to have the fault rectified.

3. WARNING: Before using the pump, it should beinspected for physical damage. The pumpshould not be used if damage is evident, andshould be returned to service personnel forrepair before being returned to use. Failure todo so may result in compromised function ofthe product, patient injury or user injury.

4. WARNING: Do not use the pump if you detectany cracks, chips and loose or bent parts, orif the buttons do not move in and out freelywhen they are pressed. Failure to do so couldcause inadvertent disconnection of the pumps.

5. WARNING: Do not push or pull on the pumps,or the IV pole may tip over or the pumps fallto the floor. Do not try to remove modularconnected pumps from the IV pole whilst theyare joined together. Either of these couldcause the administration set to separate fromthe fluid container thus spilling themedication, or the pumps themselves could bedamaged.

6. WARNING: Correct entry of data is essential inorder to ensure that the intended infusion isperformed. Before confirming any displayeddata when setting up an infusion, you shouldensure that it is correct. Failure to do so mayresult in compromised function of the product,patient injury or user injury.

7. WARNING: Dose-rate calculation requirescare in entering data. Refer to specific productdrug labelling for information on appropriateadministration techniques and dosages.Entering incorrect data may result in patientinjury or death.

8. WARNING: When delivering drugs in theepidural space, use only those medicationsspecifically indicated for epidural use.Epidural administration of other drugs couldresult in serious patient injury or death.

9. WARNING: The use of administration setsincorporating injection sites could lead to animproper or inappropriate infusion resulting inserious patient injury or death.

10. WARNING: Failure to clearly identify the pumpand administration sets could lead to animproper or inappropriate infusion resulting inserious patient injury or death.

11. WARNING: Remove any air to prevent airembolism. The presence of air within theinfusion can result in complications resultingin patient injury or death.

12. WARNING: To avoid over infusion, do notprime the infusion line when the admini-stration set is connected to the patient. Overinfusion can result in patient injury or death.

13. WARNING: The Occlusion alarm level must bechecked before starting an infusion to ensurethat it is appropriate for the infusion. Failureto do so may result in an unacceptably slowtime to Occlusion alarm, resulting in patientinjury or death.

14. WARNING: Prior to starting an infusion,inspect the fluid path for kinks, a closed clampor other obstructions. Failure to do so mayresult in the infusion not being deliveredcorrectly, resulting in patient injury or death.

15. WARNING: If using a blood pressure cuff abovethe patient’s venipuncture site take extra carein setting the Occlusion alarm pressures.Failure to do so may result in unnecessaryOcclusion alarms, resulting in patient injuryor death.

16. WARNING: The Occlusion detection systemmeasures downline pressure in the admini-stration set, but does not detect infiltration. Inaccordance with local protocol, you mustperiodically inspect the patient’s infusion sitefor signs of infiltration. Failure to do so mayresult in an unacceptably slow time toOcclusion resulting in patient injury or death.

17. WARNING: If an Occlusion alarm occurs,immediately clamp the line to the patient. Theninspect the fluid pathway to determine whathas caused the obstruction. An unintentionalbolus of medication can result in patient injuryor death.

Warnings

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W a r n i n g s a n d C a u t i o n s G r a s e b y M e d i c a l L t d .

18. WARNING: Do not run parallel infusion linesbelow the pump. Delivering a Secondaryinfusion means running a second line abovethe pump. Failure to do so may result in aninaccurate delivery of medication, resulting inpatient injury or death.

19. WARNING: Check the Secondary set carefully,since an occlusion above the pump on theSecondary line could cause the Primary fluidto be delivered instead of the Secondaryinfusion. Administering the wrong medicationmay cause serious patient injury or death.

20. WARNING: The Secondary volume to be infusedmust match the amount of fluid in thesecondary container. Primary flow resumeswhen the secondary container is empty. If thevolumes do not correspond, the wrong infusionmay be delivered which could cause seriouspatient injury or death.

21. WARNING: Correct management of batterycharging, as described in this documentationis essential to ensure that the pump canoperate on battery for the time specified.Failure to do so may result in compromisedfunction of the product or patient injury.

22. WARNING: If a backup alarm sounds, the pumpshould be immediately removed from thepatient and sent to be repaired by a GrasebyMedical qualified technician. Failure to do somay cause patient injury or death.

23. WARNING: Failure to use the power cordretainer means that the pump may beaccidentally or erroneously disconnected from

the mains. Although there is a battery backupin case this happens, the battery may not becharged sufficiently. Consequently, there is arisk of the pump not functioning which couldlead to patient injury or death.

24. WARNING: Do not open the pump housing.Refer all service faults only to qualifiedtechnical personnel. Opening the pumphousing may cause electric shock leading topatient or user injury or death.

25. WARNING: When the pump is carrying out aninfusion, to ensure that electrical safety ismaintained, only items of equipment thatconform to EN60950 are to be connected to theRS232 connector situated at the back of thepump, otherwise patient safety may becompromised.

26. WARNING: While Graseby Medical Limitedhave taken all reasonable steps to ensure thatthe pump operates correctly while underremote control, it is the responsibility of theperson who designs and implements thecontrolling device to ensure that the resultingsystem (pump and controlling device) is fit forits intended purpose. Failure to do so mayresult in compromised function of the product,patient injury or user injury.

27. WARNING: Use only Graseby Medicaladministration sets with this product. Failureto do so may result in compromised systemaccuracy leading to complications resulting inpatient injury or death.

Cautions tell you about dangerousconditions that can occur and cause damageto the pump if you do not obey all of theinstructions in this manual.

1. CAUTION: Refer all service, repair andcalibrations only to qualified technicalpersonnel. Unauthorised modifications to thepump must not be carried out.

2. CAUTION: Do not autoclave, steam sterilize,ETO sterilise or subject the pump totemperatures in excess of 55° C (131° F).Excessive temperatures may cause damage tothe pump.

3. CAUTION: To prevent serious damage to thepump it must not be immersed in any liquids orexposed to strong organic solvents. Wipe offspills immediately. Do not allow fluid orresidues to remain on the pump. Additionally,

Caut ionsthe pump is not designed to allow it to besterilised. Failure to observe these cautionsmay cause internal damage to the pump.

4. CAUTION: Carry out periodic cleaningfollowing the detailed instructions in theVolumetric Infusion Pumps Service Manual. Donot use unapproved cleaning agents.

5. CAUTION: When turning the pump on, ifscreens similar to those illustrated are notdisplayed, do not use the pump, and send thepump to authorised service personnel.

6. CAUTION: Only carry the pump by the handle.Failure to do so may result in damage to thepump, or the pump may be dropped whichcould cause internal damage to the pump.

7 CAUTION: The backlight has a limited life andmay, if used constantly, cause the light to dim.Eventually the message display may then needto be replaced. To preserve the life of themessage display, you should only turn on theMessage Display Light as described here if itis specifically required. Misuse of this featurecould lead to both battery and LCD depletion.

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C o n t e n t s

Contents

New features of version 0.71 software .............................................................. v

Chapter 1 - IntroductionIntroduction to the 500/505 pumps ............................................................. 1 - 1

Model 500 Volumetric pump ............................................................................... 1 - 1

Micro 505 Volumetric pump ................................................................................ 1 - 1

Epidural administration ...................................................................................... 1 - 2

Pump features .................................................................................................... 1 - 3

Chapter 2 - Operat ing the pumpIntroduction .................................................................................................. 2 - 1

Who should read this chapter ............................................................................ 2 - 1

What this chapter covers .................................................................................... 2 - 1

Front of the pump ........................................................................................ 2 - 2Indicators and displays ....................................................................................... 2 - 2

Programming keys ............................................................................................. 2 - 3

Rear of the pump ......................................................................................... 2 - 4Connecting the pumps to an IV pole .......................................................... 2 - 5

Switching on ....................................................................................................... 2 - 7

Switching the pump on and off ................................................................... 2 - 7Switching off ....................................................................................................... 2 - 8

Using the pump on battery ................................................................................. 2 - 8

Sounds on the Volumetric ......................................................................... 2 - 10Audio alarm ......................................................................................................2 - 10

Quiet Pump mode .............................................................................................2 - 11

Alarms and computer control ...........................................................................2 - 11

Types of infusion ....................................................................................... 2 - 12Primary .............................................................................................................2 - 12

Primary and Secondary ....................................................................................2 - 13

Primary and Bolus ............................................................................................2 - 14

Ending a Secondary infusion ...........................................................................2 - 14

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The effect of Options settings on infusions ............................................. 2 - 15Infusing with Rate and VTBI limits enabled ......................................................2 - 15

Setting up a Primary Infusion ................................................................... 2 - 16Prepare the solution .........................................................................................2 - 16

Prime the administration set - Example ...........................................................2 - 17

Load the cassette into the pump ......................................................................2 - 18

Setting the Occlusion Alarm .............................................................................2 - 18

Primary infusion 5 or 6-Step Setup ..................................................................2 - 19

During the infusion .................................................................................... 2 - 20If the infusion will not start running ...................................................................2 - 20

Infusion information displays ............................................................................2 - 21

Running Rate Change (Rate titration) .............................................................2 - 21

Security on the pump........................................................................................2 - 22

Display the Drug Label .....................................................................................2 - 23

Stop the infusion ...............................................................................................2 - 23

If an occlusion is detected ................................................................................2 - 23

Change the Occlusion alarm setting ................................................................2 - 24

Ending the Primary infusion ..................................................................... 2 - 25KVO infusion .....................................................................................................2 - 25

About Secondary Infusions ....................................................................... 2 - 26Setting up a Secondary infusion ......................................................................2 - 26

Lower the Primary solution container ..............................................................2 - 27

Prime the Secondary administration set ..........................................................2 - 27

Connect the Secondary to the Primary administration set ...............................2 - 28

About the Secondary Volume to be Infused .....................................................2 - 28

Program the Secondary infusion ......................................................................2 - 29

Secondary infusion - Bolus enabled ................................................................2 - 30

Running a Bolus infusion.......................................................................... 2 - 31Ending a Secondary infusion ...........................................................................2 - 32

Ending a Bolus infusion ...................................................................................2 - 32

Checking infusion totals ............................................................................ 2 - 33Total Volume infused ........................................................................................2 - 33

Primary totals ....................................................................................................2 - 34

Secondary totals ...............................................................................................2 - 34

Bolus totals .......................................................................................................2 - 34

Re-running infusions at the same rate .............................................................2 - 35

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C o n t e n t s

Chapter 3 - OptionsIntroduction .................................................................................................. 3 - 1

Options available ................................................................................................ 3 - 1

Using options ...................................................................................................... 3 - 2

1. Standard Message................................................................................... 3 - 32. Time Remaining ...................................................................................... 3 - 3

3. Message Display Light ............................................................................ 3 - 4Turning the light on and off ................................................................................. 3 - 4

4. Battery Test .............................................................................................. 3 - 5Using the Battery Test option .............................................................................. 3 - 5

5. Quick Rate Change ................................................................................. 3 - 7Performing Quick Rate Changes........................................................................ 3 - 7

6. Rate Taper ................................................................................................ 3 - 8To enter Rate Taper ............................................................................................ 3 - 9

To exit Rate Taper ............................................................................................... 3 - 9

To program a Rate Taper by ‘Total Time’ ..........................................................3 - 10

To program a Rate Taper by ‘Maximum Rate’ ..................................................3 - 12

Using the ‘End Early’ feature ............................................................................3 - 14

Resuming, restarting or reprogramming the Rate Taper .................................3 - 15

Programming or reprogramming the Rate Taper with Limits set .....................3 - 16

7. Volume Over Time (VOT) ....................................................................... 3 - 17To use Volume Over Time .................................................................................3 - 18

8. Dose-Rate Calculation ........................................................................... 3 - 19Dose-Rate Calculation Recovery ....................................................................3 - 19

To enter or exit Dose-Rate Calculation ............................................................3 - 20

Dose-Rate Calculation steps ...........................................................................3 - 20

Dose-Rate Calculation programming example ...............................................3 - 23

Changing the dosing rate without stopping the infusion .................................3 - 25

Changing the infusion rate without stopping the infusion ...............................3 - 26

Dose or rate change alarms .............................................................................3 - 27

Programming or reprogramming Dose-Rate Calculation with Limits set ........3 - 28

Setting Rate and VTBI limits...................................................................... 3 - 29Minimum and Maximum Infusion Rates ...........................................................3 - 29

To set the minimum and maximum infusion rate ..............................................3 - 30

Maximum VTBI ..................................................................................................3 - 31

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C o n t e n t s G r a s e b y M e d i c a l L t d .

To set the maximum infusion volume ............................................................... 3 - 31

Programming and running infusions with limits ...............................................3 - 32

KVO rate ...................................................................................................... 3 - 33Setting a KVO rate ............................................................................................3 - 33

Drug Label .................................................................................................. 3 - 34Drug Library ......................................................................................................3 - 34

Checking the current drug label .......................................................................3 - 35

Selecting a new drug label ...............................................................................3 - 35

Clearing the drug label .....................................................................................3 - 36

Chapter 4 - TroubleshootingIntroduction .................................................................................................. 4 - 1

What’s in this chapter .......................................................................................... 4 - 1Who should read this chapter ............................................................................ 4 - 1

Handling problems with the pump ............................................................. 4 - 2

Pump Messages ........................................................................................... 4 - 3Pump will not switch on ...................................................................................... 4 - 3

Programming Messages with alarms ................................................................. 4 - 3

Warning Messages with alarms ......................................................................... 4 - 3

Warning Messages with no alarms .................................................................... 4 - 7

Instrument Care ............................................................................................ 4 - 8

Specifications/StandardsSpecifications.............................................................................................. S - 1

Standards .................................................................................................... S - 9

Trumpet curves ......................................................................................... S - 10

AppendixNurse-Call Feature ....................................................................................... A - 1

Index

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v

C o n t e n t s

The information in this section isintended for technicians and cliniciansalready familiar with earlier versionsof the Graseby 500/505 volumetricpump. It summarises the changes tothe pump that appear with version 0.71of the pump software:• new menu,• new options,• new features that the menu and

options provide.To find out the software version of aparticular pump, check the instructionslabel on the right side of the pump. Ifthere are more than eight optionslisted, then the software version is 0.71or later.

For full details on how to use the pumpsee the Volumetric Instruction Manual.For information on configuring thepump, see the Technical User Manual,and for more detailed technicalinformation, obtain a copy of theVolumetric Service Manual.

New MenuA Technician Menu has been introduced,to simplify the configuration of eachpump. Some of the items on theTechnician Menu affect how the pumpbehaves; others control the options thatappear to the pump user when theypress the Options button to show theOptions menu. The configurable itemson the new Technician Menu are shownon page 12 of the Technical UserManual.

If the Technician Menu settings are leftat their factory defaults, the pumpbehaves as the previous version of thepump.

New features of version 0.71 softwareNew OptionsThe new options (and some of theprevious options) can be enabled on theTechnician Menu. This means that theycan appear when appropriate, but canbe disabled if not required. On theinstruction label on the pump, Optionsnumbered 1 to 8 are the ones thatappeared in previous versions of thepump software. The additional newoptions shown on the label are:• Primary infusion Minimum• Primary infusion Maximum• Primary Max Volume to be infused• Secondary/Bolus Minimum• Secondary/Bolus Maximum• Secondary/Bolus Max Volume to be

infused• KVO Rate• Drug Library to allow selection and

display of a drug label.

New featuresThe new menu and new options inversion 0.71 software provide a numberof new features. These fall into thefollowing broad areas:• Infusion mode features• Safety features• Display features• Servicing features.

Infusion mode featuresUsing the Technician Menu, the pumpcan be configured:• to stop at the end of a Secondary

infusion, or to continue infusing andautomatically switch to theprogrammed Primary rate;

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• to allow a Bolus infusion to beprogrammed where the volumeinfused is deducted from theprimary infusion volume to beinfused; to highlight this feature,the key previously called“Secondary” is now called“Secondary/Bolus”

• to allow the user to set a KVO ratefor an infusion, or remain at thedefault rate configured for theparticular pump;

• to use the Occlusion Alarm levelspecified for an infusion, or remainat the configured default alarmlevel;

• to allow access to a previouslyprogrammed Dose-Rate Calculationinfusion when the pump is switchedon (Dose-Rate Calculation recovery),or display the standard messages.

Safety features• a timeout safety feature has been

added. This means that whenmessages are not actioned withinthe timeout period, for examplesetting a value, the pump reverts tothe previous display.

• safety keypad lockout, this featureis only activated when operating thepump on AC power. It allows theuser to lockout the keypad aftersetting the pump up for use, so thatit can be ready for infusion at alater time.

Configurable safety features that can becontrolled on the Technician Menu are:

• automatic keypad lock after oneminute, to prevent malicioustampering, and increase patientsafety;

• preset rate and VTBI limits, so thatInfusion Rate and Volume to be

Infused are limited to a suitablerange; this prevents values beingprogrammed accidentally which areinappropriate for infusions inparticular environments (such asepidural infusions, or paediatricapplications).

Display features• configured parameters are shown on

the Message Display when the pumpis switched on.

Configurable display features that can becontrolled on the Technician Menu are:

• the backlight may be activated whenthe keypad is touched, or kept onpermanently;

• one of 30 preset drug labels may beselected and viewed as requiredduring an infusion;

• the display of micrograms (whenprogramming an infusion usingdose-rate calculation) can be shownas ‘µg’ or ‘mcg’;

• the time display may include thesuffix GMT, or the suffix can besuppressed if it is not appropriate.

Servicing featuresOn the Technician Menu, the pump canbe programmed with a pump ID to suitthe hospital protocol, and a service duedate:

• the ID, for example the serialnumber of the pump, or analphanumeric pump name, isdisplayed each time the pump isturned on;

• when a Service Date is set, the dateis displayed each time the pump isswitched on. An alarm sounds whenthe date is reached.

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In t roduct ionChapter 1

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1 — 1

I n t r o d u c t i o n

Introduct ion to the 500/505 pumps

The Model 500 is designed for use in allareas, as it can be programmed with aninfusion rate of up to 999 millilitres perhour, and a maximum volume to beinfused of 9999 millilitres.

The Graseby Medical 500 and 505Volumetric pumps are designed for usein infusion therapy in both venous andarterial infusions. They offer bothstandard and optional featuresbringing accurate fluid delivery to thepatient.

This makes them ideal for use ingeneral care, home care, and intensive/critical care areas.

The Model 500 and Micro 505 pumpsare very similar in design. Thedifferences are in colour, graphics andin the maximum rate and volume to beinfused that can be programmed for aninfusion.

Model 500 Volumetr ic pump

Read the entire contents of thismanual carefully before using thepump.

Micro 505 Volumetr ic pump

The main features of the pumps aredescribed starting on page 1-3. For fulldetails on the differences between the500 and 505, see the Specificationsection at the end of this manual.

The Micro 505 is designed for use inpaediatric/neonatal environments andfor fluid restricted patients. It can onlybe programmed with an infusion ratebelow 100 millilitres per hour, and themaximum volume to be infused is 999.9millilitres.

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Both the Model 500 and the Micro505 pumps may be used for epiduraladministration.

AnaestheticsEpidural administration ofanaesthetics is limited to short-term(not to exceed 96 hours) infusion, withindwelling catheters specificallyindicated for short-term delivery ofanaesthetic drugs.

AnalgesicsEpidural administration of analgesicsis limited to use with indwellingcatheters that are specifically indicatedfor short or long term delivery ofanalgesic drugs.

Epidura l administ rat ionTo prevent infusion of drugs notindicated for epidural use and to avoidinappropriate delivery rates whenusing the pump for epiduralapplications:

• use the pump’s Maximum Rateoption, to set a maximum infusionrate of 20 mL/h on a pump to beused for epidural administration.This feature is described fully inChapter 3, Options;

• do not use IV administration setswhich contain injection sites;

• differentiate the pump and IV setbeing used for epidural delivery fromthose being used for other routes ofadministration. A yellow EpiduralLabel Set for the VolumetricInfusion Pump (part number TPF-00306) is available from GrasebyMedical. The labels should be stuckon the front, top and sides of thepump to help staff to identify apump that is dedicated to epiduralapplication.

WARNING: The use of administration setsincorporating injection sites could lead toan improper or inappropriate infusionresulting in serious patient injury ordeath.

WARNING: Failure to clearly identify thepump and administration sets could leadto an improper or inappropriate infusionresulting in serious patient injury ordeath.

WARNING: When delivering drugs in theepidural space, use only thosemedications specifically indicated forepidural use. Epidural administration ofother drugs could result in serious patientinjury or death.

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I n t r o d u c t i o n

Pump fea turesThe main features of the 500 and 505pumps are listed below:

Easy to use featuresThe pumps have been designed to beeasy to use:

• they are easy to set up and operate,yet with all the advanced featurestypically associated with the morecomplicated infusion systems;

• they have a straightforward keypadand an easy-to-read message display;

• the unique air-in-line removalsystem allows clearing of bubbles inthe line by simply opening andclosing the door: air is preventedfrom going beyond the cassette; thisincreases patient safety, minimisesthe risk of infection and savesoperator time;

• they can be used at the bedside or astransportable equipment; using theinternal battery which also switchesin automatically if the pump isbeing used on mains power and thisis interrupted.

Use of administration setsThe pumps can only be used withGraseby Medical administration sets.These administration sets have thefollowing features:

• all Graseby Medical administrationsets incorporate a safety clip toprevent accidental free flow whenthe administration set is removedfrom the pump;

• when used with Graseby Medicalblood administration sets thepumps deliver blood and bloodproducts without significanthaemolysis of red blood cells.

Infusion mode features• accurate (± 2%) fluid delivery;• the pumps can be configured to stop

at the end of a Secondary infusion,or automatically switch to infuse atthe programmed Primary rate;

• a Bolus infusion may beprogrammed so that the volumeinfused is deducted from theprimary infusion volume to beinfused;

• KVO rate may be specified for aninfusion, or remain at the defaultrate for a particular pump;

• the pumps offer a quick rate changefeature for complete titrationcapability;

• automatic delivery of a secondarymedication (if a secondary infusionhas been set up).

Safety featuresThe pumps have been designed with ahigh emphasis on safety:

• there is an optional automatickeypad lock which preventsinadvertent operation and increasespatient safety;

• the keypad can also be lockedmanually at any time;

• a pump may be configured so thatits Infusion Rate and Volume to beInfused are limited to a suitablerange; this prevents values beingentered accidentally which areinappropriate for infusions inparticular environments (such asepidural infusions).

• the pumps have indicators that arelit to show if they are running onbattery or mains;

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• when using the battery, a test isperformed on power-up and the levelis shown on the display; manualtesting is also available;

• the pumps have an RS232 interfaceallowing connection to a computerfor external monitoring.

Display featuresApart from the standard display,pumps can be configured to show extrainformation, either as a standardmessage display or by pressing a key totoggle the display.

Standard displays are:

• the volume infused in the currentinfusion;

• the infusion rate;• the Volume to be Infused in the

remainder of the infusion.Additionally:• the rate and volume to be infused

displays are automatically adjustedto make them easy to read in anylight;

• the time remaining in the presentinfusion may be viewed;

• the total volume of fluid delivered toyour patient since the totaliser waslast cleared to be viewed; alsodisplayed with the total volume isthe total time (hours and minutes)that the pump has been in use sincethe totaliser was last cleared;

Using configurable displays:• the backlight may be activated when

the keypad is touched, or kept onpermanently;

• optionally, one of 30 preset druglabels may be selected and viewedas required during an infusion.

Occlusion Pressure featuresThese features increase safety ininfusing fluid, particularly in criticalcare areas such as neonatal andpaediatric care:

• when setting occlusion alarms, threestandard occlusion alarm settingsbetween 100 and 500 mmHg can bemade; see the Specification sectionat the end of this manual for fulldetails of the occlusion alarmvalues;

• the occlusion pressure alarm settingwhen the pump switches on isconfigurable; you can change thesetting for a particular infusionusing the Occlusion AlarmSetting key;

• when an occlusion alarm sounds, thepumping mechanism backs off toreduce downline back pressure andbolus potential (bolus potential isapproximately 0.3 mL regardless ofthe rate and the administration setused);

• when an occlusion is detected, thepump does not give an occlusionalarm immediately, but only alarmsif the occlusion pressure continuesto exceed the occlusion threshold forup to 10 seconds; however, if suchtemporary occlusions persist, thenthe occlusion alarm is generated;this helps to avoid nuisanceocclusions.

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Special infusion featuresThe pumps have a number of specialinfusion options:

• a Volume over time option allowsthe user to set the volume to beinfused and total time for theinfusion, the pump automaticallycalculating the infusion rate;

• a Dose-rate calculation option whichallows automatic calculation of theinfusion rate by entering infusiondose; patient weight (kg or lbs); drugamount in fluid container (in MG,Gm or mcg units), and volume offluid in the container, in mL;

• a Rate Tapering option allowsautomatic tapering of the infusionrate (either up or down) foradministration of IV nutrition.

Multiple use featuresWhen multiple infusion lines arerequired, two or three pumps can befitted together:

• modular side rails and hooks meanthat one, two, or three pumps maybe connected to a single IV pole; thisprovides space saving;

• the modular connection system hasa safety feature which ensures thatthe first pump must be correctlyattached to an IV pole before thesecond and third pumps can beconnected.

Servicing featuresThe pumps have been designed with anumber of features for Biomedicalengineers:

• a Service Due Indicator, allows aservice date to be set, which isdisplayed on power-up with analarm;

• special menus are provided to aid intesting, troubleshooting and service;

• the last 200 events are recorded andavailable on these menus;

• downloading of the pump history ispossible using the RS232 port witha special optional kit (Part no 0150-0673).

Together with the ability to configurethe pump using the Technician Menu,these features offers greatermanagement flexibility.

Instructions for using these functionsappear in the Technical User Guide andthe Volumetric Service Manual.

Optional featuresSome pumps are optionally fitted witha Nurse-Call Feature which allows apump to be connected to a hospitalnurse call system and signal alarmsoccurring in the pump.

Note: This feature is not available inall countries.

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Operat ing the pumpChapter 2

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What this chapter covers

This chapter introduces the Volumetricpump. It explains all the terminologythat you should understand, and thetechniques that you use to operate thepump.

In t roduct ion

These sections describe physicalaspects of the Volumetric:

• front of the pump - indicators anddisplays

• front of the pump - programmingkeys

• rear of the pump• attaching the pump to an IV pole• switching the pump on and off• using the pump on battery• sounds on the pump.

These sections explain how to programan infusion:

• types of infusion• setting up a Primary infusion• about Secondary infusions• running a Bolus infusion.This chapter does not cover the types ofinfusion that may be run if the pumphas optional features enabled. Theseare described in Chapter 3, Options.

Who should read this chapterThis chapter is aimed at all users whohave been trained in how to use theVolumetric pump.

It is not designed to be used as a self-teach manual, but should be used toreinforce the best-practice techniquesdemonstrated during training sessions.

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Front of a 500 series pumpIndicators and displays

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Programming keys

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Rear o f the pump

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Connect ing the pumps to an IV poleIn use, Graseby Medical recommendthat the pump should be connected to asuitably balanced IV pole using the poleclamp as illustrated in the diagram onthe opposite page.

The diameter of the pole must bebetween 1.2 cm and 3.8 cm (0.5 and 1.5inches).

To provide maximum stability whenusing the modular connection system,ideally, the IV pole should have 6wheels and a low centre of gravity. Thebase diameter should be 56 cm (22inches).

Attaching a single pump to an IVpoleTo attach the pump to a suitablybalanced IV pole:

1. Loosen the screw on the pole clamp.2. Hold the pump by the handle and

slip the arms of the pole clamp ontothe pole.

3. Tighten the screw on the pole clampto firmly attach the pump to thepole.

Attaching more than one pump toan IV poleWhen multiple infusion lines arerequired, you can connect up to threepumps to a single pole using the hooksand rails that make up the modularconnection system.

As all pumps have connectors on bothsides, you can use any one as the centre,

left, or right pump.

This diagram shows how three pumpsmay be connected together using theVolumetric’s modular connectionsystem:

Inspecting the modularconnectionsBefore connecting the pumps, you mustcheck that the modular connectionparts are all in good condition:

1. Carefully inspect the modularconnection system for damage,including cracks, chips, loose or bentparts.

2. Press the disconnect buttons severaltimes to make certain that thebuttons move in and out freely.

WARNING: Do not use the pump if youdetect any cracks, chips and loose or bentparts, or if the buttons do not move inand out freely when they are pressed.Failure to do so could causeinadvertent disconnection of thepumps.

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How to connect pumps togetherOnce you have inspected the modularconnection system as described in theprevious section, connect the pumps asfollows:

1. Clamp the first pump to the IV pole.This is now the "centre" pump.

Note: As you tighten the screw on thepole clamp, you automatically adjustthe modular connection hook anddisconnect button. Once the pump issecurely attached to the pole, the hook isin the correct position to allow you toconnect further pumps.

2. Take the second pump, grasping itby the handle and hold it so that themodular connector rails are directlyabove or below the connector rails ofthe centre pump.

3. Engage the edges of the modularconnector rails and slide the secondpump up or down until it isconnected to the centre pump. Whenthe connection is secure, you hear adistinct click.

4. Before releasing the handle of thesecond pump, double-check that theconnection is secure by moving thepump up and down and exertingpressure on the top of the pump.

To attach a third pump to the otherside of the first pump, repeat steps 2, 3and 4.

Moving an IV pole with pumpsconnectedIf you need to move the IV pole once thepumps are attached, always ensurethat you grasp the IV pole with onehand and steady the pumps with theother hand if necessary.

Disconnecting modularconnected pumpsYou must always disconnect modularconnected pumps one by one beforeremoving the centre mounted pumpfrom the IV pole.

Disconnect the left and right handpumps from the centre mounted pumpas follows:

1. Grasp handle of pump to beremoved.

2. Lift the pump slightly.3. Press the disconnect button and

slide the pump up or down todisconnect from the centre pump.

4. Place the pump in a location whereit will not be damaged.

WARNING: Do not push or pull on thepumps, or the IV pole may tip over orthe pumps fall to the floor.Do not try to remove modular connectedpumps from the IV pole whilst they arejoined together.Either of these could cause theadministration set to separate from thefluid container thus spilling themedication, or the pumps themselvescould be damaged.

Note: If the connection is loose, or thepumps seem to wobble, disconnectthen carefully reconnect them,making sure both edges of themodular connectors engage. Do notuse pumps where the connection isloose, but return them to a suitablyqualified technician for repair.

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Switching the pump on and off

To switch on the pump you can doeither of the following:

• press the On/Off key• open the front door by lifting the

latch.

Switch on in Quiet Pump modeIf you want to use the pump withoutany key clicks and also suppress thenon-insistent alarms, you can switch onin "quiet pump" mode:

1. Press the Silence key and keep itpressed down.

2. Press the On/Off key.Note: Quiet Pump operation iscancelled when you turn off the pump.

Self testWhen you switch it on, the pumpcarries out a series of tests to ensurethat all components are functioningcorrectly. If any electrical or mechanicalproblems are detected, or if anypotential problems are detected, then a

message is displayed and the alarmsounds. See Chapter 4, Troubleshootingfor more details on handling alarms.

Message Display at Switch onThe messages displayed when youswitch on the pump depend on whichfeatures have been enabled on thepump and whether or not it isconnected to the AC mains supply.

If all the pump options have beenenabled, the pump displays messagesto provide you with the followinginformation about itself:

• Pump Identifier• Drug Label• Primary Min Rate and Max Rate• Primary Max VTBI• Battery gauge (displayed only if the

pump is disconnected from the ACmains supply)

• Service due date.

After switching onWhen the pump has completed its selftests, it is ready for you to program,load a cassette (see page 2-18), or startan infusion. You see a screen somethinglike this:

Before switching the pump on, visuallycheck for any cracks on the case, ordamage to any part of the pump or itsconnectors. Plug the AC mains cord into

Switching on

an AC mains supply if possible. Ifnecessary, the pump can be run on itsinternal batteries, see Using the pumpon batteries, later in this chapter.

Note: If the pump is switched off andconnnected to AC power and thesaftey keypad lockout feature isactive, the pump cannot be switchedon via the keypad, see Safety keypadlockout, page 2-22.

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Switching of fFor safety reasons, the front door mustbe properly closed and any infusionmust be on Hold before you switch offthe pump.

Using the pump on bat teryThe pump contains an internalrechargeable battery. However, ineveryday use, the pump should beconnected by its cord to a suitable ACmains supply, if one is available. Thebattery is then kept fully charged, andwill continue to be charged whilst thepump is infusing.

The pump automatically uses the battery:

• if you switch on whilst the powercord is unplugged, or

• if the AC power fails whilst thepump is operating.

Switching on using the batteryWhen you switch on the pump, if it isbeing powered by internal battery:

• you need to hold down the On/Offkey to turn the pump on. If the pumpis operating on the AC mainssupply, it switches oninstantaneously when you touch theOn/Off key;

• there is a short pause whilst thepump carries out the Battery Testand displays the Battery Gaugescreen to indicate the currentbattery capacity:

Note: The battery is always testedwhen the pump is switched on, eventhough the Battery Gauge is notdisplayed during Dose-RateCalculation, DRC Recovery or RateTaper infusion start up.

Testing the batteryAt any time when operating on battery,you can check the battery capacity bycarrying out the Battery Test describedin Chapter 3, Options.

Operating using the batteryDuring operation of the pump onbattery:

• the yellow Battery indicator is lit• the Message Display light turns off

if the pump is left on Hold, unlessyou have set the ‘Backlight on’option, described in Chapter 3,Options.

Low batteryWhen you switch on the pump, andduring operation, the pump warns youwhen the battery capacity is low. If yousee the yellow Battery indicatorflashing whilst the pump is infusing,you should plug the power cord into theAC mains supply as soon as possible.

• If the pump is running an infusion,press the Hold key;

• if the front door of the pump is open,close it with the latch;

• then press the On/Off key.

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Low battery alarmsWhen approximately one hour ofoperation remains, the pump sounds analarm and displays this message:

If you see this message, plug the powercord into the AC mains supply as soonas possible.

If you decide that you must continue touse the pump on battery, anotheralarm sounds approximately half anhour before it is fully discharged.

This message is displayed:

It is essential that the pump is pluggedinto the AC mains supply at this point.

Recharging the batteryTo charge the battery, plug the powercord into the AC mains supply.

It takes approximately 10 hours torecharge a completely depleted battery.

CapacityA new, fully charged battery willoperate the pump for approximately 6hours at 100 mL/h (99.9 mL/h on Micro505).

The battery may discharge morequickly if the battery has aged and is ina poor condition even though it wasrecently charged.

Pump in storageYou should connect the pump to the ACmains supply to charge the batteryevery three months, even when thepump is not in service. This helps tomaintain the life of the battery.

WARNING: Correct management ofbattery charging, as described in thisdocumentation is essential to ensurethat the pump can operate on battery forthe time specified. Failure to do so mayresult in compromised function of theproduct or patient injury.

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Sounds on the Vo lumetr icThe Volumetric pump makes a 'click'sound as you press each key. It alsosounds an audio alarm to alert you to acondition that requires attention on thepump: either an insistent (three-tone)or non-insistent (two-tone) alarm. Theclick and non-insistent alarm do not

sound if the pump is switched on inQuiet Pump mode. See next page. As afurther safety feature, the Volumetricemits a high-pitched system alarm toindicate a problem requiring theattention of a Graseby Medicalqualified technician.

Audio alarmWhen the Volumetric pump requiresattention, it uses an audio alarm toindicate that there is a problem.

Whilst sounding the alarm, it alsodisplays a message to explain theproblem. A full list of all the alarmmessages, their possible causes andhow to solve the problem is explainedin Chapter 4, Troubleshooting.

This section explains the differenttypes of alarm sounds made by thepump.

You may hear three types of alarm fromthe Volumetric:

• insistent• non-insistent• continuous (backup alarm).

Insistent alarmThis type of alarm indicates that fluiddelivery has stopped, or cannot bestarted. It alerts you to a condition thatmust be corrected before the infusioncan be started, or continued, forexample if an occlusion is detected.

The insistent audio alarm consists ofthree tones: two high-pitched and onelow-pitched, repeated at two-secondintervals.

To silence an insistent alarm, press theSilence or Hold key. The alarm willrecur unless you correct the problem asdescribed in Chapter 4, Troubleshooting.This chapter describes each alarm, itscause and action to take.

Non-insistent alarmThis type of alarm alerts you to acondition that needs attention, but hasnot caused the infusion to stop. Forexample, you hear a non-insistentalarm if the pump is running onbatteries and the batteries are low, orif the infusion has switched to a KVOrate.

The non-insistent audio alarm consistsof two tones, one high-pitched and onelow-pitched, repeated at two-secondintervals. To silence this type of alarm:

• press the Silence or Run key tosilence the alarm without stoppingfluid delivery;

• press the Hold key to silence thealarm and stop fluid delivery.

Note: In Quiet Pump mode, there is noaudio alert for certain non-insistentalarms. See the next page for moredetails.

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In some circumstances, it may bedesirable to operate the Volumetricwithout the associated sounds.

For safety reasons, you cannot turn offthe insistent or continuous alarms, butif necessary you can operate the pumpwithout the key-press 'click' sound andcertain non-insistent alarms. This iscalled a 'Quiet Pump' infusion.

To run a 'Quiet Pump' infusion:

1. Ensure that the pump is turned off.2. Press Silence and keep it held

down.3. Turn on the pump with On/Off.The keypad click and non-insistentalarm sound is now off. The pumpremains in Quiet Pump mode until youswitch off and then on again.

Quiet Pump mode

Silent alarms in Quiet Pump modeWhen running the pump in Quiet Pumpmode, certain alarms associated with aSecondary infusion are silent. Thealarm is silent in the followingcircumstances:

• when the pump automaticallyswitches from Secondary to Primarywhen the Secondary infusion iscomplete;

• when you program the Secondaryinfusion, but press the Primary keythen the Run key without runningthe Secondary infusion;

• when you press Run to start theSecondary infusion with the Volumeto be Infused set to zero.

Alarms and computer controlIf a pump is being run under computercontrol, you can silence it from thecomputer. However, you must resolvethe problem causing the alarm on thepump.

WARNING: If a backup alarm sounds, thepump should be immediately removedfrom the patient and sent to be repairedby a Graseby Medical qualified technician.Failure to do so may cause patient injuryor death.

Continuous - backup alarmIn addition to the insistent and non-insistent operational alarms, theVolumetric pump has a fail-safebackup alarm system. This has adistinctive high-pitched tone:

• should the audio alarm system fail,then the pump sounds the backupalarm, with a 1.5 second pausebetween alarm tones;

• should an electromechanical systemfailure occur, the pump sounds thebackup alarm continuously.

If you hear the backup alarm sounding,you should immediately remove thepump from the patient and have itrepaired by a Graseby Medicalqualified technician.

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Types of in fus ionHospital protocols dictate how thePrimary, Secondary and / or Bolusfeatures are used, and the pump shouldbe configured to conform with theseprotocols.

This section summarises the typicaluse of these features of the pump.

For a Primary infusion, you set up thepump to deliver solution from a singlecontainer. This diagram shows anexample of how a pump looks when setup for a Primary infusion using aStandard administration set (8C-820)

The pump’s Volume to be InfusedDisplay shows the remaining Volumeto be Infused and on its MessageDisplay the pump shows the totalinfused so far.

For full details on how to set up aPrimary infusion: see Setting up aPrimary Infusion, page 2-16.

P r i m a r y

Using the pump, you may carry out:

• a Primary infusion

• a Primary and a Secondary infusion

• a Primary and a Bolus infusion.

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Secondary

For a Primary and a Secondaryinfusion, two containers are used:

• one to deliver the Primary infusion,for example, a hydration solution;

• a second to deliver an additionalinfusion, for example an antibioticdose; this is sometimes called a“piggyback” infusion.

The pump keeps separate totals for thePrimary and Secondary infusions: thetotal infused in the Secondary infusionis not deducted from the PrimaryVolume to be Infused.

The pump can be configured to work inone of two ways at the end of theSecondary infusion: see Ending aSecondary infusion, over the page.

For full details on how to set up aSecondary infusion:

• first follow the steps in Setting up aPrimary Infusion, page 2-19;

• then see About Secondary Infusions,page 2-26.

Secondary infusion with BolusenabledThe pump can be configured, using theTechnician Menu, to offer a Bolusinfusion as an alternative to theSecondary infusion. If the Bolus featureis enabled, you can:

• run a Secondary infusion, where thevolume infused is not deducted fromthe Primary Volume to be Infused

or• run a Bolus infusion, where the

volume infused is deducted from thePrimary Volume to be Infused.

Pr imary and Secondary

Primary

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When the Bolus feature is configured,each time you press the Secondary/Bolus key, the Message Display shows:

At this point, you would press 3 toenter Rate and Volume to be Infusedfor the Bolus, or to view the totals forthe Bolus infusion.

For full details on how to administer abolus infusion, see Running a BolusInfusion on page 2-31.

With the pump configured to offer theBolus feature, you can carry out a Bolusinfusion as an alternative to theSecondary infusion.

A Bolus infusion may be administeredat a different rate, with the volume tobe infused entered separately to thePrimary volume, just as for aSecondary infusion.

However, for a Bolus infusion, theVolume infused is deducted from thePrimary Volume to be Infused.

At the end of the Bolus, the pumpreverts to the Primary infusion at thepreviously programmed Primary rate.

The Secondary Stop feature, if enabledhas no effect at the end of a Bolus.

Primary and Bolus

The Secondary Stop feature in theTechnician Menu controls how thepump works when the Secondaryinfusion is complete.

• With Secondary Stop disabled, thepump automatically reverts to thePrimary infusion at the previouslyprogrammed rate, so that there is acontinuous flow. When the Primaryinfusion starts a non-insistentalarm sounds.

Ending a Secondary infusion• With Secondary Stop enabled, the

pump stops and sounds an alarmuntil you manually silence it andstart the Primary infusion.

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The ef fect o f Opt ions set t ings oninfusionsSome of the Options settings can affectthe way you program the infusion, whatyou can do during the infusion, or theway the pump behaves. For example, ifthe pump has the appropriate Optionsenabled on the Technician menu, youmay choose to:

• turn on the Message Displaybacklight

• set the KVO rate• select a Drug Label• program a Dose-Rate Calculation,

Volume Over Time or Rate Taperinfusion.

Infusing with Rate and VTBI l imits enabled

However, the settings which may mostaffect the way you program an infusionare Rate and VTBI limits. Such limitsrestrict the values you can use duringan infusion and their use is describedbelow.

If you need to make any changes tothese Options settings, you must do sobefore programming the infusion. SeeChapter 3, Options for full details.

If the features for setting limits areenabled on the Technician Menu, thelimit values can be set or examinedusing the Options key. They can be setindependently for Primary andSecondary infusions and may not all beenabled. If Primary Rate or VTBIlimits are enabled, you can also see thesettings displayed after the pump isswitched on.

When limits are enabled, you cannotrun an infusion with a Rate or Volumeto be infused set outside the limits.Also, you cannot change the rate whilerunning to go outside the limits. If youtry to do this, or if you program a valueoutside the limits and then press theRun key, you see the message:

Wherever possible check or set thelimits before you program the infusion,especially if you might have to give aSecondary infusion or a Bolus. Theeasiest way to check Primary infusionsettings is to look at the messagedisplay when you switch the pump on.To check Secondary infusion settings,you must use the Options key. Settinglimits is described in Setting Rate andVTBI limits on page 3-29 in Chapter 3,Options.

Limits are enabled and set for a safetypurpose (for example, where the pumpis used for Epidural administration). Ifyou are likely to be in a situation whereyou have to give an infusion in anemergency, ensure that when a pump isswitched off, the limits are left withsafe value settings.

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Note: A thick solution in this case maybe certain cytotoxic agents, lipid-basedfluids and other viscous solutions, forexample Total Parenteral Nutrition.

Height of solution container abovethe pumpIf necessary, adjust the height of thepole so that the bottom of the solutioncontainer is between 15 cm and 30 cm(between 6 inches and 12 inches) abovethe top of the pump

On Model 500, 30 cm (12 inches) may berequired for rates over 500 mL/h.

On both Model 500 and Micro 505,30 cm (12 inches) may be required whenusing thick solutions and/or60 drops/mL sets.

Sett ing up a Primary Infusion

Prepare the solut ion

Using an aseptic technique, prepare thesolution container and prime theadministration set following theinstructions provided with the set. As aguide:

1. Remove the solution container fromits packaging and remove the capfrom the fluid outlet.

2. Remove the administration set fromits packaging and close the rollerclamp.

3. Remove the cap from the spike onthe administration set and insertthe spike into the fluid outlet on thesolution container.

4. Hang the container with theadministration set on the IV poleand ensure that the container is thecorrect height above the pump.

To set up and run a Primary infusionthe main steps are:

• attach the pump to the IV pole,described on page 2-5;

• set the Options for the infusion ifappropriate, particularly Rate orVTBI Limits if they are enabled asdescribed on page 2-15;

• prepare the solution;• prime the administration set;• load the administration set into the

pump;• program the infusion;• start the infusion.

WARNING: Correct entry of data isessential in order to ensure that theintended infusion is performed. Beforeconfirming any displayed data whensetting up an infusion, you should ensurethat it is correct. Failure to do so mayresult in compromised function of theproduct, patient injury or user injury.

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With the solution container hanging onthe IV pole and the administration setspike inserted into the container, primethe administration set as follows:

Prime the administrat ion set - Example1. Squeeze the drip chamber and fill

until it is at least one third full. Thedrip chamber may fill completelyduring loading and/or an infusion.This will not adversely affect thefluid delivery or the operation of thepump.

2. Hold the cassette inverted, so thatthe roller clamp is above thecassette, as shown here.

3. Slowly open the roller clamp toallow the solution to flow throughand prime the cassette and the line.You can control the flow by movingthe roller clamp as necessary.

4. When the entire set is primed, closethe roller clamp.

You must always follow the Instructionsfor Use that accompany theadministration set to be primed. Thissection shows an example to explainthe basic priming steps to be carriedout on an administration set without abi-directional check valve, filter,injection site or c-clamp.

WARNING: Remove any air to prevent airembolism. The presence of air within theinfusion can result in complicationsresulting in patient injury or death.

WARNING: Use only Graseby Medicaladministration sets with this product.Failure to do so may result incompromised system accuracy leading tocomplications resulting in patient injuryor death.

WARNING: To avoid over infusion, do notprime the infusion line when theadministration set is connected to thepatient. Over infusion can result in patientinjury or death.

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When you switch the pump on, theOcclusion Alarm setting is always thesame, and is defined by the TechnicianMenu configuration setting.

Before an infusion, always check, and ifnecessary, change the setting to suitthe infusion by pressing the OcclusionAlarm Setting key. Continue pressingthe key until you see the setting youwant. Never use a Low setting withhigh infusion rates.

For full details, see Change theOcclusion Alarm setting, on page 2-24.

WARNING: The Occlusion alarm levelmust be checked before starting aninfusion to ensure that it is appropriatefor the infusion. Failure to do so mayresult in an unacceptably slow time toOcclusion alarm, resulting in patientinjury or death.

See the Specification section at theend of this manual for details on thepressure values for High, Mediumand Low settings.

Load the cassette into the pump

The safety clip on the administrationset is marked with arrows to indicatethe correct direction for insertion.

The pump is marked with a diagramshowing the position of the safety clipslot.

1. Open the door of the pump byraising the latch.

2. With the flat side of the cassettetowards you, and the roller clampbelow the cassette, match the fourholes in the corners of the cassettewith the four metal pins inside thepump.

3. Press the cassette into place andrun your finger down the cassette toensure that it is flat and correctlyfitted.

4. Slide the safety clip up to the baseof the cassette and push it fullyinward, into its slot.

5. Close the door, pushing the latchinto place.

Sett ing the Occlusion Alarm

With the administration set primedand the solution container hanging onthe IV pole, you can load the cassetteinto the pump as follows:

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1. If Min and Max Rates and MaxVTBI are enabled on the pump,ensure they are appropriate for theinfusion by pressing the Optionskey. To find out more see page 2-15.

2. If the infusion is for a new patient,or if you need to clear the totals forthis patient, press Total Volumethen press *.

3. Press the Occlusion AlarmSetting key to display the currentsetting and continue pressing ifnecessary to set an appropriatelevel.

4. Press the Rate key then use thekeypad to enter the infusion rate inmL/h.

5. Press the Volume to be Infused keythen use the keypad to enter thevolume in mL.

Ensure that the Rate and Volume tobe infused are correct for thisPrimary infusion then open theroller clamp. Inspect the fluid pathfor kinks, a closed clamp, or anyother upstream obstructions.

6. Press the Run key to start theinfusion.

Primary infusion setup

Once the solution is ready and thecassette is loaded into place in thepump, check that the Primary indicatoris lit. If not, press the Primary key.

WARNING: The Occlusion alarm level mustbe checked before starting an infusion toensure that it is appropriate for the infusion.Failure to do so may result in anunacceptably slow time to Occlusion alarm,resulting in patient injury or death.

WARNING: Prior to starting an infusion,inspect the fluid path for kinks, a closedclamp or other obstructions. Failure to doso may result in the infusion not beingdelivered correctly, resulting in patientinjury or death.

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During the infusionThis section explains the mainactivities you may want to carry outonce you have started the infusion.

When the infusion is running, you can:

• see the progress of the infusion fromthe information shown on thedifferent displays on the pump;

• change the infusion rate;• lock the keypad to provide security

on the pump;

• display the drug label (if thisfeature is enabled);

• stop the infusion.If you press Hold to stop the infusion,you can:

• change the occlusion alarm setting(see page 2-24);

• set up and start a Secondaryinfusion (see page 2-26).

I f the infusion wi l l not start runningThis will only occur if you have one ormore of the following features enabledon the Technician menu:

• Min and Max Rate;• Max VTBI.If you have entered a rate which isoutside the set limits, or a VTBI whichis greater than the maximum, when youpress Run you see the message:

and an alarm sounds. The Rate orVTBI display also changes to the oneused before you programmed theinfusion.

If this happens, you should:

1. Silence the alarm.2. Check the Rate or VTBI display to

see which has changed to find outwhich limit has been exceeded.

3. Check the prescription.4. Check the Min and Max Rate and

Max VTBI settings by pressing theOptions key until each is displayed.

5. Make corrections as necessary.6. Press Run to start the infusion.

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If you do not complete the rate changewithin 10 seconds, an alarm soundsand the rate reverts to the previousrunning rate, followed by a message totell you the change has not beencompleted.

If rate limits are enabled, and youenter a rate that is outside those set,an alarm sounds and you see:

The pump continues at the previousrate. Silence the alarm and check thecurrent settings using the Options key.If you need to change the rate limit, youmust first put the pump on hold.

Message DisplayThe Message Display starts at zero andcounts up in mL to show the volumeinfused so far, for example:

Rate display and Pumping indicatorThe Rate display shows the infusionrate. The Pumping indicator is ahorizontal line located at left of the Ratedisplay.

The indicator moves to show that thesolution is being infused. The speed of

the Pumping indicator isapproximately proportional to theinfusion rate.

Volume to be Infused displayThe Volume to be Infused displayinitially shows the programmedvolume. During the infusion, it countsdown to show the volume remaining forthis infusion.

Original volume to be infusedTo find out the original programmedVolume to be Infused, add the amountin the Volume to be Infused display tothe amount in the Message Display.

In fusion informat ion d isplays

Whilst the pump is running, you canchange the infusion rate. For example,you may need to adjust the initial rateonce the infusion is established.

You can also stop the infusion and thenchange the rate, but the ability tochange without stopping the delivery ofthe solution is especially importantwith some drugs, for example,vasoactive drugs.

You can carry out a running rate changeon Primary or Secondary infusions.

Once the infusion has started, to entera running rate change:

1. Press Rate.2. Enter the new rate using the

numeric keypad.3. Press Run within 10 seconds.

Running Rate Change (Rate t i t rat ion)

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To prevent any tampering with thekeypad during the infusion, there aretwo ways to secure the keypad:• manual locking• automatic locking.

Manual keypad lockingThis safety feature is always availableon the pump, whether or not theautomatic keypad locking feature isenabled.

To lock the keypad during an infusion,press the grey Keypad lock button onthe rear of the pump. The MessageDisplay confirms that the keypad islocked:

If you touch any of the keys on thekeypad once it is locked, the pump re-displays the message.

Safety keypad lockoutThe saftey keypad lockout is only activewhen operating the pump on AC power.It allows the user to ‘lockout’ thekeypad, so that after setting up thepump for use, it is ready for infusion ata later time.

To set the saftey keypad lockout, switchthe pump off and connect to an ACpower supply. Then press the keypadlock button once. If you now attempt toswitch the pump on, the keypad islocked out and the pump inactive. Thepump can only be switched on by:• pressing the keypad lock once and

then switching the pump on usingthe On/Off key

• or by opening the door.

Secur i ty on the pumpIf the AC power supply is removedduring the ‘lockout’, the feature isabandoned, pressing the On/Off keyswitches the pump on. If the AC poweris removed and reconnected without anyuser interface with the pump, thelockout remains active. When the pumpis used on battery power this feature isinactive.

Automatic keypad lockingBefore starting the infusion, you canenable the Autolock Keypad feature inthe Technician Menu.

With Autolock Keypad enabled, thekeypad locks automatically if you leavethe pump untouched for one minute.

If you touch a key, the Message Displayreminds you that the keypad has beenlocked:

Unlocking the keypadTo unlock the keypad once it is locked,press the grey Keypad lock button on therear of the pump:• for a manually locked keypad, press

the button once;• for an automatically locked keypad,

press the button twice.

To silence alarm with keypad lockedIf the pump is sounding an alarm whilstthe keypad is locked, you must:• first unlock the keypad with the

button on the rear of the pump,• then press the Silence key.

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To stop the infusion at any time:

• press the Hold key.

The pump may be configured, in theTechnician Menu, to display the DrugList.

If the Drug List is enabled, you candisplay the Drug Label that was lastselected using the Options key.

Display the Drug LabelTo display the Drug label on theMessage Display for two seconds:

• press the * key.For more information on Drug Labels,see Chapter 3, Options.

Stop the infusion

If an occlusion is detected, the Runlight remains lit, but the Pumpingindicator stops. The pump does not givean occlusion alarm immediately, butonly alarms if the occlusion pressurecontinues to exceed the occlusionthreshold for 10 seconds. This helps toavoid nuisance occlusions.

However, the pump monitors anytemporary occlusions, and if suchocclusions persist, then the occlusionalarm is generated.

If an occlusion is detected when theocclusion alarm is set to Low, the pumpalarms immediately.

I f an occ lus ion is detectedIf an occlusion alarm occursIf an occlusion alarm occurs,immediately clamp the line to thepatient. Then inspect the fluid pathwayto determine what has caused theobstruction.

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You can check the current occlusionalarm setting when an infusion isrunning if you press the OcclusionAlarm Setting key. You can change thesetting if you first put the infusion onHold, see steps in opposite column.

When you switch the pump on, theOcclusion Alarm setting is always thesame, and is defined by the TechnicianMenu configuration setting. You shouldset the alarm to be appropriate for theinfusion before pressing Run.

The occlusion alarm setting determinesthe amount of back pressure allowedbefore the pump alarms. There arethree possible settings: Low, Mediumor High.

Whilst the pump is infusing,particularly at higher infusion rates, orwith thick solutions (see Noteopposite), or with small diametercannulas, you may see the followingalarm message:

If there is no obvious reason for thealarm, the message may occur becauseyou have not selected an appropriateOcclusion Alarm Setting for theinfusion. If this is the case, you maywant to change the Occlusion AlarmSetting.

To change the Occlusion Alarm Settingduring an infusion, whether or not analarm has occurred:

1. Press Hold to silence the alarm ifnecessary, and stop the infusion.

2. Press the Occlusion AlarmSetting key once to display thecurrent setting.

3. Press the Occlusion AlarmSetting key repeatedly to displaythe available settings.

4. When the correct setting isdisplayed, press Run.

Change the Occlusion alarm sett ing

WARNING: If using a blood pressure cuffabove the patient’s venipuncture site takeextra care in setting the Occlusion alarmpressures. Failure to do so may result inunnecessary Occlusion alarms, resulting inpatient injury or death.

WARNING: The Occlusion detectionsystem measures downline back pressurein the administration set, but does notdetect infiltration. In accordance withlocal protocol, you must periodicallyinspect the patient’s infusion site forsigns of infiltration. Failure to do so mayresult in an unacceptably slow time toOcclusion resulting in patient injury ordeath.

Approximate Occlusion alarm settingsLow 2 psi, 103 mmHg, 13.5 kPa

Medium 5 psi, 259 mmHg, 34.5 kPa

High 10 psi, 517 mmHg, 68.9 kPa

When an occlusion alarm occurs, thepumping mechanism backs off toreduce down-line pressure and boluspotential (bolus potential isapproximately 0.3 mL regardless ofthe rate and the administration setused).

Note: A thick solution may be certaincytotoxic agents, lipid-based fluidsand other viscous solutions, forexample Total Parenteral Nutrition.

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The pump warns you that the infusionis complete when the Primary Volumeto be Infused reaches zero.

At this moment, the pump sounds atwo-tone alarm. You can decide to:

Ending the Pr imary in fus ion

KVO infus ionIf you press Silence to stop the alarm,the pump continues to infuse at theKVO (Keep Vein Open) rate. The KVOrate is shown on the Rate display.

Depending on how the pump isconfigured, the KVO rate may be:

• the default KVO rate of 3.0 mL/h,• the programmed infusion rate if

that was less than 3.0 mL/h;• the KVO rate specified for this

pump, see Specifying a different KVORate, below.

The Message Display shows “KVO”, aswell as the combined Primary and KVOvolume infused, for example:

The pump continues to infuse at theKVO rate. After six minutes, the twotone alarm sounds again, as a reminderthat the KVO infusion is still running.You can decide to:

• silence the alarm and stop theinfusion - press the Hold key

• silence the alarm and continue toinfuse at the KVO Rate - press theSilence key.

Specifying a different KVO rate

If the ‘KVO Rate Entry’ option has beenenabled in the Technician Menu, you canuse the Options key to specify a KVOrate, before you start the infusion.When you set the KVO rate you can goto a maximum of 10 mL/h (on a 500pump) or 3mL/h (on a 505 pump) or theMax Primary Rate if one is also enabledand set below these limits.If the programmed infusion rate is lessthan the set KVO rate, when the pumpgoes into KVO, it will continue pumpingat the programmed lower rate.For full details on how to set the KVOrate, see Chapter 3, Options.

• silence the alarm and stop theinfusion - press the Hold key

• silence the alarm and continue toinfuse at the KVO Rate - press theSilence key (see details below).

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About Secondary infusionsThe pump has the facility for you to setup and run a Secondary infusion, forexample, to:

• administer a dose of antibiotics to apatient who is already receiving aPrimary infusion;

• administer a loading dose of a drug,of a different concentration of thesame drug as in the Primarycontainer.

You use the Secondary/Bolus key toprogram a Secondary infusion. TheSecondary volume infused is kept as aseparate total. It is not deducted fromthe Primary Volume to be Infused.

Once you have started an infusion fromthe Secondary set, the solution from theSecondary container takes precedenceover the Primary infusion. For details

on what happens if the Volume to beInfused is less than the contents of theSecondary container, see page 2-27.

Secondary Rate and VTBI limits maybe set if enabled in the Technicianmenu. See page 2-15 for more details.

Bolus feature enabledIf the Bolus feature has been enabled inthe Technician Menu, you can use theSecondary/Bolus key to:

• run a Secondary infusion, wherethe volume infused is not deductedfrom the Primary Volume to beInfused;

or alternatively,• run a Bolus infusion, where the

volume infused is deducted fromthe Primary Volume to be Infused.

Sett ing up a Secondary infusion

To set up a Secondary infusion, youneed a means of combining a Primaryand Secondary infusion. This may bethe combined Primary/Secondary (8C-6200) IV Administration set fromGraseby Medical, product code 591.096.

Alternatively, use an administration setwith an injection site or Y-site (asshown here) plus a SecondaryAdministration set (not shown).

The basic steps for setting up aSecondary infusion are described in thefollowing sections:

• lower the Primary solution container;• prime the Secondary administration

set;• connect the Secondary to the

Primary administration set;• program the Secondary infusion

(with or without the Bolus featureenabled);

• start the infusion.

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You must always follow the Instructionsfor Use that accompany the particularadministration set to be primed. Eachset contains specific priminginstructions, and also gives details ofany warnings concerning the use of theadministration set.

Pr ime the Secondary admin is t ra t ion set

Open the packaging around theSecondary administration set and findthe hanger that looks something likethis:

Take the Primary container from the IVpole and use the hanger to suspend itfrom the IV pole.

Lower the Pr imary solut ion conta inerThis should lower the Primarycontainer by approximately 20 cm(eight inches). Make sure that the dripchamber on the Primary container isstill at least 15 cm (six inches) abovethe pump.

WARNING: Do not run parallel infusionlines below the pump. Delivering aSecondary infusion means running asecond line above the pump. Failure to doso may result in an inaccurate delivery ofmedication, resulting in patient injury ordeath.

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Connect the Secondary to the Pr imaryadmin is t ra t ion se tIf you are using the combined Primary/Secondary (8C-6200) IVAdministration set from GrasebyMedical, product code 591.096, followits accompanying Instructions for Use.

If you are using a separate Primary andSecondary set, then go through thefollowing steps.

1. Insert the needle from the Secondaryset into the injection site on thePrimary set.

2. Keep the Secondary clamps closeduntil you are ready to start theSecondary infusion.

3. Check that the roller clamp belowthe pump is closed, and go on toprogram the Secondary infusion.

The position of the two solutioncontainers and administration sets isshown on the diagram on page 2-13.

WARNING: Check the Secondary setcarefully, since an occlusion above thepump on the Secondary line could causethe Primary fluid to be delivered instead ofthe Secondary infusion. Administering thewrong medication may cause seriouspatient injury or death.

About the Secondary Volume to be In fusedBecause the Secondary container hangson the IV pole at a higher level than thePrimary, the entire contents of theSecondary container may be infused atthe end of the Secondary infusion. Thiscan happen even though the SecondaryVolume to be Infused is zero.

On a pump where Secondary Stop is notenabled in the Technician Menu, youmust ensure that the amount that youenter as the Secondary Volume to beInfused is equal to the volume of fluidin the Secondary container.

If the Secondary Stop feature isenabled, the pump stops infusing andsounds an alarm when the Secondaryinfusion is complete and the SecondaryVolume to be Infused has beendelivered. You can then clamp theSecondary set to prevent any more fluidfrom being infused from the Secondarycontainer.

WARNING: The Secondary volume to beinfused must match the amount of fluid inthe Secondary container. Primary flowresumes when the Secondary container isempty. If the volumes do not correspond,the wrong infusion may be deliveredwhich could cause serious patient injury ordeath.

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1. Press the Hold key if the pump isrunning.

2. If Secondary Min and Max Ratesand Max Secondary VTBI areenabled on the pump, ensure thatthey are appropriate for the infusionby pressing the Options key. Tofind out more see page 2-15.

3. Press the Secondary/Bolus key.The yellow Secondary indicator islit.

4. The Message Display shows thevolume from the previous Secondaryinfusion.

5. The Rate Display shows the lastrate used for a Secondary infusion.Press the Rate key and enter therate for the Secondary infusion, inmL/h.

6. Press the Volume to be Infused keyand enter the Secondary volume inmL. This should normally match thevolume in the Secondary container.

7. Verify that the rate and volume tobe infused settings are correctlydisplayed. Open the roller clamp onthe Secondary administration set

8. Press the Run key to start theSecondary infusion. The MessageDisplay shows the volume infused.

When the infusion is complete, seeEnding a Secondary infusion on page2-32.

Program the Secondary in fus ion

This section describes how to programthe Secondary infusion on a pumpwhere the Bolus feature is disabledon the Technician Menu.

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1. Press the Hold key if the pump isrunning.

2. If Secondary Min and Max Ratesand Max Secondary VTBI areenabled on the pump, ensure thatthey are appropriate for the infusionby pressing the Options key. Tofind out more see page 2-15.

3. Press the Secondary/Bolus key.With the Bolus feature is enabled,the Message Display tells you topress 1 for Secondary or 3 for Bolus.

4. To enter the Secondary rate, press 1.The Message Display shows thevolume of the previous Secondary orBolus infusion. The yellowSecondary indicator is lit.

5. Press the Rate key and enter theSecondary infusion rate in mL/h.

6. Press the Volume to be Infused keyto clear the display, and enter theSecondary volume in mL. Thisshould normally match the volumein the Secondary container.

7. Verify that the rate and volume tobe infused settings are correctlydisplayed. Open the roller clamp onthe Secondary administration set.

8. Press the Run key to start theSecondary infusion. The MessageDisplay shows the volume infused.

When the infusion is complete, seeEnding a Secondary infusion on page2-32.

Secondary infusion - Bolus enabledThis section shows the different screensand the additional step for a Secondaryinfusion with the Bolus featureenabled on the Technician Menu.

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Running a Bolus infusionThis section shows how to administer aBolus with the Bolus feature enabledon the pump on the Technician Menu.

1. Press the Hold key if the pump isrunning.

2. If Secondary Min and Max Ratesand Max Secondary VTBI areenabled on the pump, ensure thatthey are appropriate for the infusionby pressing the Options key. Tofind out more see page 2-15.

3. Press the Secondary/Bolus key.When the Bolus feature is enabled,the Message Display tells you topress 1 for Secondary or 3 for Bolus.

4. To enter the Bolus rate, press 3.The Message Display shows thevolume of the previous Secondary orBolus infusion. The yellowSecondary indicator is lit.

5. Press the Rate key and enter theBolus rate in mL/h.

6. Press the Volume to be Infused keyto clear the display, and enter theBolus volume in mL.

7. Verify that the rate and volume tobe infused settings are correctlydisplayed for the Bolus.

8. Press the Run key to start theBolus infusion. The MessageDisplay shows the Bolus volumeinfused so far. The volume infused isdeducted from the Primary Volumeto be Infused.

When the infusion is complete, seeEnding a Secondary or Bolus infusion onthe next page.

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The pump is configured to work in oneof two ways when the Secondaryinfusion is complete, depending on theSecondary Stop setting in theTechnician Menu.

With Secondary Stop disabled on theTechnician Menu, the pump:

• sounds a non-insistent alarm twice,and then reverts to the Primaryinfusion, running at the previouslyprogrammed Primary rate.

Alternatively, if Secondary Stop isenabled on the Technician Menu, thepump:

• stops the at the end of theSecondary infusion (is put on Hold)and sounds an insistent alarm,

• displays the message:

Ending a Secondary infusion

Ending a Bolus infusion

At the end of a Bolus infusion, thepump sounds a non-insistent alarmtwice. It then reverts to the Primaryinfusion, running at the previouslyprogrammed Primary rate.

The Secondary Stop feature does nothave any effect on a Bolus infusion.

Restarting Primary infusionIf Secondary Stop is enabled on thepump, you restart the Primary infusionas follows:

1. Press the Silence key.2. Press the Primary key.3. Press Run.

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Checking in fus ion tota lsBefore, during or after an infusion, youcan check the fluid volumes that havebeen infused, and the volumesremaining to be infused.

Tota l Volume infusedTo view the combined total volume ofall fluid infused by the pump since thetotal was last cleared, for example tocheck the fluid balance for a patient:

• press the Total Volume key.If the pump is running an infusion, thetotal volume is displayed on theMessage Display as follows:

The total volume includes the volumesfrom any of the following types ofinfusion:

• Primary• Secondary• Bolus• KVO• Rate Taper• Dose-Rate Calculation.

The Message Display also shows thetotal hours and minutes that the pumphas been in use since the display waslast cleared (higher than 99 hoursreads 100+hrs).

Clearing the Total VolumeTo clear the Total Volume on the pump,for example to reset the pump beforeprogramming an infusion for a newpatient:

• press Hold to stop the infusion, ifthe pump is infusing,

• press Total Volume.The Message Display shows the totalvolume as in this example:

• press * to reset the Total Volumeand Time to zero.

The pump can display the followingtotals:

• Total volume infused

• Primary totals

• Secondary totals

• Bolus totals

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Volume to be InfusedThe Volume to be Infused displaycounts down to show the remainingvolume to be infused for this infusion,for example:

At the end of an infusion, the Volume tobe Infused is zero.

Whilst a Primary infusion is running,the Message and Volume to be InfusedDisplays show the volumes for thePrimary infusion.

Volume infused so farDuring an infusion, the MessageDisplay counts up to show the volumeinfused so far, for example:

Whilst a Secondary infusion is running,the Message and Volume to be InfusedDisplays show the volumes for theSecondary infusion.

To view Secondary volumes aftercompleting a Secondary infusion:

1. Press the Secondary/Bolus key.2. If the Bolus feature is enabled,

press 1 to choose the Secondaryvolume.

3. The Message Display shows theinfused volume for the Secondaryinfusion as shown in this example:

Pr imary to ta ls

Secondary to ta ls

The Volume to be Infused displayshows the volume remaining for theSecondary infusion.

The Secondary volumes are keptseparate from the Primary totals. Toview the combined infusion volumepress Total Volume.

If you have carried out a Bolus infusion,you can view the volumes as follows:

1. Press the Secondary/Bolus key.2. Press 3 to choose the Bolus volume.3. The Message Display shows the

infused volume for the Bolusinfusion as shown in this example:

Bolus tota ls

The Bolus volumes affect the Primaryinfusion volumes. The volume that wasinfused as a Bolus is added to thePrimary infusion volume infused figureand deducted from the Primaryinfusion Volume to be Infused figure.

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Re-running in fus ions a t the same ra teWhen an infusion is complete, you maywant to repeat it with the same Rateand VTBI values. The Rate is stilldisplayed but you need to bring backthe previous VTBI.

You can either bring back the VTBI andstart the infusion immediately, or bringback the VTBI to check it before youstart the infusion.

To bring back the VTBI and start theinfusion immediately:

1. Press the Volume to be Infused keyTWO TIMES.The VTBI is not displayed at thispoint.

2. Press the Run key.When you press Run, the VTBIvalue for the previous infusion isdisplayed and the infusion startsimmediately.

Alternatively, to bring back the VTBI,to check it before you start the infusion:

1. Press the Volume to be Infused keyTWO TIMES.

2. Press the Hold key.When you press Hold, the VTBIvalue for the previous infusion isdisplayed but the infusion does notstart.

3. To start the infusion, press the Runkey.

Note: You can also bring back theprevious VTBI if you press the Volumeto be Infused key TWO TIMES andthen wait for 10 seconds.

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OptionsChapter 3

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IntroductionThis chapter describes the Options thatare available for the Volumetric pump.Some of the optional features allow thepump to meet the requirements ofspecial clinical situations.

The Options available for theVolumetric pump are listed on the“Start-up” instruction label on the sideof the pump. If your pump does notdisplay the Option you require, returnthe pump to your Biomedical

The first options are:1. Standard Message2. Time Remaining3. Message Display Light (Backlight)4. Battery Test

The Backlight and all options afterBattery Test only appear in the Optionmenu if they have been enabled in theTechnician Menu.

5. Quick Rate Change6. Rate Taper7. Volume Over Time8. Dose-Rate Calculation

The pump can be programmed withMinimum and Maximum infusion ratesand Maximum VTBI to limit thePrimary and Secondary/Bolus Rate andVolume to be Infused values. These areprovided by the following options:

department to have the feature enabledby a suitably trained person.

Options 1, 2 and 4 are always availableon the pump, and cannot be disabled.The other Options listed below can beenabled or disabled by a suitablytrained person, using the TechnicianMenu (see the Technical User Manual).

Do not use any of the Options withoutcorrect training.

Options available• Min Rate• Max Rate• Max VTBI• Min S/B Rate• Max S/B Rate• Max S/B VTBIThe final two options appear if theyhave been enabled in the TechnicianMenu:• KVO Rate• Drug List

WARNING: Before confirming anydisplayed data, the user should ensurethat it is correct. Failure to do so mayresult in compromised function of theproduct, patient injury or user injury.

You can go directly to options withnumbers against them using theFast access method described on thenext page.

WARNING: Correct entry of data isessential in order to ensure that theintended infusion is performed. Beforeconfirming any displayed data whensetting up an infusion, you should ensurethat it is correct. Failure to do so mayresult in compromised function of theproduct, patient injury or user injury.

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There are two ways to select an Option:

• sequential access to view allavailable options;

• fast access to take you to directly toan option.

You use fast access, as described below,using a number from 1 to 8 for thenumbered options in the list on theprevious page. The numbers are alsoshown in the Options list on the ‘Startup’ label on the right hand side of thepump.

Viewing sequentiallyTo view each available Option, pressthe Options key. Each time you press,it will take you to the next availableoption. After the final option, the nextscreen is the Standard MessageDisplay. If you press the Option keyagain at the Standard Message, you re-display the Options.

Options without a number in the list onthe previous page can only be viewed byusing this method.

Fast AccessTo go directly to one of the numbereditems, first press the Options key andthen its number on the numeric keypad,using the one shown in the list on theprevious page or on the side of thepump. For example, if you press theOptions key and then numeric key 4you are taken directly to the option totest the battery.

If a numbered option has beendisabled, nothing will happen. Pressthe Options key again to see the nextavailable option.

Using optionsValues in the Message DisplayWhen you see a Message Display whereyou need to change, enter or confirm anumerical value, the previous settingwill flash (even if no value previouslybeen entered). You can either enter anew value, or accept the existing valueby pressing the * key or by pressing theOptions key again to move onto thenext option.

To enter a new value use the numerickeypad when the value is flashing andthen press the * key. If you make amistake, do not press the Options key,wait a few seconds and the value willflash again. You can enter a valuewhenever the value is flashing. It willflash again even though you havepressed the * key. If you press theOptions key without first pressing *,any changes you make are discarded.

Using Options while infusingIf you press the Options key whilerunning a standard infusion, then theoptions where you enter values (such asrate limits) display the current values,but will not allow you to change them.Backlight and Quick Rate changeoptions can be activated. Options forprogramming other special types ofinfusions (Dose-Rate calculation, RateTaper and Volume over Time) will tellyou to place the pump on Hold.

To leave OptionsWhen you have entered a value or setan option, use the Options key to moveto the next Option, or startprogramming the pump by pressing anactive key, for example, Rate,Occlusion Alarm Setting or Volumeto be Infused.

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The Standard Message refers to thepump’s normally displayed messagewhen an alternative option is notselected.

This option displays the timeremaining until completion of thecurrent infusion.

To use the time remaining displaypress the Options key and then pressnumeric key 2, or press the Optionskey until the Message Display shows:

2. Time Remaining

If the pump is on hold, the timeremaining is displayed until anotheractive key is pressed. If the pump isrunning, time remaining is displayedfor 5 seconds.

The time remaining is displayed andrelates to the operating mode the pumpis running in: Primary, Secondary,Bolus, Rate Taper or Dose-RateCalculation (if enabled).

1. Standard MessageThe Standard Message display issimilar to the screen below:

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3. Message Display Light

To turn the light onPress the Options key then pressnumeric key 3, or repeatedly press theOptions key until the Message Displayshows the following:

Press the * key to keep the light on. Thelight will remain on until the pump isturned off, or until it is returned tonormal operation.

Turning the l ight on and off

To turn the light offPress the Options key, then press key3, or press the Options key until theMessage Display shows the following:

Press the * key to turn the backlightdisplay off.

CAUTION: The backlight has a limited lifeand may, if used constantly, cause thelight to dim. Eventually the messagedisplay may then need to be replaced. Topreserve the life of the message display,you should only turn on the MessageDisplay Light as described here if it isspecifically required. Misuse of thisfeature could lead to both battery andLCD depletion.

The Message Display has a backlightthat normally turns off one minuteafter the pump begins running, or if thepump is left on Hold while usingbattery power. It turns onautomatically with any keypress, or ifthe alarm sounds.

This option, if enabled on theTechnician Menu, allows you to keepthe Message Display’s backlight onconstantly whilst the pump is in use.

Battery operation and backlight useWhen using the pump on battery power,the backlight normally turns off afterone minute. If you turn the light on asdescribed here, the backlight remainson constantly, until you turn the option(or the pump) off.

You may need to monitor the batterycapacity if you keep the light on, as thelight uses the battery power.

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4. Battery TestThe battery is automatically tested aspart of the power on sequence, if thepump is disconnected from the ACmains supply when it is switched on.The Battery Gauge is displayed to

Using the Battery Test opt ion

indicate the approximate batterycapacity, unless the pump is in Dose-Rate Calculation Recovery or RateTaper mode.

1. Press Hold and ensure that thepump is disconnected from the ACmains supply.

2. Press the Options key and thenpress numeric key 4, or press theOptions key until the MessageDisplay shows the Battery Testscreen.

3. Press the * key to start the BatteryTest.The pump measures the batteryvoltage. After 5 seconds it displaysa Battery Gauge showing theapproximate battery capacity.

This would indicate a batteryapproximately half charged.

The Battery Test option can only beused if the AC cord is disconnectedfrom the AC mains supply and thepump is on Hold.

If the pump is disconnected from theAC mains supply whilst it is infusing,it continues to infuse andautomatically switches to use theinternal battery.

In this case, you may use the BatteryTest Option described here to test thebattery. This way, you can find out theapproximate battery capacity, withoutswitching off the pump.

WARNING: Correct management ofbattery charging, as described in thedocumentation, is essential to ensure thatthe pump can operate on batteries for thetime specified. Failure to do so may resultin compromised function of the productor patient injury.

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A fully charged battery in goodcondition will power the pump forapproximately 6 hours at 100 mL/h(99.9 mL/h on Micro 505).

4. When the test is complete, you canpress Run to restart the infusion.If the battery capacity is low, youmust connect the pump to the ACmains supply to recharge thebattery.For further information on batteriessee Chapter 2, Operating the pump,or Specifications.

This indicates a fully chargedbattery.

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The Quick Rate Change option, ifenabled, allows you to change theinfusion rate with single presses of thekeypad while the pump is running. Theoption applies while the pump isrunning or when on hold, but changescannot be made when the pump is inRate Taper, Volume Over Time orDose-Rate Calculation.

1. Press the Options key and thenpress numeric key 5, or press theOptions key until the Rate Changemessage appears.

2. Press the * key to begin changing therate. The Message Display showsthis screen for 10 seconds.

3. Change the rate:• press the 1 key to decrease the

infusion rate by 1 mL/h, or todecrease by 0.1 mL/h if the originalrate was set in 10ths mL/h, or

• press the 3 key to increase theinfusion rate by 1 mL/h, or toincrease by 0.1 mL/h if the originalrate was set in 10ths mL/h.

4. After 10 seconds the MessageDisplay changes to show the volumeinfused so far. The arrows aredisplayed as a reminder that theQuick Rate Change option is stillselected. You can repeat step 3 asrequired.

5. When you have finished with QuickRate Change, to exit and redisplaythe Standard Message:• press the Options key to display

this screen, then• press * .

5. Quick Rate Change

Performing Quick Rate Changes

The Quick Rate Change isautomatically discontinued when thepump is turned off. The next time thepump is turned on it will display theStandard Message display.

Any rate limits which are set willapply. The pump will alarm if you try toset a rate outside the limits

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6. Rate TaperThis option, if enabled, allowsautomatic tapering of the infusion rate,either up or down for theadministration of Total ParenteralNutrition (TPN).

Rate taper is programmed by settingfour infusion variables.

1. Volume

2. Total time or Maximum rate

3. Taper up time

4. Taper down time

The pump then makes the necessarycalculations and performs the ratechanges at the required times.

A Rate Taper infusion can be repeatedexactly as the previous infusion, orchanges can be made if the volume ortime requirements vary from oneinfusion to another.

This option cannot be used while theQuick Rate Change, Volume Over Timesetup, or Dose-Rate Calculation is inuse.

If the pump is switched off whilst inRate taper mode, and not connected tothe AC mains supply when it isswitched on again, the automaticbattery test is carried out, but theBattery Gauge is not displayed. If thebattery is low, the alarm sounds and awarning message is displayed.

Neither the primary or secondaryindicator lights are lit when in RateTaper.

The diagram below shows a typicalRate Taper infusion and the fourprogramming variables that must beset.

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1. Press the Hold key and then pressthe Options key repeatedly untilyou see this screen.

2. Press the * key to return to theStandard Message Display.

To enter Rate Taper

Rate and volume limitsThe highest allowable infusion rate inRate Taper is 400 mL/h (99.9 mL/h onMicro 505).

The highest allowable volume to beinfused in Rate Taper is 4400 mL(999.9 mL on Micro 505).

To exit Rate Taper

Rounding in rate stepsIf a rate step calculates to less than 1mL/h it always appears in the displayas 10ths. At 1 mL/h and higher thepump may calculate a rate step anddeliver in 10ths, however the displaywill show a rate which is rounded to thenearest whole number.

Entering hours and minutesWhen programming by total time, for atotal time of less than 10 hours, enter‘0’ before the hours digit (for example09h, 00min). The highest allowednumber of minutes is 59. For 60minutes or higher, enter the time ashours, or hours and minutes.

To end a Rate Taper infusion, you mustuse the Option key to exit the RateTaper and return to the standardoperation:

1. Press the Options key, then pressnumeric key 6, or press the Optionskey until you see this screen.

2. Press the * key then follow the stepsgiven to program by ‘total time’ onpage 3-10, or ‘maximum rate’ onpage 3-12.

To program an infusion using the RateTaper option, the pump must be onhold.

Any limits set with options (such asRate or VTBI limits) will apply. Youwill be able to program Rate Taperas normally, but you will beprevented from running theinfusion. For more details, see page3-16.

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1. Press the Options key and numerickey 6 or press the Options keyrepeatedly until the MessageDisplay shows the Rate Taperoption, then press the * key to begin.

2. Enter the volume to be infused.If an error is made while enteringthe new volume, press the Volumeto be Infused key and re-enter thecorrect setting (or alternativelypress the Volume to be Infusedkey twice to return to previoussetting).When the correct volume isdisplayed press the * key.

3. Press numeric key 1 to select ‘totaltime’.

4. Enter the hours and minutesrequired to complete the infusion.Enter the leading zero as shown inthis example for numbers less than10.If you make an error while enteringthe time, press any number keyrepeatedly until the first number inthe hour value is flashing, thenenter the correct time.

To program a Rate Taper by ‘Total Time’If you need to select the exact total timefor the Rate Taper delivery, you shouldchoose the Total Time Rate Tapermethod.

In this example for ‘Total Time’ wehave chosen the following values toprogram:

• a volume of 1500 mL to be infusedover a time period of 9 hours and 30minutes;

• taper up for 1 hour;• taper down for 45 minutes.

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When the infusion time is correctpress the * key.

5. Enter the hours and minutes for thetaper up period (enter zero hoursand minutes if you do not want totaper up).When the correct ‘Taper up’ timeperiod is entered press the * key.

6. Enter the hours and minutes for thetaper down period (enter zero hoursand minutes if you do not want totaper down).When the correct ‘Taper down’ timeperiod is entered press the * key.

7. The pump calculates the maximumrate that is required to complete theRate Taper infusion within thespecified time period.If the maximum rate is correct forthe patient press the * key.If you need to change the maximumrate, press the * key twice to takeyou back to step 2 and adjust theprogram (a longer total time may berequired).If * was pressed and this displayappears, then you need to review theprogram you have set. You will haveto adjust to the volume, time and/ormaximum rate value. Press the *key. This takes you back to step 2 toreview the program values.

8. If ready to start the Rate Taperinfusion, press the Run key or pressthe * key to review your settings. Ifyou pressed the * key to review thesettings the display will take youthrough steps 2 to 8 again.

9. If you pressed the Run key the RateTaper infusion will start. Thedisplay will count up the volumeinfused from zero.

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1. Press the Options key and numerickey 6 or press the Options keyrepeatedly until the MessageDisplay shows the Rate Taperoption, then press the * key toprogram your settings.

2. Enter the volume to be infused.If an error is made while enteringthe new volume, press the Volumeto be Infused key and re-enter thecorrect setting (or alternativelypress the Volume to be Infused keytwice to return to previous setting).When the correct volume is enteredpress the * key.

3. Press numeric key 2 to select‘maximum rate’.

4. Enter the maximum rate at whichthe infusion should be run. If anerror is made while entering themaximum rate, press the Rate keyand re-enter the correct value (oralternatively press the Rate keytwice to recall the previous setting).When the correct maximum rate isentered, press the * key.

To program a Rate Taper by ‘Maximum Rate’If you want to set the maximum rate atwhich the pump delivers the Rate Taperinfusion, choose the Maximum Ratetaper method.

In this example for maximum rate wehave chosen the following values toprogram:

• a volume of 1950 mL to be infusedat a maximum rate of 225 mL/h,

• taper up time for 1 hour and 30minutes,

• taper down time for 30 minutes.

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5. Enter the hours and minutes for thetaper up period (enter zero hoursand minutes if you do not want totaper up).When the correct ‘Taper up’ timeperiod is entered press the * key.

6. Enter the hours and minutes for thetaper down period (enter zero hoursand minutes if you do not want totaper down).When the correct ‘Taper down’ timeperiod is entered press the * key.

7. The pump calculates the length oftime in hours and minutes requiredto complete the infusion with themaximum rate entered. If the totaltime is correct press the * key.If you need to change the total time,press the * key twice to take youback to step 2, and adjust theprogram (a higher or lowermaximum rate may be required).If * was pressed and this displayappears, then you need to review theprogram you have set. You will haveto adjust to the volume, time and/ormaximum rate value. Press the *key. This takes you back to step 2again to review the program values.

8. If ready to start the Rate Taperinfusion press the Run key or pressthe * key to review your settings. Ifyou pressed the * key to review thesettings the display will take youthrough steps 2 to 8 again.

9. If you pressed the Run key the RateTaper infusion will start. Thedisplay will count up the volumeinfused from 0.

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1. With the Rate Taper infusionrunning press the Hold key.

2. Press the Options key twice to viewthe time remaining for the RateTaper.

3. Press the Options key again toaccess the “end early” display. Thisshows the actual time remaining or30 minutes, whichever is less.If the displayed time is acceptablefor the infusion rate to taper down,press the * key. If you need tochange the time displayed anynumber of minutes from 01 to 99can be entered. Press the * key whenthe correct time is displayed.

4. Press the Run key to start taperingdown immediately.If the early feature is not requiredthen press the * key to continue theRate Taper program as originallyprogrammed. If the pump is on holdpress the Run key to continue theinfusion.

5. When the rate has tapered downover the set length of time, the pumpalarms then continues to infuse atthe KVO rate.

Using the ‘End Early’ featureIf it is necessary for a patient’s RateTaper infusion to end earlier thanplanned, this feature provides analternative to stopping the pumpabruptly when it is infusing at a highflow rate.

If the infusion ends early, thepatient does not receive the fullinfusion as initially programmed.

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Rate Taper run but not completedWhen the pump is turned on again, ifthe Rate Taper was programmed andRun, but not completed, the MessageDisplay shows:

• Press the Run key to resume theinfusion, or

• press the Options key then press *to review or reprogram the RateTaper settings.

If the pump is turned off when RateTaper is selected, the current RateTaper program is stored in memory.You can use this feature of the pump toset up a program ready for later use.

When the pump is turned on again, theMessage Display depends on whether ornot the Rate Taper has been run.

Rate Taper programmed but not runWhen the pump is turned on again, ifthe Rate Taper was programmed butnot run , the Message Display shows:

Either:

• press Run to start the infusionusing the pre-programmed settings,or

• press * to review or reprogram thesettings.

Repeat a completed Rate TaperAfter completing a Rate Taper programyou can repeat the program (from itsbeginning):

1. Press the Volume to be Infused keytwice. The previous volume to beinfused appears in the display.

2. Press the Run key to start theinfusion using the previous values.

Modify previous Rate Taper volumeIf you need to repeat a Rate Taperprogram but need to change the Volume:

1. Press the Volume to be Infused keyand enter the new volume. The totaltime and/or the maximum ratechanges automatically.

2. Check that the correct volume isdisplayed then press the Run key tostart the infusion.

Modify other Rate Taper valuesIf you need to change any otherprogrammed Rate Taper values: totaltime, maximum rate, taper up time, ortaper down time, you must press theOptions key and follow the steps foreither programming Total time orMaximum rate in this chapter.

Resuming, restart ing or reprogramming theRate Taper

Any limits set with options (such asRate or VTBI limits) will apply. Youwill be able to program Rate Taperas normal, but you will be preventedfrom running the infusion. For moredetails, see page 3-16.

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Programming or reprogramming the Rate Taperwith Limits setIf any limits are set for the PrimaryRate or Max VTBI, then these willapply when you program the RateTaper or if you modify a program.Setting limits is described on page3-29.

Before you enter Rate TaperIt is worthwhile checking what valuesare set for Min and Max Primary Ratelimits and for Max VTBI before youenter Rate Taper. If they areinappropriate for the prescription, youcan then adjust them and not have theRate Taper infusion halt as describedbelow.

If you program outside the limitsThe pump tests whether the entered orcalculated values are within the limitswhen you press Run. This also appliesif you change values as described on theprevious page.

If the pump detects that the calculatedrate is outside the limits, or the VTBIis too high, then the alarm sounds andthe Message Display shows thiswarning:

Note: This happens when thecalculated rate is valid, but notacceptable because of the VTBI orinfusion rate limits set on the pump. Itis not the same as the “cannot infuse”message displayed because the ratecalculation is invalid.

To silence alarm and leave Rate TaperIf you see the Preset Limits messagewhen you are programming orreprogramming a Rate Taper infusion,

• Press the Silence key to silence thealarm. The pump automaticallyleaves Rate Taper and displays theStandard Message:

This is so that you can use the Optionskey to check and if appropriate, adjustthe preset limits, which you cannot dowhen you are in Rate Taper.

Troubleshooting Preset Limits error inRate Taper programTo find out why the Rate Taperprogram exceeds the limits, check thefollowing:

1. Check the prescription volumeagainst the Maximum VTBI limitand adjust the limit if it isincompatible with the prescription.

2. If the prescription requires that youenter a Maximum Rate, check thisagainst the Max Rate limit setting.

3. If the VTBI or Rate limits areacceptable, note all limits that areset by using the Options key. Re-enter Rate Taper and check if youhave made a mistake inprogramming the prescription.

4. Step through the program, look atthe calculated values and comparethem to the limits.

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7. Volume Over Time (VOT)To enter Volume Over TimeWith the pump on hold press theOptions key then press numeric key 7,or press the Options key until theVolume Over Time option appears.

To exit Volume Over TimeTo exit Volume Over Time whenprogramming the volume or time, pressthe Options key. The followingMessage Display appears:

Press the Options key to exit or press *to continue setting Volume Over Time.

When the pump is switched off, VolumeOver Time is cancelled. When nextswitched on, the pump resumes normaloperation.

Minimum and maximum infusiontimeInfusion time is entered as hours andminutes.

Minimum infusion time: 00 hrs 01 min

Maximum infusion time: 48 hrs 00 min

For time less than 10 hours, enter ‘0’before the hours digit (for example09 h 00 m).

The highest number of minutes thatyou can enter is 59. Times of 60minutes or higher must be entered ashours, or hours and minutes.

This option, if enabled in theTechnician Menu, allows you to set upan infusion using the volume to beinfused and the total time (with thepump automatically calculating theinfusion rate). It can be used witheither Primary, Secondary or Bolusinfusions.

Note: If rate limits are enabled and set,you may be restricted in the values youenter. Always use the Options key tocheck any limits before you enter themode. See page 3-30 for more details.

Rounding up calculated ratesIf the calculated rate is 99.9 mL/h orless the rate will be rounded to thenearest 0.1 of a mL/h. On the Model500 pump, if the calculated rate isgreater than 100 mL/h, the rate will berounded to the nearest 1 mL/h.

Volume and time value ratesIf the selected volume and time valuescalculate a rate which must be rounded,the pump calculates a revised timeappropriate to the rounded rate. Forexample, if the volume entered is 14mL and the time entered is 8 hours, theactual rate calculated will be 1.75, andthen rounded to 1.8. The time thenautomatically changes to 7 hours, 47minutes and the following displayappears:

Press the * key to accept time.

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1. With the pump on hold, press theOptions key then press numeric key7, or press the Options key until theVolume Over Time option appears.Press the * key to set the program.

2. Enter the volume to be infused.When the correct volume isdisplayed press the * key. If anincorrect value has been enteredpress the Volume to be Infused keyand re-enter the volume.

3. Enter the total infusion time inhours and minutes. If you make anerror while entering a time value,press any numeric key until the firsthour digit is flashing, then enter thecorrect time value. To start enteringvalues again from step 2, press theVolume to be Infused key.When the correct time is displayedpress the * key.

4. Press the Run key to start theinfusion, or press the * key to reviewthe settings.

5. When you press Run the MessageDisplay shows the StandardMessage. When the infusion iscompleted, the pump sounds analarm, and continues to infuse atthe KVO rate until you press Hold.

Cannot infuseIf you see this message when you pressRun, then you have entered a time/volume combination that resulted in aninvalid rate.

1. Press the * key to return to step 2and enter the correct volume andtime values.

2. Press the * key, then press Run.

To use Volume Over Time

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This option, if enabled in the TechnicianMenu, allows the automatic calculationof the infusion rate when the followingparameters are set:

• dosing rate (for example mcg/min ormcg/kg/min),

• patient weight in kg or lbs (ifrequired in dose mode selected),

• drug amount in fluid container(MG = milligrams, Gm = grams,mcg = micrograms, or units),

• volume of fluid in container (mL).Dose-Rate Calculation can be used withthe pump on hold or while running. It isonly available for a Primary infusion.

8. Dose-Rate Calculat ionWhen in Dose-Rate Calculation mode,all values for the current infusion arestored when the pump is switched off.

During a Dose-Rate Calculationinfusion, if the Drug List feature isenabled, you can press * twice to viewthe selected Drug Label.

Dose-Rate Calculation RecoveryDose-Rate Calculation Recovery is anadditional feature which can only beenabled in the Technician Menu. Itenables you to set up a Dose-RateCalculation program for later use.

To use Dose-Rate Calculation Recovery:

1. Program the Dose-Rate Calculationinfusion, see page 3-20.

2. Press Run then Hold.3. Switch off the pump. When it is next

switched on, the pump displays:

You can:• press Run to restart the previous

Dose-Rate Calculation infusion, or• press * to review the dose-rate

prescription, or enter new values foran infusion, or

• press Options then * to leave Dose-Rate Calculation and return to theStandard Message display.

Note: When you switch on the pumpwith DRC Recovery enabled, noinformation screens are displayed in theself test. However, if there is a problem,such as low battery, a warning messageis displayed with an alarm sounding.

WARNING: Dose-rate calculation requirescare in entering data. Refer to specificproduct drug labelling for information onappropriate administration techniquesand dosages. Entering incorrect data mayresult in patient injury or death.

Minimum/Maximum Rate or VTBIlimits set in Options apply to aDose-Rate Calculation program. Formore details, see page 3-28.

µg may be displayed instead of mcgin Dose-Rate Calculation displays,see the Technical User Manual.

WARNING: Correct entry of data isessential in order to ensure that theintended infusion is performed. Beforeconfirming any displayed data whensetting up an infusion, you should ensurethat it is correct. Failure to do so mayresult in compromised function of theproduct, patient injury or user injury.

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To enter or exi t Dose-Rate Calculat ionTo enter Dose-Rate CalculationTo enter the Dose-Rate Calculationdisplay press Options and numeric key8, or press the Options key until yousee the following screen.

Press the * key to program the infusion.

To exit Dose-Rate CalculationTo exit Dose-Rate Calculation, pressthe Options key until you see thefollowing screen:

Press the * key to return to theStandard Message display.

This section looks at each Dose-RateCalculation step in programming order.

• Programming the dosing rate• Programming the body weight• Programming the drug amount• Programming the volume. A complete programming example isdescribed on page 3-22.

Programming the dosing rateWhen you enter the Dose-RateCalculation option, you see a displaysimilar to the following asking you toconfirm the current dosing rate:

You can confirm the current rate bypressing *, or:• change the dosing rate mode, or• enter a new value for the dosing rate.

Changing the dosing rate modeThe pump can be configured in theTechnician Menu to display either µg ormcg (micrograms).

To change the dosing rate mode (that isthe rate units),1. Press Options to display this

screen:

2. Press * until the screen shows thedosing rate mode you want to use forthe infusion.

Dosing rate modes availableThe following dosing rate modes areavailable:• mcg/kg/min (micrograms/kilogram/

minute),• mcg/min (micrograms/minute),• MG/min (milligrams/minute),• MG/hour (milligrams/hour),• units/hr (units/hour),• MG/kg/hr (milligrams/kilogram/hour),• mcg/kg/hr (micrograms/kilogram/

hour),• MG/kg/min (milligrams/kilogram/

minute),• units/kg/hr (units/kilogram/hour).

Dose-Rate Calculation steps

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Enter new value for the dosing rateWhen you have the mode you want touse on the screen, enter the value forthe dosing rate from the keypad. Thescreen changes to show that you areentering a value and not selecting themode, as if you had just entered Dose-Rate Calculation. Press * when youhave done so.

When you enter values, the precisionwith which you can enter them dependson the range:

• 0.01 to 99.99 in increments of 0.01,• 0.1 to 999.9 in increments of 0.1,• 1 to 9999 in increments of 1.If you have chosen one of the followingmodes using patient weight (mcg/kg/min, MG/kg/hr, mcg/kg/hr, MG/kg/minor units/kg/hr), you are next asked toenter it as described in Programmingthe patient weight below.

For dosing rate modes without thepatient weight, you are next asked toenter it as described in Programmingthe drug amount, opposite.

Programming the patient weightThe Patient’s body weight follows thedosing rate entry for the followingdosing rate modes:

• mcg/kg/min,• MG/kg/hr,• mcg/kg/hr,• MG/kg/min,• units/kg/hr.You need to enter the patient weightwhen you see a display similar to thefollowing:

Press the Options key to change theweight measurement from kg to lbs orlbs to kg. The pump recalculates anyvalue entered into the new weightunits.

If you press the Options key a secondtime by mistake, you are taken back tothe beginning of programming. Justpress * to get back to entering andconfirming the patient weight.

Enter the patient weight from thekeypad. When entering the weight, theprecision depends on the units you areusing. See the Specification at the endof the manual for the increments foreach weight unit.

Press * to set the weight and move onto the drug amount.

Programming the drug amountThe drug amount entry follows thedosing rate entry or the patient weight(if a dosing rate involving weight isselected).

When you are asked to enter the drugamount display, you will see a displaysimilar to the following:

If you need to change from MG drug/bag(in this example), press the Optionskey to enter the change screen:

Press the * key repeatedly to display g,MG and mcg.

When the display is correct, enter thedrug amount value from the keypad.

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When entering the amount, the precisiondepends on the units you are using. Seethe Specification at the end of the manualfor the increments for each range.

When the dosing rate mode selectedrequires ‘units’ input, only “units/bag”appears in the Message Display.

Once you have entered the drugamount, you are next asked to enter thevolume of the bag. This is used with thedrug amount to calculate the drugconcentration.

Programming the volumeWhen you enter the volume display, yousee a display similar to the following:

For the range of volumes that can beentered, see the section on Primary andSecondary infusion in the Specificationsat the end of this manual.

Enter the number of millilitres in thefluid container. This must be thevolume when the bag is full. It isused to calculate the concentration.

When the setup is completeWhen the programming steps for theDose-Rate Calculation infusion arecompleted, the display shows that theinfusion is ready to run or be reviewed:

You will need to review if an invalidrate is calculated and the MessageDisplay shows:

As well as the Message Display whichshows the volume infused and thedosing rate, the programmed volume tobe infused appears in the Volumedisplay and the calculated infusion rateappears in the Rate display.

Calculated infusion rates may berounded up as follows:

• below 100 mL/h, rounded to thenearest 0.1 mL/h,

• above 100 mL/h, rounded to thenearest 1 mL/h.

The pump also back-calculates anddisplays the actual dosing rate beingdelivered if rounding has occurred.

Changing the volume to be infusedIf you do not want the whole bag to beinfused, you can change the volume tobe infused if the pump is on Hold andthe Message Display shows:

or when the infusion has been startedand then stopped:

To alter the volume:

• press the Volume to be Infused key• enter the new volume to be infused• press Run.Note: Changing the Volume to beinfused does not affect the programmeddosing rate or the calculated infusionrate.

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Programming the pump using afixed infusion rateOnce you have completed theprogramming steps for the Dose-Rate

Calculation infusion, you can changethe infusion rate instead of acceptingthe calculated infusion rate. When theMessage Display shows:

• press the Rate key and enter thedesired rate, then

• press the Run key.The pump will then back-calculate thedosing rate based on the new infusionrate that you have entered.

1. To enter Dose-Rate Calculation pressOptions then numeric key 8, or pressOptions until you see this screen.Press the * key to enter the dosingrate display.

2. You can either accept the dosing rateor enter a new dosing rate .

3. If you need to change the dosing ratemode press the Options key.Press the * key until the requiredmode is displayed, as described inProgramming the dosing rate on page3-20.

4. Enter the dosing rate value, thenpress the * key.

Dose-Rate Calculation programming exampleIn this example we have chosen thefollowing values to program:• dosing rate - 5 mcg/kg/min• patient weight 73 kg• drug amount in fluid container - 400

mg• volume of fluid in container - 250 mL

This example includes patientweight. Step 5 is not necessary ifyou program without it.

If you do not enter any values whenprogramming, but accept eachprevious value by pressing * atevery option, the VTBI may not becorrect for the infusion. Set it to anappropriate value before runningthe infusion. Changing it will notaffect the calculated rate.

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5. In this example, because the dosingrate mode chosen is mcg/kg/min, thepatient weight screen is displayed, asdescribed in Programming the patientweight on page 3-21.The weight is displayed in either kgsor lbs. Changing the weightmeasurement is described inProgramming the patient weight onpage 3-21.Either accept the patient weight thatis currently shown by pressing *, orenter the new weight of 73 then pressthe * key.

6. The next message asks for the drugamount in the bag.

If you need to change the entry type,see Programming the drug amount onpage 3-21.

Enter the correct drug amount in thebag and press the * key.

7. Next enter the fluid volume of the bagand press the * key.

8. Before you start the infusion it isgood practice to review your settings.Press the * key to review the programand make any necessary changes.

Note: You may also need to review if thepump finds that the values you haveentered are incompatible.

9. When your program is correct pressRun. As well as the Message Display,which shows the volume infused andthe dosing rate, the programmedVolume to be Infused appears in theVolume display and the calculatedinfusion rate appears in the Ratedisplay.

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Changing the dosing rate without stopping theinfusionThe pump allows you to change thedosing rate (thus altering the infusionrate) without stopping the infusion.

1. To change the dosing rate withoutstopping the infusion, press the *key.The current dosing rate displayed inthe Message Display startsflashing, and the infusion Ratedisplay goes blank. However, thepump continues to infuse at theoriginal rate.

2. Enter the new dosing rate valueusing the keypad.

3. Within 10 seconds of entering thenew dose, press the Run key.If a warning appears in the MessageDisplay and the pump alarms, referto Dose or rate change alarms onpage 3-27.

4. The pump calculates the new dosingrate and new infusion rate. The newdosing rate is now displayed in theMessage Display and the newinfusion rate in the rate display.The pump is now infusing at the newrate.If a warning appears in the MessageDisplay and alarms, refer to Dose orRate change alarms on page3-27.If the calculated rate is rounded upthe pump will back-calculate anddisplay the actual dosing rate beinginfused.

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Changing the infusion rate without stopping theinfusionThe pump allows the infusion rate to bechanged (thus altering the dosing rate)without stopping the infusion.

1. To change the infusion rate withoutstopping an infusion, press the Ratekey.The current dosing rate displayed inthe Message Display and theinfusion Rate display goes blank.However the pump continues toinfuse at the original rate.

2. Enter the new infusion rate usingthe keypad.

3. Within 10 seconds of entering thenew rate, press the Run key.If a warning appears in the MessageDisplay and the pump alarms, referto Dose or rate change alarms onpage 3-27.

4. The pump calculates the new dosingrate. The new dosing rate is nowdisplayed in the Message Displayand the new infusion rate in the ratedisplay. The pump is now infusingat the new rate.If a warning appears in the MessageDisplay and alarms, refer to thenext page Dose or rate changealarms.

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Dose or rate change not completedwithin 10 secondsIf the new dosing rate or infusion rate isentered, but the Run key is not pressedwithin 10 seconds, or if anotherfunction key is pressed, the new rate isdiscarded and the Message Displayreverts to the previous values, a non-insistent alarm sounds and one of thefollowing displays appear:

Press the Silence key to silence thealarm.

The pump now continues infusing atthe old rate. If you still need to changethe dosing rate press the * key to takeyou back to step 1 of Changing thedosing rate without stopping the infusionon page 3-25 or Changing the infusionrate without stopping the infusion onpage 3-26.

Dose or Rate change not acceptedIf the dosing rate or infusion rate ischanged, but the resultant calculatedrate is incorrect, the displays revert totheir previous values, the non-insistent alarm sounds, and one of thefollowing displays appear:

Press the Silence key to silence thealarm.

The pump now continues infusing atthe old rate. If you still need to make achange, press the * key to take you backto step 1 of Changing the dosing ratewithout stopping the infusion on page 3-25 or Changing the infusion rate withoutstopping the infusion on page 3-26.

Check values you want to change beforeentering them to ensure that they willresult in a valid calculated rate/dose.

Dose or rate change alarms

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Programming or reprogramming Dose-RateCalculat ion with Limits setIf any Limits are set for the PrimaryRate or Max VTBI, then these willapply when you program the Dose-RateCalculation or if you modify a program.Setting limits is described on page 3-29.

Before you enter Dose-RateCalculationIt is worthwhile checking what valuesare set for Min and Max Primary Ratelimits and for Max VTBI before youenter Dose-Rate Calculation. If theyare inappropriate for the prescription,you can adjust them and not have theinfusion halt as described below.

If you program outside the limitsThe pump tests whether the entered orcalculated values are within the limitswhen you press Run.

If the pump detects that the calculatedrate is outside the limits, or the VTBIis too high, then the alarm sounds andthe Message Display shows:

Note: This happens when the cal-culated rate is valid, but is outside theVTBI or infusion rate limits set on thepump. It is not the same as the “cannotinfuse” message displayed if thecalculation is invalid.

To silence alarm and leave DRCIf you see the Preset Limits messagewhen you are programming orreprogramming a Dose-RateCalculation infusion, Press the Silencekey to silence the alarm. The pumpautomatically leaves Dose-Rate

Calculation and displays the StandardMessage:

This is so that you can use the Optionskey to check and if appropriate, adjustthe preset limits, which you cannot dowhen you are in Dose-Rate Calculation.

Troubleshooting Limits in a DRC programTo find out why the Dose-RateCalculation program exceeds thelimits, check the following:

1. Check the prescription volume (thevolume in the bag) against the VTBIlimit and adjust the limit if it isincompatible with the prescription.

2. The rate calculated will remain inthe LED display when you are takenout of Dose-Rate Calculation. Checkthis against the Rate limit setting.

3. Check the value for the VTBI sinceyou may have accepted all values fora previous Dose-Rate calculationprogram and this will not haveupdated the VTBI from the bagvolume.

4. If the VTBI or Rate limits areacceptable, note all limits that areset by using the Options key. Re-enter Dose-Rate Calculation andcheck if you have made a mistake inprogramming the prescription.

If you change the rate while runningIf you change the rate (either the dosingrate or the pump infusion rate) whilerunning, and exceed the limits, thenpress Run, the pump alarms butcontinues at the programmed rate.

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Sett ing Rate and VTBI l imitsYou can limit the infusion Rates andVTBI (volume to be infused) values foreach pump. When you set up aninfusion, the pump rejects a Rate orVTBI value that is not within theMinimum/Maximum rate limits, or isgreater than the maximum VTBI.

For example, you should set amaximum rate on a pump that isintended for use in an Epiduralapplication, or set a maximum VTBI ona pump to be used in a neonatalenvironment. Setting rate limits is alsocalled Rate Capping.

Rate Taper, Volume Over Time andDose-Rate Calculation are also affectedby limit settings.

The following Options are used to limitthe infusion rates and volumes to beinfused on the pump:

Minimum and Maximum Infusion Rates

For Primary infusions:

• Min Rate, Max Rate, Max VTBI.

For Secondary or Bolus infusions:

• Min S/B Rate, Max S/B Rate,Max S/B VTBI.

To define the ranges, the items must beenabled on the Technician Menu, andthen set using the Options key.

See page 3-32 for more details on howlimits affect programming an infusion.

If the Primary ‘Min Rate’ and ‘MaxRate’ are enabled in the TechnicianMenu, their current settings aredisplayed when you switch on the pump.If the defaults have not been changed(on a Model 500), the screen looks likethis:

The Secondary/Bolus Maximum andMinimum rates are not displayed whenyou switch on the pump, even if they areenabled and set.

Entering ratesRates must be entered as wholenumbers: they cannot include a decimalpoint. If the Min Rate is set to zero,there is no lower limit. The Max Ratemay be set to 999 (on a Model 500) or99 (on a Micro 505).

The instructions on the followingpages explain how to set values forthe (Primary) Minimum andMaximum Rate and MaximumVTBI. Once you have understoodhow to change these values, youwill find that you can set theSecondary/Bolus minimum andmaximum rates in the same way.

Unless the display includes S/B,the rate being changed is alwaysthe Primary.

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1. Press the Options key repeatedlyuntil you see the Minimum Ratedisplay. The current minimuminfusion rate flashes, showing thatyou can change this value.

2. Enter a new rate, using the numerickeypad, then press the * key toconfirm.If it is correct, to leave the rateunchanged, just press *.If the pump finds that the rate isinvalid, the number continues toflash, so you should repeat this step.

3. With the value for Min Rate static,press the Options key to displaythe flashing Maximum Primaryrate.

4. Enter a new rate then press * to setthe value. Just press * if you want toleave the maximum rate unchanged.

You can now do one of the following:

• press the Options key once to moveon to the next Option;

• press the Options key repeatedly tomove through all the Options thathave been enabled on the pump. Youcan stop when the StandardMessage is displayed on the screen,indicating that the pump is ready tobe programmed, or carry on until youreach the Min Rate screen again,where you can make further changes;

• turn the pump off then on again, tosee the new primary minimum andmaximum values in the messagesdisplayed in the power up sequence.

To set the minimum and maximum infusion rateIf the Options are enabled, you canchange either or both values. This sectionexplains how to change both values.

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1. Press the Options key repeatedlyuntil you see the Max VTBI display.The current maximum VTBIflashes, showing that you canchange this value.

2. Enter a new VTBI, using thenumeric keypad, then press the *key to confirm.If it is correct, to leave the VTBIunchanged, just press *.If the pump finds that the rate isinvalid, the number continues toflash, so you should repeat thisstep.

3. Press the Options key to take youto the next option.

To set the maximum infusion volume

This Option is to limit the volume thatmay be programmed for a singleinfusion. The Max VTBI is 9999 (on aModel 500) or 999 (on a Micro 505),There is no lower limit for the VTBI.

If the Primary Maximum VTBI isenabled, the current setting isdisplayed when you switch on thepump.

If the default has not been changed, (ona Model 500) the screen looks like this:

Maximum VTBIThe Max Secondary/Bolus VTBI is notdisplayed, even if it is enabled.

The example here shows how to setthe Maximum VTBI for the Primaryinfusion. The process is the same forsetting the Maximum VTBI for theSecondary/Bolus infusion.

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Programming and running infusions with l imits

If limits are set and you try to run aninfusion, the pump will prevent youfrom running with a rate or VTBI valueentered outside the limits. Thisincludes special infusion modes such asVolume over Time, Rate Taper andDose-Rate calculation. In the latter twoinfusion modes, the pump behaves in aslightly different way.

For Rate Taper, instructions onprogramming with limits set aredescribed on page 3-16.

For Dose-Rate Calculation,instructions on programming withlimits set are described on page 3-28.

If you change rates while running or putthe pump on hold and change thevolume, the limits are checked whenyou press Run. The pump continues toinfuse at the previous rate when anerror is detected during a rate changewhile running.

Rate limit settings also affect QuickRate changes.

When the pump detects a value whichis outside the set limits it sounds analarm and the Message Display shows:

Silence the alarm and enter a valuewhich is valid for the limits. Theprevious value is restored to the LEDdisplay.

If are using Quick Rate change, and tryto move outside the rate limits, thepump will alarm with the limitsexceeded message, and the rate LEDwill show the limit setting. If you arechanging the rate while the pump isrunning, the infusion will continue atthe limit rate.

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KVO rateThe pump automatically switches to aKVO infusion when the programmedinfusion ends. The default rate for KVOis 3.0 mL/h, or the programmedinfusion rate if that was less than 3.0mL/h.

The KVO option, if enabled in theTechnician Menu, allows you to set adifferent KVO rate.

The pump remembers the value enteredas described here, and uses it as theKVO rate. You cannot set the KVO rateto zero.

The range for the KVO rate must bewithin the following limits:

500 0.1 to 10.0 mL/hMicro 505 0.1 to 3.0 mL/h.

1. Press the Options key until you seethe KVO rate display. The currentvalue flashes, showing that you canenter a new value.

2. Enter the new KVO Rate using thenumeric keypad, then press * toconfirm.If the rate is correct, press Optionsto move on to the next Option.

In the unusual situation that the rateyou enter is not accepted, then the MaxPrimary Rate limits are set below thevalue you wish to enter. The MinPrimary Rate does not affect the KVOentry.

Sett ing a KVO rate

When you set the KVO rate, if the MaxPrimary Rate is also enabled and setbelow these limits, then that will definethe maximum KVO value you can enter.If the programmed infusion rate is lessthan the set KVO rate, when the pumpgoes into KVO, it will continue pumpingat the programmed lower rate.KVO rates cannot be changed when aninfusion is running, but if you press theOptions key, the current setting isdisplayed.

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Drug LabelThe Drug List feature, if enabled in theTechnician Menu, allows you to use theOptions key to select a drug label froma predefined list that is stored in thepump.

When the Drug List is enabled, theselected drug label is displayed for twoseconds when you switch on the pump,for example:

Drug Library

If no drug label has been selected, thescreen is shown like this:

The selected Drug Label is displayedfor two seconds if you press * when thepump is on hold, or infusing.

If you press the Options key when aninfusion is running, you will also seethe current label, but will not be able tochange it.

This is a complete alphabetical list ofthe drug labels retained in the pump’smemory. Due to the number ofcharacters that the pump can displaysome of the drug names have beenshortened or abbreviated.

Acetylcysteine

Alfentanil

Aminophylline

Carboplatin

Cisplatin

Cyclophosphamide

Dextrose

Dextrose/Saline

Dobutamine

Dopamine

Doxapram

Doxorubicin

Droperidol

Epidural

Fentanyl/Bupiv

Fluorouracil

Hartmanns

Heparin

Morphine

Nitroglycerine

Nitroprusside

Oxytocin

Propofol

Prostaglandin

Remifentanil

Ritodrine

Ropivacaine

Saline

Syntocinon

TPN

The drug label provides a visualreminder of the name of the drug,but it does not control any pumpfeatures.It is your responsibility to ensurethat the correct drug name isselected.

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1. Press Hold if the pump is infusing.2. Press the Options key until you see

the Drug Label display. It shows thename of the drug that is currentlystored in the pump.

3. Press * to change the drug.4. To select the drug label, press

• the 1 key to scroll down throughthe list, or

• the 3 key to scroll up through thelist.

5. When the required drug label isdisplayed, press the * key to confirmthe name.

6. This display shows that the selecteddrug is now stored in the pump asthe Drug Label. Press the Optionskey to take you to the next option.

7. When you see the Standard MessageDisplay, press * to show the DrugLabel for two seconds.

Select ing a new drug label

Checking the current drug label

• Switch the pump off and then on, or• Press * when the pump is on hold, or

infusing.

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O p t i o n s G r a s e b y M e d i c a l L t d .

Clearing the drug label1. Press Hold if the pump is infusing.

2. Press the Options key until you seethe Drug Label display.

3. Press * to display this screen.

4. Press * to clear the label anddisplay this screen.

5. Press the Options key repeatedly toreturn to the Standard MessageDisplay.

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Troubleshoot ingChapter 4

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T r o u b l e s h o o t i n g

The chapter contains two sections:

• warning messages with alarms,divided into Continuous (backup)alarm, Insistent alarms and Non-insistent alarms;

• warning messages with no alarms.

The chapter lists the possible causesand recommended action to take foreach of the warning messages.

What ’s in th is chapter

In t roduct ionThis chapter covers all the errormessages and alarms, displayed by theVolumetric, that notify you of anyoperating problem.

If you cannot solve the problem afterreading this chapter, the pump shouldbe inspected and repaired by a suitablyqualified technician, or returned toGraseby Medical at the address on theback cover of this Instruction Manual,in order to have the fault rectified.

The chapter does not contain details ofthe Volumetric pump System errors orwarnings that indicate a problem thatcan only be solved by the Biomedicalengineering department, or by returningto the distributor/factory. These aredescribed in the Volumetric ServiceManual.

You should read this chapter to find outhow to solve any problems that arisewhilst you are using the Volumetricpump.

You are likely to be in one of thefollowing groups:

• Biomedical engineeringdepartment, needing to find outwhat alarms may arise during thenormal operation of the pump

Who should read this chapter• People being trained, who have

access to the Instruction Manual asadditional training material

• People who have been trained, whoneed a concise summary to remindthem of the Volumetric pump’salarms and a description of what todo if the pump sounds an alarm.

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T r o u b l e s h o o t i n g G r a s e b y M e d i c a l L t d .

CAUTION: Refer all service repair andcalibrations only to qualified technicalpersonnel. Unauthorised modifications tothe pump must not be carried out.

WARNING: You should ensure that theperformance offered by the pump is fit forthe intended purpose. Failure to do somay result in compromised function ofthe product, patient injury or user injury.

WARNING: Do not use a faulty pump. Ifthe pump detects a fault when it is firstturned on, or if it develops a fault duringoperation then a continuous system alarmsounds. The pump must be referred to asuitably qualified technician or returnedto Graseby Medical in order to have thefault rectified.

Handl ing problems with the pumpMost problems in using the pump aresignalled by alarms whoseaccompanying messages are describedin the rest of this manual.

You should also use your experience inusing the pump to take action if thepump behaves as if it is faulty. Followthe warnings and cautions on this pageto take appropriate action to send thepump to a suitably qualified technicianfor checking.

Pump wil l not switch onIf the pump does not switch on whenthe On/Off key is pressed whenconnected to an AC power supply.Check that the keypad lockout featureis not active, see Safety keypad lockout,page 2-22.

WARNING: Before using the pump, itshould be inspected for physical damage.The pump should not be used if damageis evident, and should be returned toservice personnel for repair before beingreturned to use. Failure to do so mayresult in compromised function of theproduct, patient injury or user injury.

WARNING: Do not open the pumphousing. Refer all service faults only toqualified technical personnel. Openingthe pump housing may cause electricshock leading to patient or user injury ordeath.

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4 — 3

T r o u b l e s h o o t i n g

Pump Messages

Continuous (back up) alarmsWhen a continuous alarm occurs, the pump automatically stops the fluid delivery.

Message display Possible causes Action

Electrical or Do not use.mechanical problem. Pump needs to be repaired by

a qualified technician orreturned to Graseby Medical.

Potential pump Turn pump off, then on.problem detected. If alarm persists, remove

pump from use. Pump needs tobe repaired by a suitablyqualified technician orreturned to Graseby Medical.

Messages are divided into those where an alarm sounds and those which justdisplay a message.

Warning Messages with alarms

Message display Possible causes Action

Rate or VTBI limits Correct the value or change thehave been set and you limits if appropriate.are trying to programa value outside theselimits.

or

You have entered a Correct the value.Bolus VTBI greaterthan the Primary VTBI.

Programming Messages with alarms

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T r o u b l e s h o o t i n g G r a s e b y M e d i c a l L t d .

Insistent alarms (pump stops infusing)

Message display Possible causes Action

Air detected in the To remove air:cassette. 1. Close the lower roller clamp.

2. Open the door latch.3. Wait briefly for the cassette

to fill.4. Slowly close the door latch.5. Repeat if necessary.

or

Cassette loaded Make sure cassette isbackwards. properly loaded (flat side out,

pillow side in).

Battery is depleted. AC power cord must beplugged in to continue infusion.

Tubing safety clip To load the safety clip:is not correctly loaded. 1. Close lower roller clamp.

2. Open the door.3. Place safety clip in the slot.4. Close the door.5. Open the lower roller clamp.

Door was opened Always press the Hold keywhile the pump and close the roller clampwas running. before opening the door.

To restart the infusion:1. Press Silence.2. Close the door.3. Press Run.

Problem detected 1. Open the door.above the pump as 2. Check clamps and tubingthe door was being for any restrictionsclosed. 3. Reload cassette if necessary.

4. Close the door.

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T r o u b l e s h o o t i n g

Insistent alarms (continued)

Message display Possible causes Action

Insufficient flow from 1. If the fluid container isthe container to the empty, replace it. pump. 2. Raise the height of the fluid

container so that the bottomof the drip chamber is 15-30cm (6 to 12 inches) above thetop of the pump.

3. Open the upper clamp ifclosed, remove any rest-riction to the upper tubing.

4. Replace the admin set ifthere is damage to the spikeor other admin set problem.

Pressure below pump Open the lower roller clamp,exceeds the Occlusion remove any restriction to theAlarm Setting. lower tubing. Change the

Occlusion Alarm Setting ifnot appropriate for infusion.Verify patient catheter ispatent.

Pump is on hold for Press the Silence or Hold key2 minutes with the to silence the alarm.door closed, Press the Run key to start theor 6 minutes with the infusion, or turn the pump offdoor open. if not in use.

Secondary/Bolus Press the Silence or Hold keyinfusion ended and to silence the alarm.Secondary Stop has Press the Primary keybeen enabled on the Press Run to start the PrimaryTechnician Menu. infusion.

Note: In Medium or High occlusion alarm settings, when downline pressure exceedsthe alarm threshold, the motor pauses, the Run key remains lit and the Pumpingindicator stops. If within 10 seconds the pressure drops back below the threshold,pumping resumes and the alarm does not sound (if pressure remains high, thealarm sounds). If repeated pressure spikes occur, causing the pump to enter thisfiltering mode for a total of 30 seconds, measured over the last 4 minutes that thepump was infusing, the alarm sounds. Occlusions detected in the Low occlusionalarm setting cause an immediate alarm.

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Infusion rate change Press the Silence or Run keywas attempted, while to silence the alarm. Re-enterrunning but not the running rate change, seecompleted. Chapter 2 Operating the pump.

Secondary infusion Press Hold then Secondary key,was programmed but Re enter the VTBI and Rate.the Primary was run. Press the Run key.

Message display Possible causes Action

Dose-rate calculation Press the Silence or Run toprogram setup silence the alarm, if necessarystarted with the re-enter the Dose-ratepump running; calculation program setup.dosing parametersnot completed.

Running dosing rate Press the Silence or Run keychange was attempted, to silence the alarm. Re-enterbut not properly the running dose change, seecompleted. Chapter 3 Options.

The entered dose Press the Silence or Run keyor calculated rate to silence the alarm. Re-enteris incorrect. the parameters.

The infusion is Press the Silence or Run keycomplete and the to silence the alarm andpump has switched continue the KVO delivery. Theto KVO rate. pump re-alarms every 6 mins.

orpress the Hold key to silencethe alarm and stop infusing.

Battery nearly Plug in the AC power cord, ifdepleted (1/2 hour or possible,less remains). or

Press the Silence or Run keyto silence the alarm for 6minutes and continue runningthe infusion.

Non-insistent alarms (pump continues to infuse)

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4 — 7

T r o u b l e s h o o t i n g

Message display Possible causes Action

Keypad Lock/unlock Press the Keypad Lock/unlockbutton on rear of the button on the rear of the pumppump has been to unlock the keypad.pressed.

Keypad Auto lock Press the Keypad Lock/unlockbutton has been button on the rear of the pump,enabled. twice to unlock the keypad.

Note: The keypad willautomatically lock 1 minuteafter the last key is pressed.

Quick rate change See Chapter 3 Optionsoption has beenselected

The Rate taper See Chapter 3 Optionsoption has beenselected.

The rate taper Infusion values must beprogram or changed, see Chapter 3volume over time Options, Programming a rateprogram cannot be taper or Programming volumeinfused as entered. over time.

Dose-rate calculation The infusion values mustprogram cannot be be changed, see Chapter 3infused as entered. Options, Programming dose

rate calculation).

Warning Messages with no alarms

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T r o u b l e s h o o t i n g G r a s e b y M e d i c a l L t d .

Periodic cleaning of the pump housingand inside surface of the door isrecommended. Unplug the power cordand use a sponge or cloth lightlydampened with a solution of warmwater and a mild, non-stainingdisinfectant/cleaner. Do not usecleaning agents which could damagethe outer pump housing.

The Service Manual containsinformation on which cleaning agentsmay or may not be used, and how toperform cleaning.

Instrument CareCAUTION: Carry out periodic cleaningfollowing the detailed instructions in theVolumetric Infusion Pumps ServiceManual. Do not use unapproved cleaningagents.

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Specif icat ions/Standards

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S p e c i f i c a t i o n

Specif icat ions

General

Weight 5 kg (11 pounds).

Dimensions including pole clampHeight 28 cm (11 inches).Width 21.5 cm (8.6 inches).Depth 23.5 cm (9.45 inches).

Temperature Operating 18° to 40° C (64° to 104° F)Storage -25° to +55° C (-13° to 131° F).

Relative humidity Operating 30% to 75% (non-condensing).Storage 30% to 75% (non-condensing).

Pressure range Operating 50 kPa to 106 kPaStorage 19 kPa to 106 kPa

Immunity levels Immunity levels are the full levels specified inEN60601-1-2 (radiated immunity is 3 V/m andESD immunity is 3 kV contact and 8 kV air).

Free flow protection The pump mechanism operates the safety clip onthe administration set.

Head-height From bottom of drip chamber to top of pump

Model 500 15 cm (6 ins) minimum for flow rates <500 mL/h30 cm (12 ins) minimum for flow rates >500 mL/h30 cm (12 ins) when using 60 drops/mL sets30 cm (12 ins) when using thick solutions*

Micro 505 15 cm (6 ins) minimum30 cm (12 ins) when using 60 drops/mL sets30 cm (12 ins) when using thick solutions*

* certain cytotoxic agents, lipid-based fluids andother viscous solutions, for example TotalParenteral Nutrition.

Self test Dual microprocessors independently test each other.

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S p e c i f i c a t i o n G r a s e b y M e d i c a l L t d .

Maximum over infusion Under a single-fault condition, the maximum overinfusion which may occur is 12.5% over theselected flow rate. Larger inaccuracies aredetected by the pump, and cause the pump to stopinfusing and to alarm.

Air detect system Air bubbles are detected by electronic opto-encoder detection device (with self-checkingsensors) located on cassette housing.

Accuracy ± 2% of displayed rate and volume to be infused.The quoted accuracy is ±2% for a long-terminfusion.Below rates of 1 mL/h this accuracy may not beachieved for a short-term infusion.During the total infusion time the accuracyaverages out (see trumpet curves in this chapter).

Accuracy measurement equipment50 mL glass measurement burette graduated in0.1 mL increments and traceable to NationalInstitute of Standards and Technology orappropriate international standards bureau.

Test solution Sterile water or normal saline at roomtemperature (70°F ±5°/21°C ±3°).Graseby standard (primary), 20 drops/mL, non-checkvalve administration set (8C820).

Testing conditionsModel 500 Fluid level in the solution container 46 cm (18

inches) above top of the pump, rate set at999 mL/h and volume to be infused of 49 mL.

Micro 505 Fluid level in the solution container 46 cm(18 inches) above top of the pump, rate set at99.9 mL/h and volume to be infused of 25.0 mL.

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S p e c i f i c a t i o n

PowerAC power supply Internally configured for either

100-120 V AC, 200 mA, 50/60 Hz.or,

220-240 V AC, 80 mA, 50/60 Hz.

Battery type Rechargeable, sealed lead-acid, 12 Volt, 1.3 Ah.

Battery operating time 6 hours at 100 mL/h (99.9 mL/h on Micro 505),with approximately 1/2 hour warning ofdischarged battery.

Battery recharge time Approximately 10 hours, depending on theoperating conditions. The batteries will becharging during an infusion.

Leakage current 100 to 120 V less than 20 microamps ungroundedor,

220 to 240 V less than 50 microamps ungrounded

This is measured between the ground stud andthe earth protective prong of the AC mainsconnector.

Over-current protection

Voltage AC line fuse Thermal fuse Battery fuse

100 to 120 V 200 mA 130° 1.0 amp

220 to 240 V 2 x 80 mA 130° 1.0 amp

Note: All fuses are time delay fuses

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S p e c i f i c a t i o n G r a s e b y M e d i c a l L t d .

Primary and Secondary Infusions:

Rate range

Model 500 Range Increment0.1 to 99.9 mL/h 0.1 mL/h1 to 999 mL/h 1 mL/h

Micro 505 Range Increment0.1 to 99.9 mL/h 0.1 mL/h

Volume to be infused

Model 500 Range Increment0.1 to 999.9 mL 0.1 mL1 to 9999 mL 1 mL

Micro 505 Range Increment0.1 to 999.9 mL 0.1 mL

Rate Taper Infusions:

Rate range

Model 500 Range Increment0.1 to 99.9 mL/h 0.1 mL/h1 to 400 mL/h 1 mL/h

Micro 505 Range Increment0.1 to 99.9 mL/h 0.1 mL/h

Volume to be infused

Model 500 Range Increment0.1 to 999.9 mL 0.1 mL1 to 4400 mL 1 mL

Micro 505 Range Increment0.1 to 999.9 mL 0.1 mL

Time range

Model 500 & Micro 505 Range Increment0 to 59 minutes 1 minute0 to 48 hours 1 hour

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S p e c i f i c a t i o n

Volume Over Time Infusions:

Rate range

Model 500 Range Increment0.1 to 99.9 mL/h 0.1 mL/h1 to 999 mL/h 1 mL/h

Micro 505 Range Increment0.1 to 99.9 mL/h 0.1 mL/h

Volume to be infused range

Model 500 Range Increment0.1 to 99.9 mL 0.1 mL1 to 9999 mL 1 mL

Micro 505 Range Increment0.1 to 99.9 mL 0.1 mL1 to 999 mL 1 mL

Time range

Model 500 & Micro 505 Range Increment0 to 59 minutes 1 minute0 to 48 hours 1 hour

Dose-Rate Calculation Infusions:

Dose range

Range Increment0.01 to 99.99 0.010.1 to 999.9 0.11 to 9999 1

Body weight range

Units Range IncrementKilograms (kg) 0.10 to 99.99 kg 0.01 kg

0.1 to 453 kg 0.1 kgPounds (lbs) 0.22 to 99.99 lbs 0.01 lbs

0.2 to 999 lbs 0.1 lb.

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S p e c i f i c a t i o n G r a s e b y M e d i c a l L t d .

Drug amount modes/range

Mode Range IncrementMG drug/bag 0.01 to 99.99 0.01

0.1 to 999.9 0.11 to 99999 1

Gm drug/bag 0.01 to 99.99 0.010.1 to 99.9 0.11 to 999 1

mcg drug/bag 0.01 to 9.99 0.010.1 to 99.9 0.11 to 9999 1

units/bag 0.01 to 99.99 0.010.1 to 999.9 0.11 to 99999 1

Rate range

Model 500 Range Increment0.1 to 99.9 mL/h 0.1 mL/h1 to 999 mL/h 1 mL/h

Micro 505 Range Increment0.1 to 99.9 mL/h 0.1 mL/h

Volume to be infused range

Model 500 Range Increment0.1 to 999.9 mL 0.1 mL1 to 9999 mL 1 mL

Micro 505 Range Increment0.1 to 999.9 mL 0.1 mL

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S p e c i f i c a t i o n

Occlusion sensing

Alarm levels (approximate values)

Pressure units Low Medium High

mmHg 103 mmHg 259 mmHg 517 mmHg

psi 2 psi 5 psi 10 psi

kPa 13.5 kPa 34.5 kPa 68.9 kPa

Time to occlusion

Maximum (measured +25%) delay times for activation of the “Occlusion belowpump” alarm:

Rate Low setting High settingmaximum time maximum timeto alarm to alarm

1 mL/h 11 min, 5 sec. 1 hour, 10 min.

25 mL/h 15 sec. 2 min, 35 sec.

KVO rate

Default KVO rate

3.0 mL/h, or at the programmed rate if set at less than these values.

Configurable KVO rates

Model 500 0.1 to 10.0 mL/h

Micro 505 0.1 to 3.0 mL/h

AccessoriesFor a complete list of Administration Sets, please contact Graseby Medical or yourlocal distributor.

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S p e c i f i c a t i o n G r a s e b y M e d i c a l L t d .

Symbols used on the pump

Front panel symbols

Battery is charging/mainspower applied.

Audio alarm silence button.

Side panel symbols

Use pump only in uprightposition.

Rear panel symbols

Attention: consultaccompanying documents.

Data input/output.

CF Application(cardiac floating)

Audio alarm volume control.

Alternating current.

Nurse call option (only ifoption is fitted)

Inside battery door symbols

Attention: dangerousvoltages, risk of electricshock if the housing isopened.

Equipotential point.

Internal battery.

Dispose of in anenvironmentally safemanner.

Battery symbols

Recycle battery

Dispose of in anenvironmentally safemanner.

~

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S p e c i f i c a t i o n

StandardsElectrical Safety

Classified as Internally Powered Equipment Class 1, Type CF (Cardiac Floating) insulation on all inputs.

Design Standards

EN 60601-1, EN 60601-1-2, IEC 601-2-24 (Draft).

Fluid Ingress Protection

IPX 1 Drip proof

CE Marking

The CE mark demonstrates that the pump conforms to the requirements inthe European Council Directive 93/42/EEC concerning medical devices.

The number 0473 identifies the Notified Body under which the QualitySystems operated within Graseby Medical Ltd are assessed.

Disposal

When the time comes to dispose of the pump, its batteries, or any of itsaccessories, do so in the best way to minimise any negative impact on theenvironment.

You may be able to use special recycling or disposal schemes. To find outabout these contact your local waste disposal service. Separate any otherparts of the equipment where arrangements can be made for their recovery,either by recycling or energy recovery.

Important: Existing national or local regulations concerning waste disposalmust take precedence over the above advice.

PatentsUSA 5401256

510321454294855017192

GB 2247765France 2715073

0473

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S p e c i f i c a t i o n G r a s e b y M e d i c a l L t d .

The curves were developed whiletesting the Model 500 using a GrasebyMedical Standard Adult Set, 8C-820administration set.

The curves for the Micro 505 areidentical since both pumps have thesame pumping mechanism.

Trumpet curvesThe trumpet curve represents the worstcase rate error in any given observationwindow over the whole infusion period.

These trumpet curves were preparedaccording to the requirements of IEC601-2-24.

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S — 1 1

S p e c i f i c a t i o n

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S p e c i f i c a t i o n G r a s e b y M e d i c a l L t d .

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Appendix

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A - 1

A p p e n d i x

Nurse-Cal l FeatureSome pumps are fitted with a Nurse-Call feature which makes these pumpscompatible with most existing hospitalnurse-call systems.

A Graseby Medical pump equippedwith the nurse-call feature may beconnected to the hospital's system byinserting a 0.25 inch system plug into

the Nurse-Call Connector (seeillustration, below) on the pump's rearpanel.

Once connected, any activation of thepump's various audio alarms alsoactivates the hospital nurse-callsystem.

Symbol Definitions:

Nurse-CallAttention -consult accompanying documents

Note: This feature is not availablein all countries.

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A p p e n d i x G r a s e b y M e d i c a l L t d .

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Index

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I n d e x — 1

I n d e x

IndexSymbols5 Step Setup 2 - 19

AAccessing options 3 - 2Accessories S - 7Accuracy

of pump (spec) S - 2Administration set

loading cassette 2 - 18loading problem alarm 4 - 4priming 2 - 17

Air detect system S - 2Air in cassette 4 - 4Alarms

audio backup 2 - 11dose/rate change 3 - 27insistent 4 - 4low battery 2 - 9messages 4 - 3non-insistent 4 - 6occlusion below pump 2 - 24overview 2 - 10programming messages 4 - 3warning messages 4 - 3

Audio alarm 2 - 10Automatic keypad locking 2 - 22

BBack pressure 2 - 24Backlight 3 - 4Backup audio alarm 2 - 11Bag

height above pump 2 - 16, 2 - 27Bag height above pump S - 1Battery

battery test option 3 - 5recharging 2 - 9specification of S - 3too low 4 - 4using the pump on 2 - 8

Bolusending 2 - 32feature enabled 2 - 26setting up and running 2 - 31totals 2 - 34

Buttonsee also Keysunlock keypad 2 - 22

CCassette

loading into pump 2 - 18CE Marking S - 9Change rate

dosing rate change 3 - 25quick rate change option 3 - 7running rate change 2 - 21warning messages 4 - 6

Clampattach pump to IV pole 2 - 5roller clamp on admin set 2 - 17warning 4 - 4

Clipsafety 2 - 18, S - 1

Connectingpump to IV pole 2 - 5secondary admin set 2 - 28

Continuous - backup alarm 2 - 11

DDesign standard S - 10Diagram

front of pump 2 - 2loading cassette 2 - 18modular connection system 2 - 5primary infusion 2 - 12rate taper infusion 3 - 8rear of pump 2 - 4secondary infusion 2 - 13

Dimensions of pump S - 1Disconnect

modular connected pumps 2 - 6

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I n d e x G r a s e b y M e d i c a l L t d .

Displayinfusion information 2 - 21light 3 - 4on pump 2 - 2

Disposal of pump S - 9Door

open alarm 4 - 4Dose-Rate Calculation 3 - 19

example 3 - 23recovery 3 - 19warning messages 4 - 6

Dosing rate 3 - 20Download history 1 - 5Drug amount 3 - 21Drug Label

display 2 - 23example 3 - 34option 3 - 34selecting 3 - 35

EElectrical safety standard S - 9Ending

bolus infusion 2 - 32primary infusion 2 - 25rate taper infusion 3 - 9secondary infusion 2 - 32

Epidural administration 1 - 2

FFast Access to Options 3 - 2Faulty pump 4 - 3Fluid Ingress protection S - 9Free flow protection S - 1Front of the pump 2 - 2

symbols appearing on S - 8Fuses S - 3

GGiving set

load the cassette 2 - 18priming 2 - 17

Graphtrumpet curve S - 10

HHeight

bag above pump 2 - 16, 2 - 27, S - 1no flow warning 4 - 5

Highocclusion alarm setting 2 - 24

History on pump 1 - 5Hold

alarm 4 - 5key 2 - 20

IIndicators

'Battery operation' 2 - 8'Mains operation' 2 - 2'Primary infusion' 2 - 2'Pumping' 2 - 21'Secondary/Bolus infusion' 2 - 2

Infusionbolus 2 - 31change rate while running 2 - 21effect of options on 2 - 15KVO 2 - 25, 3 - 33limits 3 - 29options available 3 - 1overview of types 2 - 12primary 2 - 19ranges of rates/times/volumes S - 4restore previous rate 2 - 35secondary 2 - 26stop 2 - 23volume infused 2 - 33Volume Over Time 3 - 18

Insistent alarm 2 - 10, 4 - 4Instrument care 4 - 8IPX1 S - 10IV pole 2 - 5

KKeypad lock

manual or automatic 2 - 22warning message 4 - 7

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I n d e x — 3

I n d e x

Keyshold 2 - 20programming 2 - 3unlock keypad 2 - 22

Kg or lbs 3 - 21KVO

alarm message 4 - 6default rate S - 7infusion 2 - 25option 3 - 33specify rate 2 - 25

LLabel

show drug 3 - 34Leakage current S - 3Library

of drug labels 3 - 34Light

backlight on/off 3 - 4message display 3 - 4

Limitseffect on infusion 2 - 15effect on rate taper 3 - 9in dose-rate calcs 3 - 19programming rate taper 3 - 16setting rate and VTBI 3 - 29

Loading dose 2 - 26Lock keypad 2 - 22Low

battery alarms 2 - 9occlusion alarm setting 2 - 24

MMass units 3 - 20Maximum infusion rate

for rate taper 3 - 12KVO 2 - 25range available on pump S - 4setting limit 3 - 29

Maximum VTBI 3 - 31Medium

occlusion alarm setting 2 - 24Message Display

at switch on 2 - 7

option for backlight 3 - 4rate and VTBI 2 - 21Volume to be Infused 2 - 34

Messages, warning 4 - 3Micro 505 1 - 1Minimum infusion rate

on pump S - 4setting 3 - 29

Model 500 1 - 1Modular connection system 2 - 5Multiple pumps on a pole 2 - 5

NNo flow above pump 4 - 5Non-insistent alarms 2 - 10, 4 - 6Nurse-Call Feature 1 - 5

OOcclusion

below pump message 2 - 24, 4 - 5detection 2 - 23

Occlusion Alarm 2 - 23, 4 - 5approx values of settings 2 - 24, S - 7change the setting 2 - 24setting 2 - 18

Options 3 - 1'Battery Test' 3 - 5'Dose-Rate Calculation' 3 - 19'Drug Label' 3 - 34effect on infusions 2 - 15fast access to 3 - 2'KVO Rate' 3 - 33'Max/min rate and VTBI' 3 - 29'Message Display Light' 3 - 4'Quick Rate Change' 3 - 7'Rate Limit' 3 - 29'Rate Taper' 3 - 8'Standard Message' 3 - 3'Time Remaining' 3 - 3using 3 - 2'Volume Over Time' 3 - 17'VTBI limit' 3 - 29

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I n d e x G r a s e b y M e d i c a l L t d .

PPatient weight

in dose-rate calculation 3 - 19Kg or lbs 3 - 21

Poleclamp 2 - 5saver 2 - 5

Power supply 2 - 7, S - 3Preset limits

alarm message 4 - 3effect on infusions 2 - 15error message on Run 2 - 20setting 3 - 29

Pressure, see Occlusion AlarmPrimary Infusion

5- or 6-step setup 2 - 19ending 2 - 25overview 2 - 12setting up 2 - 16totals 2 - 34

Primeadministration set 2 - 17secondary admin set 2 - 27

Problemshandling 4 - 2

Programmingalarms 4 - 3keys 2 - 3KVO rate 3 - 33mass units 3 - 20patient's weight 3 - 21primary infusion 2 - 19rate taper infusion 3 - 9secondary infusion 2 - 29volume over time infusion 3 - 18

Pumpfeatures 1 - 3indicators and displays 2 - 2programming keys 2 - 3service alarm 4 - 3sounds 2 - 10switching on 2 - 7

Pumping indicator 2 - 21, 2 - 23

QQuick Rate Change option 3 - 7Quiet Pump Mode 2 - 7, 2 - 11

RRate

change in D-R calc 3 - 25change while running 2 - 21quick rate change option 3 - 7setting min/max limits 3 - 29titration 2 - 21

Rate change not completed 4 - 6Rate Taper 3 - 8

end early feature 3 - 14preset limits set 3 - 16program by max rate 3 - 12program by total time 3 - 10restart or reprogram 3 - 15

Re-run infusion 2 - 35Rear of the pump 2 - 4

symbols appearing on S - 8Recharging the battery 2 - 9Recovery

dose-rate calculation 3 - 19Restore infusion rate 2 - 35Roller clamp 2 - 17Running rate change 2 - 21

SSafety

clip 2 - 18, S - 1clip alarm message 4 - 4dose/rate change alarms 3 - 27, 4 - 6rate and VTBI limits 3 - 29

Safety keypad lockout 2 - 22Secondary infusion

alarm 4 - 6bolus enabled 2 - 30ending 2 - 14, 2 - 32programming 2 - 29secondary stop 2 - 28setting up 2 - 26totals 2 - 34VTBI 2 - 28

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V o l u m e t r i c I n f u s i o n P u m p I n s t r u c t i o n M a n u a l

G r a s e b y M e d i c a l L t d .

I n d e x — 5

I n d e x

Securityon pump 2 - 22

Self test 2 - 7, S - 1Service

due date display 2 - 7pump service warning 4 - 3servicing features 1 - 5

Silence key 2 - 7, 2 - 11, 2 - 22Solution

prepare for infusion 2 - 16thick S - 1

Sounds 2 - 10Standard Message

display option 3 - 3Standards S - 9Start up

label showing options 3 - 1on battery 2 - 8switching on 2 - 7

Stopinfusion 2 - 23

Storage of pump S - 1Switching off 2 - 8Switching on 2 - 7

using the battery 2 - 8System check alarm 4 - 3

TTaper, rate 3 - 8Technician Menu 3 - 1Test

battery 3 - 5conditions S - 2

Thick solutions, warning S - 1Time

rate taper program 3 - 10to occlusion S - 7volume over time program 3 - 17

Time Remainingdisplay option 3 - 3

Titration (rate) 2 - 21Total infusion volume

Bolus 2 - 34Primary 2 - 34Secondary 2 - 34

Total Volumechecking 2 - 33clearing 2 - 33

TPN 3 - 8Troubleshooting 4 - 2

preset limits and rate taper 3 - 16, 3 -28

preset limits exceeded 2 - 20Trumpet curves S - 10Tubing set, see Administration set

UUnit of measure 3 - 21Unlock keypad 2 - 22

VVoltage S - 3Volume

checking infused totals 2 - 33set the VTBI 2 - 19VTBI key 2 - 3

Volume Over Time 3 - 17Volumetric

standards S - 9VTBI

dose-rate calculation 3 - 22secondary 2 - 28setting limit 3 - 29

WWarnings

messages - no alarm 4 - 7Weight

Kg or lbs 3 - 21of pump S - 1patient's 3 - 19programming in D-R calc 3 - 21

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Page 125: Graseby Instruction Manuals

Graseby Medical Ltd.Graseby Medical Ltd.Graseby Medical Ltd.Graseby Medical Ltd.Graseby Medical Ltd.Colonial Way, Watford, Herts, UK, WD24 4LGTelephone: +44 (0)1923 246434, Facsimile: +44 (0)1923 231595http://www.graseby.co.uk

For further information, please contact your local distributor orGraseby Medical direct on +44 (0)1923 246434

Part No. 0166-0027-B

February 2002

© 2002 Graseby Medical Ltd Smiths Medical - A part of Smiths Group plc