MedSystem III with Dose Rate Calculation and Drug List Editor Directions for Use

TABLE OF CONTENTS INTRODUCTION 1 2 4 6

GETTING STARTED

ALARMS, ADVISORIES AND PROMPTS 35 35 36 37 41 41 41

MAINTENANCE 43 45 53 56 57 59

GLOSSARY ABBREVIATIONS, ACRONYMS, UNITS OF MEASURE...

61

GLOSSARY

SPECIFICATIONS... CHECK-IN... CLEANING... INSPECTION REQUIREMENTS... SERVICE INFORMATION... WARRANTY...

MAINTENANCE

RESPONDING TO AN ADVISORY, ALARM OR FAULT MESSAGE... ALARM RESPONSE KEYS... ADVISORIES... ALARMS... FAULT... WATCHDOG... OTHER CONDITIONS...

GETTING STARTED

7 11 11 11 12 13 16 17 19 20 21 24 27 30 32 33 33

ALARMS, ADVISORIES AND PROMPTS

WARNINGS AND CAUTIONS... PREPARING THE INFUSION... PREPARING THE ADMINISTRATION SET... LOADING THE SET... FRONT PANEL OVERVIEW... PROGRAMMING PAGE... PROGRAMMING PRIMARY FUNCTION... MAKING CHANGES WHILE INFUSING... PROGRAMMING OPTION... KVO STATUS... SECONDARY MODE... DOSE RATE CALCULATOR (DRC) USING A SPECIFIC DRUG NAME... DOSE RATE CALCULATOR PROGRAMMING WITH DRUG?... DEVICE... CONFIG... NOTE... BATLOG...

INTRODUCTION

ABOUT THE PUMP... FEATURES... SYSTEM COMPONENTS... SYMBOLS...

GENERAL CONTACT INFORMATION Customer Advocacy For clinical and technical questions, feedback, and troubleshooting assistance. Phone, toll-free, within the United States and Canada: (800) 854-7128, Ext. 7812

Technical Support For technical information related to maintenance procedures and service manual support. Phone: Outside the United States: (858) 458-6003 Toll-Free, within the United States : (800) 854-7128, Ext. 6003 Toll-Free, within Canada : (800) 227-7215 (Eastern) OR (800) 667-2335 (Western) For more detailed information, refer to the “Service Information” section of this document.

INTRODUCTION About the Pump INTRODUCTION

The MedSystem III® Drug List Editor Multi-Channel Infusion Pump is intended for use in today’s growing professional healthcare environment, including healthcare facilities and home care, for use on adults, pediatrics and neonates. The MedSystem III® instrument is intended for facilities that utilize infusion pumps for the delivery of fluids, medications, blood and blood products using continuous or intermittent delivery through clinically acceptable routes of administration; such as, intravenous (IV), intra-arterial (IA), subcutaneous, epidural, enteral, or irrigation of fluid spaces. The MedSystem III® Drug List Editor Multi-Channel Infusion Pump features: • Three independent fluid delivery systems in the space of one. • Compact size: - reduces bedside clutter - simplifies patient transport • Easy to set up and use, yet provides advanced features. • Accurate delivery of a variety of fluids. • Uses administration sets that provide free-flow protection. Contraindications: None known.

INTRODUCTION 1

Features Multi-channel Fluid Delivery System The instrument combines three independent infusion channels in an unparalleled small size. ®

Lightweight/portable

MORE OPTIONS

STANDARD DISPLAY

ON/OFF

START STOP

®

®

DLE

The pump with pole clamp weighs just over 5 pounds and is easy to transport.

A

B

C

Unique, rotating pole clamp The pump may be attached to a variety of surfaces.

Dose Rate Calculator (DRC) The pump calculates a volumetric or dose rate based on values entered for patient weight, drug concentration (drug amount and diluent volume) and dosing parameters.

Drug List Editor (DLE) The pump drug list can be customized using Drug List Editor software.

Six Device Types available Six available Device Types with configurable parameters (maximum and minimum rates, maximum volumes, baseline and maximum pressures, and air-in-line thresholds) to achieve specific clinical applications: General Purpose Neonatal Controller Pressure

Operating Room General Purpose II Operating Room II

Free-flow Protection The MedSystem III® system Administration Sets contain a cassette that provides protection from free-flow conditions. To remove the cassette from the pump, the cassette’s slide clamp is pulled to full extension, occluding the tubing and preventing fluid from flowing.

2 INTRODUCTION

A: Stopped DRUG? Wt ---- KG= 0.0 LB A:Conc ------mg/---- ml A:Dose ------mcg/kg/min A:Rate ------ml/h A:VR 1 ml (Vol Rem) A:VI 0 ml DI 0.0 mg Press Select to choose line Clear Select

Features (Continued)

INTRODUCTION

Monitoring System The instrument continuously monitors pump conditions and alerts with adjustable audio tones and visual messages.

Data Monitoring The pump can be configured to communicate with a remote computer, such as a centralized patient monitoring nurse’s station. The COMM receptacle is compatible with RS-232 cabling. A communications manual that describes the programming and hardware involved is available.

®

MORE OPTIONS

STANDARD DISPLAY

ON/OFF

START STOP ®

®

A

B

DLE

C

Field Maintenance Software (FMS) The pump can be modified to accommodate specialized clinical applications. The Device Type parameters, occlusion limit, and air-in-line threshold can be configured with the FMS software. A:

Secondary Mode Allows the user to program two different rates of infusion to run sequentially.

Infusing Secondary

A: Secondary Rate 100 ml/h A: Sec VolRem (VR) 100 ml A: Sec Time(TR) 1 hr A: Sec VolInf(VI) 1 ml since 12:37p 01 Feb 02 Stop Affects Secondary Fast Select

Syringe Delivery Accommodates 20cc to 60cc syringe.

Full Range of Delivery Rates Rates from 0.1 to 999 milliliters per hour.

Battery Capacity A new fully-charged battery provides 6 to 8 hours of operating time with rates at 125 ml/h per channel.

INTRODUCTION 3

System Components FRONT PANEL Instrument Keys Display Screen

®

Softkey Pads Channel Indicator Lights Green: • Steady - infusing on AC power

MORE OPTIONS

STANDARD DISPLAY

ON/OFF

START STOP

®

®

• Flashing - infusing on battery power

DLE

Red: • Slow flashing - Advisory • Rapid flashing - Alert Channel Select Keys CASSETTE Portion of administration set, inserts into cassette holder.

A

B

C

Pressure Dome Slide Clamp

Piston

Tubing Collar

LOWER ASSEMBLY

Air-in-Line Sensor Detects bubbles of air during infusion.

4 INTRODUCTION

Tubing Collar Recess Holds tubing collar in place.

Pump Latch Mechanism Drives the cassette piston to move fluid through the tubing.

System Components (Continued) CONNECTOR PANEL before removing AC adapter from pump.

External Power External power receptacle connects with power cord. Plug Symbol

EXTERNAL POWER 6-9 V

AC Adapter Power Cord 120V/60 Hz three-pronged grounded adapter with 4-pin locking connector.

COMM

Green light on indicates AC power is connected; batteries are charging. COMM Communications line receptacle connects with RS-232. Container Hook One hook on each side of the instrument. Rotating Latch Allows clamp to spin 360° and position at every 90°. Adjustable Pole Clamp Jaw with clutch feature, mounts pump to a pole or bedside. NOTE: The MedSystem III® instrument is designed to function in any orientation. However, the effectiveness of the administration set air trap is diminished when the instrument is in other than vertical position.

EXTERNAL POWER 6-9 V

COMM

Attaching Pole Clamp To attach the pole clamp, position the clamp jaw over the mounting surface and turn the knob until the clamp is tightened and the pump feels secure. When the knob is as tight as possible, continued turning will make it click and spin freely without over-tightening. INTRODUCTION 5

INTRODUCTION

Re move clip from connector

NOTE: When inserting or removing connectors to the receptacles, avoid excessive force or twisting. To remove AC adapter from pump first remove clip that is on connector.

Symbols

+

75

IPX1

UM NP P

R

ST

J

VOLUME

IC INFUSIO TR

UL

Protection against fluid ingress: Drip Proof. Attention: Refer to accompanying documentation.

! LI

Canadian and U.S. Certification Mark: Products bearing this mark have been tested and certified in accordance with applicable U.S. and Canadian electrical safety and performance standards (CSA C22.2 No. 601.1, UL 2601-1 and IEC 60601–2–24).

ED 2 50

MM-YYYY

U.S. Certification Mark: Products bearing this mark have been tested and certified in accordance with applicable U.S. electrical safety and performance standards (UL 544). Manufacturing Date: Number adjacent to symbol indicates the month and year of manufacture. Consult operating instructions.

Explosion risk if used in presence of flammable anesthetics.

Only

Caution: Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.

2

Product is Single-Use, Do not reuse.

DEHP

Product contains DEHP in the fluid pathway.

Product does not contain DEHP in the fluid pathway.

LATEX

Product is latex-free. Product incorporates SmartSite® Needle-Free Valve Ports and should not be accessed by a needle.

XX ml

XX

Approximate priming volume. Drops per milliliter specification for I.V. set will be identified on drop symbol.

Expiration date for I.V. set will be identified near hour glass symbol.

6 INTRODUCTION

GETTING STARTED NOTE: Although the MedSystem III® instrument is built and tested to exacting specifications, it is not intended to replace the supervision of IV infusions by medical personnel. The user should become thoroughly familiar with the features and operation of the MedSystem III® instrument and exercise vigilance in its utilization.

Only

Definitions

GETTING STARTED

WARNING This heading alerts the user to potential serious outcomes (death, injury or serious adverse events) to the patient or user. CAUTION This heading alerts the user to take special care for the safe and effective use of the device.

Warnings and Cautions To ensure proper performance of the MedSystem III® instrument and to reduce potential injury, observe the following precautions: Epidural Administration The MedSystem III® instrument can be used for epidural administration of anesthetic and analgesic drugs. This application is only appropriate when using analgesics and anesthetics labeled for continuous epidural administration and catheters intended specifically for epidural use. Use only a MedSystem III® instrument 28 Series set, without a ‘Y’ connector or injection port, for epidural infusions. • Epidural administration of anesthetic drugs: Use indwelling catheters specifically indicated for short term (96 hours or less) anesthetic epidural drug delivery. • Epidural administration of analgesic drugs: Use indwelling catheters specifically indicated for either short term or long term analgesic epidural drug delivery.

WARNING Epidural administration of drugs other than those indicated for epidural use could result in serious injury to the patient. WARNING It is strongly recommended that the infusion pump, source container and MedSystem III® Administration Set used for epidural drug delivery be clearly differentiated from those used for other types of administration.

GETTING STARTED 7

Warnings and Cautions (Continued) WARNING This instrument is designed to stop fluid flow under alarm conditions other than Low Battery and KVO. Periodic patient monitoring must be performed to ensure the infusion is proceeding as expected. WARNING This infusion device is a positive pressure delivery system, capable of developing positive fluid pressures to overcome widely varying resistances to flow encountered in practice, including resistances to flow imposed by small gauge catheters, filters and intra-arterial infusion. It is neither designed nor intended to detect infiltrations and will not alarm under infiltration conditions. WARNING Hospital personnel must ensure the compatibility of the drugs as well as the performance of each channel as part of the overall infusion. Potential hazards include drug interactions, inaccurate delivery rates, inaccurate pressure alarms and nuisance alarms. WARNING Use only MedSystem III® instrument 28 Series administration sets. The use of any other set may cause improper instrument operation, resulting in an inaccurate fluid delivery or other potential hazard. WARNING The use of positive displacement infusion devices ported together with gravity flow infusion systems into a common IV site may impede the flow of common “gravity only” systems, affecting their performance. Hospital personnel must ensure the performance of the common IV site is satisfactory under these circumstances. WARNING References in this document to specific drugs and drug doses are for example only. Refer to specific drug product labeling for information concerning appropriate administration techniques and dosages. Parallel Infusions There are no contraindications regarding the use of the MedSystem III® instrument with any other positive displacement infusion device when ported together into a common IV site location.

8 GETTING STARTED

Warnings and Cautions (Continued) User Precautions To ensure proper performance of the MedSystem III® instrument and to reduce potential injury to the operator, observe the following precautions:

Administration Sets • A list of approved IV sets recommended by ALARIS Medical Systems for use with the MedSystem III® instrument is listed on the Set Compatibility Card. The use of any other set may cause improper instrument operation, resulting in inaccurate fluid delivery. • Before operating the instrument, verify that the administration set is free from kinks and installed correctly in the instrument. • MedSystem III® administration sets are disposable, have a sterile fluid path and are intended only for one time use. Do not resterilize. • Always power on the instrument before inserting the set. • Do not insert a cassette into a channel with a SERVICE prompt. • Remove any cassettes from channel(s) requiring service. • Ensure the cassette is properly installed before starting infusions. • For set replacement interval, refer to facility protocol and/or government standards (such as CDC guidelines in the United States). • For IV push medication (put instrument on hold), clamp tubing above the port. • Flush port(s) per facility protocol. • Discard administration set per facility protocol.

GETTING STARTED

• Disconnect from mains (AC) and battery power when performing maintenance. • Do not open the instrument case. There are no user serviceable parts inside. The case should only be opened by qualified service personnel using proper grounding techniques. When the case is opened, an electrical shock hazard exists which can result in serious injury to persons and instrument component damage.

F

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Artifacts It is normal for an infusion device to produce nonhazardous currents when infusing electrolytes. These currents vary proportional to the infusion device flow rate. When the ECG monitoring system is not functioning under optimal conditions, these currents may appear as artifacts, simulating actual ECG readings. To determine if ECG abnormalities are caused by patient condition or the ECG equipment, place the infusion device on hold. If the ECG readings become normal, the ECG equipment requires attention. Proper setup of the ECG equipment should eliminate these artifacts. Reference the appropriate ECG monitoring system documentation for instructions on setup and maintenance. GETTING STARTED 9

Warnings and Cautions (Continued) User Cautions (Continued) Dropping/Jarring Should an instrument be dropped or severely jarred, it should be immediately taken out of use and inspected by qualified service personnel, to ensure its proper function prior to reuse.

T AR ST OP ST

®

RE MO NS TIO OP

®

E

DL

RD DA AN AY ST PL DIS

O

N/

O

FF ®

C B A

Operating Environment Not for use in the presence of flammable anesthetics.

DANGER Explosion risk if used in the presence of flammable anesthetics.

Radio Frequency Interference Operating the system near equipment which radiates high energy radio frequencies (electrosurgical/cauterizing equipment, portable radios, cellular telephones, etc.) may cause false alarm conditions. If this happens, reposition the device away from the source of interference or turn off the device and manually regulate the flow with the clamp and/or monitor the vital parameters using an appropriate clinical alternative.

WARNING Use of accessories or cables other than those specified may result in degraded electromagnetic compatibility performance of this device.

Other Precautions • The AC adapter must be connected to a properly grounded, 3-wire receptacle (“Hospital Use” or “Hospital Grade”). • Avoid excessive force or twisting of detachable power cords when inserting or removing connector terminals. • Use AC adapter indoors only. • Do not stack instruments on top of each other.

10 GETTING STARTED

Preparing the Infusion

Prepare solution container in accordance with the manufacturer’s instructions. • A syringe can be used as the container for the IV fluid to be infused. Syringe sizes from 20cc to 60cc of such as the B-D and Monoject brands can be used.

Pressure Dome Slide Clamp

Tubing Collar

Connect the container to the IV set. Prime the MedSystem III® instrument administration set in accordance with the Administration Set Directions for Use.

Clear portion of cassette

Preparing the Administration Set It is important to prime the set properly to eliminate air bubbles. Ensure the cassette slide clamp is pushed in completely so tubing is not occluded. Invert the cassette so tubing is up. Slowly open the regulating clamp and establish fluid flow to fully prime the set. Gently tap the cassette and ‘Y’ sites as necessary to remove all air. Gently massage the pressure dome to ensure no air bubbles are trapped.

WARNING An open regulating clamp and slide clamp can cause a free-flow condition and may result in serious injury to the patient.

Loading the Set 1.

Close the regulating clamp before inserting and removing the cassette to reduce the risk of free flow.

2.

Ensure cassette slide clamp is pulled out (in the closed position) prior to loading.

3.

Press

4.

With tubing down, use a 45-degree upward motion to insert cassette into channel.

5.

Push on clear portion of cassette until completely seated. Then push in slide clamp flush with entire cassette.

6.

Pull down gently on tubing collar. Press with thumb to seat tubing collar in recess beneath cassette.

A

to turn pump on.

A A

NOTE: Three beeps sound when inserted properly.

GETTING STARTED 11

GETTING STARTED

NOTE: The Model 8631A Syringe Holder is available as an accessory that provides a convenient place to hold syringes while they are being used as containers for IV fluid. The Syringe Holder is designed to be easily installed and removed from the top of the pump and to support up to three syringes. Do not use the Syringe Holder as a handle to carry the pump.

Front Panel Overview Instrument Control Keys ON/OFF Key Turns the pump on and off.

STANDARD DISPLAY Key

MORE OPTIONS Key

START/STOP Key

Allows the user to Allows the user to display additional display Standard Display softkey functions. page to view infusion settings for all channels.

Starts or stops infusion on selected channel.

Standard Display Page Status Line Displays infusion status (Infusing; Stopped; Standby; KVO; ALARM; FAULT; SERVICE) for each channel. NOTE: Status line in selected channel is highlighted.

Infusion Rate Volume Remaining (ml)

ON/OFF

STANDARD DISPLAY ®

MORE OPTIONS

START STOP

MedSystem III® DLE

Stopped

Standby

Standby

125

25

95

ml/h VR: 996.2 VI: 12.8

ml/h VR: 138.8 VI: 26.9

ml/h VR: 93.2 VI: 16.8

Volume Infused (ml) Prompt Line

Start affects channel C STNDBY

Cntrst

GP

Displays messages that prompt the user to make programming choices and/or take appropriate actions. Softkey Prompts Displays function of specific softkey. STNDBY Appears in softkey information line when is pressed during infusion. Cntrst (Contrast) Brightens or dims display. GP When pressed, indicates full name of selected Device Type on the prompt line. NOTE: Additional softkey prompts are displayed by pressing .

Softkey Pads (4)

12 GETTING STARTED

A

B

C

Programming Page Selected channel is indicated by the letter displayed at the beginning of the first five lines. Status Line Displays infusion status for selected channel.

Volume Remaining

MORE OPTIONS

STANDARD DISPLAY

ON/OFF

START STOP

MedSystem III® DLE A: Stopped A: Primary Rate 25 ml/h A: Pri VolRem (VR) 250 ml A: Pri Time(TR) 10h 00m A: Pri VolInf (VI) 10 ml since 12:37p 01 Feb 02 ®

Time Remaining Volume Infused Date/Time Displays when volume infused was last cleared and infusion began.

Press Select to choose line Prompt Line

Select

Fast

Displays messages that prompt the user to make programming choices and/or take appropriate action. Softkey Prompts

A

B

C

Displays function of specific softkey. Select – Moves highlight bar through the programmable infusion parameters.

↑ – Increases highlighted value. ↓ – Decreases highlighted value. Fast ↑ – Increases or decreases Fast ↓

highlighted value at greater increments.

GETTING STARTED 13

GETTING STARTED

Infusion Rate

To turn pump on Press . • Upon start-up, the instrument performs an automatic selftest. Listen for a “beep” to ensure that the audio alarm transducer functions properly. • Instrument Information page is momentarily displayed. • Continuing to hold down ON/OFF key will keep the Information page on the display. • When the ON/OFF key is released, the Standard Display page is displayed. To turn pump off Press and hold . • Display disappears. • Pump is turned off. To view infusion settings for all active channels Press

.

• Standard Display page is displayed. To activate additional Standard Display softkey prompts With the Standard Display page displayed: 1.

Press

once.

• TotVol, Device, Config, and Note softkeys appear. 2.

Press

again.

• Batlog and DemoWD softkeys appear. To select channel and display Programming Pages Press

,

or

.

• Selected channel programming page is displayed. With programming page displayed: To program infusion 1.

Press Select to choose value to change. • Value is highlighted.

2.

Scroll through values using ↑, ↓, Fast ↑ or Fast ↓. • ↑ and Fast ↑ increase highlighted values in single or multiple increments.

14 GETTING STARTED

To program infusion (continued) • ↓ and Fast ↓ decrease highlighted values in single or multiple increments. • Pressing ↑ or ↓ changes direction of the Fast ↑ or Fast ↓.

• Highlight remains flashing until Enter is pressed. If Enter is not pressed, the entry incomplete advisory will sound. 3.

Press Enter to accept new value. GETTING STARTED

• Highlight moves to next programmable value if channel status is Stopped or Standby. • If status is Infusing, highlight remains on selected value. 4.

To recall a previous value after a new value is introduced but not entered, press . • Recall soft key appears.

5.

Press Recall. • Number returns to previous value.

6.

Press

.

• Infusion starts or stops immediately, unless the channel’s programming is incomplete, or if an advisory, alarm, or fault condition exists on selected channel. To access alarm information • ALARM is displayed in affected channel status line. • Alarm condition is displayed on the Standard Display of the affected channel. Press affected channel

,

or

See the ALARMS, ADVISORIES AND PROMPTS section of this manual for more alarm information.

.

• Alarm Information page is displayed for that channel. To activate additional Programming Page softkeysys With the programming page displayed: 1. Press . 2.

Press 2° Sec to access Secondary page OR

3.

See the GETTING STARTED section of this manual for information on the use of the Dose Rate Calculator function.

Press CalcOn to access Dose Rate Calculation page.

GETTING STARTED 15

Programming Primary Function To set primary rate 1.

Press

,

or

.

• Programming Page is displayed. • Rate is highlighted. 2.

Press Select if current rate is desired OR

3.

Press ↑, ↓, Fast ↑ or Fast ↓ to change rate. • Value flashes.

4.

Press Enter to confirm.

A:

Stopped A: Stopped A: Primary Rate Rate 100 ml/h A: Primary 100 ml/h A: Pri VolRem (VR) 500 A: Pri VolRem (VR)ml500 ml A: Pri Time(TR) A: Pri Time(TR)05h 00m 05h 00m A: Pri VolInf(VI) A: Pri VolInf(VI) 1 ml 1 ml since 12:37p 01 Feb01 02Feb 02 since 12:37p Press Select to choose line line Press Select to choose Fast Fast Select Select

• Highlight moves to volume remaining (VR)

TTo set primary volume remaining (VR) 1. 2.

Press Select if current VR is desired OR Press ↑, ↓, Fast ↑ or Fast ↓ to change VR. • Value flashes.

3.

Press Enter to confirm. • Primary time remaining (TR) is calculated automatically based on VR and rate.

A:

Stopped

A: Primary Rate 100 ml/h A: Pri VolRem (VR) 500 ml A: Pri Time(TR) 05h 00m A: Pri VolInf(VI) 1 ml since 12:37p 01 Feb 02 Press Select to choose line Fast Select

• Highlight moves to volume infused (VI).

To clear primary volume infused (VI) 1. 2.

Press Select if current VI is desired

A:

OR Press Clear to reset volume infused to zero.

A: Primary Rate 100 ml/h A: Pri VolRem (VR) 500 ml A: Pri Time(TR) 05h 00m A: Pri VolInf(VI) 800 ml since 12:37p 01 Feb 02 Press Select to choose line Clear Select

• Date and time are cleared. • Clear softkey switches to Recall. 3.

5.

Press Enter to confirm OR Press Recall softkey to recall previous VI, date and time. THEN Open regulating clamp on administration set.

6.

Press

7.

• Channel starts infusing. • Current date and time are entered. Press

8.

OR • Display reverts to Standard Display page after one minute. Verify settings.

9.

Verify solution flow from primary container.

4.

to begin infusion.

16 GETTING STARTED

A:

Stopped

Stopped

A: Primary Rate 100 ml/h A: Pri VolRem (VR) 500 ml A: Pri Time(TR) 05h 00m A: Pri VolInf(VI) 0 ml since ----Press Enter or Recall Recall Enter

Making Changes While Infusing To titrate or change primary rate during infusion 1.

Press , or . • Programming Page is displayed. • Rate is highlighted.

2.

Press ↑, ↓, Fast ↑ or Fast ↓ to change Rate • Value flashes.

3.

Press Enter to confirm. • New rate begins infusing immediately. GETTING STARTED

To change volume remaining during infusion 1.

Press

,

or

.

• Programming Page is displayed. • Rate is highlighted. 2.

Press Select to highlight VR.

3.

Press ↑, ↓, Fast ↑ or Fast ↓ to change VR. • Value flashes.

4.

Press Enter to confirm. • Infusion continues with new volume remaining To clear volume infused during infusion NOTE: When the channel VI is cleared, that volume is not subtracted from the volume on the TotVol page.

1.

Press

,

or

.

• Programming Page is displayed. • Rate is highlighted. 2.

Press Select to highlight VI.

3.

Press Clear then Enter to reset volume infused to zero. • Date and time are cleared. • Clear softkey switches to Recall.

4.

Press Enter to confirm • Infusion continues with volume infused reset to zero. • Current date and time are entered OR

5.

Press Recall softkey to recall previous VI value, date and time.

GETTING STARTED 17