Imed 960, 965 Service manual

r

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and

insert

into

label

holder

on

spine

,11

binder

of

960A/

965A

|P

pi

T

WARNINGS, CAUTIONS AND NOTICES

USE ONLY

PROPER

HOSPITAL

GROUNDING.

GRADE

POWER

GROUNDING

ACHIEVEDBYCONNECTIONTOA

GRADE".

DANGER:

CAUTION:

WARNING: REPLACE

EXPLOSION

OF

FLAMMABLE

RISQUE

PRESENCE D'ANESTHESIQUES INFLAMMABLES.

TO

REDUCE

REMOVE

QUALIFIED

HAZARD,

ANESTHETICS.

D'EXPLOSION,

RISK

COVER

SERVICE

FUSE

OR

AS

SUPPLY

RELIABILITY

RECEPTACLE

DO

NOT

NE

PAS

OF

ELECTRICAL

BACK.

PERSONNEL.

MARKED.

CORD

USEINTHE

EMPLOYER

SHOCK,

REFER

TO

INSURE

CAN

ONLY

MARKED

PRESENCE

EN

DO

SERVICING

BE

"HOSPITAL

NOT

TO

JSJ

IPR

CAUTION:

TO

MAXIMIZE

RECOMMENDED

OPERATED

THE

IN

CONTROLLED

IN

DROPPED AT

CHECKED

PRIOR

BEFORE

SERVICE

THAT

AN

BETWEEN

THE

TO

CONNECTING

NOTE

LIFEOFTHE

THIS INSTRUMENT

ENVIRONMENT

68°F

EVENT

BY

A

USE

(20°C)

WARNING

ANY

BIOMEDICAL

FOR

AND 77°F

THE

INSTRUMENT

TIME, IT MUST BE

PATIENT

"REFER

INSTALLED

BE

THAT

IS

(25°C).

TECHNICIAN

CARE.

TO

MANUAL'

BATTERY,ITIS

STORED

TEMPERATURE

IS

AND

pi

NOTICE

JIPJ

r

fw

Product

to

design

change

without

containedinthis

of

issue.

This

publication

provided

in

repairing

solely

IMED

and/or

contains

for

specifications

notice.

manualiscurrent

the use of

infusion pump/controllers.

The

IMED

technical

information

as ofthe

proprietary

are

subject

personnel

date

data

Noneofthe

duplicated

other

than

IMED

infusion

component parts thereof.

of

the

information

the

usertosubstantial

information

nor

mayitbe

for

the

repair

pump/controllers

contained

utilizedinany

and

maintenance

and

Any

unauthorized use

herein

liability,

herein

manner

the

may

of

subject

be

r

f^

Copyright0

9775 Businesspark Avenue

San

Diego, CA 92131-1699

(619)

All Rights

PrintedinU.S.A.

U.S.

Other Patents Pending

1990 by

566-9000

Reserved

Patents

IMED

3,985,133

Corporation

PREFACE

imed

'

(IW

This manual contains operation and maintenance

instructions for

of

Volumetric/Microvolumetric

These instruments are grouped

configurations

figure:

CONFIGURATION

Foster

Hightower

Product

PI

Inprovement

Technical

particular configuration is

reference

the

which

REFERENCE

information

code

and/or

IMED Model 960A/965A

Infusion

into

are definedinthe

SOFTWARE

F

HT

PIP

that is

unique

identified

the

software

Pumps.

three

following

DISPLAY

None

P0.6/P1.4/P1.5

P4.xx

to a

by the

version

series

displayed during initialization.

The information provided herein is intended for

use by technical personnel responsible for

servicing

into six sections and is presented

these

products.

The

material is divided

as

follows:

Section 1 - Descriptive Information; Section 2 -

Preparation for Use; Section 3 - Operating

Instructions;

Section 4 -

Functional

Description

and Schematic Diagrams; Section 5 -

Maintenance Instructions;

Section

6 -

Parts

Lists

and Assembly Drawings.

This manual

Additional by contacting

ment

and

The

960A/965A

supersedes

IMED

P/N 960-9010-00.

copies of this manual may be obtained

IMED's

ordering IMED

Customer Service Depart

Part

No. 960-9200-00.

International

Addendum

P/N

960-

9208 supplements this manual for support of the

220V

versions

of

these

instruments.

€$Sl

7^

ips

RECORD

OF

CHANGES

imecl

•PT

Date

05/01/90

DescriptionofChange

Initial

Issue

By

JD/MOW

(

F

<BB

imed

TABLE

section

•pj

SECTION

1 -

description

1.0

1.1

1.2

1.3

1.4

1.5

2 -

2.1

2.2

2.3

2.3.1

2.3.2 Pre-operational

2.3.2.1 Electrical Leakage Test 2-3

2.3.2.2 Electrical Ground Test 2-3

2.3.2.3 Dielectric Test 2-3

2.3.3

2.3.3.1 Test Requirements 2-3

2.3.3.2

introduction

operating

PHYSICAL

USER

CHARACTERISTICS

INTERFACE

OPERATING

ADMINISTRATION

PREPARATION

FOR

INTRODUCTION

PRE-OPERATIONAL

OPERATIONAL

Pre-operational Check

Abbreviated Test

Procedures

characteristics

SPECIFICATIONS

SETS

USE

MECHANICAL

PERFORMANCE

Battery

Electrical

Operational

OF

CONTENTS

!.!!!!."!.'

'.'.'.'.'.'.

!!!!!!!

INSPECTION

CHECK

Charge 2-3

Inspection 2-3

Performance

Test

'.

!

'...'.

n

1-1

i.i

i_2

1-2

1-5

2-1

2-3 2-3

f

SECTION

^pi

t

3 -

OPERATION

3.1

3.2 CONTROLS

3.3

3.3.1 Setup Procedure 3-4

3.3.2 Starting an Infusion 3-4

3.3.3 During the Infusion 3-5

3.3.4 Infusion Complete 3-5

3.3.5 Stopping an Infusion 3-5

3.3.6 Changing Rate or

3.3.7 Resetting Volume Infused 3-5

3.3.8 Clearing Alarms 3-6

INTRODUCTION

AND

INDICATORS

NORMAL

OPERATION 3.4

VTBI

during an

' "

Infusion

3-1

3.1

3-1

3-5

r

f™

SECTION 4 - PRINCIPLES OF OPERATION

4.1 INTRODUCTION 4-1

4.2

4.2.1 Physical Description

4.2.1.1 Pumping Mechanism

4.2.2 Functional Operation

4.2.2.1 Pumping Mechanism 4-2

4.3

4.3.1 Functional Description 4-2

4.3.1.1 Microprocessor System 4-2

4.3.1.2 Prime Mode Logic 4-2

4.3.1.3

4.3.1.4 Photosensor System 4-5

4.3.1.5 Alarm

4.3.1.6 Volume and Rate Inputs 4-6

4.3.1.7

4.3.1.8 Power Supply 4-6

MECHANICAL OPERATION 4-1

ELECTRICAL/ELECTRONIC OPERATION 4-2

Operate

Malfunction Alarm 4-6

Logic 4-5

System

4-1

4-1 4-1

4-1

4-5

in

imecl

4.3.2 Detailed Circuit Description 4-6

4.3.2.1

4.3.2.2 Microprocessor

4.3.2.3 Keypad Entry and 7-Segment

4.3.2.4 Circuit Enabling 4.9

4.3.2.5

4.3.2.6 Prime Mode Logic . . , 4-10

4.3.2.7 Operate

4.3.2.8 Rate Compensation 4-11

4.3.2.9 Volume To Be Infused Logic

4.3.2.10

4.3.2.11 Forward/Reverse Logic . 4-11

4.3.2.12 Alarm

4.3.2.13

4.3.2.14 Pressure Adjustments 4-19

4.4

4.4.1 Functional Descriptions 4-20

4.4.1.1 Microprocessor System 4-20

4.4.1.2 Prime Mode Logic 4-20

4.4.1.3 Operate Logic , 4-20

4.4.1.4

4.4.1.5 Alarm

4.4.1.6 Volume and Rate Inputs

4.4.2 Detailed

4.4.2.1 Microprocessor System . , 4-22

4.4.2.2

4.4.2.3 Displays . . . . 4-23

4.4.2.4

4.4.2.5 Battery Charger 4-23

4.4.2.6 Ultrasonic AIL Detector 4-24

Main

Circuit Board Logic 4-7

System

Power

Motor

Liquid

ELECTRICAL7ELECTRONIC

Photo-sensor

Keypad Back

Supply

Logic

Direction Control

Systems

Crystal Display

System

Circuit

Descriptions 4-22

Entry

Up

Battery

(LCD)

OPERATION

Display

Logic 4-9

[ [

..

[ . [

4-7

'

4-9

4-10

4-11 4-11

4-12

4-19

4-20

'

4-22

.'

4-22 4-23

SECTION

5.1

5.2

5.2.1 Cleaning Instructions

5.2.3

5.2.3.1

5.3

5.4

5.4.1

5.4.2

5.4.2.1

5.4.2.2

5.4.2.1

5.4.2.2

5.4.2.3 Angle

5.4.2.4

5.4.2.5 Cassette Nest Removal 5-9

5.4.2.6 AirInLine

5.4.2.7

5.4.2.8

5.4.3

5.4.3.1

5.4.3.2

5.4.3.3

5.4.3.4

5 -

MAINTENANCE

INTRODUCTION

PREVENTIVE

Electrical

Battery

TROUBLESHOOTING

DISASSEMBLY

Separating

Front

Main Front

Power

Keypad Door

Invertor

Hall

Disassembly

Valve Shaft

Shuttle

Angle

Shuttle

MAINTENANCE

!!!!!!!

Inspection

Voltage

Check

'.'.'.'.'.'.'.'.'.

the

Case

Pump

Logic

Panel

Assembly

Effect

Assembly

Board

Assembly

and

Display

Assembly

Plate

Assembly

Removal

Detector Removal 5-9

Removal . . . 5-10

Sensor

of the

Drive

Motor

Plate

Circuit

Assembly

Disassembly

Removal

Board

Removal

Harness

Angle

Motor

Removal 5-10

Removal

Card

Removal

Removal 5-9

,[

' "

Removal

Plate

Assembly

!!!!!!!!!

!!!!!!!

5-1

^

5-2

5-8

'.

5-8

5-8 5-8

5-9

5-10

5-11

p»

imecl

5.4.4

wn

5.4.5

5.4.5.1

5.4.5.2

w\

5.4.5.3

5.4.5.4

5.4.5.5

5.4.5.6

5.4.5.7

5.4.6 Chassis Assembly Disassembly

5.4.6.1 Battery Removal

5.4.6.2

5.4.6.3 Transformer Removal 5-12

5.5 REASSEMBLY

5.6 COMPREHENSIVE OPERATIONAL PERFORMANCE TEST 5-15

5.6.1

5.6.2 Qualitative Operational Performance Test 5-15

5.6.3 Quantitative Operational Performance Test 5-15

5.6.3.1 Equipment Requirements 5-15

5.6.3.2 Test Setup 5-15

5.6.3.3 Rate/Volume Inhibit

5.6.3.4 Prime Inhibit

5.6.3.5 Volume Infused

5.6.3.6 Normal Operation

5.6.3.7 Walk-Away Alarm

5.6.3.8 Door Alarm

5.6.3.9 Power Off

5.6.3.10 Purge Pressure

5.6.3.11 Operate (up stroke) Pressure Test Procedure 5-18

5.6.3.12

5.6.3.13 Downstroke Occlusion Pressure

5.6.3.14 Operate

5.6.3.15 AIL Detector

5.7

5.7.1

5.7.2 Battery Alarm Check 5-20

5.7.3 Occlusion Calibration 5-21

5.7.4 Battery Charger Adjustment

5.7.5 Plunger

5.7.6 Valve

5.7.7

5.7.8 Occtusion

Front

Panel

Rear

Pump

Chassis Assembly Removal

Pole

Clamp

AC

Power

Sonalert

Audio

Nurse

Line

Cord

Assembly Disassembly

Assembly

Entry

Module

Removal

Silence

Call

Switch

Receptacle

Clip

Removal

Disassembly

Removal

."!!!!

!!!!!!!

\\\

5-11

.'

5-11

''

5-11

5-12

'

5-12

.'

5-12

Power

Battery

Electrical

Volume-Rate

ADJUSTMENT AND CALIBRATION 5-20

Equipment

Ultrasonic AIL Detector Calibration Procedure 5-22

Supply

Backup

Board

Inspection

Test

Reset

Test

Memory

Test

(Upstroke)

Test

Removal

Test

Procedure 5-17

Inhibit

Test

Procedure 5-17

Test

Procedure 5-17

Test Procedure 5-18

Procedure 5-18

Pressure Test

Procedure 5-19

Requirements

Limit

Adjustment 5-22

Drive

Shaft Check and Adjustment

Calibration

(Alternate

(PIP)

Test

Procedure 5-17

Test

Procedure 5-18

Procedure

Method)

(Alternate)

.[

5-12

5-13

5-15

5-19

5-20

5-21

5-22 5-23

SECTION 6 - ILLUSTRATED PARTS BREAKDOWN

6.1 INTRODUCTION 6-1

INFUSION

WARRANTY

IMED INTERNATIONAL

DEVICE

SERVICE

DISCREPANCY

CENTERS

OFFICES

REPORT

(IMED

Form

9000-x

6-1

1/90)

imed

LIST

Figure

1-1

1-2

2-1

2-2 Nurse

3-1

4-1

a

4-2 Stepper

4-3 4-4

4-4a Ultrasonic AIL Detector Schematic 4-24

4-5

4-5a Power/Display Board (PIP/P4.x) Sheet 1of5 . . . . 4-27

4-5a Power/Display Board

4-5a

4-6

4-6 4-6

4-6a

4-7 Angle

4-7a

4-8 Power Supply

4-9 Battery Backup

4-10

4-10a Interconnect 4-10b Interconnect

4-10c

4-1

Od

4-11 4-11a

5-1

5-2

5-3

5-4

5-5

6-1

6-2

6-3a

6-3b

6-4a Parts

6-4b

6-5

6-6

6-7 6-7a

6-8

6-9

6-10

6-11

6-12

Title

IMED

Audio

96QA/965A

960A/965A

960AJ965A

Stepper

960A/965A

Main

Power/Display

960A/965A Volumetric

Characteristics

Front

Call

Test

Controls

Functional

Motor

Functional

Logic

Board

Power/Display

Front

Front Front

960A/965A

Angle

Interconnect

960A

965A

Universal

Open-ended

AIL

Typical

960A/965A

Parts

Parts Parts

Parts

Panel

Panel Panel

Plate

Assy.

Assy. Assy.

Front

Board

Diagram

Diagram Diagram

Diagram

AIL

Detector

AIL

Detector

Test

AIL

PCB

Board

Pressure

Test

Identification

Identification Identification

Identification

Infusion

and Rear Operating Features 2-2

Light

and

Indicators

Block

Pulse Phasing 4-12

Phase

Sequencing

Block

Schematic . . . 4-26

(PIP/P4.x)

Board

(PIP/P4.x)

(Display

(Display (Display

Panel

Schematic 960A 4-36

Schematic

Board

Schematic 960A/965A 4-38

Board

(PIP/P4.x)

960A

965A (Foster) . . . . 4-42

965A

960A

(Optical) (Optical)

Station

Setup

Diagram

Board)

Board) Board)

Assy.

(Display

965A

(Foster)

(Hightower)

(PIP/P4.X)

Schematic Schematic

Simulator Test

Station

Data

Sheet

960A/965A

960A

965A

960A Angle

965A

960A/965A

9S0A/965A

960A/965A

9S0A/965A

Setup

Final

Front

Angle

Door

Shuttle

MLB Power&Display

Front

Rear

Power

Battery

OF

FIGURES

Page

Pump 1-0

.'

1.4

2-3

'.'

3-2

(Foster)

(Hightower)

(PIP/P4.x)

Sheet 2 of 5 4-28

Sheet 3 of 5 4-29

Sheet

4 of 5 4-30

Sheet

5 of 5 .'.' '

Schematic

Schematic Schematic

Board)

Schematic

Sheet 1 of 3

Sheet 2 of 3 Sheet 3 of 3

Schematic

(F)

(F) (F)

(HT)

...'.

' ' ' '

'.,.'

*

4-13

.'.

4-21

4-31

4-32

4-33 4-34

4-35

4-37

4-39 m

4-3

4-4

4-40

4-41

4-43

4-44 )

' '

4-45 4-46

5-16

5-23

Plate

Plat

Plate

Assembly

Pump

Assembly

Circuit

Card

Assembly

Circuit

Case

Panel

Card

Assembly

CCA

Assembly

Supply

Back-Up

Assembly

CCA

Keyboard

PCB

(PIP/P4.X)

and

Assembly

Display

(HT)

(PIP/P4.X)

'.'.'.'.'.'.

. . . . . .

'.

5-23

5-24

5-25

6-3

6-6

6-9

6-10

6-13

6-17

6-19

6-21

6-25 6-31

6-33

6-36

6-40

6-43

6-45

J

f^?,

1

f*$$

]

1

m

-J

{

^

m

J

'

m

*!

j

*.

I

-J

<m

J

1

ft»'

—

VI

imed

Table

1-1

1-2

1-3

3-1

3-2

4-1

5-1

5-2

5-3

5-4

6-1

6-2 6-3

6-4a Parts

6-4b Parts

6-5 Parts

6-6 6-7 Parts

6-7a Parts

6-8

6-9

6-10

6-11

6-12 Parts

Title

Operating

Performance

Administration

960A/965A

Alarm/Prompt

Microprocessor

Troubleshooting/Fault

Malfunction

TableofTorque

Parts

Parts Parts

Parts

Parts Ust

Parts

Requirements

specifications

Sets

Controls

and

Messages

Signal

Isolation

Alarm

Codes

Values

List-960A/965A

List

960A

Angle

List

965A

Angle

List

960A/965A

List

9S0A/965A

List

960A/965A

List

9S0A/965A

960A/965A

List

96QA/965A

List

9S0A/965A

List

960A/965A

List

9S0A/965A

Door

Shuttle MLB

Power

Front

Rear Case

Power

Battery

LIST

OF

TABLES

Indicators-Functional

Functions

Guide

(P0.x/1.x)

(PIP/P4.X)

Final

Assembly

Front

Angle

Plate

Pump

Circuit

Assembly

Circuit

and

Panel

Supply

Back-Up

Plate

Card

Display

Assembly

Circuit

Assembly

Assembly Assembly

Board

Card

Assembly

CCA

Card

PCB

Assembly

PCB

Description

(HIGHTOWER)

Assembly

Keyboard

...[..........

'

.'

!

and

Display

(HT)

.

Page

1_3

1-3

1-5

3-3

3.6

4-8

5.3

5-4

5-6

5.14

6-2

6-4 6-8

6-11

6-15

6-18

6-20 6-22

6-26

6-32

6-34

6-37

6-42

6-44

•^w

VII

imed

Figure

============

1-1.

IMED

9G0A/965A

1-0

Volumetric

======

Infusion

Pump

imed

r

SECTION

1.0

INTRODUCTION

This section contains a description of the operating and physical characteristics plus the

operating requirements

specifications for the

965A

Micro

Volumetric

administration sets compatible

instruments

are

listedatthe

and

IMED

Infusion

performance

960A Volumetric

with

end

Pumps.

of

IMED

each of these

this

section.

and

The physical and operational characteristics of

the

960A

and

965A

are

identical in

respects.

differ

face italic print.

1.1

The

Infusion

electro-mechanically

Those

from

OPERATING

IMED

characteristicsofthe

the 960A

Model

willbeidentified

CHARACTERISTICS

960A&965A

devices are electronically controlled,

driven,

piston

pumps. The 960A is designed delivery

965A

cations.

sets configured

of drugs and

fluids

to adult patients. The

is designed for pediatric/neonatal appli

Both

instruments

with

utilize

a snap-in cassette pump.

most

965A

by

Volumetric

(syringe)

primarily

administration

for the

that

bold

type

An

automatic priming feature is incorporated to facilitate preparing the administration set. A tactile

keypad allows the user to enter infusion rate and

volume to be infused

and

VTBI

are shown on seven-segment

displays. A backlighted

Volume

Infused, operator prompts and alarm

(VTBI).

LCD

The selected rate

LED

panel displays

messages. Table 1-1 defines the operating range

of the rate and instrument. Once

VTBI

parameters for each

set

up and started, both

instruments operate on a semi-automatic basis.

While

microprocessor monitors the

in-line

selected

an

infusion

is in progress, the instrument's

fluid

column for air-

and occlusion pressure. When the

volume

has

been

infused,

the

instrument

automatically changes over to the "keep vein

open

visual

(KVO)"

INFUSION

rate

and

COMPLETE

initiatesanaudio

alarm.

and

1 -

DESCRIPTION

In addition to controlling and monitoring the

infusion, the instrument's microprocessor

diagnostic program

appropriate action in the event of an open door,

the battery not chargingoreither a hardware or

software

The instruments can be operated on battery

power for a limited period of time. The length of

operating time available on battery power is

dependent upon the delivery rate used.

operating on AC power the battery charger is

recharging or maintaining the battery at

charge.

1.2

The 9S0A/965A instruments have the

physical characteristics:

Height: 11.75 inches (29.6 cm)

Width: 10.00 inches (25.4 cm)

Depth: 6.00 inches (15.2 cm)

Weight -14.75 pounds (6.7 kg) The

retardant plastic material housing and support for

components

is molded in two

rear

system

Although

are

built

malfunction.

the

and

specifications

not

intendedtoreplace

by

medical

We

urge

professional

use

of

PHYSICAL

case

is molded from a high-impact, flame

case

assemblies.

personnel

the

user

standard

this

equipment.

CHARACTERISTICS

and

pole clamp assembly. The case

pieces

will

NOTE:

IMED

tested

and

detect

Models

to

exacting

and

960AJ965A

standards,

the

supervision

of

IV

infusions.

to

exercise

of

careinthe

and

provides the

the

internally mounted

which form

initiate

they

a

following

the

While

full

are

front and

1-1

imocl

'

FRONT

Software

The front

CASE

Release

case

ASSEMBLY

P-0.x/1.x

Instruments

assembly contains the front panel

assembly, main logic board, invertor, angle plate assembly,

cassette

air in line detector

Software

Release

Thefront case assembly contains the

display

and

boot,

door assembly.

REAR

Software

cassette

CASE

Release

boards,

nest,

The rear case assembly contains the battery,

power input module, sonalert, audio control

switch,

assembly, power supply board, transformer line cord clip.

Software

The

power

battery

assembly and line cord clip.

1.3

The

panel assembly,

nurse call connector, pole clamp

Release

rear case assembly contains the

input

module,

backup

USER

960AJ965A

INTERFACE

nest, shuttle boot assembly,

and

door assembly.

P-4.x

Instruments

angle plate

air-in-line

ASSEMBLY

P-0.x/1.x

P-4.x

Instruments

sonalert, audio control

board,

transformer,

user

interface

the

administration

assembly,

detector

Instruments

pole

includes

keypad,

shuttle

assembly

battery,

clamp

the

set

installation

power

and

AC

and

AC

switch,

front

area and the rear panel assembly.

FRONT

PANEL

The front panel assembly employs four controls

to

operate

the

instrument.

The

ON/STOP

control

is an alternate action type switch used to turn the

instrument

On

and

Off.

The

PRIME

ON/OFF

control initiates operation of the pumping mechanism for approximately 1 minute,

is

setto"000M.

The

VOL INF

RESET

clear the volume infused register and the

panel display to "0",ifactuated

setto"0000".

The

START

when the

control

initiates

if

the rate LCD

VTBI

will

operation of the pumping mechanism,ifthe rate

and

VTBI

are

set

toavalue

>0.

Fourteen arrow ®(2) controls are used to

program the instrument for a specific infusion. Six

arrow controls

which

displays in three seven-segment

are

used

to input the infusion rate

LED

windows.

the

LED

Eight

arrow

VTBI

which displays in four seven-segment

controls are used to

windows. An amber backlighted "PRESS"

input

indicator (above the START control) illuminates with

an accompanying audio alarm if the START

control is not pressed

and/or

VTBI

while

The backlighted

"VOLUME INFUSED"

after the power

has

the instrument is operating a series of 5

sequence

across

following

an

infusion

LCD

panel displays the

since

been

a change in rate

is in progress.

the

last

reset

off for 4 hours.

or "0"

While

dashes

the LCD panel. Eleven visual

messages are displayed on the panel in response

to

instrument

operator. In addition to the

LED indicator

OPERATING

when

the

ADMINISTRATION

The

set

plastic door

shuttle

arm

must be

fitting

engaged

will

close. The

alarm

flashes

andared

instrument

installation

and

includes

and

air in line

properly

to the shuttle arm before the door

set

conditions

when

LED indicator

is in

SET

INSTALLATION

areaisbehind

or to

LCD

the

ALARM.

the

cassette

detector.

prompt

panel a green

instrument

the

The

is

flashes

AREA

clear

nest,

cassette

the

seated in the nest and plunger

tubing must be inserted into

the air in line detector to enable starting the

will

pump. The pump

is

opened

REAR

during an infusion.

PANEL

stop and alarm if the door

The rear panel controls include the AUDIO

silence switch. When permitted the audio alarm can be silenced temporarily by pressing the

AUDIO

Software

A

switch.

NURSE

Release

CALL

P-0.x/1.x

instruments

connector is provided. When an

external Nurse Call system is connected to the

instrument,

facility's

enters

is

1.4

OPERATING

the

960A/965A

will

activate

Nurse Call systemifthe instrument

an

alarm

condition.

SPECIFICATIONS

the

The operating specifications for the 960A & 965A are divided into operating requirements and

performance specifications. These requirements

and

specifications

and

1-2 respectively.

are

delineated in

Tables

1-1

1-2

_

Table 1-1. Operating Requirements

imed

Parameter

Power Required:

Battery:

Nurse Call System Power

Limitations: (P-O.x/1 .x Software

Instruments

ONLY)

Operating Temperature Range:

Operating

Storage Temperature: * Storage

Humidity

Humidity:

*

Parameter

Range:

See

NOTE

108-132

(secondary),

Sealed

Maximum

24

VAC,

0.3

Amps

50-60

Hz,

nominal,

Single

Lead-Acid,6VDC,10Amp-Hr

recommended Voltage/Current

VDC/500

mA

(Leakage current 100

40°F (5°C) to 104°F (40°C)

40% to 95% Relative

Humidity,

-40°F (-40°C) to 158°F (70°C)

on

Warning,

40% to 95% Relative

Caution

and

Notice

Humidity,

page inside of the

Table 1-2. Performance Specifications

Specification

Fusedat0.4A

<|>t2wire

non condensing

Specification

plus

uA

maximum)

front

(primary)

Ground

cover.

5.0A

Operating Principle:

Operating

RATE

range:

VOLUMETOBE

Keep

Vein

Open

Occlusion

Air In

Battery Operation:

Line

Pressure:

Detection:

INFUSED

(KVO)

rate:

range:

Electronically

type

pump

1-999

0.1-99.9

1-9999

0.1-999.9

1

0.1

18 psi nominal

Software

Optical (5 Elements)

Software

Ultrasonic

mL/hr

10 hours at 125

mL/hr in

mL

in 1

mL in

Release

controlled,

in 1

mL/hr

0.1

mL

0.1

P-4.x

mL/hr

electro-mechanically

increments

mL/hr

increments

mL

P-0.x/1.x

Instruments

increments

Instruments

(with

new,

fully

charged battery)

driven

piston/cylinder

10

hours

at 50

=

1-3

mL/hr

(with

new,

fully

charged

battery)

imecl

Battery Charging:

_/

Instrument Operating at 125

mL/hr:

Instrument-Off:

Automatic

ALARMS/PROMPTS:

Audio

Prime:

Characteristics:

AUDIO

MALFUNCTION

ALARM

PROMPT (F)

PROMPT

WALKAWAY

"PRESS"

ADVISORY

TYPE

(HT)

20

hours

7

hours

Stops

second

after

approximately1minute;

press

AIRINLINE,

BATTERY, RATE

AUDIO

CONTINUOUS

INTERMITTENT

CONTINUOUS CONTINUOUS

DOOR

000,

NOT

OFF

AUDIBLE

manual

of PRIME ON/OFF control

OCCLUSION,

OPEN,

CHARGING,

and

PRESS

SOUND

WARBLE

BEEP

INFUSION

NOT

OPERATING,

SET 0000

stop

capability

COMPLETE,

RATE

VOLUME,

AUDIO

SILENCE

NO

YES

LOW

NOT

SET

with

000,

VOLUME,

The

960A

and

Laboratory's

the

Canadian

Equipment

965A

Volumetric Infusion Pumps comply with the

544,

Medical

and

Standard Association's

specifications.

Dental

NOTE

Equipment

C22.2

No.

(Second

125-M1984,

Underwriter

Edition,asamended)

Electromedical

and

1

fHS

1

1-4

p

imed

•fR>

1.5

The following administration

with

965A

in

ADMINISTRATION

the

960A

Micro

Table

Reorder

Number

1-3.

9200

9201

9205

9210

9211

9214

Volumetric

Infusion

ACCUSET™

ACCUSET

ACCUSET Administration

ACCUSET

ACCUSET Closed System Vented Administration

ACCUSET

SETS

sets

available for

Infusion

Pump

and

Pump are listed

Table

Administration

1-3.

Set

Administration Set

Set

Closed System Vented

Closed

System

Nonvented

use

Administration

Description

960A

with

Microbore

with

Microbore

with

Macrobore Patient Extension

Administration

Sets

Patient Extension

Patient Extension and 0.22

Set

Administration

with

0.22

Set

with2Injection

Micron

Filter

Sites

Filter

9215

9216

9219

9224

9230

•MB

9235

9251

9252

9381

9382

9510

9512

ACCUSET

ACCUSET Closed System Nonvented Administration

ACCUSET

Chamber

ACCUSET

Chamber

ACCUSET

Set

ACCUSET

SECONDARY20Vented

SECONDARY20Nonvented

GRAVISET™20Vented

GRAVISET20Nonvented

Closed System Nonvented Administration Set

Closed

Closed System

System

Primary

Vented

Administration

Nonvented

Vented

Quick

Nonvented

ADD-i-MED™

ADD-i-MED

Secondary

Administration

Secondary

Administration

Primary

Administration

Set

Administration

Spike

Quick

Vented

Nonvented Administration

Administration

(without

spike

Administration

Set

with

Set

with

Drip

(without

Set

0.22

Metered

Chamber)

Drip

Chamber)

Set

Micron

Filter

Chamber

Administration

and

Drip

and

Drip

Set

9515

9517

GRAVISET

20 Vented

Primary

20 Nonvented

with

Primary

0.22

with

1-5

Micron

0.22

Filter

Micron

Administration

Filter

Administration

Set

imecl

9550

9552

9555

9557

9630

9635

9260

9261

9269

9271

GRAVISET20Vented

ADD-i-MED

GRAVISET20Nonvented

GRAVISET20Vented

Administration

Set

ADD-i-MED

GRAVISET20Nonvented

Administration

ACCUSET

Administration

ACCUSET

Administration

MICROSET™

MICROSET

Chamber

MICROSET

Micron

filter

Set

Closed

Administration

Closed

System

Set

System

Set

Administration

System

Closedsystem

Primary

ADD-i-MED

Primary

ADD-i-MED

NON-PVC

Set

with

Vented

Nonvented

965A

with

Patient

Administration

with

Primary

with

Primary

Extension

Check

with

Check

with

Quick

Set

Check

Spike

and 0.22

Set

with

Valve

Spike

with

Administration

Valve

(without

Administration

and

0.22

and

Drip

(without

Micron

Metered

Chamber

Set

Micron

0.22

Micron

Chamber)

Drip

Chamber)

Filter

Chamber

Filter

and

Set

Filter

Drip

022

9274

9276

MICROSET

Chamber

MICROSET

Micron

Filter

Closed

System

Nonvented

Administration

Set

with

Metered

Chamber

and

Drip

r

0.22

1-6

p*

imed

2.1

INTRODUCTION

This

section

initial

the

inspection and pre-operational checkout of

IMED

965A

contains

960A

Micro

information relative to

Volumetric

Infusion

SECTION

Pump and

Pump.

2 -

the

These

procedures include a mechanical inspection,

electrical inspection, pre-operational battery

charge and a performance check to ensure that the instrument operates properly and has not

been damaged during shipment or storage.

2.2

PRE-OPERATIONAL

INSPECTION

The

960A/965A

thorough testing shipping

production

prior

container has been designed to protect

instruments have undergone

control

to shipment

MECHANICAL

and

quality

from

the

factory.

assurance

The

the instrument against damage under normal

shipping conditions; nevertheless, internal

physical

and/or electronic component damage could have

occurred without leaving a visible signature.

Therefore, it is recommended that the

following

inspection procedure be performed upon receipt

of the instrument at the user's

1. Carefully remove the instrument from the shipping container. (It is recommended the

shipping material

be

saved

facility.

in the event the

instrument has been damaged and must be

returned to the factory for service or repair.)

2. Inspect the exterior

case,

front

and

rear, for

holes, cracks, scratches, broken or damaged

controls, missing components and/or screws.

PREPARATION

5. Check the cassette nest for damage or

distortion.

6. Inspect proper

7. Inspect the

8. Install an approved administration

instrument

correctly

9. Actuate

front panel

the rear panel to ensure proper operation

(see

10. Inspect the power cord for damage, bent

prongs

11. Exercise the pole clamp mechanism to

ensure

In

evidence

the

not

the

has

for

instrument

liability for repair

2.3

FOR

the

carrier's

returnadamaged

factory

authorized

authorization

USE

the

shuttle

installation.

Air-in-line

to

and

each

and

Figure 2-1 for location of controls).

or deformed connector.

freedom

event

of

shipping

before

boot

for

cutsortears

detector for damage.

ensure

the

door

the

cassette

closes.

of the keypad controls on the

the

Audio silence switch on

of

movement.

NOTE

the

instrument

damage,

agent

immediately. Do

instrument

the

carrier's

repairs.

to

Contact

return

the

for repair regardless

costs.

OPERATIONAL

PERFORMANCE

shows

notify

set

seats

to

agent

IMED

of

CHECK

and

for the

3. Inspect the green tinted covering the Rate and

clear window on the

or

cracks.

4.

Ensure

the

the top, bottom,

door

fits

and

LCD

flush

side.

Lexan®

VTBI

windows

displays and the

panel for scratches

with

the

case

at

Prior to the first operational use and

routine maintenance or servicing of the

960A/965A, it is strongly

operational performance

recommended

checkbeperformed.

The operational performance check consists of

two

phases;

a Pre-operational Electrical

Inspection to check the electrical integrity of the

instrument for compliance with regulatory agency

2-1

following

that an

any

irned

"

CASSETTE

AIR-IN-LINE

ON

STOP

VALVE

SHUTTLE

DETECTOR-

CONTROL

SHAFT-

NEST.

AfU

DOOR-

-OPERATING

-ALARM

LCD

DISPLAY

RATE (ML/HR)DISPLAY AND

'

INDCATOR

VOLUME

DISPLAY

PRESS

.131111110

-

START

VOLUME

PRIME

INDCATOR

ALARM/PROMPT

TOBE

INFUSED

AND

INDCATOR

CONTROL

INFUSED

ON/OFF

CONTROL

(ML)

CONTROL

FRONT

CORDCLIP

AC INPUT MODULE

A

FUSE

HOLDER

Figure

2-1.

960A/965A

REAR

Front

and Rear Operating Features

2-2

POLE

CLAMP

SONALERT

AUDIO

SILENCE

SWITCH

NURSE

CALL

IP-OxSoftwareInttrunwntt

CONNECTOR

ONLY)

imecl

requirements and an operational performance test

to verify instrument performance.

2.3.1

The

fully

able

Pre-operational Check Battery Charge

instrument

charged condition. However, since consider

time

could

is shipped

elapse

between

with

the

batteryina

shipping

and

first

use, a pre-operational battery charge is

recommended. Connect the

suitable

for

24

AC

hours.

outlet

and

allow

AC

power cord to a

the

batterytocharge

2.3.2 Pre-operational Electrical Inspection

The pre-operational electrical inspection

an

electrical

check

andadielectric

leakage test, a

test.

CAUTION

ground

includes

continuity

Some of these tests are inherently

hazardous. Safeguards for personnel and

property

should

be

employed

when

conducting such tests. Tests should only

be performed by qualified personnel.

CSA Standard C22.2 No. 125 for Risk Class 2

Equipment.

2.3.3 Abbreviated Operational Performance

Test

The

following

designedtoensure

controls and indicators is

operational performance test is

each

of the 9Q0A/965A

functioning

properly

and

check the operability of all the features available in the normal operating modes.

2.3.3.1

The

Test

following

Requirements

items of laboratory equipment and

supplies are required to conduct the operational

performance

1. ACCUSET Closed System

administrative

2. IV

3.

Standard

4. Nurse Call Test (Software Release P-0.x/1.x

Solution

tests:

Container

IV

Pole

set

Light

ADD-i-MED

(see

figure 2-2)

ONLY)

2.3.2.1 Electrical Leakage

Test

Perform an electrical leakage current measure

ment in compliance with Underwriters Labora

tories Canadian Standards Association

C22.2

Leakage

microamperes.

2.3.2.2

Perform

measurement

(UL)

544

for

Patient Care

Equipment

(CSA)

No.

125 for

currents

Electrical

Risk

Class 2 Equipment.

aretobe

Ground

less

Test

than

an electrical ground impedance

in compliance with UL 544 for

Standard

100

Patient Care Equipment and/or CSA Standard

C22.2 impedance between the

power cord plug and the grounding

rear

2.3.2.3

Performadielectric

with

No.

125

for

Risk

case

should

Dielectric

not

Class 2

grounding

exceed

Test

Equipment.

100

milliohms.

on the

point

on the

withstand testincompliance

UL 544 for Patient Care Equipment and/or

and/or

The

5.

Hemostat

6. Empty fluid container

7. Gas

8. Fluid

9. Fluid simulator,

10.

a—OE

2.3.3.2

tight

syringe: 100

simulator,

Test

magnet (door alarm override).

NURSE

CALL

PUJC

clear

opaque

•V

ALKALINE

+ l I

—HI

I—

fluid

Figure 2-2. Nurse Call Test

Test

Procedures

microliter

fluid

390 OHU,

capacity

I/4W.3X

WV

Light

The following tests and associated procedures

are

presented

efficient, qualitative

operability.

in a

sequence

check

of instrument

that

provides an

LLD

2-3

\

imed

•

INITIAL

SETUP

1. Mount pump onIVpole (leave AC power

cord

unplugged).

2. Spike

3. Install Nurse Call

and

hangIVfluid container above the

instrument, then

fill

Test

connector. (Software

drip

Light

Release

chamber

2/3

in the Nurse Call

P-0.x/1.x

full.

ONLY)

NOTE

Test

procedures

that

refer to operation

the Nurse Call Test Light are applicable

ONLY

Release

TEST

to

instruments

P-O.x

SEQUENCE

installed.

with

Software

1. Press ON/STOP key and check:

•

The

valve

position

the down position

and

shaft

the

will

hometothe

shuttle

arm

will

10 o'clock

home

NOTE

The

"PRESS"

indicators

test

check.

2. Plug the AC power cord into a suitable

outlet

• The

and

"NOT

check:

and

OPERATING

do

not

flash during

CHARGING"

message

LED

the

self-

wall

extinguishes

The

•

LCD panel backlight illuminates.

of

3. If

4. If VTBI not "OOOO7"000.0",

5.

6. Open the

to

rate

not

MOOO7"00.0"I

"OOOO7"000.0".

If

"VOLUME

VOL

INF

display on the

INFUSED"

RESET.

door.

LCD

"DOOR

panel (red

indicator and alarm audio

Nurse Call

test

light remains illuminated.

set

to "OOO7"00.0".

set

to

is not

OPEN"

"O'TO.O",

message

ALARM

will

remain active).

press

will

•

LCD

Panel-"VOLUME

"8888"/"888.8" illuminates for 3

then

reverts

to "VOLUME

INFUSED"

seconds,

INFUSED"

last volume infused value or "07*0.0", if

the

power

hours

has

been

off for more than 4

• Operating/Rate graphics - illuminate

steadily for 3 seconds, then go blank

• Alarm/Prompt messages display

for

seconds, then go blank except for

OPERATING"

which display steadily and

which cator

flashes.

flashes

The Nurse Call test

•

RATE

•,8887"88.8H

and

momentarily, then display

in the Rate and

and

The

and

VTBI

Displays show

and

"88887"888.8"

"P-X.X"

"NOT CHARGING"

"AIRINLINE"

red

ALARM LED indi

the

alarm

audio

light

illuminates

"96.0"or"96.5"

(X.X

refers to the

installed software revision) in the =2 seconds

followed

by reversion to the

last confirmed infusion parameters or

"OOO7"00.0"

power

and "00007"000.0", if the

has

been

off for >4

hours.

and

3

"NOT

sounds.

VTBI

for

7.

Install

cassetteinthe nest and

affix

to shuttle arm. Press tubing into the Air In

Line

detector.

Do

not

connected

8. Ensure

9. Press

priming.

•

"AIRINLINE"

"NOT

steadily on the

and

• Rate and

and

10.

Checktoensure

tubing

finish.

prime

all

PRIME

visual

—-/—.-

set.

Close

the

WARNING

with

the

door.

administration

to a patient.

clamps are open.

ON/OFF key once to initiate

message

OPERATING"

LCD

alarm

VTBI

indications

displays

will

message

panel and the audio

will

respectively for 960

Allow

all air is

the auto-prime

cleared

flash and

will

show ---/-.-

plunger

will

display

continue.

A/965A.

from the

cycle

set

to

2-4

11.

Check

allowing instrument to remain idle

observe:

• After 45/80

12.

Set

25/70.0

•

walk

away

alarm

seconds

flashes,

flashes, the audio alarm

"NOT

OPERATING"

Nurse Call test

rate to 125/50.0

mL,

then press START and check:

All

indicators reflect

light

mLThr

red

illuminates.

normal

(operator

"ALARM"

message

sounds

and

VTBI

operation.

alert)

and

indicator

and

to

by

the

•

"INFUSION

on

the

COMPLETE"

LCD

message

• Operating/Rate graphics sequence at

rate

•

Audio

• Nurse Call test light illuminates

• Rate display alternates between

"1257"50.0"

18.

Press

•

Audio

•

"AUDIO

LCD panel.

Alarm

AUDIO

alarm

sounds

and

Silence

silences

"17"0.r

switch

mL/hr.

and

OFF" message appears on the

imecl

flashes

KVO

check:

13. Place hemostat on the

check:

• ALARM

•

OPERATING

indicator

indicator extinguishes

• Operating/Rate graphics

•

"OCCLUSION"

OPERATING"

panel

•

Audio

• Nurse Call test

Alarm

displays steadily on the

sounds

distal

tubing

flashes

extinguish

message flashes and

light

illuminates

• Pumping mechanism stops.

14.

Remove

check:

•

All

15.

Place

check:

• ALARM

•

OPERATING

• Operating/Rate graphics

•

"OCCLUSION"

OPERATING"

panel

•

Audio

• Nurse Call test

•

Pumping

16. Remove the hemostat, press

check:

•

All

17. Set

await Infusion Complete alarm, then check:

• ALARM

•

OPERATING

the hemostat, press

indicators

reflect

hemostat on the

indicator

indicator extinguishes

Alarm

sounds

mechanism stops.

indicators

VTBI

to 5/2.0

reflect

indicator

START

normal

proximal

flashes

operation.

tubing

extinguish

message flashes and

displays

light

steadily

illuminates

START

mL,

flashes

normal

press

operation.

START

extinguishes

and

on the

and

"NOT

LCD

and

"NOT

LCD

19.

Press

20.

Open

set, install the test magnet over the door

sensor

fluid

OPTICAL AIR

configured

step

21. Press

START

•

22.

Slide

the

•

23.

Slide

the

•

24. Expose the third

• ALARM

•

ON/STOP to

the door, remove the administration

and

put the filled portion of the clear

simulatorinthe

IN

with

Ultrasonic

#32).

ON/STOP,

and

check:

All

indicators reflect normal operation.

the clear

first

sensor

All

indicators

the clear

second

All

OPERATING

Audio

sensor

indicators reflect

indicator

Alarm

shut

down

AIL

detector.

LINE

set

fluid

to

air

reflect

fluid

TEST

simulator

to

(If

AIL

detector proceed to

VTBI

to 100/40.0, press

and

check:

normal

air

and

normal

sensor

to air

flashes

indicator extinguishes

sounds

• Operating/Rate graphic extinguishes

•

"AIRINLINE"

OPERATING"

• Nurse Call test light illuminates

• Pumping mechanism stops.

25.

Remove

and

all sensors

check:

•

All

indicators reflect normal operation.

message

flashes and

message displays steadily

invert

see

fluid,

simulator

press

then

START

the

instrument.

instrument is

downtoexpose

operation.

downtoexpose

check:

operation.

and

check:

"NOT

install

so

and

2-5

imed

26. Slide simulator up to expose the lower 3

sensors

•

to

air

and

check:

All

indicators reflect normal operation.

27. Slide simulator up to expose the lower 4

sensors

•

• OPERATING indicator extinguishes

•

ALARM

Audio

to

air

indicator

Alarm

and

sounds

check:

flashes

• Operating/Rate graphic extinguishes

•

"AIRINLINE" OPERATING"

• Nurse Call

message

test

light illuminates

flashes and

"NOT

displays steadily

• Pumping mechanism stops.

28.

Press

simulator

START

•

ON/STOP,

and

so

and

All

indicators reflect normal operation.

remove

replace with the

all

sensors

check:

see

the

clear

opaque

fluid,

fluid

then

press

29. Slide the simulator up to expose the lower 2

sensors

«

• OPERATING indicator extinguishes

•

ALARM

Audio

to

air

indicator

Alarm

and

sounds

check:

flashes

• Operating/Rate graphic extinguishes

•

"AIRINLINE"

OPERATING"

• Nurse Call

message

test

light illuminates

flashes and

"NOT

displays steadily

• Pumping mechanism stops.

30.

Press

simulator

START

ON/STOP, reposition the

so

all

and

sensors

check:

see

fluid, then

opaque

press

ULTRASONIC

32.

Press

START

•

All

33. Slide the fluid simulator down to

sensor

•

ALARM

AIR

IN

LINE

TEST

ON/STOP,

and

check:

set

VTBI to 100/40.0,

indicators reflect normal operation.

expose

to

air

and

check:

indicator

flashes

• OPERATING indicator extinguishes

•

Audio

Alarm

sounds

• Operating/Rate graphic extinguishes

•

"AIRINLINE"

OPERATING"

• Pumping mechanism

• Nurse Call

34. Reposition liquid,

•

All

35.

Press

•

Instrument

36.

Remove

sensor

detector.

fluid

press START and check:

indicators reflect normal operation.

ON/STOP

the

and

Remove

message

stops

test

light illuminates.

simulator so sensor

and

check:

shuts

down.

test

the

magnet

fluid

the

from

simulator

Nurse

flashes and

displays steadily

the

door

from

Call

Test

from the Nurse Call receptacle, if appropriate.

The instrument is now ready for patient

service.

See

Section

3 -

OPERATION

for

standard operating procedures.

will

the

care

1

press

"NOT

see

AIL

Light 6

(w?k

•

All

indicators reflect normal operation.

31. Slide the simulator down to

4

sensors

•

ALARM

to

air

indicator

and

check:

flashes

expose

• OPERATING indicator extinguishes

•

Audio

Alarm

sounds

• Operating/Rate graphic extinguishes

•

"AIRINLINE"

OPERATING"

•

Nurse

Call

• Pumping mechanism

message

test

light illuminates

flashes and

displays steadily

stops.

the upper

"NOT

1

2-6

imed

SECTION

3.1

INTRODUCTION

This

section

procedures

Vo

umetric

Volumetric

intended to provide maintenance technicians

a basic understanding of

including

system.

Although

and tested to exacting specifications,

the

replace

in

the

The

professional

utilization

describes

for

operationofthe

Infusion

the

audio

the

instrument

the

supervision

user

is

of

the

recommended

IMED

960A

Pump

Pump.

and

960A&965A

role of medical personnel

urged

standards

the

and

The

instrument

visual

NOTE

is

not

intended

ofIVinfusions.

to

exercise

of

instruments.

the

965A

Micro

information

operation

alarm/prompt

are

built

to

care

in

the

is

with

3 -

OPERATION

3.2

The

operate

Figure

3-1.

italics,

CONTROLS

controls

Items

and

the

960A

3-1

and

uniquetothe

listed

AND

INDICATORS

indicators

and

965A

with

descriptionsinTable

965A

usedtosetupand

are

illustrated

are

presented

in

3-1

•

imed

ED

OPERATING

VOLUME

tssmmm

AIRINLINE OCCLUSION

INFUSION LOW

BATTERY DOOR MALFUNCTION

V

RATE

tt

-0-

ON

STOP

OPEN

(ML/HR)

tr

43-

INFUSED

tasaaaai

COMPLETE

-L? 43-

ON/OFF

PRIME

laataaaa

j

960A

niff™

NOT

OPERATING

RATE NOT

CHARGING

SET

0000

AUDIO

VOLUME

tr

-0-V43-

VOL

INF

RESET

^. J

88

as&ssaaa

NOT

000

VOLUME

OFF

TOBE INFUSED

u

tt

J3-

PRESS

START

ALARM

88]

J

(ML)

-a

43-

IPFR&TIMfti'!'|V^Il\/

VOLUME

AIR IN OCCLUSION INFUSION LOW

DOOR

MALFUNCTION

RATE

tr

43- 43-

INFUSED

LINE

COMPLETE

BATTERY

OPEN

0.1 ML/HR U

(ML/HR)

tr

ON

STOP

NOT

OPERATING

RATE NOT

CHARGING

SET

0000

AUDIO

VOLUMETO BE INFUSED (ML)

-t?

43-

ON/OFF

PRIME

•a

43-

VOL

RESET

965A

8 8

NOT

000

VOLUME

OFF

-cr

tr

43- 43- 43-

^RESS

INF

START

fti

ARM

8.8

tr

Figure

3-1.

960A/965A

Controls

3-2

and

Indicators

Wl

imecl

Control/Indicator

OPERATING

ALARM

Indicator

ALARM/PROMPT

RATE

(ML/HR)

Controls/Display

VOLUMETOBE

Controls/Displays

ON/STOP

Control.

Display

INFUSED

Table

(ML)

3-1

960A/965A

- Functional Description

Green

Red

condition.

Backlighted

INFUSED"

on and either the last Volume Infused value or

Operating/Rate sequencing graphics; and eleven

alarm/prompt messages, when appropriate.

Six

into

separately controlled. Digits do not rollover.

Eight

infused

separately controlled. Digits do not rollover.

Applies

mode. When in

powered down except for the microprocessor

remains powered for 4 hours.

Controls

and

Indicators

Functional Description

LED

that

LED

that flashes when the instrument isinan

arrow

(0)0

the three

arrow

into

flashes

LCD

panel that displays:

message

controls

RATE

®@

controls

the

four

when

the

instrumentisinfusing.

"VOLUME

whenever

the

instrument

usedtoinputaninfusion

digit

displays. Each

usedtoinputavolumetobe

VTBI

digit

displays. Each

system power to the pump when in the

the

STOP

mode, the instrument is

digit

power

"0";

is

digit

ON

which

alarm

is

rate

is

PRIME

START

VOLUME

RESET) Control

•PRESS"

AUDIO

fpl

ON/OFF

Control

INFUSED

Indicator

Switch

Control

RESET

(Rear Panel)

(VOL

INF

Operates the

±3) when the rate is set to 000

manually stopped by actuating the PRIME ON/OFF

control during the automatic

Initiates

rate and/or

restarts an infusion

condition.

Clears the

INFUSED"

"00007*000.0".

Illuminates if

within

VTBI

Temporarily

When silencing is invoked,

conditions will be

10 seconds

during an infusion.

pumping

mechanism

(00.0).

priming

for

63 ±3 seconds

Priming

sequence.

operation of the pumping mechanism,

VTBI

changes input during an infusion and

following

Volume

display, when actuated

Infused register and

the

START

following

silences the audio alarm when

sounded

clearing of an alarm

"VOLUME

with

the

VTBI

control

has

not

been

the changing of rate and/or

permitted.

NOTE

subsequent

upon

occurrence.

alarm

can be

confirms

actuated

(72

set to

3-3

imed

3.3

NORMAL

OPERATION

5. If

Rate

not

"OOO7"00.0",

setto"0007*00.0".

The following

steps

necessary

and the 965A

procedures

to

operate

Micro

Volumetric Infusion Pumps.

describe in detail the

the 960A Volumetric

Operating instructions are also provided in the

Operator's Manual.

3.3.1

1. Attach the 960A/965A to the

2. Plug

3. Spike

Setup

power

the

outlet.

and

Procedure

AC

power

hang the

IV

pole.

cord into a suitable AC

IV

fluid

container in

accordance with accepted hospital

procedures.

4.

Press

instrument,

•

the

ON/STOP

then

check:

LCD

Panel-"VOLUME

"88887"SSS.S"

then

reverts

last volume infused

power

has

illuminates for 3

to

"VOLUME

been

off for

controltoturn

INFUSED"

value

or 0/0.0, if the

more

than4hours

on

the

seconds,

and

• Operating/Rate graphics - illuminates goes

steadily for 3 seconds, then

blank

6. If

7.

8. Open the door.

VTBI

not "OOOO7"000.0",

"00007*000.0".

If

"VOLUME

INF

RESET.

INFUSED"

"DOOR

is not

OPEN"

display on the LCD panel (red

indicator and alarm audio

9.

Install

to shuttle arm.

Line

Do

connected

10. Ensure all clamps are open.

11.

Press

priming.

•

cassette in the nest and

Press

detector.

not

Close

WARNING

prime with

toapatient.

PRIME

ON/OFF

"AIRINLINE"

OPERATING"

and

the operating/rate graphic

the

LCD

panel.

alarm

indications

tubing into the

the

message

The

will

door.

administration

control

audio

continue.

set

to

"0",

press

message

ALARM

will

remain

affix

once

will

flash, "NOT

will

display steadily

will

and

visual

VOL

will

active).

plunger

Air-ln-

set

to initiate

flash on

•—

-

• Alarm/Prompt

seconds,

OPERATING"

"AIR IN LINE" ALARM

alarm

•

RATE

"8887*35.8"

audio

and

messages

display for 3

then go blank except for "NOT

LED

which

indicator

sounds

VTBI

and

displays steadily and

flashes.

flashes

Displays show

"QBQ8"/"888.8"

The

and

momentarily, then display "96.07*96.5" in

the Rate

"P-X.X" (where

X.X

and

the installed software revision) in the

for =2

last

"0000TOOO.O",

for

The

indicators do not flash during

test

seconds

set

values

>4

hours.

"PRESS"

check.

followed by reversion to the

or

"OOO7"00.0"

if the power

NOTE

and

OPERATING

has

and

been off

the

red

the

refers to

VTBI

LED

self-

• Rate and

VTBI

displays

will

and -—/--.- respectively.

12.

Checktoensure

tubing set, then

manually

stop

all

airiscleared

press

PRIME ON/OFF to

priming or allow automatic

cycle to complete.

13. Attach administration

set

to the patient's

indwelling venipuncture device.

14. Use

15. Use

3.3.2

RATE

VTBI

Starting

arrow @@ controls to

arrow

an

Infusion

1. Press START to begin the infusion, then

check:

•

The

OPERATING

LED

indicator

• The Operating/Rate graphic begins

sequencing

3-4

show —

from

set

VTBI.

flashes

/-.-

the

RATE.

_

imed

r

M

The

"NOT

extinguishes.

If START is not pressed,

OPERATING"

illuminated.

Rate and/or VTBI entry

indicator

display(s) will flash,

an

audio

not

pressed

data entry,

3.3.3 During

1.

The

VOLUME

2. The

OPERATING

graphic

OPERATING"

NOTE

message

Within

plus

prompt

within5minutes

the

ten

the

Rate

will

pump

Infusion

INFUSED

LED

will

flash and sequence respectively.

message

the

"NOT

will remain

seconds

the

"PRESS"

and/or VTBI

as

appropriate, and

sound.IfSTART

of

will

shut

down.

value

will

and Delivery/Rate

of

the

increment.

3. Various alarm conditions may arise require operator attention. An alarm message

will

be displayed on the

ALARM LED will

will

sound.

Alarm/Prompt

recommended

See

messages

actions.

flash

Table 3-2 for a

LCD

and

and the

panel, the red

the

alarm

listing

the

last

which

audio

of the

last

is

will

•

LCD

panel

battery

will

remain backlighted and

will

continue to charge as

the AC power cord is connected to an

power

source.

3.3.6 Changing Rate or VTBI during an

Infusion

1.

Use

the

arrow

@®

controlstoinputanew

rate

and/or

• New rate and/or

VTBI.

VTBI

value

will

appear

the respective display.

2.

Press

the

START

controltoconfirm

initiate the new parameter(s).

• If START is not

seconds,

an audio prompt

and/or

The

instrument

the

3.3.7

control is

Resetting

the

VTBI

"PRESS"

display

NOTE

will

rate

Volume

pressed

will

sound

will

continue

and/or

pressed.

Infused

within

indicator will flash,

and

10

the rate

flash.

to

infuse

VTBI until

long

and

the

as

AC

in

at

JPB

3.3.4 Infusion Complete

1. When the programmed volume to be infused

has

been

delivered,

an

INFUSION

KVO

infusion.

• The

"INFUSION

flash

LED

will

sound.

on the

flash

• The infusion rate

mL/hr or 0.1

the

instrument

COMPLETE

COMPLETE"

LCD

panel, the red

and

an

audio

will

change to

mL/hr)

and

will initiate

alarm and begin a

message

ALARM

alarm

"1" or "0.7"

will

KVO

(1

will

flash alternately with the programmed rate

on the Rate display.

3.3.5

1.

Stopping

Press

the

an Infusion

ON/STOP

control:

• Pumping mechanism

•

All

indicators and displays

will

stop

will

extinguish

will

1. Use the arrow

@®

display to "0000" or "000.0".

2.

Press

VOL

INF

"VOLUME

"0"or"0.0"

RESET

INFUSED"

"INFUSION COMPLETE"

display

"OPERATING"

flashing

LED

Operating/Rate graphic

rate

ALARM

audio

3. Use the arrow

display to

4.

Press

•

"OPERATING"

the

LED

alarm

will

0®

the

desired value.

START

indicator

control:

LED

• "INFUSION COMPLETE"

extinguish

controls to

control:

value

indicator

will

sound.

controls to

indicator

set

will

reset

message

will

reflect

flash

and

set

the

will

message

the

will

stop

KVO

flash

will

VTBI

to

the

VTBI

3-5

imed

•

"ALARM"

alarm

• Operating/Rate graphic

programmed delivery rate.

If

the

instrumentisstopped

infusion, the valve shaft

audio

LED

will

indicator

silence

NOTE

will

extinguish and

will

reflect

during an

will

stop at its

present position. To load a

turn

"home"tothe

3.3.8 Clearing

1.

RefertoTable

and

Table 3-2. Alarm/Prompt Messages

NOTE

the

Response

instrument

loading position.

Alarms

on.

The

3-2.

Alarm/Prompt

Procedures.

new

valve

cassette,

shaft

Message

first

will

Alarm

applicable ONLY to instruments with Software Release

Message/Presentation

VOLUME

AIR

Audio

OCCLUSION

Audio

Nurse

INFUSION

Visual - Flashing

Audio-Alarm Nurse

LOW

Visual - Flashing

Audio-Alarm Nurse

INFUSED

Visual-Continuous Audio-None

IN

LINE

Visual - Flashing

-

Alarm

Nurse

Call-On

Visual - Flashing

-

Alarm

Call-On

COMPLETE

Call-On

BATTERY

Call-On

responses

XXXX

that refer to operation of the Nurse Call feature are

Cause

Normal display of value in volume

infused register.

Air bolus detected by the

AIL

sensor. Pumping stops.

Tubing in line pressure exceeds

occlusion pressure

stops. Can occur during

normal operation.

Volume

switches to

Infused

KVO

limit.

Pumping

priming

equals

VTBI.

delivery rate.

or

Pump

Battery charge has dropped to 5.8 V

threshold. Pumping continues.

voltage drops to 5.4 V, a

MALFUNCTION alarm will

and

pumping

will

stop.

If

activate

P-0.X/1.X

None. Reset to

Clear air

START.

Clear

Set

instrument

Plug instrument AC power cord

into

installed.

Response

from

occlusion;

up another infusion or turn

off.

a suitable

"0"

as required.

tubing; Press

Press

AC

START.

power source.

DOOR

OPEN

Visual - Flashing

Audio-Alarm

Nurse

MALFUNCTION

Call-On

Visual - Flashing

Audio-Alarm

Nurse

Call-On

Door

is opened

during

Malfunction

the

stops (except Malfunction

an

infusion.

detected in any one of

monitored

code displays in

LOW

Infused quantity.

while

priming

Pumping

parameters.

BATTERY).

3-6

or

stops.

Pumping

Volume

If

priming,

PRIME

close door and press

ON/OFF

twice.Ifinfusing,

close door and press START.

Instrument must be repaired by

biomedical

returningtoservice.

BATTERY,

into

AC

technician

before

If LOW

plug AC power cord

outlet.

Table 3-2. Alarm/Prompt Messages

imed

jpi

IB

Message/Presentation

NOT

OPERATING

Visual

Audio•None Nurse

RATE

Visual-Flashes

Audio

RATE

Visual-Flashes

Audio

NOT

- Steady

Call-On

NOT

000

- Prompt

000

- Prompt

CHARGING

Visual - steady

Audio-None

SET

0000

VOLUME

Visual -

Audio

flashes

- Prompt

twice

Cause

Instrument power on, but has not pressed.

message

sounds.

PRIME

Rate

flashes

ON/OFF

set

>000 (00.0).

After

and

control pressed

START control pressed Rate

set

to 000 (00.0;.IfSTART

pressed

"ALARM" indicators flash

again, "PRESS"

START

=45 seconds,

alarm audio

with

the

and

alarm

audio sounds; otherwise, after 45

seconds

OPERATING"

alarm

"ALARM"

audio

indicator&"NOT

message flash and

sounds.

Instrument power on, with the AC

power

VOL

with

cord not

source.

INF

VTBI

connectedtoan

RESET

set

control

>0000 (000.0).

pressed

with

AC

Response

Press

START, or turn instrument

power off.

Set

Rate to 000 (00.0;, then press

PRIME

Set

then

ON/OFF.

Rate to a value >000

press

START.

(00.0),

Plug AC power cord into an AC

power

Set

press

outlet.

VTBI

to 0000 (000.0;, then

VOL INF RESET.

SET

'p

VOLUME

Visual -

Audio

flashes

- Prompt

twice

START

set pressed

"ALARM" indicators flash

control pressed

to 0000 (000.0/ If START

again, "PRESS"

with

and

VTBI

alarm

Set

VTBI to a

(000.0;, then

value

press

>0000

START.

audio sounds; otherwise, after 45

seconds

"NOT

jpi

AUDIO

OFF

Visual - Steady

Audio-Silenced

and

AUDIO

while

"ALARM"

OPERATING"

audio

alarm

switch

indicator

and

message flash

sounds.

(rear panel) pressed

an audio alert is sounding.

After temporary delay, audio

will

resume. May be silenced again,

permissible.

if

temporarily

PRESS

Visual•Flashes

Audio

- Prompt

Rate and/or

infusion,

and

START

rate

10 seconds have elapsed

START

control

and/or

VTBI

control

pressed

VTBI

changed

not

actuated

twice

setto000

during

with

or

an

Press

VTBI

START.

START,orset

to a value >0, then press

rate and/or

(00.0;/oooo (000.0;.

3-7

Imed 960, 965 Service manual

Specifications and Main Features

Frequently Asked Questions

User Manual