Alaris imed Gemini PC-2TX User manual

<x ALARIS
MEDICAL SYSTEMS
em»
imc
Gemini
pc-2Txe
VOLUMETRIC
INFUSION
PUMP/CONTROLLER
MAINTENANCE
MANUAL

WARNINGS,
CAUTIONS
AND
NOTICES
CAUTION:
FEDERAL
(USA)
LAW
RESTRICTS
THIS
DEVICE
TO
SALE
BY
OR
ON
THE
ORDER
OF
A
PHYSICIAN.
USE
ONLY
HOSPITAL
GRADE
POWER
SUPPLY
CORD
TO
INSURE
PROPER
GROUNDING.
GROUNDING
RELIABILITY
CAN
ONLY
BE
ACHIEVED
BY
CONNECTION
TO
A
RECEPTACLE
MARKED
"HOSPITAL
GRADE”.
DANGER:
EXPLOSION
HAZARD,
DO
NOT
USE
IN
THE
PRESENCE
OF
FLAMMABLE
ANESTHETICS.
WARNING:
TO
PREVENT
UNRESTRICTED
FLOW,
CLOSE
CLAMP
WHEN
FLO-STOP
IS
OPEN.
CAUTION:
TO
REDUCE
RISK
OF
ELECTRICAL
SHOCK,
DO
NOT
REMOVE
COVER
OR
BACK.
REFER
SERVICING
TO
QUALIFIED
SERVICE
PERSONNEL.
WARNING:
REPLACE
FUSE
AS
MARKED.
|
CAUTION:
BEFORE
CONNECTING
"REFER
TO
MANUAL"
©
NOTE
TO
MAXIMIZE
THE
SERVICE
LIFE
OF
THE
INSTALLED
BATTERY,
IT
IS
RECOMMENDED
THAT
THIS
INSTRUMENT
BE
STORED
AND
OPERATED
IN
AN
ENVIRONMENT
THAT
IS
TEMPERATURE
CONTROLLED
BETWEEN
68°F
(20°C)
AND
77°F
(25°C).
WARNING
IN
THE
EVENT
THE
INSTRUMENT
IS
DROPPED
AT
ANY
TIME,
IT
MUST
BE
CHECKED
BY
A
BIOMEDICAL
TECHNICIAN
PRIOR
TO
USE
FOR
PATIENT
CARE.

WARNINGS, CAUTIONS AND NOTICES
WARNING:
To
PREVENT
UNRESTRICTED
FLOW,
CLOSE
ROLLER
CLAMP
WHEN
FLO-STOP®
IS OPEN.
/ | \ CAUTION: REFER TO MANUAL
TYPE
CF
(Equipment
useable
for
direct
cardiac
applications)
ALTERNATING
CURRENT
‘
REPLACE FUSE ONLY WITH SAME TYPE AND RATING
EQUIPOTENTIAL GROUND POINT: IF THE INTEGRITY OF THE
ХУ
EQUIPOTENTIAL
EARTH
CONNECTION
OR
HOSPITAL
EARTH
SYSTEM
IS
IN
QUESTION,
OPERATE
THE
INSTRUMENT
USING
(os
INTERNAL
BATTERY
POWER.
'
IPX1 DRIP PROOF
ii

Product design and/or specifications are subject to
change without notice. The information contained
in this manual is current as of the date of issue.
NOTICE
None
of
the
information
contained
herein
may
be
duplicated
nor
may
it
be
utilized
in
any
manner
other
than
for
the
repair
and
maintenance
of
IMED®
This publication contains ALARIS Medical
Systems™ proprietary data provided solely for the
use of technica! personnel in repairing IMED®
Gemini
infusion
pump/controllers
and
the
component
parts
thereof.
Any
unauthorized
use
of
the
information
contained
herein
may
subject
the
user
to
substantial
liability.
Gemini infusion pump/controllers.
This
manual
may
not,
in
whole
or
in
part,
be
copied,
photocopied,
reproduced,
translated,
or
converted
to
any
electronic
or
machine-readable
form
without
prior
written
consent
of
ALARIS
Medical
Systems,
Inc.
ALARIS Medical Systems, Inc.
10221 Wateridge Circle
San Diego, CA 92121 USA
[phone]
SCopyright
2000
ALARIS
Medical
Systems,
Inc.
All
Rights
Reserved
Printed in USA
U.S.
Patents
4,617,014;
4,689,043;
4,690,673;
4,725,205;
4,728,265;
4,836,752;
4,909,710;
4,920,336;
4,954,046;
4,859,927;
4,764,166;
305,151.
AU
580,184;
586,594;
590,179;
601,664;
607,1
12;
622,088;
596,552;
604,477.
CA
1,235,033;
1,258,212;
1,300,977;
1,280,647;
1,296,791;
2,020,926;
1,296,
092;
1,238,832,
AT
0,225,158.
BE
0,225,158.
FR
0,225,158;
283,614; 315,312;
0,431,726; 0,238,227.
GB
0,225,158;
283,614;
315,312;
0,431,726;
0,238,227.
NL
0,225,158;
283,614.
IT
0,225,158;
283,614.
SE
0,225,158;
283,614.
CH
0,225,158.
DE
P3686558.3;
P3772,556.9;
3871721T2;
P6908208;
P3774598.
TW
UM52721.
JP
#3
17544705;
888181687
25:478190238
7%;
###196716885;#885179311985:;4###17303955.
Other
US
and
Foreign
Patents
Issued
and
Pending.
IMED®, Gemini
PC-2TX®
and
Flo-Stop®
are
registered
trademarks
of
ALARIS
Medical
Systems,
Inc.
iii

PC-2TX
PREFACE
This manual contains operation and maintenance
instructions for the IMED® GEMINI PC-2TX® series
of Volumetric Infusion Pumps/Controllers (“PC-
2TX”). The information provided herein is intended
for use by technical personnel responsible for
servicing these products. The material is divided
into seven sections and is presented as follows:
Section 1 - Description, Section 2 - Preparation for
Use; Section 3 - Operation; Section 4 - Principles
of Operation; Section 5 - Maintenance; Section 6 -
Illustrated Parts Breakdown; Section 7 - Calibration
and Preventative Maintenance.
iv
Additional copies of this manual may be obtained
by contacting your nearest ALARIS Medical
Customer Service Department.
This manual P/N 143648 supersedes PC-2TX
Maintenance Manual, Part No. 1325-9201-00,
1325-9208-00, and 141881.
The features of the 220V model of the PC-2TX
have been incorporated into this manual. Text or
graphics that are related exclusively to the 220V
model are identified with a (AB) symbol.

A
SECTION
7
-
CALIBRATION
AND
PREVENTATIVE
MAINTENANCE
7.1
INTRODUCTION
に
ο
ἶἶΐἀ{ἶῑῴῄζ{ἵὤζἶἵὤ.
7.2
PREVENTIVE
MAINTENANCE
ан,
нь.
7.3
CALIBRATION
PROCEDURES
...........................
7.3.1
Strain
Beam
Calibration
.................................
7.3.1.1
Calibration
Equipment
Requirements
.......................
7.3.1.2
CalibrationProcedures
..................................
7.3.2
Door
Sear
Adjustment
................,..................
7.4
COMPREHENSIVE
OPERATIONAL
PERFORMANCE
TEST
7.4.1
Electrical
Inspection
..................,..,..............
7.4.1.1
ElectricalleakageTest..................................
7.4.1.2 Electrical Ground Test
7.4.1.3 Dielectric Test (Optional)
7.4.1.4 Battery Runtime Test
7.4.2
Qualitative
Operational
Performance
Тез
...................
74.3
Quantitative
Operational
Performance
Test
..................
7431
Eguipment
Reguiremenis
................................
743.2 Test Procedures
| © WARRANTY
SALES AND SERVICE OFFICES
TECHNICAL
SERVICE
MANUAL
SUPPLEMENTS
vii

PC-2TX
LIST OF FIGURES
Figure
Title
Page
1-1 IMED GEMINI Model PC-2TX Volumetric infusion Pump/Controller
1-2
Audio
Characteristics
..............................,,..,,......,..,,................
1-6
2-4
PC-2TX
Front
and
Rear
Panel
Operating
Features
.................,..................,..
2-2
2-2
Air-In-Line
Simulator
.........................
0
페이
K
n
a
2-6
2-3
PC-2TX
Abbreviated
Test
Data
Sheet
.................................................
2-7
3-1
PC-2TX
Front
Panel
Controls
and
Indicators
.......,....,...............................
3-2
4-1
PC-2TX
Pumping
Mechanism
.......-.......
знании
ани
иен
нуна
4-2
4-2
PC-2TX
Signal
Flow
and
Interconnect
Diagram
..........................................
4-3
4-3
Cross
Section
of
Strain
Beam
Assembly
.................................
0...
4-5
4-4
AIL
Detector
Cross
Section
........................................................,..
4-9
45
Slide
Clamp
Detector
Cross
Section
...................................................
4-10
4-6
AIL/SCD
Board
Schematic
(P/N
1840-5012)
.............................................
4-11
4-7
Logic
Board
1340-5048
(Sheet
t
of
3)
.............,................................,...
4-15
4-7
Logic
Board
1320-5048
(Sheet
2
of 8)
..................................................
4-17
4-7
Logic
Board
1320-5048
(Sheet
3
of 3)
.....................,............................
4-19
4-8
Display
Board
1320-5049
(Sheet
1
of
4)
...........................,....................
4-21
4-8
DisplayBoard1320-5049(Sheet20f4)
............................................
4-23
4-8
Display
Board
1320-5049
(Sheet
3
of
4)
................................................
4-25
4-8
Display
Board
1320-5049
(Sheet
4
of
4)
....................,......................,....
4-27
4-9
Power
Supply
Board
1320-5054
(Sheet
1
of 8)
...........................................
4-29
49
PowerSuppiyBoard
1320-5054
(Sheet20f3)............................................
4-31
4-9
Power
Supply
Board
1320-5054
(Sheet
3
of
3)
........,..................................
4-33
4-10
Motor
Controller
Board
1320-5001
(Sheet
1
0Î 3)
.......,.............
eee.
4-35
4-10
Motor
Controller
Board
1320-5001
(Sheet
2
of
3)
...............,....,....................
4-37,
4-10
Motor
Controller
Board
1320-5001
(Sheet
3
of
8)
.........................................
4-39:
6-1
Parts
Identification
-
PC-2TX
Pump
Assembly
.
.......,...,...............................
6-4
6-2
Parts
Identification
-
Front
CaseAssembiy(Sheet1).
...................................
6-7
6-2
Parts
Identification
-
Front
Case
Assembly
(Sheet
2).
.....................................
6-9
6-3
Parts
Identification
-
DOOr
ASSEMblY
eneret
eve
6-12
6-4
Parts
Identification
-
Rear
Case
Assembly
{Sheet
1)
......................................,
6-15
6-4
Paris
Identification
-
Rear
Case
Assembly
(Sheet
2)
.......................................
6-17
6-5
Parts
Identification
Pole
Clamp
Assembly
..........,.............,......................
6-19
6-6
Parts
Identification
-
Power
Supply
Board
CCA
......,..............,.....................
6-26
6-7
Pertsidentification
-DisplayBoardCCA
..............................................
6-29
6-8
Parts
Identification
-
Logic
Board
CCA
e
6-35
6-9
Parts
Identification
-
Motor
Controller
CCA
..........................,......,.......,....
6-41
7-1
Universal
Test
Station
Setup
...............,..:.,,,.,.....4......
ere.
7-5
7-2
Air-in-line
Simulator.
............................
1...
lee
7-7
7-3
PC-2TX
Test
Data
Sheet
............................................................
7-8

LIST OF TABLES
Table
Title
Page
1-1
Product
History
............................................4.4..
iii
ee.
1-4
1-2
Operating
Reguirements
........................
1.000.
1-5
1-3
Performance
Specifications
............................,..........................
τς
1-5
1-4
ο
ος
αμ
ED
1-7
3-1
Description
of
Controls
and
Indicators
............,..................................
3-3
3-2
Visual
MessageDisplays
.................................
1...
3-51
4-1
RS-232-C
Communications
Data
Port
Signal
Definitions
............................
2
2,
4-13
5-1
Troubleshooting
Guide
k
5-7
5-2
PC-2TX
Error
Log
Codes
ss
eee
eo
5-10
5-3
Table
of
Torque
Values
............,.......,.................................
이
이
5-27
6-1
Paris
List
-
PC-2TX
Pump
Assembly
..........................................
6-2
6-1a
Parts
List
-
PC-2TX
Pump
Assembly
220V
νι
νεο
ον
ων
ee
k
ος
6-2
6-2
Parts
List
-
Front
Case
Assembly
.
...........,...,..........,..........................
6-5
6-3
Partslist-DoorAssembiy.................................
0.00
la
6-11
6-4
Paris
List
-
Rear
Case
Assembly
..............,...,..................................
6-13
6-5
Parts
List
-
Pole
Clamp
Assembly
.....................................................
6-14
6-6
Parts
List
-
Power
Supply
Boardg
CCA
eee.
6-21
6-7
Paris
List
-
Display
Board
CCA
に
k
k
6-27
6-8
Parts
List
-
Logic
Board
CCA
00000
eo
n
k
nn
6-30
6-9
Paris
List
-
Motor
Controller
Board
CCA
.........,......................................
6-36

PC-2TX
GoD |o sm 000
GEES O vem O a Gü
리디아 리사 上 ie
imed Gemini Pc2Tx
El
06000)
fO®
©
Of)
519000
“DEDO
re
(>)
Hooon
Figure
1-1.
IMED®
GEMINI
PC-2TX®
Volumetric
Infusion
Pump/Controller
x

PC-2TX
SECTION
1
-
DESCRIPTION
1.1 INTRODUCTION
This
section
includes
general
operating
character-
istics,
physical
description
and
operating
specifi-
cations
for
all
versions
of
the
IMED®
GEMINI
PC-2TX®
Volumetric
Infusion
Pump/Controller
(PC-
2TX").
1.2 OPERATING CHARACTERISTICS
The GEMINI Model PC-2TX is a two channel
volumetric
infusion
pump/controiler
used
in
the
administration of intravascular drugs and fluids.
Both
channels
are
capabie
of
independent
operation
in
either
the
Pump
or
Controller
delivery
mode.
The
pumping
mechanism
employs
linear
peristaltic
action.
The
peristaltic
action
is
provided
by a series of 12 cam-actuated fingers that
sequentially collapse then release, in a ripple-like
action, the soft pumping segment of a GEMINI
administration
set.
This
action
produces
a
positive
pressure
at
the
outlet
side
and
a
vacuum
on
the
inlet
side
of
the
pump,
thereby
delivering
a
continuous flow of infusion solutions reliably,
accurately and with a high degree of safety.
The
two
channel
configuration
enables
a
variety
of
infusion
techniques
including
independent
primary,
simultaneous
primary
and
sequential
secondary.
Independent
and
simultaneous
primary
infusions
can
deliver
either
a
specified
volume
or
the
entire
contents
("ALL")
of
a
solution
container.
Use
of
the
ALL
setting
requires
installation
and
connection
of
an
Empty
Container
Detector
(ECD)
which
is
available
as
an
optional
accessory.
Sequential
secondary
(piggyback)
infusions
with
independently
defined
delivery
parameters,
for
both
the
primary
and
secondary
solutions,
can
be
provided
on
each
channel.
Operational contro! of the PC-2TX is affected
through
the
control
and
indicator
panel
on
the
front
of
the
instrument
and
the
Audio
Control
switch
on
“the rear of the instrument. Basic operating
instructions
are
printed
on
the
right
side
of
the
instrument
case.
Functional
control
is
provided'by
a
16
bit
micro-processor
with
a
stored
program
that
includes
a
Maintenance
mode
to
monitor
instrument
performance,
an
audio/visual
alarm
subsystem
to
alert
operators
to
abnormal
conditions
and
redundancy
checks
to
confirm
system
accuracy.
1.3 OPERATING CONDITIONS
The
PC-2TX
can
be
operated
independently
{Normal
Operation)
or
as
a
computer
controlled
device
(Computer
Operation).
Normal
operation
includes
the
Controller
and
Pump
modes
plus
a
Maintenance
mode.
Computer
operation
includes
Monitor
and
Computer
Control
modes.
NORMAL OPERATION
SYSTEM OPTIONS
The
systems
option
mode
allows
the
operator
to:
e Adjust contrast of the LCD display
ο Set the Time of Day clock
9 Enable Anesthesia Mode
. Set up Computer Control
e
Check System Configuration
The
System
Configuration
screen
displays
the
current
status
of
the
following
selectable
features:
NOTES
To
enter
the
Configuration
Setup
mode:
press
and
hold
the
"OPTIONS/EDIT"
switch
at
power
up.
Bold
face
type
indicates
factory-default
settings.
る Clock Setup: Military or AM/PM
9
Factory
Set:
Factory
default
settings
YES
or
NO
e
Maximum
Rate:
Max
usable
rate
1-999
mL/hr
e
C2
Port:
Baud
300,
600,
1200,
2400,
4800,
9600,
19200;
(Data
Frame
is
set
to
N81);
Serial
No.
XXXX.
ο
Aux
Port:
No
Port
:
9
PCS
Mode:
P
or
C
or
S
Channel
delivery
mode
selection
plus
mode
lock/unlock
1-1

PC-2TX
® Delayed Start: Enabled or Disabled
e Drug Calc: Enabled or Disabled
e Multidose: Enabled or Disabled
e Dose Display: Fixed or Temp
e Battery Mode: Disabled Normal High
e Key Audio: Enabled or Disabled
e Alarm Audio: Profile 1, 2 or 3
® Switch(over) Audio: Enabled or Disabled
e Tamper Mode: Enabled or Disabled
e Language: English
9 Anesth. Mode: Enabled or Disabled
e Comp. Ctrl.: Enabled or Disabled
® Dynamic Press: Enabled or Disabled
e Press. Trend: Enabled or Disabled
e Vol. Time Inf: Enabled or Disabled
e S/W Version: SCX.XX.XX.X
e MC Version: X.XX
e. C2S/N: XXXX
e CRC: XXXX/Checksum: XXXX
CONTROLLER MODE
In the CONTROLLER mode, the PC-2TX js pro-
grammed to control the infusion of a specific
volume of IV solution. The instrument senses and
responds to patient-side pressure and container
height in a manner similar to a gravity infusion. The
instrument's pressure sensor measures the
hydrostatic pressure from the bottle and compares
that pressure against distal tubing in-line pressure.
When in-line pressure exceeds pump input
pressure, an occlusion condition exists and an
alarm is initiated. Actual delivery pressure is directly
proportional to container height; increasing
container height raises and decreasing the height
reduces occlusion pressure. Controller mode
occlusion pressure tolerance is +12 (30.5cm)
inches from the bottle height. Transient surges in
patient-side pressure of <60 seconds duration will
produce a LOW FLOW condition which stops the
infusion while the pressure is above the occlusion
threshold. Pressure transients above the occlusion
threshold >60 seconds duration or cumulative time
required to compensate for volumetric deficiency
caused by periods of Low Flow in excess of 30
minutes will cause an occlusion alarm.
PUMP MODE
In the PUMP mode of operation, the instrument
employs a preset occlusion pressure limit of 10 +2
psi (69 +14 kPa) predicated on a nominal container
height of 24 inches (61 cm) and a delivery rate >30
mU/nr, For delivery rates <30 mL/hr, the occlusion
pressure is rate dependent to ensure timely
detection of occlusion conditions. Any transient
distal in-line pressure above this limit will generate
a patient-side occlusion alarm.
Software Releases through 3.9.9.4
The PC-2TX, when operating in the Pump Mode,
can be locked into a rate-independent (10 psi)
occlusion pressure mode. This mode will result in
significantly increased time-to-occlusion for rates
<30 mUhr.
Software Release 4.10.14.0 and Subsequent
A Selectable (S) pressure mode allows an
occlusion pressure to be selected between 0.5 psi
(25 mmHg) and 10 psi (617 mmHg) in 25 mmHg
incremenis. A high occlusion pressure selection
coupled with a siow infusion rate will result in an
increase in time-to-occlusion.
MAINTENANCE MODE
The
maintenance
mode
is
intended
solely
for
use
by
biomedical
technicians
to
perform
servicing
and
maintenance
actions
and
must
never
be
used
when
the
PC-2TX
is
connected
to
a
patient.
The
maintenance
mode
provides
biomedical
service
personnel
access
to
the
closed
loop
maintenance
test
routines
and
operating
history
logs.
Maintenance mode menu includes:
る S/C board iest and displays
ο M/C board test and displays
ㆍ Press [off] to exit
The
S/C
board
test
and
display
sub-menu
includes
an Error Log display with a 100 entry register.
COMPUTER OPERATION
MONITOR MODE
The Monitor mode allows a host computer to
monitor infusion status and instrument
performance.
Monitor
mode
is
enabled
when
a
host
computer
is
connected
to
the
PC-2TX
through
the
Communications Data Port and the Monitor
indicator is illuminated.
COMPUTER CONTROL
The Computer Control mode allows an infusion,
once set up, to be controlled and monitored by a
host computer installation.

1.4 USER INTERFACE
Instrument control and operation is accomplished
through the 30 keypad controls, the central
information display and the independent channel
information displays. Infusion parameters are
programmed into the instrument using the
appropriate keypad controls. Rate and Votume-to-
be-Infused (VTBI) are input separately for each
channel. Rate and VTBI for secondary infusions
(piggyback) are also programmable, independent of
the
primary
infusion
parameters,
for
each
channel.
Visual Prompt and Advisory messages with
accompanying audio alerts are provided to assist
operators
in
setting
up
the
instrument
for
operation.
infusion completions, alarm conditions and
software-detected malfunctions are signaled by
both audio and visual alerts; hardware-detected
malfunctions are signaled by an audio warning.
Delayed Start, Multidosing and Drug Calculation
infusions, when these features are enabled, are
programmed via the Channel Options menu.
The rear panel of the PC-2TX is configured with an
ECD connection for each channel, a connector to
accept a Nurse Call line, and a standard RS-232-C
communications data port for interfacing with a host
сотрщег.. ::
iMED® GEMINI Series disposable administration
sets are required for use with the GEMINI family of
Infusion Pump/Controllers.
1.5 PHYSICAL DESCRIPTION
The PC-2TX instrument has the following physical
characteristics:
Height: 10.8 inches (27.4 cm) -
Width:
11.8
inches
(30.0
cm)
with
pole
clamp
Depth: 7.3 inches (18.5 cm) with pole clamp
Weight:
=18
pounds
(8.2
kg)
including
power
cord
The PC-2TX instrument consists of two major
assemblies: the front and rear cases.
FRONT CASE
The front case consists of a metalized, high-impact,
injection
molded,
plastic
case/insert
which
houses
and supports: the pumping chamber access doors,
the peristaltic pumping mechanisms, pressure
transducers
(strain
beams),
Air-in-line,
Slide
clamp
and
Flo-Stop
detectors,
keypad,
the
channel
and
central
displays,
the
display
CCA,
logic
CCA
and
motor
control
CCA.
REAR CASE
The
rear
case
assembly
consists
of
a
die-cast
aluminum
shell
which
mounts
and
supports
internally:
the
battery,
transformer
harness
assembly,
audio
oscillator,
power
supply
CCA
and
communication
harness
assembly.
The
exterior
of
the
rear
case
supports
the
pole
clamp,
power
entry
module,
ECD
storage,
power
cord
retention
strap,
power
cord
retention
bracket
and
the
equipotential
grounding
point
on
the
220V
model.
1.6 PRODUCT HISTORY
The
initial
release
of
the
GEMINI
PC-2TX®
Infusion
Pump/Coniroller
was
in
April
1994.
Since
that
time
a
number
of
changes
have
occurred.
Refer
to
Table
1-1
for
product
history.
1.7 OPERATING SPECIFICATIONS
The
PC-2TX
Operating
Specifications
are
subordinated
into
Operating
Requirements
and
Performance
Specifications
which
are
delineated
in
Tables 1-2 and 1-3 respectively.
1.8 ACCESSORIES
The
accessories
approved
for
use
with
the
PC-2TX
are listed in Table 1-4.

PC-2TX
Model
1325A
1325B
1325C
1325D
Table 1-1. Product History
History
Initial release of product Software version 3.9.9.4.
ADDED
TX
Feature
set
-
Volume/time
dosing,
Selectable
output
pressure,
Dynamic
Pressure
Readout,
Pressure
Trending
(History),
7
segment
display
checking added with Software version 4.10.14.0.
*
Rate
display
test
enabled,
Audio
Failure
“Pop-up
box",
added
with
Software
version
5.10.18.4.
«
Incorporated
Corrective
Drug
Application
with
Software
version
7.05.05.0.
*
Software
versions
7.05.05.0
and
earlier,
will
not
recognize
a
year
entry
beyond
1999
in
the
Clock
Entry
menu.
Introduced
Software
version
1.85.
The
current
PC-2TX
System
Configuration
may
be
viewed
by
pressing
Options/Edit
key
to
bring
up
the
Systems
Options
Menu,
then
pressing
#5
Keypress,
to
access
the
System
Configuration
listing.
Revision Matrix:
Revision #
1325A
1325B
1325BX (220
1325C
1325CX (220
1325D
1326AX (220
1
PC-2TX PC-2TX PC-2TX
3.9.9.4, 4.2.8.0, 5.10.18.4 7.05.05.0
4.5.24.0, 4.10.14.0,
4.12.9.0, 5.1.18.0,
5.2.4.0
X
Revision "A" - Initial Revision
Revision "B" - Software Upgrade for Units to enhance operation.
Revision
"C"-
Software
Upgrade
to
correct
a
specific
drug
calculation
concentration
for
the
drug
Esmolol
(Brevibloc),
to
be
incorrectly displayed.
Revision
"D"-
Mandatory
Upgrade
to
incorporate
with
Software
Revision
1.85,
or
1.86.
Note’:
1325/1326x
= a
number
associated
with
a
particular
model,
and
software
version,
ie.,
1325A
could
be
3.9.9.4
or
一
5.10.18.4 etc.
Note
All
PC-2TX's
have
a
Maintenance
or
Diagnostic
Mode.
To
access
this
mode:
hold
in
the
Audio
Contro!
switch
on
the
panel and then press Power On.keypress.
CAUTION:
The
“Fractional”
and
“Integer”
Pumping
Mechanisms
are
not
interchangeable.
1-4

PC-2TX
Table
1-2.
Operating
Requirements
Parameter
Power Required:
_ Rated Input Power: ED
Electrical Leakage:
Electrical Shock Protection:
Level of Protection against Electrical
Shock:
Level of Protection against fluid
ingress:
Battery:
Battery Recharge:
Instrument Off or Operating:
Nurse Call System Power Limitations:
Operating Temperature Range:
Operating Humidity Range:
Storage Temperature:
Storage Humidity:
Table 1-3.
Parameter
Operating Principle:
Mode of Operation:
Specification
110V:
90-132
VAC,
current
draw
0.1
Amps
nominal
(.36
Amps
max),
10
Watts,
fused
at
0.4
A,
50-60
Hz,
3
wire,
Single
220V:
220-240
VAC,
0.15
Amps
nominal,
fused
at
200mA,
50/60
Hz,
3
wire,
Single
10 VA
Less than 100 microamps
Class 2, Internally powered equipment
Type CF equipment
IPX1
Sealed lead-acid, 6 VDC, 12 Amp-Hr
New
batteries
will
recharge
to
90%
of
capacity
in
8
hours
and
will
return
to
a
fully
charged
condition
within
16
hours.
For
maximum
battery
life,
battery
should
be
fully
recharged
after
each
discharge.
Maximum
recommended
Voltage/Current
24
VDC/500
mA
40°F
(5°C)
to
104°F
(40°C)
0%
to
95%
Relative
Humidity,
non-condensing
-40°F
(-40°C)
to
158°F
(70°
C)
0%
to
95%
Relative
Humidity,
non-condensing
at
35°C
Performance Specifications
Specification
Linear Peristaitic
Continuous

PC-2TX
Operating Range:
Pump and Controller modes:
Rate:
Volume-to-be-Infused (VTBI):
Keep Vein Open (KVO) Rate:
Occlusion Pressure -
Controller Mode:
Pump Mode:
Selectable Mode:
Air-In-Line Detection:
Secondary (Piggyback):
Nurse Cail Feature:
Communications Data Port:
Channel Display Indicators:
ALARM:
STANDBY:
INFUSING:
Battery Operation:
0.1
-
999
mL/hr
in
0.1
mL/nr
increments
to
99.9
mL/hr
and
4
ml/hr
increments
from
1
to
999
mL/hr
(Controlier
mode
maximum
recommended
rate
is
500
mL/hr)
0.1 - 9999 mL in 0.1 mL increments to 999.9 mL and 1 mL
increments from 1 to 9999 mL.
NOTE
Fractional
VTBI
vaiues
cannot
be
used
with
rate
values
>100
mL/hr.
1
mL/hr
for
delivery
rates
>
1
mL/hr,
or
set
delivery
rate
if
<1.0
mU/hr
container height (+12" or +30.5 cm)
10
+2
psi
(69+14
kPa)
(at
delivery
Rates
below
30
mL/hr
occiusion
pressure
is
flow
rate
dependent
to
ensure
rapid
response
to
occlusion
conditions).
The
"10
psi
mode”
can
be
invoked
during
SYSTEM
CONFIGURATION
thereby
setting
occlusion
pressure
to
1042
psi
(69+kPa)
for
all
rates.
(NOTE:
Time
to
occlusion
at
rates
<30
mL/hr
will
be
significantly
increased).
25-517
mmHg
(0.5-10.0
psi)
in
25
mmHg
(0.5
psi)
increments.
Ultrasonic
Dual
rate
programmable
Activates
an
externally
powered
system
in
the
event
of
an
Alarm,
Malfunction
or
selected
Advisories
EIA
Standard
RS-232-C.
Requires
standard
9
pin
subminiature
D
connector
Red LED - flashes during alarm condition
Amber
LED
-
illuminates
when
channel
is
programmed
for
a
delayed start and awaiting start time
Green
LED
-
flashes
when
channel
is
actively
infusing
With
a
new,
fully
charged
battery,
approximately
7.5
hours
with
two
channels
operating
at
125
mL/hr.
Minimum
recommended
run
time
is
4
hours.
NOTES
To
maximize
battery
life,
recharge
battery
for
10
hours
between
consecutive
battery
operations.
Failure
to
fully
recharge
the
battery
between
consecutive
battery
operations
will
reduce
battery life.
1-6

Audio Characteristics:
PC-2TX
VOLUME SILENCE
AUDIO
TYPE
AUDIO
PERIOD
VAR/FIXED
YES/NO
(1) MALFUNCTION ΠΠ an m ПА ом
OFF MAXIMUM NO
600 msec ON, 0.5 sec OFF, 75db FIXED
600 msec ON, 3 sec OFF...
(2) KEY CLICK | ON
OFF VARIABLE NO
30 msec ON (Once)
{3} ALARM ΠΠΠΠΠΛΠΠΠῃ ON
n OFF
Profile
1
500
msec
ON,
1500
msec
OFF,
VARIABLE
YES
500 msec ON, 1500 msec OFF...
LL om
OFF
Profile
2
400
msec
ON,
1
sec
OFF,
VARIABLE
YES
100 msec ON, 400 msec OFF...
NUL on
OFF
Profile
3
400
msec
ON,
500
msec
OFF,
VARIABLE
YES
400 msec ON, 500 msec OFF...
(4) PROMPT LILLA | | | ON
OFF
100
msec
ON,
2
sec
OFF...
VARIABLE
YES
(5) ADVISORY | | ON
OFF
100
msec
ON,
15
sec
OFF...
VARIABLE
YES
(6) CHANGEOVER | | | | | ON
OFF
100
msec
ON,
400
msec
OFF
(6
beeps}
VARIABLE
YES
(7) ILLEGAL KEY Il on
OFF
100
msec
ON,
100
msec
OFF
(2
beeps)
VARIABLE
No
Figure 1-2. Audio Characteristics
Table 1-4. Accessories
Part No. Description
1303
Communications
Emulator
Plug
(optional)
3299-100 Calibrated Tubing (optional)
1308
Universal
Empty
Container
Detector
(ECD)
20-2370-7 Syringe Holder
1-7