The IVAC® Volumetric Pump - Models 571 and 572 automatically regulates the infusion rate of IV solutions using a linear
peristaltic, volume displacement mechanism to regulate fluid flow at the prescribed rate. The pump can be operated with
a Flow Sensor and is compact and robust enough for most patient situations.
The IVAC® 571 Volumetric Pump operates in primary infusion mode only.
The IVAC® 572 Volumetric Pump has a primary and secondary infusion mode.
Product Familiarity
Ensure that you are fully familiar with the pump by carefully studying the Directions for Use (DFU) prior to operation and
prior to attempting any repairs or servicing. As part of continuous improvement, product enhancements and changes are
introduced from time to time.
Purpose of this Manual
This Technical Service Manual describes how to set up, test and maintain the following IVAC® Volumetric Pumps:
Model 571
Model 572
This manual is intended for use by personnel experienced in medical equipment testing and maintenance procedures .
Conventions Used in this Manual
BOLDUsed for Display messages/values, self-test codes, controls and indicators referenced in this manual, for
example, CAL RATE, test code 11, ON/OFF switch.
'Single quotes'Used to indicate cross-references made to another section of this manual. For example, see
Chapter 2, 'Configuration and Calibration'.
underlineUsed to indicate a link to another section within this manual.
ItalicsUsed to refer to other documents or manuals. For example, refer to the relevant Directions for Use
(DFU) for further information. Also used for emphasis, for example, ...if the gap still measures less
than...
Wherever this symbol is shown a Hints & Tips note is found. These notes provide useful advice or
information that may help to perform the task more effectively.
Wherever this symbol is shown a Toolbox note is found. These notes highlight an aspect of test
or maintenance that is important to know about. A typical example is drawing attention to a
software upgrade that you should check has been installed.
Prior to using this pump, carefully read the Operating Precautions described in the Directions for Use
(DFU).
This pump contains static-sensitive components. Observe strict precautions for the protection of
static sensitive components when attempting to repair and service the pump.
An explosion hazard exists if the pump is used in the presence of flammable anaesthetics. Exercise
care to locate the pump away from any such hazardous sources.
Dangerous Voltage. An electrical shock hazard exists if the casing of the pump is opened or
removed. Refer all servicing to qualified service personnel.
This pump is protected against the effects of radio frequency emissions and is designed to be
M
fail safe if extremely high levels of interference are encountered. Should false alarm conditions
be encountered, either remove the source of the interference or regulate the infusion by another
appropriate means.
If the pump is dropped, subjected to excessive moisture, humidity or high temperature, or otherwise
suspected to have been damaged, remove it from service for inspection by qualified service
personnel.
Introduction and Start Up
When connected to an external power source, a three-wire (Live, Neutral, Earth) supply must be
used. If the integrity of the external protective conductor in the installation or its arrangement is in
d
doubt, the pump should be operated from the battery.
The English switch panel controls and indicators are described below. For information on overlays in other languages,
refer to the relevant DFU. See also Appendix B, 'Spare Parts Listing' for switch panel part numbers.
Increases or decreases infusion rate and pressure and volume values. Three
UP/DOWN
columns for faster/slower increase or decrease:
Left = 100's, Centre = 10's, Right = units (or in micro mode Left = 10's,
Centre = units, Right = fractions).
CLEAR
TOTAL VOLUME INFUSED
PRESSURE LIMIT
READ PRESSURE
Clears total volume infused when both switches are held down together.
Displays total volume infused value (primary + secondary volume infused).
Sets the Information Display to continuously monitor volume infused.
Displays or changes the occlusion pressure alarm level limit.
Displays the IV infusion site pressure.
Sets the Information Display to continuously monitor infusion pressure.
(Model 572 only). Switches between PRIMARY and SECONDARY infusion
PRIMARY/SECONDARY
CRIS
modes. Allows displays of VTBI or rate setting of one mode while operating
in another.
On Model 572: only used in Self-test mode.
On Model 571: hidden switch, only used in Self-test mode.
RATEChanges the infusion rate.
VOLUME TO BE INFUSED
(VTBI)
Sets the value of Volume To Be Infused. Displays volume remaining to be
infused.
RUN/HOLD
Starts and stops pump infusion. Silences/cancels alarms and advances
start-up instruction messages.
ON/OFFTurns the pump on and off.
AC POWER INDICATOR
BATTERY INDICATOR
0
With a Flow Sensor in use, an illuminated ("0") in the Information Display window indicates a drop is
detected by the flow sensor in the drip chamber.
When illuminated, indicates the pump is connected to an AC power supply
and the battery is being charged.
Flashes to indicate the pump is operating on battery power.
Flashing Displays When the pump is operating on battery power, both Displays flash on/off.
Rear Panel
PRESSURE UNIT SELECTOR
SWITCH
RESET SWITCHResets the circuit breaker.
Sets the displayed pressure units. Millimetres of mercury (mmHg) or
Centimeters of water (cmH20).
1. Press the RUN/HOLD switch to place the pump on hold.
2. Press the R AT E switch.
3. Use the JK switches to set the new rate.
4. Restart the pump at the new rate by pressing the
HOLD
switch.
RUN/
Clearing the total Volume Infused
1. Press the RUN/HOLD switch to place the pump on hold.
2. Press and hold the TOT VOL INF switch and the K
switch directly above simultaneously for 2 seconds until
display shows
3. Resume infusion by pressing the RUN/HOLD switch.
000.0.
Changing the Volume To Be Infused
1. Press the RUN/HOLD switch to place the pump on hold.
2. Press the VOL TO BE INF switch.
3. Set new volume by pressing the JK switches. OFF can
also be selected when a flow sensor is in use, see Notes
below.
4. Restart the pump by pressing the
Notes:
1) Without a flow sensor in use, a VTBI value must be entered,
otherwise, the pump will be unable to operate.
2) With a flow sensor in use, a VTBI value isn't required and
OFF can be selected if required.
RUN/HOLD switch.
Adjusting the maximum pressure limit
(Occlusion pressure alarm level)
1. Simultaneously press and hold the LIMIT PRES
switch whilst using the JK switches to adjust
the pressure limit.
2. Release the LIMIT PRES switch.
Note: Pressure value will be displayed in
cmH20 depending on unit selected. See 'Pressure
Unit Selector'.
mmHg or in
Reading the pressure
1. Press and hold the READ PRES switch. Wait at least
10 seconds to allow reading to stabilize.
Note: Pressure value will be displayed in
in cmH20 depending on unit selected. See 'Pressure
Unit Selector'.
mmHg or
Selecting alternating display of total
volume infused
1. Press and release the TOT VOL INF switch three
times within 2 seconds while the pump is infusing or
on hold.
On Model 572, the display will alternate between
primary or secondary infusion and total volume
infused.
On Model 571, the display will continuously
show the total volume infused.
Selecting alternating display of infusion
pressure
1. Press and release the READ PRES switch three times
within 2 seconds while the pump is infusing or on
hold.
On Model 572, the display will alternate between
primary or secondary infusion and infusion
pressure.
On Model 571, the display will continuously
show the infusion pressure.
Operating on Battery Power
The pump operates on battery power when it is disconnected from the AC power. The battery power indicator, the
Information and Numeric Displays will flash whenever the pump is on battery power. In the event of a power failure, the
pump will automatically continue to operate on battery power.
Two alarms indicate the condition of the pump's battery:
LOW BATT alternating with the selected volume or pressure status. This indicates that approximately 30 minutes of
operating time remains on battery power
LOW BATT (constant). This indicates that the battery is discharged. Connect the pump to an AC power supply to
recharge the battery.
Note: The pump's battery is designed for limited duration use. Wherever possible, the pump should be used connected
to an AC power supply. If the pump is to be taken out of service for an extended period, it is good practice to charge the
battery periodically to ensure full capacity.
This mode of operation supports automatic secondary infusions ("piggybacking") in the same pump channel. When
the secondary VTBI reaches zero, a transition tone will sound and the primary settings will automatically take effect.
Secondary mode can be used where a second, independent VTBI is required, and also when an automatic rate change is
required.
When the pump is programmed and delivering in the secondary mode, the primary infusion is temporarily stopped and
fluid is drawn from the secondary (higher) container. Delivery from the primary container resumes when the fluid level in
the secondary line is level with the fluid in the primary container.
Notes:
1) The primary fluid container must hang lower than the secondary fluid container to allow the secondary infusion to
run.
2) On completion of the secondary infusion the pump will automatically return to primary infusion.
Secondary
Starting the Pump with Secondary Infusion
1. Load the primed set. See 'Loading the IV Infusion Set' earlier in this
chapter for instructions.
2. Prepare the secondary infusion using a secondary solution container
and the IVAC® "52" Series back check valve set; lower the primary
container. See Figure 1-3 below.
Prime the secondary IV infusion set in accordance with the set
Directions for Use
Attach a secondary IV infusion set to the upper Y-site of the
primary IV infusion set
3. Press the
up in PRIMARY mode.
4. Use the JK switches to set the primary rate.
5. Press
6. Set primary VTBI if required.
7. Press the SEC switch to place the pump into SECONDARY mode. The
pump will sound a four beep verification tone.
8. Use the JK switches to set the secondary rate.
9. Press the
10. Set secondary VTBI by using the JK switches.
11. Press
ON/OFF switch to power on the pump. Pump always starts
VOL TO BE INF if required.
VOL TO BE INF switch.
RUN/HOLD to start secondary infusion.
Primary
container
Back Check
valve
Y-Site
container
IV Infusion set
patient end
WARNING:
Secondary infusion applications using a back check
valve set must have a VTBI setting equal to the
volume in the secondary container; this will require
consideration of such variables as factory overfill,
medication additions, priming volume, etc.
Underestimating the volume will cause remaining
secondary solution to be infused at the primary rate;
overestimating will result in primary solution being
infused at the secondary rate.
When using a flow sensor it must be positioned on the
primary IV infusion set (as shown in Figure 1-4). Correct
placement of a flow sensor is essential for proper
operation.
Verifying a value in one mode while operating in another
1. Press and release the appropriate (current) mode switch. For example, SEC.
2. Within two seconds press the switch representing the information to be displayed. For example, PRI.
Changing the infusion manually to primary mode
1. Press the RUN/HOLD switch to set pump on hold.
2. Press the PRI switch; pump sounds a three beep verification tone and goes into PRIMARY mode.
Flow Sensor
A flow sensor (part number 180) is used to detect an empty solution container. It is connected to the drip chamber and
when a drop is detected in the drip chamber an illuminated ("0") appears in the Information Display.
When not in use, the flow sensor can be stored on the pump handle.
Pole Clamp Accessories
The following pole clamp accessories allow the pump to be mounted on conventional IV poles:
Universal Pole Adapter (part number 6767)
Pole Adapter (part number 5767A)*
Pole Clamp Accessory (part number BC100A)*
* must be used in conjunction with each other.
Refer to Chapter 6, 'Spare Parts Replacement Procedures' for assembly information.
Self-test mode is used to access a number of configuration and test routines which are designed to test and verify many
of the pump functions, defaults and calibrations without requiring internal inspection. Configuration settings are also
accessed via self-test mode.
Each test is accessed by selecting a Test ID number as shown in the table below.
Test IDDescription
001Software Revision Display
002Configuration Status Display
003Flash Display Test
004Segment Display Test
005Sequence Display Test
006EEPROM Test and Data Display
007A/D Channels Test
008Rate Calibration Display/Set
009 *Configuration Rate Display/Set
010Maximum Rate Display/Set
011 *VTBI Configuration Display/Set
012Pressure Display
013Pressure Calibration Set
014Maximum Occlusion Pressure Limit Display/Set
015Default Occlusion Pressure Limit Display.Set
016Alarm History Display/Clear
Entering Self-Test Mode
1. Press the RUN/HOLD and ON/OFF switches
simultaneously until the display turns on. Initially,
the current software revision level is displayed.
2. Press the RUN/HOLD switch. The Information
Display will read: TEST ID and the Numeric
Display will read: 002 which means the pump is
ready to start test 002.
Note: The display may bypass the display of the
software revision level and advance directly to
TEST ID 002, depending on how long the RUN/
HOLD switch is held down.
3. Use the
required.
J K switches to select the Test ID
The three columns of JK switches
allow faster/slower increments:
Left = 100's
Centre = 10's
Right = Units
017Switch Test
018AC Power Run Time Display/Reset
019Battery Run Time Display/Reset
020Secondary Mode Completion Tone Display/Set
021Air-In-Line Test
022I/O Port Test
023Language Display/Set
024CIM ID Display/Set
025Alarm Tone Display/Set
026*AIL Alarm Threshold Display/Set
027System Vacuum Display
028Enter Operational Setup Mode
029Burn-In Test
030Not used
031*Infusion Mode Configuration Display/Set
* A mode select jumper (part number 132350) must be
used to change settings, see 'Mode Select Jumper' for
further details.
Test Execution
1. After selecting the Test ID number (see above),
press the RUN/HOLD switch to start the test.
In order to perform certain tests and to change any pump settings, a mode select jumper must be installed.
Procedure:
1. With the pump off, remove the test connector cover from the back of the rear case.
2. Connect the mode select jumper (part number 132350) to the test connector, orientating the jumper so that CR1 is at
the top.
3. Place the pump in self-test mode then select and carry out the test(s) as required.
4. When the test is complete, switch the pump off and remove the mode select jumper from the test connector.
5. Refit the test connector cover.
Configuration Settings
Enter Self-Test mode. See 'Entering Self-Test Mode' in previous section for instructions.
Note: For default settings refer to Appendix C 'Configured Options'.
Test IDSettingAction/Data Displayed
009
010
011
Rate Configuration
RATE CFG
Maximum Rate
MAX RATE
VTBI Configuration
VTBI CFG
Display and/or set the current rate range.
STANDARD = rate range of 001 to 999 ml/h
ALL RATE = rate range of 0.1 to 999.9 ml/h. Note: Use this setting where
fractional flow rates are required.
To change the setting:
Install the mode select jumper. See 'Mode Select Jumper'.
Press the CRIS (lower hidden switch on Model 571) and VOL TO BE INF
switches together and wait for a click.
Press the J unit (right column) switch to select STANDARD or the K unit
switch to select ALL RATE.
Display and/or set the maximum infusion rate.
999 = set to STANDARD rate configuration (ml/h). This rate cannot be changed.
0.1 and 999.9 = set to ALL RATE configuration (ml/h).
Note: Rate configuration is set in Test 009.
To change the maximum rate setting (for ALL RATE configuration):
Press and hold the PRI (upper hidden switch on Model 571) while using the
J K switches to adjust the value.
Display and/or set the Volume To Be Infused (VTBI) limit. VTBI limit ranges are:
MACRO = 1 to 9999 ml, MICRO = 0.1 to 999.9 ml.
If set to ALL RATE configuration (see Test 009), VTBI CFG can be set to MACRO
or MICRO.
If set to STANDARD rate configuration, VTBI CFG is set to MACRO and is not
adjustable.
To change the VTBI limit (for ALL RATE configuration):
Install the mode select jumper. See 'Mode Select Jumper'.
Press the CRIS (lower hidden switch on Model 571) and VOL TO BE INF
switches together and wait for a click.
Press the J unit switch to select MACRO or the K unit switch to select
MICRO.
Display and/or set the maximum occlusion pressure limit. Pressure values are
displayed in MMHG or CMH20 depending on the pressure units selected. See
'Selecting Pressure Units' for further information.
This pressure limit setting determines the upper limit of the pumps' variable
pressure range thereby fixing the upper limit when the LIMIT PRES switch is
used during normal operation.
To change the setting:
Press and hold the PRI (upper hidden switch on Model 571) while using the
J K switches to adjust the value.
Press the RUN/HOLD switch to save the new value.
Page 16
Configuration & Calibration
Configuration Settings (continued)
Test IDSettingAction/Data Displayed
Display and/or set the default pressure limit.
Pressure values are displayed in MMHG or CMH20 depending on the pressure
Default Occlusion
015
Pressure
DEFAULT
Secondary Mode
020
Completion Tone
(Model 572 only)
023Language
units selected. See 'Selecting Pressure Units' for further information.
This setting determines the occlusion pressure limit at power up.
To change the setting:
Press and hold the PRI (upper hidden switch on Model 571) while using the
J K switches to adjust the value.
Press the RUN/HOLD switch to save the new value.
Display and/or set the audible tone that sounds when the SECONDARY infusion
finishes and switches to PRIMARY infusion.
1 CLICK = one-click tone
4 BEEPS = four-beeps tone
To change the setting:
Press the J unit switch to select 4 BEEPS or the K unit switch to select 1
CLICK
.
Display and/or set the language to be displayed. Languages are ENGLISH, DUTCH, FRENCH, GERMAN, ITALIAN, SPANISH or SWEDISH.
To change this setting:
Press the J K unit switches to scroll through list and select language.
024
CIM ID
CIM ID
025Alarm Tone
AIL Alarm Threshold
026
UL AIR
Setting is not in use. OFF = CIM not in use, 001 to 999 = CIM ID number
Important: Ensure the setting is OFF.
To change setting to OFF:
Press and hold the VOL TO BE INF switch while using the J K switches to
select OFF.
Press the RUN/HOLD switch to save the new setting.
Display and/or select the alarm tone volume level.
Approximate decibel volumes are:
HI TONE = 90 db
MED TONE = 80 db
LOW TONE = 70 db
To change the setting:
Press the J unit switch to select alarm tone.
WARNING: Take any necessary precautions against prolonged exposure to the
HI TONE alarm as this may result in hearing damage.
Display and/or set the air bubble length maximum value. This value is the
nominal air bubble threshold in microlitres used for air-in-line detection. Value
must be between 50 and 150 microlitres.
To change the setting:
Install the mode select jumper. See 'Mode Select Jumper'.
Press the CRIS (lower hidden switch on Model 571) and VOL TO BE INF
switches together and wait for a click.
Press the J K switches to enter the value (in 10 µl increments).
Display and/or set the pump infusion mode.
PRI ONLY = PRIMARY infusion mode only (Model 571).
SEC/CRIS = PRIMARY and SECONDARY infusions modes. (Model 572).
031
Infusion Mode
INFM CFG
To change the setting:
Install the mode select jumper. See 'Mode Select Jumper'.
Press the CRIS (hidden switch on Model 571) and VOL TO BE INF switches
together and wait for a click. Press the J unit switch to select PRI ONLY or
The pressure units can be configured to be displayed as millimetres of mercury (mmHg) or
as centimeters of water (cmH20).
To select the pressure units:
Set the Pressure Unit Selector switch on the rear panel to the required position.
Pressure Unit
Selector Switch
Calibration Procedures
Vacuum System Calibration (Test 27)
Equipment required:
50ml syringe
Pressure gauge
"52" Series IV infusion set
Procedure:
1. Remove the battery cover from the pump to
allow access to the Accessory Interface Board.
See Chapter 6, 'Spare Parts Procedures' for
instructions.
2. Prepare a modified IV infusion set as follows:
Completely remove the clear membrane
cover from the white pressure sensing disc.
Ensure no membrane remains as this could
compromise the integrity of the vacuum
Attach the air-filled IV infusion set to the
syringe. Use the luer fitting on the distal end
of the set or cut approximately 1 inch (2.5
cm) off the distal end and press the tubing
firmly into the tip of the syringe. Ensure a
good seal is formed between the two devices
Splice a T-fitting into the IV infusion set
tubing approximately 1 foot (30 cm) up from
the syringe attachment. Connect the pressure
gauge to the T-fitting port
Push the syringe plunger in until it stops
3. Load the modified IV infusion set into the pump
and close the door. Ensure that the set tubing is
not kinked.
4. Enter self-test mode and select test 027. See 'Entering
Self-Test Mode' for instructions.
5. Press the RUN/HOLD switch to enter the Vacuum Display mode and display VAC MMHG.
6. Pull the syringe plunger out until the pressure gauge reads -95 mmHg and immediately clamp off tubing below the
pump to hold the vacuum stable.
7. Adjust the vacuum detect potentiometer R45 on the Accessory Interface Board until the numeric display on the
pump reads -95 ± 5 mmHg.
Note: R45 is the upper potentiometer on the Accessory Interface Board.
8. Perform the 'Vacuum Retention Verification' procedure as detailed in
Chapter 3, 'Routine Maintenance'.
Proximal
End of Set
Pressure
Gauge
Syringe
Do not adjust the lower
potentiometer, R4, this
is pre-adjusted during
manufacture.
1. Remove the chassis from the body. See Chapter 6, 'Spare Parts Procedures' for instructions.
2. Attach the jumper of the test jumper cable between connector J7 on the Logic Board and connector P7 on the
Accessory Interface Board.
3. Connect the battery pack to the battery connector.
4. Set up equipment as shown below.
Note: Set the pressure unit selector switch (on the back panel of the pump) to the same units as the air pressure
source.
Proximal
End of Set
Pressure
Gauge
Reservoir
Air
Pressure Source
5. Enter self-test mode, press the RUN/HOLD switch and select test 12. Press the RUN/HOLD switch again to display the
pressure MMHG (or CMH20).
Ensure the pump is connected to the AC power supply for approximately 30 minutes before continuing with this
calibration.
6. Enter self-test mode, press the RUN/HOLD switch and select test 13. Press the RUN/HOLD switch again to display
PRES CAL.
7. With the door open and no set loaded, adjust the zero potentiometer (R20 on the Analog Board) so the pump reads
000 ±1 mmHg (or 000 ±1.4 cmH20).
8. Install an IV infusion set, close the door and apply a test pressure of 000 mmHg (000 cmH2O) to the distal end of the
set. Record the reading displayed as the PI offset value.
9. Apply a test pressure until the meter reads 400 mmHg (544 cmH2O) and adjust the span potentiometer (R23 on the
Analog Board) so the pump reads 400 mmHg ±2 (544 cmH20 ±10 ) plus the offset value, PI, recorded in the previous
Step.
10. Return the test pressure to 000 mmHg (000 cmH2O), bleed off any air from the IV infusion set then remove the IV
infusion set.
Note: If the set is removed when still under pressure may result in damage to the pressure sensing disc film.
11. Leave the door open and reverify that the pump reads 000 ±1 mmHg (000 ±1.4 cmH2O). If not, repeat the procedure
from Step 7, until no further adjustment of the zero and span potentiometers is required.
12. Press the J unit and RATE switches simultaneously for a minimum of one second to set the 000 mmHg (000 cmH2O)
calibration point.
13. Reload the IV infusion set and apply test pressure until the meter reads 400 mmHg (544 cmH2O). When the pressure
reading is stable, press the TOT VOL INF and the
the 400 mmHg (544 cmH2O) calibration point.
Both Steps 12 and 13 must be performed to correctly set the calibration parameters. Performing
only one step will result in the message RECONFIG REQD when the pump returns to operation.
14. Press the RUN/HOLD switch to return to test 13 and turn the pump OFF. Remove the IV infusion set (first bleeding off
any pressure).
15. Disconnect the battery pack from the battery connector.
16. Remove the test jumper cable and reassemble the pump.
17. Perform the 'Dry Set Pressure Verification' procedure as detailed in Chapter 3, 'Routine Maintenance'.
J 100 switches simultaneously for a minimum of one second to set
There are two types of rate accuracy associated with the pump, these are System Rate Accuracy and Pump Rate Accuracy.
System Rate Accuracy is the rate accuracy of the pump when used with a standard "52" Series infusion set. Due to slight
variations in between sets, the system accuracy of the pump is ± 5%. Pump Rate Accuracy is the absolute rate accuracy of
an individual pump which can only be determined with the use of a characterised set.
The following procedure describes how to calibrate the Pump Rate Accuracy. For instructions on how to verify Pump Rate
Accuracy, see 'Rate Accuracy Verification' in Chapter 3, 'Routine Maintenance'.
Characterised Sets (part number 191806)
Must be used for rate accuracy calibration
Sets are labeled with a serial number, a nominal volume and an expiry date (180 days from the date
the set was characterised)
Handle sets with care at all times. Sets must not be pressurised. Prior to loading or removing from
the pump, manually open the auto-pinch-off mechanism. Do not stretch the set excessively
Record the number of times each set is used in a log book. A set must not be used for more than 20
rate runs.
Equipment required:
Characterized set (191806)
Stopwatch
Class A burette (50 ml) with 0.1 ml
graduations
Preparation:
1. Set up the equipment as shown.
The vertical distance from the
fluid level of the container to
the pump pressure transducer
should be 34 ±4 inches
The burette zero line should
be within ± 2 inches from the
pump pressure transducer.
Verify that the inside of the
wall is free of droplets
Ensure fittings are secure and
there is no leakage through
the 3-way stopcock
Ensure that the air has been
purged from the characterised
set and all equipment
2. Close the set roller clamp.
3. Plug the pump into the AC mains
and turn the pump ON.
1. Enter self-test mode, press the RUN/HOLD switch and select test 8. Press the RUN/HOLD switch again to display CAL
RATE.
2. Press and hold the PRI switch then use the JK switches to enter an initial rate calibration of 37. Press the ON/OFF
switch to turn the pump off.
Note: Ensure a characterised set is loaded and the burette is free of droplets.
3. Turn the pump ON and set the pump to Primary rate = 800 ml/h, VTBI = OFF, TOT VOL INF = 000.0 (or, if not using a
flow sensor, set the pump to Primary rate = 800 ml/h, VTBI = 100 ml, TOT VOL INF = 000.0).
4. Press the RUN/HOLD switch to start the pump and simultaneously start the stopwatch. Allow the pump to run for 3
minutes (180 seconds) then press the RUN/HOLD switch to put the pump on hold.
5. Verify that the volume in the burette is 40.0 ± 0.4 ml. If not, repeat the test.
If the percentage of error is greater than ± 1%, use the following formula to determine the new CAL RATE number:
Formula to determine new CAL RATE number
Final CAL RATE number =
(actual volume)-1 ) x 200
[
Example:
Final CAL RATE number =
[
Set the CAL RATE number to 41 in Test 8 while pressing the PRI switch.
6. Repeat the above calibration procedure until the actual volume is within ±1% of the expected volume indicated on
the characterised IV infusion set.
Flow Sensor Check (where flow sensor is in use) 35
Performance Verification Procedure 36
Page 23
Routine Maintenance
Routine Maintenance
For routine maintenance, the following tests and procedures should be performed in addition to the tasks described in
the section 'Physical Inspection and Clean'.
Refer to the relevant DFU for the recommended routine maintenance period.
Self-Test Functions
The self-test functions are a series of test routines which are designed to test and verify many of the pump functions and
defaults without requiring internal inspection. These tests are accessed by entering Self-Test mode and selecting a Test ID
number as shown in the table below.
1. Enter Self-Test mode. See 'Entering Self-Test Mode' in Chapter 2 for instructions.
2. Proceed through the series of tests, referring to the table below for details of each test.
Note: For details of other tests such as the configurable options and calibration settings, see Chapter 2, 'Configuration
& Calibration'.
Test
ID
001
002
003Display Flash Test
TestAction/Description
Software
Revision
Configuration
Status
Displays the current software revision level, e.g. REV 3.01.
Verifies whether or not the configuration data is valid.
CONFIG/VALID = configuration data is valid
OR,, where not valid, a message indicates which configuration is required to be set:
SET RATE CAL = see Test ID 008
SET RATE CONFIG = see Test ID 009
SET RATE MAX = see Test ID 010
SET VTBI CONFIG = see Test ID 011
SET PRES CAL = see Test ID 013
SET PRES MAX = see Test ID 014
SET PRES DEFAULT = see Test ID 015
SET AIR LIMIT = see Test ID 026
SET INF MODE CONFIG = see Test ID 031
Verify that the segments of both Displays light and the battery indicator flashes as follows:
Information Display: all positions show ******** alternating with 00000000.
Numeric Display: all positions show 8888 alternating with 0000. The two decimal points also
flash.
Battery indicator: flashes alternately on and off.
Verify that both Displays show various characters and the battery indicator flashes as follows:
Information Display: repeatedly cycles through the 64-character set (A to Z, 0 to 9 and ASCII
characters). All positions must show the same character at the same time.
Numeric Display: repeatedly cycles through numbers 0 to 9. All positions must show the same
character at the same time.
Battery indicator: flashes alternately on and off.
Verify that both Displays show numbers, one position at a time (and the battery indicator
flashes) as follows:
Information Display: numbers 0 to 7 appear sequentially, left to right.
Numeric Display: numbers 0 to 3 appear sequentially, left to right.
Battery indicator: flashes alternately on and off.
Verify that both Displays cycle through numeric sequences (and the battery indicator flashes)
as follows:
Information Display: ignore this 128-byte location reading.
Numeric Display: counts from 001 through 128.
Page 24
Routine Maintenance
Self-Test Functions (continued)
Test
ID
007
TestAction/Description
Verify the eight A/D channels (0 through 7) as follows, using the
each channel.
Note: The Information Display shows the Channel number being tested (0 through 7) and the
Numeric Display shows a value representing the analog input to the A/D convertor.
Channel 0 = Flow Sensor Test
Information Display: All positions show 0's, 00000000.
Numeric Display: Value must be greater than 195 (no obstruction in the light path), or less
than 185 (light path is obstructed).
Channel 1 = Drop Reference
Information Display: All positions show 1's, 11111111.
Numeric Display: Value must read 210 ± 8.
Channel 2 = Battery Monitor
Unplug the pump from AC power.
Information Display: All positions show 2's, 22222222.
Numeric Display: New battery reading must be greater than or equal to 140. A reading of less
A/D Converter
than 140 indicates a discharged or bad battery.
Test
Plug the pump into AC power.
J and K switches to select
012Read Pressure
Read Alarm
016
History
Channel 3 = Pressure
Information Display: All positions show 3's, 33333333.
Numeric Display: value between 0 and 500.
Channel 4 = Flow Sensor Detect
Information Display: All positions show 4's, 44444444.
Numeric Display: Value less than 20 (flow sensor not plugged in) or more than 80 (flow sensor
plugged in).
Channel 5 = Vacuum Detect Signal
Information Display: All positions show 5's, 55555555.
Numeric Display: Value between 110 and 277 (with set installed).
Channel 6 = Not used. Ignore reading.
Channel 7 = Not used. Ignore reading.
Verify the pressure level reading sensed by pressure transducer. Note: To ensure a valid
reading, the pump should be powered on for at least 30 minutes prior to this test.
Information Display: CMH20 or MMHG (per pressure unit selection switch position on back
panel).
Numeric Display: Without set installed, shows value between -28 and +14 cmH20 or between
-20 and +10 mmHg.
Read the last 16 alarm or error messages (alarm stack).
The most recent alarm or error is always displayed first.
Information Display: All positions show *'s, ******** are displayed initially, followed by
repeated cycle of the last 16 alarm messages.
Numeric Display: Blank
To clear the alarm stack:
Press and hold the READ PRES switch and the J 100 switch for at least 2 seconds, until
Information Display: Initially shows SWCH TEST. Press each switch and verify the
corresponding code is displayed:
Switch:Display code:Switch:Display code:
TOT VOL INF
PRI
RATE
LIMIT PRES
SEC
VTBI
READ PRES
TL V INF
PRI
RATE
LIMT PRS
SEC
VTBI
READ PRES
CRIS
J 100
K 100
J 10
K 10
J Unit
K Unit
CRIS
UP 100
DN 100
UP 10
DN 10
UP 1
DN 1
Notes:
1) The ON/OFF switch does not have a code.
2) The Numeric Display remains blank.
Read/clear the total number of hours that the pump has run on AC power.
Information Display: AC HRS
Numeric Display: Number of hours on AC power.
To reset the total AC power hours to 0000:
Press and hold the READ PRES switch and the J 10 switch for at least 2 seconds.
Read/clear the total number of hours that the pump has run on battery power.
Information Display: BATT HRS
Numeric Display: Number of hours on battery power.
To reset the total AC battery hours to 0000:
Press and hold the READ PRES switch and the J unit switch for at least 2 seconds.
021Air-In-Line Test
022I/O Port Test
System Vacuum
027
Test
Verify air-in-line sensor operation. To run test:
Load an air-filled or fluid-filled IV infusion set.
Information Display: 00000000 = fluid detected in IV infusion set and door is closed.
10000000 = air detected in IV infusion set or door is open.
Numeric Display: UAIL
Read data on the various input ports. Press the
J and K switches to select each port.
Information Display: Shows the 8 input port data bits in binary format.
Numeric Display: Indicates which port is being examined:
000 = display port, Display U7. 008 = switch port, Display U5. 016 = Logic U20. 048 = A/D end
of conversion, U22. 064 = Logic U21. 080 and 081 = parallel I/F ports. 096, 097, 098 and 099
= serial I/F ports. 128 = timer of Logic U14. 129 = Logic U23. 130 = Logic U24.
Key troubleshooting tests:
Port 016
bit 0 = rotation sensor 1
bit 1 = rotation sensor 2
bit 2 = set sensor
bit 3 = air-in-line sensor
Port 064
bit 7 = door sensor
Read the vacuum level being applied by the vacuum system when an IV infusion set is loaded
and the door is closed.
Information Display: VAC MMHG
Numeric Display: Current vacuum value that is generated to hold the pressure sensing disc in
place.
To run the test, following the instructions in 'Vacuum Retention Verification' later in this
chapter.
The pump exits self-test mode and starts operational set up mode.
Allows pump to run (burn-in) without setting up an IV solution bag, fluid and drain.
Warning:
This test must only be run in a workshop environment for verification that internal failures have
been corrected. Full performance verification testing must then be carried out.
To run test: Load an air-filled IV infusion set and close the door. Enter self-test mode, select
test 029, press the RUN/HOLD switch then, within two seconds, press and hold the PRI and
CRIS switches together. Pump will start running at maximum rate and rate can be changed by
pressing the RATE switch and using the
J and K switches.
Upgrading Software
The latest version of software available for Model 571/572 is V3.01. Perform upgrades by acquiring the software upgrade
kits specified in the spare parts listing.
Equipment required:
Software upgrade kit
Software Upgrade Kits Available
Pump ModelPart Number
145071
571/572
145070
KIT,UPGRD,REV 3.01,570
(EPROM only)
SERV ASSY,MEM,REV3.01,570(BOM)
(includes EPROM fitting and removal instructions)
Software
Version
3.01
3.01
Vacuum Retention Verification (Test 27)
The pump's vacuum system can be tested and verified by performing the following Vacuum Leak Test.
Procedure:
1. Enter self-test mode and select test 27. Press the RUN/HOLD switch to enter the Vacuum Display mode and display
VAC MMHG.
2. Load an IV infusion set and close the door.
3. Verify that the numeric display shows a reading of -250 or more negative.
4. Allow the reading to stabilise for 5 to 10 seconds, then record the value, for example, -337.
5. After 30 seconds, verify that the vacuum value has not decreased by more than 5, for example -332.
If the pump fails this test:
Check the following things, replacing and repeating the test as necessary:
Face of the pressure transducer
Replace the test IV infusion set
Y-clip, door latch pin, door latch
Pressure transducer/vacuum assembly
Perform the 'Vacuum System Calibration' procedure, see Chapter 2. for instructions.
Without an IV infusion set loaded, turn the pump ON, set rate to 125 ml/h then press the RUN/HOLD switch.
Verify that the LOAD SET message is displayed.
With the pump running, open the door. Verify that the pump stops, alarms and the message DOOR is
displayed. Verify that the automatic pinch-off clamp has stopped the flow by checking that no drops are
falling in the drip chamber.
Load a fluid-filled IV infusion set. Turn the pump ON, set rate to 125 ml/h then press the RUN/HOLD switch
to start infusing. Tilt the drip chamber of the set to induce air bubbles into the IV infusion set. Verify that
when the air bubble enters the pump, the pump alarms, stops and displays the message AIR IN LINE. Turn
the pump OFF and remove the test loop.
Load an empty, air-filled IV infusion set. Turn the pump ON then press the RUN/HOLD switch to start the
pump. The pump should not run; verify that the AIR IN LINE message is displayed. If the pump does run,
refer to Chapter 4, 'Troubleshooting'.
Block the light in the flow sensor (with a finger or other suitable object) to simulate a faulty flow sensor.
Press the RUN/HOLD switch to resume infusing. After a short time, verify that the pump stops, alarms and
the display message alternates between FLOW and SENSOR.
Press the RUN/HOLD switch to place the pump on hold. Hold the VOL TO BE INF switch and press the K
unit switch until OFF is displayed. Press the RUN/HOLD switch to start the infusion. After approximately one
minute, close the roller clamp. Verify that the pump stops running, the alarm tone sounds and the display
message alternates between BOTTLE and CLAMP.
Press the RUN/HOLD switch to place the pump on hold. Set VTBI to 60 ml by first pressing the VOL TO BE INF switch then the
infusing. After approximately one minute, close the roller clamp to create an upstream occlusion.
Verify that the pump stops running, alarms and displays UPSTREAM OCCLUSION.
JK switches. Set rate to 900 ml/h then press the RUN/HOLD switch to start
TIME OUT
PRESSURE LIMIT
EXCEEDED
(DOWNSTREAM
PRESSURE
EXCEEDED)
Press the RUN/HOLD switch to place the pump on hold. Verify that the pump takes 2 minutes ±10 seconds
to alarm after the last switch has been pressed. TIME OUT is displayed, and the rate is still shown.
See 'Downstream Pressure Occlusion Test' procedure later in this chapter for instructions.
Battery Power Check and Operation Test
Before performing this test, it is recommended that the battery is charged to full capacity by
connecting the pump to AC mains for a minimum of 16 hours.
1. Remove power cord from the AC power socket.
2. Press the ON/OFF switch to turn the pump on. Verify that the battery indicator flashes on and off.
3. Set rate to 499 ml/h then press the RUN/HOLD switch to start the pump. Verify that the pumping indicator bar
appears on the Information Display and that it rotates rapidly.
4. (Optional) Verify that the pump continues to run for a minimum of 15 minutes without alarming LOW BATT.
5. Plug the power cord back in to AC power socket.
Flow Sensor Check
See 'Physical Inspection and Clean' for instructions.
Take an IV infusion set and cut the tubing a couple of inches below the drip chamber, discarding the drip chamber.
Connect the air pressure source to the freshly cut proximal end of tubing.
Insert the distal end of the modified set into a container of water.
3. Close the roller clamp. Adjust the air pressure to 10 psi.
4. Load the modified IV infusion set. Close the door then open the roller clamp.
5. Open the door and verify that (after an initial spurt of bubbles) no further bubbles are seen coming from the distal
end of the tubing into the water bottle.
If bubbles continue, replace the auto-pinch mechanism. Refer to Chapter 6, 'Spare Parts Replacement Procedures' for
When servicing the pump, the Mechanism Leak Test must be performed to verify the integrity of
the pumping mechanism.
Misalignment of the pumping mechanism can result in the pressure plate and the mechanism's cam
followers failing to pinch the IV infusion set tubing sufficiently, thereby allowing the pump to leak
fluid at low rates or when stopped.
Procedure:
1. Prepare a special Pressure Test Set as follows:
Take an IV infusion set and cut the tubing a couple of inches
below the drip chamber, discarding the drip chamber.
With a knife, carefully remove the membrane cover from the
white pressure sensing disc, see Figure 3-2. Ensure no membrane
(rough edges) remain—the surface of the pressure sensing disc
should be as flat as possible after the membrane is removed.
Cut out a piece of mylar to match the shape and size shown
below.
Cut away
membrane cover
Firmly press
mylar cap
over slot
Mylar Cap
Shape
Remove the adhesive backing and firmly press the mylar onto the
surface of the pressure sensing disc so that it covers the vertical
slot and is centered on the disc. See Figure 3-3
The distal end (bottom) end of the set may be cut to adapt it for
connecting to the air pressure source.
Figure 3-2
Figure 3-3
2. Load the special pressure test set, with 15.0 psi (775 mmHg) air pressure at the distal end, into the pump and close the
door.
Change the special Pressure Test Set after 20 uses, or if signs of wear are visible on the silicone
section or if any leak in the set is observed.
3. Run the top end of the pressure test set into the water bottle and below the water level (as shown below).
4. Open the pressure test roller clamp to pressurise the set.
5. Verify that the pressure (that the transducer is seeing) is not greater than 300 mmHg when set is fully pressurised. To
do this read the pressure using test 12 (Enter self-test mode, press the RUN/HOLD switch and select test 12).
Warning: A pressure reading greater than 499 mmHg may result in damage to the transducer.
If a high pressure reading is noted, check the following:
The pressure sensing disc is positioned correctly.
The mylar cap is adhered tightly and correctly on the pressure sensing disc.
The height of the mylar cap matches the Myler Cap Shape shown above.
6. Connect the pump to the AC mains then turn the pump ON, entering self-test mode.
7. Press the RUN/HOLD switch and select the burn-in test 29, then within two seconds, simultaneously press and hold
the PRI switch and the CRIS switch.
Verify that the pump is running at 999 (or 999.9 ml/h).
8. Set the rate to 20 ml/h (or 20.0 ml/h) by simultaneously pressing the R AT E switch and the J K switches. Run the
pump for at least one minute. Verify that no bubbles are visible in the water bottle.
If air bubbles are visible in the water bottle, the pump fails the test.
If the pump fails the test, verify set up and repeat the test as required, otherwise, return the pump to the
manufacturer.
9. Turn the pump OFF.
10. Close the roller clamp slowly. Open the door to release any pressure trapped in the pressure test set and carefully
remove the set from the pump.
Note: Take care not to stretch the silicone segment of the set as correct segment length is critical to the mechanism's
There are two types of rate accuracy associated with the pump, these are System Rate Accuracy and Pump Rate Accuracy.
System Rate Accuracy is the rate accuracy of the pump when used with a standard "52" Series infusion set. Due to slight
variations in between sets, the system accuracy of the pump is ± 5%. Pump Rate Accuracy is the absolute rate accuracy of
an individual pump which can only be determined with the use of a characterised set.
The following procedure describes how to verify the Pump Rate Accuracy. For instructions on how to calibrate the Pump
Rate Accuracy, see 'Rate Accuracy Calibration' procedure in Chapter 2.
Equipment required:
Characterized set (191806)
Stopwatch
Class A burette (50 ml) with 0.1 ml graduations
Characterised Sets (part number 191806)
Must be used for rate accuracy calibration
Sets are labeled with a serial number, a nominal volume and an expiry date (180 days from the date
the set was characterised)
Handle sets with care at all times. Sets must not be pressurised. Prior to loading or removing from
the pump, manually open the auto-pinch-off mechanism. Do not stretch the set excessively
Record the number of times each set is used in a log book. A set must not be used for more than 20
rate runs.
Preparation:
1. Set up the equipment as shown.
The vertical distance from the
fluid level of the container to
the pump pressure transducer
should be 34 ±4 inches
The burette zero line should
be within ± 2 inches from the
pump pressure transducer.
Verify that the inside of the
wall is free of droplets
Ensure fittings are secure and
there is no leakage through
the 3-way stopcock
Ensure that the air has been
purged from the characterised
set and all equipment
2. Close the set roller clamp.
3. Plug the pump into the AC mains
and turn the pump ON.
1. Set the pump to Primary rate = 800 ml/h, VTBI = OFF, TOT VOL INF = 000.0 (or, if not using a flow sensor, set the pump
to Primary rate = 800 ml/h, VTBI = 100 ml, TOT VOL INF = 000.0).
2. With the pump displaying START PRIMARY or ON HOLD PRIMARY, press the RUN/HOLD switch to start the pump
and simultaneously start the stopwatch. Allow the pump to run for 180 seconds (3 minutes) ± 0.5 seconds then press
the RUN/HOLD switch to put the pump on hold.
3. Measure the volume in the burette and calculate the percentage of volume error using following formula:
Formula to calculate the percentage of volume error
% volume error =
x 100
n
Where:
b = volume in burette
n = nominal volume as indicated on the
characterised set
4. If the % volume error is ± 2% or less, the pump is within the correct specification. If not, repeat the test.
If the pump fails a second time, perform the 'Rate Accuracy Calibration' procedure. See Chapter 2 for instructions.
Downstream Pressure Occlusion Test
Procedure:
1. Connect an IV infusion set to a fluid container. Prime the set to ensure that air is completely
expelled.
2. Verify and, if necessary, adjust the DEFAULT pressure setting (test 015) and the MAXIMUM
(test 014) occlusion pressure setting to 500 mmHg.
3. Connect a fluid pressure gauge to the luer end of the set.
4. Turn the pump ON and set the pump to VTBI = 100 ml, Primary rate = 499 ml/h.
5. Connect the pump to the pressure gauge by closing the three-way stopcock. Start the pump
and allow it to run until it alarms DOWNSTREAM PRESSURE EXCEEDED.
6. Verify that the pressure gauge reads between 11.0 and 14.0 psi.
7. Open the stopcock to relieve the pressure.
If the pump fails to alarm as stated, perform the 'Dry Set Pressure Calibration' procedure.
To ensure the pump remains in good operating condition, it is important to keep it clean and carry out the routine
procedures described below.
Routinely clean the pump, especially if spillage has occurred.
Before cleaning always switch OFF and disconnect from the AC power supply. Never allow fluid to
enter the casing and avoid excess fluid build up on the pump.
Keep pump upright to prevent fluid entry around the pressure transducer.
Do not use aggressive cleaning agents as these may damage the exterior surface of the pump.
Do not steam autoclave, ethylene oxide sterilise or immerse this pump in any fluid.
Unplug the power cord from the AC wall outlet before cleaning. Do not allow fluids to enter the pump case.
Clean the exterior surfaces (the outer case top, bottom, sides; the switch panel, the front panel and inside the door)
with a cloth dampened with warm water, or a mild non-abrasive detergent (such as commercially available dish
cleaning liquid) mixed with water.
Note: Alcohol, ammonia, acetone, benzene, phosphoric acid, xylene and similar solvents can erode (wear away pit)
or otherwise damage the cam followers and other surfaces of the pump. The cam followers must be kept clean using
a solution of warm water and a mild non-abrasive detergent, and inspected for possible erosion according to the
procedure outlined on the following page, see 'Inspecting and Cleaning the Mechanism'.
Check that labels are flat, legible and fully adhered. Replace as necessary.
Inspect the case for loose or damaged components and replace if necessary.
Inspect the circuit breaker for damage.
Inspect the AC power supply plug and cable for damage.
Inspect the door assembly for damage. Check that the door pivots freely and latches securely.
Inspect the mechanism for fluid spill residue or foreign matter. Open the door and inspect the exposed cam followers,
the pressure plate and tubing pincher. Clean any surfaces where solution has accumulated.
(A) (B)
(B)
(C)
(A) (B) (C)
Pressure
Transducer
Clean crevices (A) using a soft-bristle brush,
such as a one-inch paint brush, dipped in the
mild detergent solution (see above). Pat dry
all moistened areas with a cloth then leave the
door open for at least 15 minutes to air-dry
crevices.
Manually actuate points (B) by pressing then
releasing each part to verify that it moves freely.
After cleaning is complete, if required and
where heavy spillage has required extensive
cleaning, lubricate the tubing pincher and the
sides of the mechanism (C) using a siliconebased grease.
cleaning agents on the surface of the
pressure transducer.
Page 35
Routine Maintenance
Physical Inspection and Clean (continued)
Inspecting and Cleaning the Mechanism
Open the door and inspect/clean the exposed cam followers, the pressure plate and tubing pincher.
Clean any surfaces where fluid spill residue is noted, referring to the cleaning instructions above for appropriate
cleaning method.
Check the Cam Followers for cleanliness and erosion:
Shine a flashlight into the cam followers. The followers should be clean and shiny. A dull appearance may indicate
erosion. If the followers appear to be dirty or are dull, clean per the following procedure.
Clean the Cam Followers:
Clean the surface of the cam followers using a cotton-tipped applicator dampened in a solution of warm soapy water
and a mild non-abrasive detergent (such as commercially available dish cleaning liquid). Rinse the cam followers with
a soft cloth or cotton-tipped applicator dampened in water then allow the cam followers to dry.
Check the Cam Followers for erosion after cleaning:
If, after cleaning the cam followers, they are still dull, replace the mechanism assembly per replacement instructions in
Chapter 6 of this manual, or return the pump to the manufacturer.
Verify that the Pressure Plate is not bent, cracked or deformed.
Verify that the Tubing Pincher opens and closes freely (without sticking).
If the pincher is sticking or is hard to actuate, remove the pincher cover and inspect for contamination or inadequate
lubrication. Remove assembly and clean if necessary. See Chapter 6, 'Spare Parts Replacement Procedures' for pincher
removal instructions.
If required, apply a coating of silicone lubricant to cavity in front panel. Refit the pincher, pincher spring and pincher
cover following the instructions in Chapter 6.
Flow Sensor Check (where flow sensor is in use)
Clean the flow sensor by wiping over with a cloth, lightly dampened with warm water and a
standard disinfectant/detergent solution. Ensure the connector does not get wet. Dry flow sensor
before use.
To aid cleaning of flow sensors which have been heavily soiled, contaminated or if the handles
operation is not free, the flow sensor may be immersed and soaked in clean soapy water.
Activating the spring mechanism of the sensor whilst immersed will assist in cleaning the inside of
the mechanism. After cleaning, the sensor should be allowed to dry fully prior to use.
CAUTION: the plug of the sensor should not be immersed as damage will occur.
Check that labels are flat, legible and fully adhered. Replace as necessary.
Check that lenses are clean and clear and show no sign of cracks.
Inspect the body of the flow sensor for damage.
Check that the sliding action of the flow sensor operates smoothly.
Use this troubleshooting guide to help identify the cause of errors and faults which may occur as a result of damage
to the pump or failure of an internal component. The following tables list the error messages and general faults and
describe what action to take to resolve the problem. For information on alarm procedures and messages, refer to the
relevant DFU.
If the nature of the problem is unclear, enter self-test mode and step through the self-test functions
to check that the main functions of the pump are operating correctly. See Chapter 3, 'Routine
Maintenance' for details.
Test 016 READ ALARM HISTORY displays the sixteen most recent malfunction messages. To run test
016, enter self-test mode and select the test. See Chapter 3 for instructions.
Error Messages
MessageFailureAction/Replace
AIR IN LINEAir in IV infusion set detected by air-in-line
sensor.
IV infusion set removed from air-in-line detector
or is not installed in lower tubing guides.
AIR IN LINE
non-flow sensor
operation
persistent
AIR IN LINE
BOTTLE CLAMP
flow sensor
operation only
CHECK DISC
non-flow sensor
operation only
COM LINE
only when pump
connected to a CIM
Air in IV infusion set detected by air-in-line
sensor.
Empty container; clamp closed, upstream
occlusion, flow sensor mispositioned, tubing/
bottle venting incorrect.
Air-in-line transmitter or receiver failure.
VCO or timer failure.
Foreign matter lodged between pressure
transducer and pressure disc.
Pressure sensing disc improperly seated in
retainer.
Communication with external device has been
disconnected.
Purge air from IV infusion set. Check air-in-line
sensor is clean.
Check IV infusion set is properly installed in the airin-line detector and into lower tubing guides.
Purge air from IV infusion set.
Check VTBI is set.
Check equipment set up.
Replace air-in-line receiver on the front panel.
Replace air-in-line transmitter on the door.
Replace Accessory Interface Board.
Check equipment set up
Remove pressure disc, inspect and remove any
foreign matter then re-install disc.
Open and close door to reestablish vacuum.
If problem persists, check for blocked vacuum
ports or leaks. See FIX ME Q actions.
Upgrade software to Rev 3.01.
Check connections; Check that external device is
functioning.
Important: Test 024 CIM ID must be set to OFF
when CIM is not in use.
Downstream restriction, kinked tubing, clogged
filter, or pressure limit exceeded.
Communication error between pump and
external device.
Check overall setup, eliminate cause of alarm and
restart pump. Verify that maximum or default
pressure settings are not set too low for intended
clinical application.
Check connections; Check that external device is
operating correctly.
Important: Test 024 CIM ID must be set to OFF
when CIM is not in use.
Page 39
Troubleshooting
Error Messages (continued)
MessageFailureAction/Replace
FIX ME 0Microprocessor execution error.Replace U28, U29 on Logic Board; Replace U1 on
Logic Board.
FIX ME 1Logic Board component failure (CRC check error). Replace U13 on Logic Board; Replace U1 on Logic
Board; Replace U28, U29 on Logic Board.
Replace Logic Board.
FIX ME 2Microprocessor failure (CPU error).Replace U1 on Logic Board.
If problem persists, follow FIX ME 1 actions.
FIX ME 3RAM contents lost following loss of power. (RAM
error). Occurs at power up after reconnection of
AC and battery power.
FIX ME 4Watchdog reset failure.
Microprocessor, Watchdog or Interconnect cable
failure.
FIX ME 5Numeric Display segment failure.
Flex cable not correctly installed at J3.
Display driver circuit or checking circuitry failure.
FIX ME 6Numeric Display digit select failure.Run tests 03 and 17 to identify faulty digit or
FIX ME 7Segment check circuit failure.Remove power to Logic Board to power down
FIX ME 8Mechanism flag not detected at proper time
(Motor revolution period error).
Insufficiently lubricated mechanism.
Failed or misaligned rotation sensor optics.
Flag loose, mispositioned on mechanism cam
pulley.
Slipping mechanism cam or motor pulleys.
Failed cable assembly.
Failed Logic Board components.
Failed motor drive circuitry on Power Regulator
Board.
Failed or misaligned motor; misaligned front
panel.
Cam followers damage; jammed cam follower
assembly.
Failed pressure plate.
Recycle power ON/OFF switch; Replace U28, U29
on Logic Board.
If problem persists, follow FIX ME 1 actions.
Replace U7, U8 on Power Regulator Board; Replace
U14 on Logic Board; Replace interconnect cable.
Reseat flex cable into J3 ensuring cable tabs are in
line with connector tabs.
Run Tests 03, 04 and 05.
If Display and Front Panel switches function
properly and do not stick then replace DS1-DS3.
Replace flex cable.
Replace Display Board.
Clean any dried solution in mechanism then
lubricate along edges of cam followers.
Verify pulleys do not slip; verify motor rotates and
is not binding.
Rotate motor by hand, run test 22 and observe
port 16, bits 0 and 1.
Check red/black motor wires for damage.
Replace motor.
Replace pulley belt.
Replace Power Regulator Board.
FIX ME 9Microprocessor malfunction (Background
execution error).
FIX ME AMotor current not detected during power-up
(Motor shutdown failure).
Failed Logic Board or Power Regulator Board
components.
Failed motor.
Replace interconnect cable (Logic Board to power
Regulator Board).
Replace Logic Board.
Replace Power Regulator Board.
Replace motor.
Page 40
Troubleshooting
Error Messages (continued)
MessageFailureAction/Replace
FIX ME BU14 on Logic Board failed power-up test
(Counter timer failure).
FIX ME CWatchdog circuit failure at power-up.Replace U7, Y1 on Power Regulator Board; Replace
FIX ME DSpeaker checker failure at power-up.Replace speaker; Replace U4 or Power Regulator
FIX ME ESpeaker failure at power-up.
Speaker disconnected or failed.
FIX ME FA/D converter failure at last power-down.Replace U35 on Logic Board; Replace Logic Board
FIX ME GWatchdog check failure at last power-down.Replace U7 on Power Regulator Board; Replace
FIX ME HIncorrect pressure applied during pressure
calibration or internal adjustments out of
tolerance.
Replace U14 on Logic Board; Replace U1, U13 on
Logic Board.
Replace Logic Board.
Power Regulator Board.
Replace U14, U24 on Logic Board; Replace Logic
Board.
Board.
Replace speaker; Replace Power Regulator Board.
or Analog Board.
Check power supply reference voltage: On Power
Regulator Board, test point = positive side of C16,
limits 5.12 ±0.01 VDC; if not adjust R36.
Power Regulator Board.
Ensure correct calibration pressures are used, see
'Dry Set Pressure Calibration' procedure.
Verify that pressure unit selection switch is in the
correct position.
Replace vacuum/pressure transducer assembly.
FIX ME JPressure transducer failure.Check pressure adjustments, see FIX ME H.
Replace pressure transducer/vacuum assembly.
FIX ME KCIM ID entered without a CIM connected.Change CIM ID setting to OFF, see test 024.
FIX ME LEEPROM failureReplace U27 on Logic Board; Replace U23 on Logic
Board.
FIX ME MAir-in-line failure.Replace air-in-line receiver on the front panel.
Replace air-in-line transmitter on the door.
Replace Accessory Interface Board.
FIX ME NMotor rotation direction is reversed.
One or both motor rotation sensors failed.
FIX ME PSet sensor failure:
Set sensor detection failed when tested.
Sensor exposed to direct sunlight on latch side
of pump.
FIX ME QVacuum system failure.Install new IV infusion set and run test 27. Verify
Check that connectors J13 and J16 on Accessory
Interface Board are not reversed.
Replace rotation sensor assembly.
Locate pump away from direct sunlight.
Replace the set sensor assembly.
that the vacuum reading is -250 or more negative
when door is closed.
Clean face of pressure transducer and check for
damage.
Check and replace Y-clip, door latch pin and door
latch as necessary.
Replace pressure transducer/vacuum assembly.
FIX ME RVacuum detect circuit failure.Replace Accessory Interface Board.
FIX ME SPump was operating in Secondary or CRIS mode
yet configured as PRI ONLY in test 031. (Infusion
mode error).
FLOW SENSORDrops splashing in drip chamber. Drip chamber
too full.
Improper secondary set.
Flow sensor mispositioned or removed/installed
while pump is running.
persistent
FLOW SENSOR
LOW BATT
alternating with
the selected
volume or pressure
status
LOW BATTBattery discharged; insufficient charge to
Flow sensor lenses obscured.
Flow sensor wiring open or short-circuited.
Analog Board circuitry failure.
Battery is almost discharged. Approximately 30
minutes of run time remain. Pumps continues to
run but sounds a low-pitched, audible tone to
alert user.
operate pump.
The pump will sound an alarm and stop
operating.
Replace U1 on Logic Board.
Replace U28, U29 on Logic Board.
If problem persists, follow FIX ME 1 actions, then
FIX ME L actions as necessary.
Check for proper flow sensor set up and eliminate
problem. For ambulation, slightly lower drip
chamber fluid level if necessary.
Check for damage to flow sensor wiring from
receptacle to Logic Board.
Replace Analog Board, then Logic Board.
Operate on AC power. The battery will recharge
while operating on AC power.
Operate on AC power. The battery will recharge
while operating on AC power.
Note: A fully discharged battery can be recharged
to a full charge in approx. 24 hours with the pump
turned off and connected to AC power.
persistent
LOW BATT
(even after
charging)
RECONFIG
REQUIRED
SET OUTIV infusion set removed or improperly loaded.
persistent
SET OUT
TIME OUT2 minutes have elapsed since pump put on hold
Weak battery.
Battery charge circuit out of adjustment or
malfunctioning.
A/D converter (U16 on Logic Board) or Power
Regulator Board component failure.
Invalid configuration or calibration data.Run test 02 and identify invalid configuration then
Incorrect IV infusion set used.
Set sensor does not detect that IV infusion set is
loaded.
Door sensor does not detect door is closed.
Magnet broken, missing from door latch or
magnet polarity reversed.
or since last switch was pressed.
A switch is stuck or has been pressed and held
for more than 1 minute.
Check battery voltage is 14.4 ± 0.05 VDC.
If necessary, adjust R10 on Power Regulator Board
to achieve 14.4 ± 0.05 VDC.
set configuration as necessary.
If problem persists, run full self-test and perform all
calibration procedures.
Load IV infusion set properly using correct IV
infusion set.
Check set sensor and door sensor using test 22.
Check for damaged or missing door latch magnet.
Check magnet polarity is correct.
Press the RUN/HOLD switch twice to continue
infusion.
Fuse blown.
ON/OFF switch failure.
Power Regulator Board or Logic Board circuitry
failure.
Bad battery.
Battery is disconnected, has a wiring problem or
has failed.
Reset circuit breaker once. If it trips again,
disconnect from AC power then:
Check mains inlet for fluid ingress.
Check power lead for damage.
Replace Power Regulator Board.
Replace transformer.
Run test 17.
Test switches while opening and closing door.
Replace or reposition flex cable routed to J3.
Replace Bezel/Switch Panel assembly.
Replace Display Board.
Replace fuse F1 on Power Regulator Board.
Replace Bezel/Switch Panel assembly.
Check battery voltage is 14.4 ± 0.05 VDC, adjust
R10 on Power Regulator Board if necessary.
Replace Power Regulator Board or Logic Board.
Replace clad fuse on Power Regulator Board. If fuse
blows repeatedly, verify that the battery charge
voltage is 14.4 ± 0.05 VDC, adjust R10 on Power
Regulator Board if necessary.
Replace battery.
Scrambled or
frozen Display
Momentary
Display
Knocking noiseDirt build-up around pressure plate.Clean and inspect pressure plate.
Fuse blown (F1),
intermittent FIX
ME 0, FIX ME 3 or
halted alarms
Microprocessor malfunction.
Faulty flex cable.
Pump has automatically shut off due to low
battery charge.
3/8" test connector cover screw shorted out.Replace 3/8" screw with 1/4" screw (300330).
Replace Y1 on Logic Board; Replace U1 on Logic
Board.
Check flex cable connection at J3 of Display Board.
Replace Logic Board.
The IVAC® Volumetric Pump, Models 571 and 572 are designed to be serviced generally to major assembly level.
The main circuitry within the pump is contained on five printed circuit boards (PCBs): Logic PCB, Power Regulator PCB,
Display PCB, Accessory Interface PCB, Analog PCB and a switch panel.
Cardinal Health will make available, on request, circuit diagrams which will assist appropriately qualified technical
personnel to repair those parts of the device which are designated by the manufacturer as repairable.
Logic PCB
Contains the main processor module, memory circuits, I/O
circuits and associated support circuitry which provide
the control functions for almost all the aspects of the
pump. It drives and monitors all other modules using the
program code stored in the EPROM and the RAM ICs.
Main Processor
Consists of an 8-bit microcontroller with an internal
clock generator, vectored interrupts and 64k byte
addressing capability. The processor gets instructions
from the program memory (EPROM U1 and RAM U28,
U29) and then executes them.
Power Control Circuit (& On/Off Switch)
Consists of flip flop (U18) and gate (U17) which are
powered from the VRAM supply so are operational
even when the pump is off. The ON/OFF switch
enables power to the system. It uses a single push
switch on the front panel to toggle the flip flop (U18).
Note if the battery voltage falls below 10.2V, the
microprocessor asserts the OFF signal to toggle U18
into the power-off condition as if the ON/OFF switch
has been pressed.
Wait-State Generator
Memory Address Decoder
Decoding used to select EPROM U13 and RAMs U28
and U29 is provided by various logic circuits.
Read Only Memory (ROM)
The software program is stored in ROM (U13).
Electrically Erasable Programmable Read Only
Memory (EEPROM)
U27, a 128 byte EEPROM is used to retain important
user information such as calibration constants and
operating parameter configurations.
Random Access Memory (RAM) and RAM test
U28 is the read/write memory type and a second RAM,
U29, and various ICs form a hardware RAM test circuit.
I/O Decoding
A/D Converter
Analog Input Signals
Output Ports/Input Ports
Programmable Interval Timer
Data Bus Buffer
Power Regulator PCB
The Power Regulator PCB provides system power supplies,
AC line and battery charging functions, motor control,
watchdog and alarm driver circuits.
Transformer, Rectifier and Filter
Line Regulator
Performs two functions, it is the main power source
when the pump is connected to AC power and it keeps
the battery charged by providing a nominal charge
voltage of 2.35V per cell. The circuit uses an integrated
circuit (U1) , configured as a fixed-frequency pulse
modulation regulator.
AC Line Indicator
AC Power Signal
Power Control Circuitry
+5L Regulator
5.12V Reference and VRAM Regulator
5V Switching Regulator
Clock/Dividing Chain
Crystal Y1, with associated components form a crystal
oscillator which clocks a binary counter. This counter
provides a signal which in turn drives certain circuitry
such as the watchdog alarm and provides timing for the
line regulator and motor control circuitry.
Watchdog
Watchdog pulses enable this circuit to perform an
integrity check on the microprocessor, generating an
alarm if pulses are not received within a defined timing
window.
Alarm Circuitry
Motor Control Circuitry
The microprocessor drives the motor by stepping the
current through each motor winding in the correct order
to cause the motor shaft to turn. Digital signals from
the Logic PCB determine the direction and duration of
the current and the winding is increased/decreased to
ensure sufficient torque to move the mechanism and
to hold its position. The motor control circuit controls
current across a bridge to the windings of the stepper
motor using a pulse width modulation technique.
Battery
The sealed lead acid battery pack consists of six cells each
with a potential of 1.8V to 2.40V, connected in series, a clad
fuse (F2), and a 1.5A fuse (F1). The battery pack is rated at
Consists of two separate circuits, the drop discriminator
which monitors the flow status and the pressure amplifier
which amplifies the output of the pressure transducer.
Drop Discriminator
The drop discriminator circuitry is only active when
a flow sensor is in use. The circuitry consists of a
synchronous demodulator, differential amplifier, an LED
driver, an AGC (automatic gain control) circuit and drop
simulator circuitry.
Pressure Amplifier
The pressure amplifier circuitry comprises four
functional blocks: the chopper/modulator input, the
instrumentation amplifier, the demodulator and the
output amplifier.
Accessory Interface PCB
Comprises the ultrasonic air-in-line detector and the
vacuum detection circuitry. It also acts as an interface
between the Logic PCB and various sensors and
periphery devices including the door sensor, pressure
sensor, Display PCB, motor and the rotation sensors.
Transducer/Vacuum Assembly
The pressure transducer and the vacuum unit make up
this assembly.
Pressure measurement is detected by the pressure
sensor. Pressure sensor readings are provided by the
transducer output voltage taken from a bridge circuit
on the pressure transducer diaphragm.
A cylinder within the pump provides a vacuum to
ports surrounding the front face of the pressure
transducer to ensure firm coupling between the
pressure sensor disc pad of the IV infusion set and the
diaphragm of the transducer.
Display PCB
This board comprises four 7-segment numeric displays,
two 4-digit alphanumeric modules, battery and AC
power LEDs and display circuitry which includes address
decoders, display drivers, and check circuitry. The bezel/
switch panel is an extension of the Display Board via P2.
Mechanism
The motor drives the timing pulley which in turn drives
the CAM, turning the rotation flag. The rotation flag
passes through the two rotation sensors. The function of
these two rotation sensors is to verify that the motor is
turning the correct direction.
Mains Inlet, Circuit Breaker and
Transformer
The AC line voltage is connected to the step-down
transformer through the circuit breaker. The secondary
output of the transformer provides a nominal 24 VAC
which is rectified through a full-wave rectifier, rectified
and converted into an unregulated DC voltage.
Air-In-Line Detector System
Comprises two parts: the air-in-line receiver on the front
panel and the air-in-line transmitter on the door. These
parts sandwich the IV infusion set tubing when the door
is closed and together with the air-in-line drive and
detect circuit they ultrasonically sense air in the fluid
path.
Ensure the pump is disconnected from the AC power supply and switched off before attempting to
service the pump
The pump contains static-sensitive components. Observe strict ESD precautions at all times
Batteries should be disposed of as outlined by the local country regulations: do not send back to
the manufacturer
Only use Cardinal Health recommended spare parts
Following all spare part replacement and repair activities, testing must be performed in accordance
with the Performance Verification Procedure (PVP), see Chapter 3, 'Routine Maintenance'
Separating the Chassis and the Body
Replacement Procedure
1. Remove the two screws and washers securing the battery access cover then remove the battery access cover and
shield.
2. Slide out the battery pack and unplug the battery connector.
3. Remove the two screws from the bottom of the pump case.
4. Remove the two screws and two washers from the back panel of the chassis assembly.
5. Unplug the interconnect cable from the Accessory Interface Board.
6. Grasp and gently lift the battery housing then slide the chassis assembly out of the case.
7. Remove the one screw securing the earth wire to the mechanism assembly.
8. Reassemble in reverse order.
Refitting note:
Tuck the battery connector harness
(with large ferrite bead attached) into
the space at the top left of the battery.
If intermittent FIX ME 0, FIX ME 3 errors
are experienced, a blown fuse (F1),
halted alarms or the test connector
cover screw (item (D) is a 3/8" screw,
replace with 1/4" screw (300330).
1. Remove the four screws and washers securing the
transformer assembly. Remove the transformer
assembly.
2. Remove the Power Regulator Board retainer.
3. As required, cut away heat shrink then desolder and
remove the black and white wires from the circuit
breaker.
4. Disconnect the cable harness from the Power
Regulator Board (J1).
5. Reassemble in reverse order.
Refitting note: When refitting the transformer,
circuit breaker and AC line filter, it is important
to ensure that the transformer wires are placed
under the Power Regulator Board retainer (D)
without being pinched:
1. Position the retainer.
2. Place wires under tab guide of retainer.
3. Secure transformer with the four screws.
(D) Power Regulator Board Retainer
(C) Transformer
Transformer Cover
(B) Washer (x4)
(A) Screw (x4)
Transformer
Circuit Breaker
Heat shrink
Spare Parts
Item Description Part Number
A SCREW,MACH 8-32X1 1/2 PNH PHH 301126
B WSHR,SPLIT,.168X.296X.040,PS 300037
C ASSY,XFMR,220V 571/572(BOM) 139009
D RETAINER,PW BD 125383
1. Remove the knurled nut which secures the circuit breaker button to the rear panel.
2. Desolder and remove the black and white wires, cutting away heat shrink as required. Disconnect the crimp
connectors. Remove the circuit breaker.
3. Remove the two screws from the mains inlet on the outside of the rear panel and the two kep nuts securing the AC
line filter on the inside.
4. Disconnect the blue, brown and ground lug wires from the AC line filter.
5. Slide the AC line filter out from the back, removing the two adapters (one adapter on Models XBX, XCX).
6. Reassemble in reverse order.
Refitting notes:
When refitting the AC line filter:
Place one of the adapters over on the AC line filter with the
thick section at the top. Slip the AC line filter through the
back then place the 2nd adapter over the filter with the
thick section at the bottom.
Ensure the AC line filter is orientated so that the earth pin is
nearest to the outer edge of the pump.
(F) Washers (x2)
(B) Kep Nut (x2)
Models XBX, XCX
(A) Circuit Breaker
Heat shrink
(B) Kep Nut (x2)
Knurled Nut / Circuit Breaker Button
(E) Screw (x2)
(D) AC Line Filter
(C) Adapter
Transformer
(C) Adapter (2nd)
not on Models XBX, XCX
Ground Lug
Spare Parts
Item Description Part Number
A BREAKER,CIRCUIT,571/572 137441
B NUT,KEP 6-32 S PL 300036
C ADPT,LINE FILTER,56X/57X/220V 125389
D FILTER,EMI,LINE,120/250,1A 304746
E SCREW,MACH 6-32X3/4 PNH PHH 300360
F WSHR,FL,M 6,BRASS,NICKEL PLT 303736
A NUT,HEX 6MM METRIC,3.2MM THK 303742
B NUT,HEX METRIC, M6, 5MM THK 303740
C WSHR,FL,M 6,BRASS,NICKEL PLT 303736
D WASHER,EXT T LKG,6MM,CS CAD PL 303737
E LBL,GND SYM 123273
F WSHR,COLOR CODE,YEL/GRN,NPS 303739
G CONN,PLUG 0.984 MTG STUD 303734
1. Disconnect the speaker harness from the Power Regulator Board (J2).
2. Remove the speaker assembly by breaking it loose from the battery housing.
3. Remove the two nuts securing the battery housing to the rear panel assembly.
4. Remove the CE panel and rear panel as required.
5. Reassemble in reverse order.
Refitting note:
Use Loctite 38050 to fix the speaker in place.
(D) CE Panel
(E) Rear Panel
Speaker harness
(A) Speaker Assembly / Loctite 38050
(B) Nut (x2)
(C) Battery Housing
Models XBX, XCX
Spare Parts
A ASSY,SPEAKER,56X/57X(BOM) 125425
B NUT,KEP 6-32 S PL 300036
C HSG,BATT,56X/57X 125318
D KIT,CE PANEL,571/2 136853
E ASSY, PANEL REAR ,RFI,571/572XB 137851
To replace the components within the body assembly, follow the instructions in the relevant sections of this chapter.
These sections are:
Separating the Chassis and the Body
Y-Clip, Pressure Transducer/Vacuum Assembly
Door Sensor Assembly
Air-In-Line Receiver Assembly
Pincher Mechanism
Mechanism Assembly: Rotation Sensor Assembly, Motor, Timing Pulleys, Belt
Accessory Interface Board
Separating the Front Panel Assembly from the Case
Cover Assembly, Handle, Bumpers, Fastener Clips
Important note: The Front Panel and the Door are not serviceable.
If replacement of these components is required, contact your local Cardinal Health Affiliate Office or
Distributor for advice.
Y-Clip, Pressure Transducer/Vacuum Assembly
Replacement Procedure
1. Remove the one screw and two washers securing the Y-clip. Remove the Y-clip.
2. Remove the two mounting screws securing the pressure transducer to the front panel.
3. Remove the two screws securing the vacuum unit to the front panel.
4. Pull the tubing (which connects the pressure transducer and the vacuum unit) out of the retaining clip.
5. Disconnect the vacuum unit connector (J10) and the pressure transducer (J15) from the Accessory Interface Board,
removing cable ties as required.
6. Withdraw the pressure transducer/vacuum assembly from the body.
7. Remove the plunger spring from the vacuum unit as required.
8. Reassemble in reverse order.
Spare Parts
Item Description Part Number
A CLIP,Y,570 132801
B WSHR,FL,.174X.380X.032,PS 300038
C SCREW,MACH,6-32X3/16,PNH,PHH 304209
D SCREW,MACH 8-32X1/4 PNH PHH 300055
E SERV ASSY,PRES,VACUUM,57X 141176
F SPRING,PLUNGER,56X/57X 133246
G SCREW MACH 6-32 X3/8 PNH PHHSS 303938
H CLIP,CORD,.18 DIA,ADH BK,NYL 303106
1. Unfasten the one retaining clip which secures the door sensor assembly to the inside of the front panel.
2. Disconnect the wiring harness (J11) from the Accessory Interface Board, removing cable ties as required.
3. Withdraw the door sensor assembly.
4. Reassemble in reverse order.
Refitting note:
Insert the door sensor assembly through the front panel, mount on peg and secure with clip.
To provide a clear view of the fitting area, the
illustration below shows the door removed. The door is
not serviceable.
If a replacement door is required, contact your local
Cardinal Health Affiliate Office or Distributor for advice.
Cable Tie
(A) Fastener Clip
(B) Door Sensor Assembly
Spare Parts
Item Description Part Number
A FSTNR,SPD NUT LKG 0.250 SSTUD 302902
B ASSY,DOOR SNSR BD,56X/57X(BOM) 132536
1. Remove the two screws securing the air-in-line receiver assembly to the front panel.
2. Disconnect the wiring harness from the Accessory Interface Board (J1) and pull the wiring harness free of the silicone
fixing on the inside of the front panel.
3. Remove the air-in-line receiver assembly, drawing the wiring harness out through the front panel hole..
4. Reassemble in reverse order.
To provide a clear view of the fitting area, the
illustration below shows the door removed. The door is
not serviceable.
If a replacement door is required, contact your local
Cardinal Health Affiliate Office or Distributor for advice.
(B) Air-In-Line Receiver
(A) Screw (x2)
Front Panel Back View
Spare Parts
Item Description Part Number
A SCREW,CAP,4-40X1/4,BUTH,HXSO 304172
B ASSY,AIL,RECEIVER,57X(BOM) 133996
Refitting note:
Secure the wiring
harness with
adhesive silicone,
RTV 162 as shown
1. Remove the one screw securing the pincher mechanism to the front panel.
2. Remove the cover plate, spring and the pincher.
3. Reassemble in reverse order.
Refitting note:
Use Loctite 243 on the securing screw.
To provide a clear view of the fitting area, the
illustration below shows the door removed. The door is
not serviceable.
If a replacement door is required, contact your local
Cardinal Health Affiliate Office or Distributor for advice.
(E) Pincher
(D) Spring
(C) Cover
(A/B) Screw / Loctite
Spare Parts
Item Description Part Number
A SCREW,CAP 6-32X1/4 FLH HXSO 301164
B ADHESIVE LOCTITE 243 0000ME00672
C COVER,PINCHER,56X/57X(BOM) 125321
D SPRING,CAM,56X 125768
E PINCHER,56X/57X 133248
To carry out repairs and/or replacement of the body assembly components, follow the instructions in the relevant
sections of this chapter.
Important: Breakdown of the mechanism assembly is limited to replacement of the motor, the rotation
sensor assembly, the two timing pulleys and the timing belt only. Do not attempt to disassemble the
Front Panel Assembly any further.
If repair of any other mechanism components is necessary, contact your local Cardinal Health Affiliate
Office or Distributor for advice.
Rotation Sensors
Timing Pulley (large)
Mounting Plate
Timing Pulley (small)
Rotation Sensor Assembly
Replacement Procedure
1. Disconnect the rotation sensor assembly wiring harness from
the Accessory Interface Board (J16 = back sensor, J13 = front
sensor), removing cable ties as required.
2. Remove the one screw which secures both rotation sensors.
Withdraw the rotation sensor assembly.
3. Reassemble in reverse order.
Refitting note:
After fixing the rotation sensors, rotate the motor timing pulley
and adjust the rotation sensor slot to ensure that the optical flag
rotates freely.
Motor
Belt
To J13
To J16
To J14
(B) Screw
(A) Rotation Sensors
Spare Parts
Item Description Part Number
A ASSY,HARN,ROTN SNSR,56X/57X 125445
B SCREW,MACH 4-40X5/8 PNH PHH 300347
1. Disconnect the motor connector (J14) from the Accessory
Interface Board, removing cable ties as required.
2. Holding the motor in place, use a flexible or right-angled
screwdriver to remove the two screws which secure the motor
to the motor mounting plate.
3. Remove the motor.
4. Measure and record the distance between the small timing
pulley and the motor surface.
5. Loosen the set screw which secures the small timing pulley to
the motor then pull up to remove it.
6. Reassemble in reverse order, referring to 'Refitting notes' on the
next page.
To provide a clear view of the fitting area, the mechanism is shown here broken
down, however, breakdown of the mechanism assembly is limited to replacement of
the motor, the rotation sensor assembly, the two timing pulleys and the timing belt.
Do not attempt to disassemble the Front Panel Assembly any further.
Timing Pulleys, Belt
Replacement Procedure
1. Loosen the set screw securing the large pulley
timing assembly then pull up to remove it from
the cam shaft.
2. Remove the belt from around the pulley as
required.
3. Reassemble in reverse order, referring to
'Refitting notes' on the next page.
(A) Timing Pulley (large)
Set Screw
Cam Shaft
(B) Belt
(C) Timing Pulley (small)
(D) Motor
(E) Screw (x2)
Spare Parts
Item Description Part Number
A ASSY,TIMING PULLEY,57X(BOM) 131002
B BELT,TMG 79GRV 0.080P 302878
C PULLEY, TMG 24 GRV 0.080P 302876
D MOTOR 4-WIRE 56X57X 10013683
E SCREW,MACH 6-32X3/8 PNH PHH 300034
1) When refitting the motor, align the two diagonal motor mounting holes with the motor mounting plate before
securing the motor in place with the two screws. Use Loctite 243 on the two screws.
2) When refitting timing pulley (small) onto a replacement motor, install it at the same height as recorded from the old
motor.
3) When refitting the belt, verify the belt tension by pushing on the belt between the pulleys. The belt should easily push
(> 5 pounds of force) by approx. 0.1 to 0.2 inches. Tighten or loosen the belt as required:
Loosen the two motor screws and hold the motor to the mounting plates
Push motor towards the front of the case to lessen belt tension OR pull the motor towards the rear of the case to
increase belt tension.
Retighten the two screws and recheck belt tension.
4) Position timing pulley (large) onto the cam shaft just far enough to keep it off the mechanism plate then tighten the
set screw. When replacing the timing pulley (large), tighten the set screw onto the flat of the cam shaft to ensure
correct flag orientation.
Turn timing pulley (large) so the flag on the timing pulley passes through the optical sensors freely. Ensure the flag
does not rub the sensors. If so, loosen the rotation sensor fixing screw, reposition the flag then retighten the rotation
sensors screw ensuring the rotation sensors do not move.
1. Unplug all cables connected to the Accessory Interface Board, including the flex cable (J12).
2. Using a right-angled Phillips screwdriver, remove the 3 screws and 1 washer securing the Accessory Interface Board to
the case.
3. Withdraw the Accessory Interface Board from the body, removing the strain relief pad from between the case
standoffs as necessary.
4. Reassemble in reverse order, referring to 'Refitting notes' on the next page.
To provide a clear view of the fitting
area, the illustration below shows a
front view of the case. Fitting is only
carried out from the rear of the case.
Standoff
(B.3) Strain Relief Pad
(B.2) Shield
(B.1) Flex Cable
(A) Accessory Interface Board
If a strain relief pad (B.3) is not present, fit pad (145271) between the Accessory Interface Board
J12 connector
(C) Washer
(B.4) Screw (x3)
and the case by positioning it between the mounting standoffs on the case
Ensure that the shield (B.2) is the larger-size shield (141574) which covers all exposed leads in
the path of the flex cable as shown below. Check the part number and replace existing shield as
necessary
1) When refitting the flex cable, first carefully route the cable through the front panel and door grommets then connect
it to J12 connector.
It is important to firmly seat each pin into the connector using a birch stick (or equivalent tool or method), otherwise
intermittent contact may occur resulting in Display errors
2) When refitting the Accessory Interface Board take care not to loosen the flex cable connection at J12 or to move the
strain relief pad from its position between the standoffs.
Apply the shield
to the area of the
board shown, on
the clad side.
1. Remove the two kep nuts securing the ground strap between the cover (inside top of case) and the front panel.
2. Unfasten the six retaining clips securing the front panel to the case. Separate the front panel assembly from the case.
3. Reassemble in reverse order.
Refitting note:
1) Use silicone (clear RTV coating, inner bond 140) around the case edge when refitting the front panel to the case.
To provide a clear view of the fitting area, the
illustration below shows the door removed. The door is
not serviceable.
If a replacement door is required, contact your local
Cardinal Health Affiliate Office or Distributor for advice.
Front Panel
Ground Strap
(A) Fastener Clip (x6)
(B) Kep Nut (x2)
Spare Parts
Item Description Part Number
A FSTNR,SPD NUT LKG 0.250 SSTUD 302902
B NUT,KEP 6-32 S PL 300036
1. Using a right-angled Phillips screwdriver, remove the two screws securing the handle to the case. Remove the handle.
2. Remove the four screws which secure the bumpers to the bottom of the case. Remove the bumpers.
3. Reassemble in reverse order.
Refitting note:
When refitting the handle, use adhesive on the two
fixing screws.
(A.2) Screw (x2)
(A.1) Mylar Shield
To provide a clear view of the
fitting area, the illustration below
shows a front view of the case.
Fitting is only carried out from the
rear of the case.
(A.3) Handle
Case Cover
(Part of cover assembly A, not
available separately)
To replace the components within the door assembly, follow the instructions in the relevant sections of this chapter.
These sections are:
Separating the Chassis and the Body
Bezel/Switch Panel, Display Board
Pressure Plate
Door Latch
Door Latch Pin
Air-In-Line Transmitter Assembly
Set Sensor, Pressure Disc Plunger
Pincher Cam Block
Important note: The Door and the Front Panel are not serviceable.
If replacement of these components is required, contact your local Cardinal Health Affiliate Office or
Distributor for advice.
Bezel/Switch Panel, Display Board
Replacement Procedure
1. Remove the four screws securing the bezel/switch panel and Display Board to the door assembly.
2. Ease the bezel/switch panel and Display Board assembly away from the door until it is possible to disconnect the
interconnect flex cable connector (H) from the back of the Display Board (J3).
3. Remove the four caps from the Bezel ground posts.
4. Remove the three screws securing the Display Board to the bezel/switch panel.
5. Carefully separate the Display Board and the bezel/switch panel then disconnect the flex cable connector (J2) from the
Display Board.
6. Disconnect the set sensor cable harness connector (J1) and the air-in-line harness connector (J4) from the Display
Board then remove the Display Board.
7. Remove the interconnect flex cable by sliding the cable out through grommets in the door and front panel.
8. Remove the mylar shield (L) from the Display Board as required.
To provide a clear view of the fitting area, the door is shown below removed from its hinges.
Important: Do not remove the door from its hinges for servicing or replacement purposes.
If the door is damaged or a replacement is required, contact your local Cardinal Health Affiliate Office
or Distributor for advice.
(D/E) Screw (x4) / Loctite
(C) Hinge Pin
(A) Bezel/Switch Panel
(A.1) Foam
(B) Display Board
(F) Grommet, front panel
(G) Connector
(H) Interconnect flex cable.
See also 'Far Side View' below.
1) When refitting the Display Board, fold the interconnect cable as shown in the 'Far Side View' illustration (see previous
page).
2) Use Loctite 243 on the four screws (D) which secure the bezel/switch panel and Display Board to the door assembly.
3) Adhere the mylar shield on the solder side of the Display Board, centered on, and against the edge of the interconnect
cable connector, J3.
4) When refitting the interconnect flex cable carefully slide it through the front panel and door grommets. If necessary
lightly grease the cable with lub grease 33 (0000ME00452), on a cotton swab. It is important to ensure any grease is
wiped away from exposed cable using alcohol and lint-free cloth. If foreign matter remains, failure of the front panel/
Display Board may occur. See also 'Accessory Interface Board' for additional refitting notes.
Spare Parts
Item Description Part Number
A ASSY,BEZEL/OVLY,ENG,571(BOM) 139002
A ASSY,BEZEL/OVLY,ENG,572(BOM) 138999 (Models XBX, XCX)
A ASSY,BEZEL/OVLY,FREN,571(BOM) 139000
A ASSY,BEZEL/OVLY,DUT,571(BOM) 139001
A KIT,BEZEL/OVLY,SPAN,571(BOM) 139003
A KIT,BEZEL/OVLY,ITAL,571(BOM) 139004
A ASSY,BEZEL/OVLY,SWED,571(BOM) 139005
A KIT,BEZEL/OVLY,GER,571(BOM) 139006
A SERV ASSY,BEZEL/OVLY,ENG,570 133207 (Model XAX)
A.1 FOAM,0.062TX0.125W GREY 302932
B SERV ASSY,DSPL BD,57X(BOM) 139007
* DSPL,7/SEG,ORANGE,COM CATH.400 302274 (DS3-6 on Display Board)
* DIODE,LED,YEL,MV53154/HLMP3465 302762 (DS7,8 on Display Board)
* DISPLAY,LED,RED,5X7 DOT MATRIX 303899 (DS1,2 on Display Board)
* CONN,HDR,LTCH,4P,1X4,RA,AU 302797 (J1 on Display Board)
C PIN,GRV 0.125X1.25 S ALLOY 302053
D SCREW,CAP 4-40X5/8 HXSO 302466
E ADHESIVE LOCTITE 243 0000ME00672
F GROMMET,FLEX STRIP 125359
G CONN,FL FLEX RTANG 11P 0.100C 303612
H FLEX CBL,RFI,571/572 139753 (Models XBX, XCX)
H CBL,FLEX,56X/57X 140787 (Model XAX)
J SCREW,MACH 4-40X1/4 PNH PHH 300345
K CAP,GROUND,POST,571/572 137653
L SHIELD,MYLAR,56X/570 125413
1. Mark the face of the pressure plate to ensure it can be refitted with the correct top side upwards.
2. Remove the four screws and washers securing the pressure plate to the door.
3. Remove the pressure plate and two coil springs seated in the door recesses.
4. Reassemble in reverse order.
Important:
Each pressure plate is mated to the cam followers during manufacture burn-in. If the pressure
plate is damaged or a replacement is required, contact your local Cardinal Health Affiliate Office or
Distributor for advice.
Correct top-side-up orientation of the pressure plate must be observed when it is refitted.
Refitting notes:
1) Install the pressure plate with the correct top side upwards using the mark made on face when removed.
2) Use Loctite 243 on screws when refitting the pressure plate.
(A) Spring (x2)
Pressure Plate
(B) Washer (x4)
(C/D) Screw (x4) / Loctite
Spare Parts
Item Description Part Number
A SPR,CPRSN,.360X.813X.813X.035,MW 302900
B WSHR,FL,.187X.438X.020,BLK,SS 301594
C SCREW,MACH 8-32X3/8 PNH PHH 301522
D ADHESIVE LOCTITE 243 0000ME00672
2. Remove the two curved spring washers and the door latch.
3. Remove the magnet cover and magnet as required.
4. Reassemble in reverse order.
Refitting notes:
1) When refitting the magnet, ensure the south pole faces outwards, secure magnet in place using loctite and cover.
2) Fit the two curved spring washers into the latch recesses outwardly, convex.
3) Fit the groove pin flush with the outside surface of the door.
(A) Groove pin
(B) Cover
(C/D) Magnet / Loctite
See Inside View
(F) Spring Washers (x2)
When refitting the
door latch, apply
lub grease 33
(0000ME00452) on
a cotton swab, to
entire length of slot
inside the latch.
(E) Latch
Inside View
Spare Parts
Item Description Part Number
A PIN,GRV 0.125X1.25 S ALLOY 302053
B COVER,MAGNET 125337
C MAGNET,MAGNETIZED,CO 90C98A 302425
D ADHESIVE LOCTITE 496 0000ME00753
E ASSY LATCH,GNRC,(BOM) 132777
E ASSY,LATCH,ENG,(BOM) 132776 (with label)
F SPRING,CVR,WSHR U-138-0045S 301591
1. Break loose and remove the one screw and two washers securing the pincher cam block, they are glued in place.
2. Remove the pincher cam block.
3. Reassemble in reverse order.
(C) Pincher Cam Block
(B) Washer (x2)
(A) Screw
Refitting notes:
Fit and adjust the pincher cam block as follows:
1) Loosely secure the pincher cam block with the one screw and two washers.
2) Open the pump door and insert a 0.125" pin gauge in the clamp of the pincher mechanism on the front panel. The
pin must sit vertically and the pin tip must sit below the pressure plate. Locating it any higher will result in inaccurate
adjustment of the pincher cam block.
3) With the pincher cam block free to move but loosely held in place by the securing screw, close the pump door over
the pin gauge. Slide the securing screw to the right until the pincher cam block rests solidly against the pincher then
tighten the securing screw, taking care not to strip the plastic threads.
4) Apply Loctite 420 to the back of the door and around the pincher cam block. Allow to dry for a minimum of 10
minutes before removing the pin gauge.
5) Insert a 0.110" pin gauge in the clamp of the pincher mechanism on the front panel. The pin must sit vertically and the
pin tip must sit below the pressure plate.
6) Close the pump door. Verify that the pin drops out of the pincher mechanism. If not, readjust the pincher cam block.
Spare Parts
Item Description Part Number
A SCREW,MACH 4-40X1/4 PNH PHH 300345
B WSHR,FL,.4BA T2 ST/STA2 0000ME00310
C PINCHER,CAM,56X/57X 125368
A LBL,FLOW SNSR PLCMT,ENG,57X 132152
A LBL FLOW SNSR PLCMT GER 571 135383
A LBL,FLOW SNSR PLCMT,FREN,570/1 132712
A LBL,FLOW SNSR PLCMT,DUT,571 137695
A LBL FLOW SNSR PLCMT SWED 571 137693
A LBL FLOW SNSR PLCMT SPAN 571 137694
A LBL FLOW SNSR PLCMT ITAL 571 137692
B LBL,PRES XDCR,ENG,57X(BOM) 133215
B LBL,PRES XDCR,GER 125452.01
B LBL,PRES XDCR,FREN 125452.02
B LBL,PRES XDCR,SWED 125452.04
B LBL,PRES XDCR,SPAN 125452.05
B LBL,PRES XDCR,ITAL 125452.06
C LBL,VPVP,ENG,572(BOM) 135990
C LBL VPVP ENG 571 (BOM) 138658
C LBL VPVP GER 571 (BOM) 135590
C LBL VPVP FREN 571 (BOM) 135589
C LBL,VPVP,DUT,571(BOM) 137658
C LBL VPVP SWED 571 (BOM) 137651
C LBL VPVP SPAN 571 (BOM) 137656
C LBL VPVP ITAL 571 (BOM) 137649
D LBL START UP ENG 571 (BOM) 138656
D LBL,START-UP,ENG,572(BOM) 137463
D LBL, START-UP, GER, 571 (BOM) 137841
D LBL, START-UP, FREN, 571 (BOM) 137839
D LBL,START-UP,DUT,571(BOM) 137329
D LBL START UP SWED 571(BOM) 137646
D LBL START UP SPAN 571(BOM) 137333
D LBL START UP ITAL 571(BOM) 137642
E LBL CE MARK INST MDD 136933
F LBL,CAUT,ENG 125392
F LBL,CAUT,GER 125407.01
F LBL,CAUT,FREN 125407.02
F LBL,CAUT,DUT 125407.03
F LBL CAUT SWED 125407.04
F LBL CAUT SPAN 125407.05
F LBL CAUT ITAL 125407.06
G ASSY,BEZEL/OVLY,ENG,572(BOM) 138999 (Models XBX, XCX)
G SERV ASSY,BEZEL/OVLY,ENG,570 133207 (Model XAX)
G ASSY,BEZEL/OVLY,ENG,571(BOM) 139002
G KIT,BEZEL/OVLY,GER,571(BOM) 139006
G ASSY,BEZEL/OVLY,FREN,571(BOM) 139000
G ASSY,BEZEL/OVLY,DUT,571(BOM) 139001
G ASSY,BEZEL/OVLY,SWED,571(BOM) 139005
G KIT,BEZEL/OVLY,SPAN,571(BOM) 139003
G KIT,BEZEL/OVLY,ITAL,571(BOM) 139004
H LBL,HANDLE,UPR,572 135992
H LBL HANDLE UPR 571 135539
I LBL,HANDLE,LWR,ENG,57X 132394
I LBL HANDLE LWR GER 571 135382
I LBL, HANDLE, LWR, FREN, 57X 132713
I LBL HANDLE LWR DUT 571(BOM) 137685
I LBL HANDLE LWR SWED 571(BOM) 137683
I LBL, HANDLE, LWR, SPAN, 571 137684
I LBL HANDLE LWR ITAL 571(BOM) 137682
J LBL,PRESS TO OPEN,ENG 125393
J LBL,PRESS TO OPEN,GER 125451.01
J LBL,PRESS TO OPEN,FREN,56X/57X 125451.02
J LBL,PRESS TO OPEN,DUT 125451.03
J LBL PRESS OPEN SWED 125451.04
J LBL,PRESS TO OPEN,SPAN 125451.05
J LBL PRESS OPEN ITAL 125451.06
K LBL,FLOW ARROW,ENG 125497
K LBL,FLOW ARROW,GER 125450.01
K LBL,FLOW ARROW,FREN,56X/57X 125450.02
K LBL,FLOW ARROW,DUT 125450.03
K LBL FLOW ARROW SWED 125450.04
K LBL FLOW ARROW SPAN 125450.05
K LBL FLOW ARROW ITAL 125450.06
L LBL,TBG POSN,57X 133208
L LBL TBG POSN GER 571 135386
L LBL,TBG,POSN,FR/CAN,570 133430
L LBL TBG POS DUT 571(BOM) 137690
L LBL TBG POS SWED 571(BOM) 137688
L LBL TBG POS SPAN 571(BOM) 137689
L LBL TBG POS ITAL 571(BOM) 137687
M LBL,S/N RPLCMNT 125569
N LBL,NAME RATING,ENG,571/572 137496
N LBL,NAME RATING,FREN,571 137960
N LBL,NAME RATING,DUT,571 137847
N LBL NAME RATING SWED 571 137648
N LBL NAME RATING SPAN 571 137848
N LBL NAME RATING ITAL 571 137644
R LBL PUSH TO RESET GER 571 137476
R LBL,PUSH TO RESET,FREN,571 137475
R LBL,PUSH TO RESET,DUT,571 137330
R LBL PUSH TO RESET SWED 571 137645
R LBL PUSH TO RESET SPAN 571 137845
R LBL PUSH TP RESET ITAL 571 137641
The following information is for reference purposes only. For more detailed specifications refer to relevant DFU.
Infusion
Rate range1 to 999 ml/hSTANDARD RATE range
0.1 to 999.9 ml/hALL RATE range, with user selectable maximum rate
Volume infused range0.1 to 9999.9 ml/h
KVO rate5.0 ml/h or at current set rate whichever is less
Critical volumeMaximum incremental volume delivered in case of failure will not exceed 8.75 ml
System Accuracy±5%
Infusion SetIVAC "52" Series Volume Infusion sets
Occlusion pressureMaximum: 500 mmHg (680 cmH20)
Mode of operationContinuous
Electrical
Battery typeLead acid, sealed, rechargeable. Automatically charges when the pump is connected to AC
power
Battery life5 hours @ 125 ml/h with a fully charged, new battery
Battery recharge timeApproximately 24 hours from discharge to 100% charge
Power requirements220 to 240V AC; 50/60 Hz; 0.25A; 3-wire grounded system
Memory retention At 25°C, with a fully charged, new battery, the volatile memory configuration information will be
retained for at least 6 months
Ground current leakageMaximum 100µA rms (ungrounded) at 220 Vrms to meet EN/IEC 60601-1
Protection against
electrical shock hazards
Class I
Physical
WeightApproximately 6.5 kg
Case materialBlue enameled aluminium
DimensionsW H D
12.7 cm 29.2 cm 19.3 cm
Environmental
IPX ratingIPX1
Temperature Relative humidity Atmostpheric pressure
Operating limits+5°C to +40°C 20% to 90% non-condensing 700 - 1060 hPa
Transport/storage limits-40°C to +60°C 10% to 100% 500 - 1060 hPa
• The use of any accessory, transducer, or cable with the IVAC® Volumetric Pump other than those specified may result in
increased emissions or decreased immunity of the pump.
• The IVAC® Volumetric Pump should not be used adjacent to or stacked with other equipment, however if adjacent
or stacked use is necessary, the IVAC® Volumetric Pump should be observed to verify normal operation in the
configuration in which it will be used.
Caution:
• The IVAC® Volumetric Pump is a CISPR 11 Group 1 Class A Medical Equipment System and intended for use by
healthcare professionals only.
• Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed, put into service and
used according to the EMC information provided in the accompanying documents.
• Portable and Mobile RF communications can affect Medical Electrical Equipment.
• Operating the pump near equipment which radiates high energy radio frequencies (electro surgical or cauterizing
equipment, portable radios, cellular telephones, etc.) may cause false alarm conditions. If this happens, reposition the
pump away from the source of interference or turn off the pump and manually regulate the flow.
Guidance and Manufacturer’s Declaration – Electromagnetic Emissions
The IVAC® Volumetric Pump is intended for use in the electromagnetic environment specified below.
The customer or the user of the IVAC® Volumetric Pump should assure that it is used in such an environment.
Emissions Test Compliance Electromagnetic Environment – Guidance
CISPR 11
RF Emissions
CISPR 11
RF Emissions
EN 61000-3-2
Harmonic Emissions
EN 61000-3-3
Voltage Fluctuations,
Flicker Emissions
Group 1
Class A
Class A
Complies
The pump uses RF energy only for its internal function in the normal
product offering. Therefore, its RF emissions are very low and are not
likely to cause any interface in nearby electronic equipment.
The pump is suitable for use in all establishments, other than
domestic, and those directly connected to the public low-voltage
power supply network that supplies buildings used for domestic
purposes.
Important: The IVAC® Volumetric Pump has been assessed to the following standards;
EN/IEC 60601-1-2:1993 (Models 571XAX, 572XAX & 572XBX)
EN/IEC60601-1-2:2001 (Models 571XBX & 572XCX).
Guidance and Manufacturer’s Declaration - Electromagnetic Immunity
The IVAC® Volumetric Pump is intended for use in the electromagnetic environment specified below.
The customer or the user of IVAC
® Volumetric Pump should assure that it is used in such an environment.
Immunity Test
EN 61000-4-2 Electro-
Static Discharge (ESD)
EN 61000-4-4
Electrical Fast Transient,
Burst (EFT) (Note 3)
EN 61000-4-5
Power Line Surge
(Note 3)
EN 61000-4-8 Power
Frequency Magnetic Field
(50/60 Hz)
EN 60601-1-2
Test Level
±6 kV contact
±8 kV air
±2 kV for power
supply lines
±1 kV for input/
output lines
±1 kV Line(s) to
Line(s)
±2 kV Line(s) to
Earth
3 A/m 400 A/m 50 Hz
Compliance Level
±8 kV contact (Note
2)
±15 kV air (Note 2)
±2 kV for power
supply lines
N/A (Note 4)
±1 kV Line(s) to
Line(s)
±2 kV Line(s) to
Earth
(Note 2)
Electromagnetic Environment – Guidance
Floors should be wood, concrete, or ceramic tile.
If floors are covered with synthetic material, the
relative humidity should be at least 30 %.
Mains power quality should be that of a typical
commercial or hospital environment.
Mains power quality should be that of a typical
commercial or hospital environment.
Power frequency magnetic fields should be at
levels characteristic of a typical location in a
typical commercial or hospital environment.
EN 61000-4-11
Voltage Dips, Short
Interruptions, and Voltage
Variations
(Note 3)
Note 1—UT is the AC mains voltage prior to application of the test level.
Note 2—Compliance levels raised by EN 60601-2-24.
Note 3—Performed at the Minimum and Maximum Rated Input Voltage.
Note 4—Cardinal Health recommends using signal cables of less than 3 meters in length and this requirement is applicable only if signal cables are 3
meters or more in length. (EN 60601-1-2:2002, Clause 36.202.4)
<5 % UT (Note 1)
(>95 % dip in UT)
for 0.5 cycle
40 % UT
(60 % dip in UT)
for 5 cycles
70 % UT
(30 % dip in UT)
for 25 cycles
<5 % UT
(>95 % dip in UT)
for 5 sec
<5 % UT
(>95 % dip in UT)
for 0.5 cycle
40 % UT
(60 % dip in UT)
for 5 cycles
70 % UT
(30 % dip in UT)
for 25 cycles
<5 % UT
(>95 % dip in UT)
for 5 sec
Mains power quality should be that of a typical
commercial or hospital environment.
If the user of the pump requires continued
operation during power mains interruptions, it is
recommended that the pump be powered from
an uninterruptible power supply or a battery.
The pump does employ an internal short
duration battery.
Guidance and Manufacturer’s Declaration—Electromagnetic Immunity
LIFE SUPPORT Equipment
The customer or the user of the IVAC
Immunity Test
EN 61000-4-6
Conducted RF
EN 61000-4-3
Radiated RF
The IVAC
EN 60601-1-2
3 V rms
150 kHz to 80
MHz
3 V/m
80 MHz to 2.5
GHz
® Volumetric Pump is intended for use in the electromagnetic environment specified below.
® Volumetric Pump should ensure that it is used in such an environment.
Test Level
Compliance
Level
10 V rms
(Note 3)
10 V/m
(Note 3)
Portable and mobile RF communications equipment should be used no
closer to any part of the pump, including cables, than the recommended
separation distance calculated from the equation applicable to the
frequency of the transmitter.
Recommended Separation Distance
3.5d = [-----] √P
V
1
12d = [-----] √P 80 MHz to 800 MHz
V
2
12d = [-----] √P 80 MHz to 2.5 GHzE
1
23d = [-----] √P 800 MHz to 2.5 GHzE
1
Electromagnetic Environment – Guidance
where P is the maximum output power rating of the transmitter in watts
(W) according to the transmitter manufacturer and d is the recommended
separation distance in meters (m).
a
Field strengths from fixed RF transmitters, as determined by an
electromagnetic site survey, b should be less than the compliance level in
each frequency range. c
Interference may occur in the vicinity of equipment marked with the
following symbol:
Note 1—At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2—These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures,
objects, and people.
Note 3—Compliance levels raised by EN 60601-2-24.
a The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to 2.5 GHz are intended to
decrease the likelihood that mobile/portable communications equipment could cause interference if it is inadvertently brought into patient areas. For
this reason, an additional factor of 10/3 is used in calculating the recommended separation distance for transmitters in these frequency ranges.
b Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and
FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF
transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the pump is used exceeds
the applicable RF compliance level above, the pump should be observed to verify normal operation. If abnormal performance is observed, additional
measures may be necessary, such as re-orienting or relocating the pump.
c Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 10 V/m.
Recommended Separation Distances for LIFE SUPPORT Equipment between
portable and mobile RF communications equipment and the IVAC
The IVAC
The user of the IVAC
portable and mobile RF communications equipment (transmitters) and the IVAC
Rated Maximum Output
Power of Transmitter
® Volumetric Pump is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.
® Volumetric Pump can help prevent electromagnetic interference by maintaining a minimum distance between
to the maximum output power of the communications equipment.
Separation Distance According to Frequency of Transmitter
W
150 kHz to 80 MHz
Outside ISM bands
3.5
d = [------] √P
V
1
150 kHz to 80 MHz
In ISM bands
12
d = [------] √P
V
2
® Volumetric Pump
® Volumetric Pump as recommended below, according
m
80 MHz to 800 MHz
12
d = [ ------] √P
E
1
800 MHz to 2.5 GHz
23
d = [------] √P
E
1
0.01 0.030.120.120.23
0.1 0.110.380.380.73
1 0.351.201.202.30
10 1.113.803.807.28
1003.5012.0012.0023.00
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be determined using the
equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the
transmitter manufacturer.
Note 1—At 80 MHz and 800 MHz, the separation distance for the higher frequency range apply.
Note 2—The ISM (Industrial, Scientific, and Medical) bands between 150 kHz and 80 MHz are 6.765 MHz to 6.795 MHz; 13.553 MHz to 13.567 MHz; 26.957
MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
Note 3—An additional factor of 10/3 is used in calculating the recommended separation distance for transmitters in the ISM frequency bands between
150 kHz and 80 MHz and in the frequency range 80 MHz to 2.5 GHz to decrease the likelihood that mobile/portable communications equipment could
cause interference if it is inadvertently brought into patient areas.
Note 4—These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects,
and people.
Information on Disposal for Users of Waste Electrical & Electronic Equipment
U symbol on the product and/or accompanying documents means that used electrical and electronic products should
This
not be mixed with municipal waste.
If you wish to discard electrical and electronic equipment, please contact your Cardinal Health affiliate office or distributor
for further information.
Disposing of this product correctly will help to save valuable resources and prevent any potential negative effects on human
health and the environment which could otherwise arise from inappropriate waste handling.
Information on Disposal in Countries outside the European Union
This symbol is only valid in the European Union. The product should be disposed of taking environmental factors into
consideration. To ensure no risk or hazard, remove the internal rechargeable battery and dispose of as outlined by the local
country regulations. All other components can be safely disposed of as per local regulations.
Battery Removal
Removal Procedure
Remove the two screws and washers securing the battery access
cover then remove the battery access cover and shield.
Slide out the battery pack and unplug the battery connector.