Alaris GP Plus Infusion Pump Service Manual
Alaris GP Plus Infusion Pump Service Manual
s
Alaris® GP Volumetric Pump
Contents
General Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Introduction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Product Familiarity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Purpose of this Manual. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Conventions Used in this Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Licensing Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
General Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Features of the Pump. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Configuration and Calibration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Service Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Entering Service Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Factory Defaults. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Near End Of Infusion (NEOI) Warning Configuration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .14
Data Set Transfer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Calibration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Preventative Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Preventative Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Visual Inspection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Recommended Cleaning and Storage. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Cleaning the Pump. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Storing the Pump. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .23
Cleaning and storing the Infusion Set. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Cleaning the door. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Cleaning the Flow Sensor. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Updates. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Upgrading firmware. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Battery Test and Replacement. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Replace the Main Battery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Test Verification/PVP (Service Mode). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
PVP Work Flow . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Alarms Functionality. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
User Interface. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Power Supplies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Sensor Tests. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
COMMS Test. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Occlusion Test. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Occlusion Test (Optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Volumetric Accuracy. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Performance Verification Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
Log Downloads. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
PC Setup (first time only) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
PC Setup (second time). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
1 General Information
Introduction
The Alaris® GP Volumetric Pump series (hereinafter referred to as ‘Pump’) are small lightweight volumetric infusion pumps that provide
accurate and reliable infusions over a range of rates.
The pump is designed to meet the infusion requirements as specified in the Directions For Use (DFU) for all hospital departments
including general wards, critical and intensive care, operating rooms and accident and emergency rooms.
This pump is suitable for use by appropriately trained clinicians or nurses. This pump can be used for intravenous infusion modes.
Supporting fluid & drug therapy, blood transfusions and parenteral feeding.
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.
It is intended for use by personnel experienced in medical equipment testing and maintenance procedures.
'Single quotes' Used to indicate cross-references made to another section of this manual. For example, see Chapter 2,
'Configuration & Calibration'.
Italics Used 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 an Update note is found. A typical example is drawing attention to a software
upgrade that should be confirmed has been installed.
Wherever this symbol is shown an Important note is found. These notes highlight an aspect of test or
A maintenance that is important to know about.
Licensing Information
This product uses zlib ([Link] © 1995-2005 Jean-loup Gailly and Mark Adler
Technician Mode uses the lwIP communication stack ([Link]
© 2001, 2002 Swedish Institute of Computer Science. All rights reserved.
Redistribution and use in source and binary forms, with or without modification, are permitted provided that the following conditions
are met:
1. Redistributions of source code must retain the above copyright notice, this list of conditions and the following disclaimer.
2. Redistributions in binary form must reproduce the above copyright notice, this list of conditions and the following disclaimer in the
documentation and/or other materials provided with the distribution.
3. The name of the author may not be used to endorse or promote products derived from this software without specific prior written
permission.
THIS SOFTWARE IS PROVIDED BY THE AUTHOR “AS IS” AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT LIMITED TO,
THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE ARE DISCLAIMED. IN NO EVENT SHALL THE
AUTHOR BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT
NOT LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE, DATA, OR PROFITS; OR BUSINESS INTERRUPTION)
HOWEVER CAUSED AND ON ANY THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT (INCLUDING NEGLIGENCE OR
OTHERWISE) ARISING IN ANY WAY OUT OF THE USE OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
General Precautions
w Attention consult accompanying documents: Prior to using this pump, carefully read the Operating Precautions
described in the Directions for Use (DFU).
V This pump contains static-sensitive components. Observe strict precautions for the protection of static sensitive
components when attempting to repair and service the pump.
B 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.
m 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 high energy radio frequency emissions and is designed to be fail
M 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.
®
Al
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.
When connected to an external power source, a three-wire (Live, Neutral, Earth) supply must be used. If the
d integrity of the external protective conductor in the installation or its arrangement is in doubt, the pump should
be operated from the battery.
Alaris®
GP
Door
Display
Softkeys
Chevrons
Run
Bolus Mute
Hold
Pressure
Options
Battery indicator
AC power indicator On/Off
Door Lever
Handle
RS232/Nursecall connector
(cover removed for clarity)
IR communications port
Potential Equalisation
(PE) Connector
Service Mode can be accessed via a three-digit access code that is entered using the following procedure:
1. Hold down b and turn the pump on a.
2. Enter the access code 212 using the f keys and the NEXT softkey.
3. When the code shows on screen, press OK to confirm.
Select the required option using the f keys and the OK softkey.
For the Alaris® GP Volumetric Pump the options will be as follows:
Factory Defaults Load a default data set. Confirm to perform a cold start.
SELECT WITH
QUIT OK
For the Guardrails® and Plus software pumps the options will be as follows:
CQI Events Download For future implementation
Data Set Transfer
Configuration
Upload a data set to pump.
This menu comprises a list of options which are
SERVICE
configurable by the user. CQI Events Download
Calibration This menu comprises a list of calibrations which can be Data Set Transfer
performed by the user.
Configuration
Test Verification/PVP Performance Verification Procedure Tests.
Calibration
Factory Defaults Load a default data set. Confirm to perform a cold start.
Test Verification/PVP
Factory Defaults
SELECT WITH
QUIT OK
Factory Defaults
Select the required option using the f keys and the OK softkey.
Default Data Set Replace the current data set with a default data set.
Cold Start Confirm Confirm clearing and resetting the data set and
calibration data to the factory defaults.
FACTORY DEFAULTS
Clear CQI Log File* Confirm clearing all pump history and resetting the data
set to the factory default. Default Data Set
* Alaris® GP Guardrails® Volumetric Pump and Alaris® GP Guardrails® Volumetric Cold Start Confirm
Pump (with Plus software) only.
Clear CQI Log File
Note: For pumps with
Plus software the option
order will be:
• Default Data Set
• Clear CQI Log File
SELECT WITH
• Cold Start Confirm
QUIT OK
******
All data set and ******
WARNING!
cal
data will be reset to
default!
The pump will require a
full calibration before
returning to clinical use.
QUIT OK
Configuration
Select the required option using the f keys and the OK softkey.
Date/Time Sets the current date and time used for event logging. SERVICE CONFIGURATION
Software Versions Displays the pump software versions.
Date/Time
Serial Number Configure the displayed serial number. Software Versions
Pump Reference Pump specific text to be displayed in user mode at start Serial Number
up. (20 characters max.) Pump Reference
Language Configure the Language used for display messages. Language
Backlight & Contrast Adjust the Backlight and Contrast values Backlight & Contrast
Current Data Set File Displays the current data set file details. Current Data Set File
SELECT WITH
QUIT OK
Date/Time
ADJUST WITH
QUIT NEXT OK
Software Versions
• Press OK to exit after verifying Software Version fitted, display will vary depending on software version fitted.
Serial Number
Write Success: .
ADJUST WITH
QUIT NEXT OK
Pump Reference
---------------------
ADJUST WITH
QUIT NEXT OK
Language
Dimming = 25%
ADJUST WITH
QUIT PARAM OK
QUIT OK
NEOI Warning
1. Select the required NEOI status can be enabled or disbaled by pressing ON or
OFF. NEAR END OF INFUSION
Note: ON is shown when the NEOI is disabled and OFF is shown when the NEOI
is enabled.
2. Press ACCEPT to confirm.
Note: ACCEPT will not be shown until after the first toggle of the status. Enabled
In Service Mode select Data Set Transfer using the f keys and the OK softkey.
1. Using the Alaris® GP Transfer Tool select data set to be uploaded.
2. Press the RS232 or IrDA softkey to select the Comms mode being used.
3. Connect the pump to PC.
4. Press the START softkey to begin transfer.
5. Please ensure the data set ID shown on the pump is identical to the one transferred.
6. Press PASS softkey to confirm correct transfer and exit.
7. To transfer the data set to another pump repeat steps 2 to 6.
In Service Mode select Data Set Transfer using the f keys and the OK softkey.
1. Using the Guardrails® Editor V3.1 Transfer Tool Transfer Tool select data set to be uploaded.
2. Connect the pump to PC.
3. Press the START softkey to begin transfer.
4. Please ensure the data set ID shown on the pump is identical to the one transferred.
5. Press ACCEPT softkey to confirm correct transfer and exit.
6. To transfer the data set to another pump repeat steps 2 to 5.
Caution: Loading the Data Set Transfer Tool software is considered a non-clinical service activity. Interconnecting the
A pump with a PC may cause the safety or electromagnetic environment to change while the connection exists. The
threat of higher leakage currents or EMI disturbances may be present. Disconnect the IrDA or RS232 cable connection
at both ends following software upload activities.
Upload data set to an Alaris® GP (Guardrails®) Volumetric Pump (with Plus software)
Equipment required:
• Alaris® Editor V4.2 Software Kit (1000SP01462) or Alaris® Transfer Tool Software Kit (1000SP01463)
• RS232 cable (1000SP01183)
• USB to RS232 Converter cable (1000EL00979)
• USB to RS232 converter 4 way hub (1000EL00980) - optional
• PC - for requirements see Upgrading Firmware PC requirements
Using the Alaris® Transfer Tool allows an approved data set to be uploaded to a pump (with Plus software).
Warning -
A At no time should the Alaris® Transfer Tool be used to upload to a pump while the pump is connected to a patient.
In Service Mode select Data Set Transfer using the f keys and the OK softkey.
1. Select the Data Set Upload button (Ctrl+U). The Data Set Upload Wizard is displayed. Click Next to continue.
2. Select the serial port(s) required to transfer the data set to the pump(s). Click Next to continue.
3. Click the Select Dataset button and Open the required data set. The selected data set and path are displayed. Click Next to
continue.
4. Enter the data set ID and click Validate. If the data set ID entered matches the ID of the selected data set the Next button will
become available. Click Next to continue.
5. The data set selection is now complete. Click Finish. The file information is updated to show the File used, Data Set and
Supported Pump Types.
6. Connect the pump to PC.
7. Press the START softkey to begin transfer.
8. When the transfer is complete, the pump will validate the data then display Transfer Complete. The transfer status will be shown as
Data Set Deployed to the Pump.
Note: Please ensure the data set ID shown on the pump is identical to the one transferred.
9. Press ACCEPT softkey to confirm correct transfer and exit. The transfer status will be shown as Deployed.
10. Switch off the pump by holding the power button for 3 seconds and disconnect from the PC.
11. If multiple uploads are required, connect the next pump and repeat from step 5.
12. When all uploads are complete, click Menu > Exit to close the Transfer Tool.
Caution: Loading the Transfer Tool software is considered a non-clinical service activity. Interconnecting the pump
A with a PC may cause the safety or electromagnetic environment to change while the connection exists. The threat of
higher leakage currents or EMI disturbances may be present. Disconnect the IrDA or RS232 cable connection at both
ends following software upload activities.
Calibration
Select the required option using the f keys and the OK softkey.
1. Wait for the pressure sensors to park.
2. Ensure that an infusion set is not installed.
CALIBRATION
Zero Point Cal
3. Press the START softkey.
Pressure Cal
4. Pump will countdown for 15 seconds.
Volumetric Cal
5. Press the ACCEPT softkey. Battery Cal
6. Press the PASS softkey.
SELECT WITH
QUIT OK
Pressure Calibration
Equipment required:
• Calibrated Pressure Gauge, minimum specification of
• Accuracy = 0.10% of full scale
• Full scale = 1500mmHg
• Pressure Calibration Set (1000SP01422) Use to calibrate 10 pumps and then
CALIBRATION
change Zero Point Cal
Set up equipment as per figure 2-1 and allow 30 seconds before proceeding. Pressure Cal
Select the required option using the f keys and the OK softkey.
Volumetric Cal
Battery Cal
1. Turn 3-way tap to close from atmosphere.
2. Press the START softkey.
3. Apply a pressure of 200mmHg and pump will countdown for 15 seconds.
4. Press the ACCEPT softkey.
5. Apply a pressure of 800mmHg and pump will countdown for 15 seconds.
SELECT WITH
6. Press the ACCEPT softkey.
QUIT OK
7. Turn 3-way tap to vent to atmosphere.
8. Turn 3-way tap to close from atmosphere.
9. Press the NEXT softkey to proceed to Verification Procedure.
Verification Procedure
Software version v1.7 x and below Software version v1.9.x and above
10. Apply a pressure of 200mmHg and wait for 5 seconds. 10. Apply a pressure of 500mmHg and wait for 5 seconds.
11. Press the NEXT softkey. 11. Press the NEXT softkey.
12. Apply a pressure of 400mmHg and wait for 5 seconds. 12. Turn 3-way tap to vent to atmosphere.
13. Press the NEXT softkey. 13. Press the PASS softkey.
14. Apply a pressure of 600mmHg and wait for 5 seconds.
15. Press the NEXT softkey.
16. Apply a pressure of 800mmHg and wait for 5 seconds.
17. Press the NEXT softkey.
18. Turn 3-way tap to vent to atmosphere.
19. Press the PASS softkey.
Pressure source
(50ml/100ml syringe or
similar device)
Pressure
Gauge Vent to Alar s®
GP
atmosphere
Volumetric Calibration
Select the required option using the f keys and the OK softkey.
1. Load the primed Infusion Set (60793) into the Pump and set-up as shown in
Figure 2-2 below and adjust the fluid level so that the meniscus is level with the
CALIBRATION
zero mark. Zero Point Cal
2. Press START to begin. Test will run and fluid will be delivered into the burette. Pressure Cal
3. When Volume delivered! is displayed, check accumulated air in line value Volumetric Cal
is less than 100µl then enter the volume delivered into the burette using the Battery Cal
f keys and the OK softkey. If accumulated air in line value is greater
than 100µl then repeat test.
4. If no calibration is required (Volume delivered within limits of 19.4ml to 20.5ml)
then press PASS to confirm and exit.
5. If the Calibration value is changed automatically then press VERIFY and repeat
steps 2 to 4. SELECT WITH
6. If the pump still fails replace the Platen and Fingers then repeat the calibration QUIT OK
procedure.
VOLUMETRIC CALIBRATION
Rate 125ml/h
VTBI 20.0ml
Cal Value 920
Acc’d Air 0µl
450mm
± 20mm
Al r s
GP
START to begin...
QUIT DETAILS START
Battery Calibration
Select the required option using the f keys and the OK softkey.
1. Connect AC Mains to the Pump and press CAL to begin.
2. When calibration is complete it will display CALIBRATION SUCCESS or
CALIBRATION
CALIBRATION FAILURE. Press PASS to confirm successful calibration or REPEAT Zero Point Cal
to perform calibration again. Pressure Cal
Volumetric Cal
Battery Cal
SELECT WITH
QUIT OK
3 Preventative Maintenance
Preventative Maintenance
To ensure the pump remains in good operating condition, routine and preventative maintenance inspections are required. Routine
maintenance inspections should be performed by hospital/facility before each use, see Directions For Use for details.
Preventative maintenance inspections should be performed at least every year.
For the preventative maintenance inspection the following should be performed:
• Full visual inspection of the pump, internal and external
• Fitting of all updates required
• Battery test and/or replacement
• Clean the pump
• Performance Verification Procedures
Following all spare part replacement and repair activities, testing must be performed in accordance with the
A Performance Verification Procedure (PVP). Additional testing and calibration may be required after certain repairs
are completed, see table in Chapter 6 ‘Corrective Maintenance’ for more information.
Visual Inspection
Open the pump, as per Chapter 6 ‘Corrective Maintenance’ and visually inspect the interior of the pump.
Visually inspect the exterior of the pump checking the following:
• Labels should be replaced as required if not flat, legible or fully adhered.
• Check Keypad for any sign of wear and replace as required.
• Case components must be checked for damage and replaced if necessary.
• Check the pole clamp is not damaged and that it functions correctly.
• Inspect the AC power supply plug and cable for damage.
• The case should be clean and free from IV solution residue, especially near moving parts.
• Check for dried solution deposits on accessible areas of pumping mechanism.
Door Removal
1. emove the screw securing the lower hinge lock.
R
2. Open the lower hinge lock.
3. Pull the door away from lower hinge pin and lift up to remove the door.
4. Clean the door.
5. Refit door in reverse order. Ensure screw is refitted with a torque of 70cNm.
Updates
Upgrading firmware
Recommended at the next service: If the Alaris® GP Guardrails® Volumetric Pump (SKU: 80263UN01-G) has
software versions V1.9.0 then upgrade to software version V1.9.2 or greater.
Mandatory: If the Alaris® GP Volumetric Pump (SKU: 80263UN01 or 80063UN01) has software versions V1.7.8 or
earlier then upgrade to software version V1.7.18.
Mandatory: If the Alaris® GP (Guardrails®) Volumetric Pump (with Plus software) (SKU: 9002MED01 or
9002MED01-G) has software versions V2.1.12 or earlier then upgrade to software version V2.1.14.
Complete and return the 'Software Upgrade Record' in the 'Appendix' section after performing any software
A upgrade.
Requirements
• PC
Minimum hardware system requirements: Software requirements:
• 1GHz Pentium processor • 512MB RAM • Microsoft Windows 2000 (service
pack 4), or XP (service pack 2)
• 1GB of free space on the system hard drive • CD ROM drive
• Available configurable RS232 9 pin serial or • Keyboard
USB communications ports
Preparation
• Load the SMU software onto the PC
• Connect RS232 connector (using USB to RS232 converter if required) to each pump being updated
• Disconnect the Battery
• Remove the Battery Compartment Plug
Battery
Compartment
Plug
Software Upload
1. Through the Rear Case, there is a set of three dip switches on the bottom of the Control PCB. Switch 1 should be ON and switches 2
and 3 should be OFF.
2. Using a small flat blade screwdriver or round ended tweezers configure the dip switch settings
to:
a) Switch 1 = OFF
b) Switch 2 = ON
c) Switch 3 = ON
3. Start the SMU facility to upload the software.
12. Refit the Battery Compartment Plug, this prevents fluid ingress.
13. Power up the pump in Service Mode, enter access code 212, then select Configuration > Date/Time and set the current date and
time.
If the Control, Interface or RS232 PCB is replaced, the pump must be re-programmed.
A
Battery pack
Battery Cover
The battery pack used in this Alaris® Volumetric Pump is manufactured by CareFusion and includes a proprietary
A PCB (printed circuit board) designed specifically for the Alaris® Volumetric Pump, and in conjunction with Alaris®
Volumetric Pump software, controls battery use, charge and temperature. Any use of battery packs that are not
manufactured by CareFusion in the Alaris® Volumetric Pump is at your sole risk, and CareFusion does not provide
any warranty for or endorsement on any battery packs that are not manufactured by CareFusion. CareFusion’s
product warranty shall not apply in the event the Alaris® Volumetric Pump has suffered damage or premature wear,
or malfunctions or otherwise operates incorrectly, as a result of use with a battery pack that is not manufactured by
CareFusion.
Select the required option using the f keys and the OK softkey.
PVP Work Flow Performance Verification Procedure (PVP) tests. TEST/VERIFY
Alarms Functionality Test the Alarms function correctly.
User Interface Display, Keypad, LEDs and Audio Tests. PVP Work Flow
Power Supplies Test AC Mains and Battery operation. Alarms Functionality
Sensor Tests Perform tests on the pump sensors. User Interface
Comms Tests RS232, IrDA and Nurse Call Tests. Power Supplies
Sensor Tests
Comms Tests
SELECT WITH
QUIT OK
Alarms Functionality
1. Press the START softkey to begin.
2. Pump starts an infusion.
3. Check all alarms sound and display correctly.
4. Alarms to test are:
• AC Mains Disconnect
• Door Open
• Upstream occlusion
• Air In Line
5. When all the alarms have been tested press the PASS softkey if all the alarms worked correctly or REPEAT softkey if alarms still need
to be checked.
ALARMS FUNCTIONALITY
AC Mains
Door Open
Upstream Occ
Air In Line
User Interface
Select the required option using the f keys and the OK softkey.
Chequerboard Display Chequerboard Test. USER INTERFACE
Keypad Tests Perform Keypad Test to check all keys work when pressed.
LED Tests Check all LEDs display in correct order.
Chequerboard
Audio Tests Check Primary and Secondary Audio sounders. Keypad Tests
LED Tests
Audio Tests
SELECT WITH
QUIT OK
Chequerboard Pattern
QUIT
Keypad Tests
1. Press the START softkey to begin.
2. Press all the keys and a P will indicate each key to pass.
3. Press PASS softkey to confirm pass and exit.
KEYPAD TESTS
[ .] [ .] [ .]
[ .] [ .] [ .] [ .]
[ .] [ .] [ .]
[ .] [ .] [ .]
START to begin...
START
LED Tests
1. Press the START softkey to begin.
2. Check LEDs are displayed correctly and P to pass. If an LED is not displayed then
press O to fail.
LED TESTS
3. Press PASS softkey to confirm pass and exit. Safety Processor
Primary Red
Secondary Red
Primary Amber
Secondary Amber
Start
Stop
Battery
START to begin...
QUIT START
Audio Tests
1. Press the START softkey to begin.
2. Check Audio sounds are correct and P to pass. If Audio sounds are not correct
then press O to fail.
AUDIO TESTS
3. Press PASS softkey to confirm pass and exit. Primary Audio
Working
Test
Secondary Audio
Test
START to begin...
QUIT DETAILS START
Power Supplies
Select the required option using the f keys and the OK softkey.
AC Mains Test Tests the AC mains removal detection. POWER SUPPLIES
Battery Test the battery. To perform calibration see Chapter 2
'Configuration & Calibration'. AC Mains Test
Battery
SELECT WITH
QUIT OK
AC Mains Test
1. Press the START softkey to begin.
2. Check AC Mains connected/disconnected is correctly indicated and press P
softkey or press O softkey if not correctly detected.
AC MAINS TEST
3. Press PASS softkey to confirm pass and exit.
AC Connection
START to begin...
QUIT DETAILS START
Battery
1. Review the battery information.
2. Press the DETAILS softkey to see further battery details. BATTERY CALIBRATION
3. Press QUIT softkey to exit.
Serial No 1001
Current 0mA
FCC 2714mAh
Chrg Remain 2477mAh
Rel Chrg 91%
Temperature 25°C
QUIT DETAILS
Sensor Tests
In Sensor Tests menu select required test using the f keys and the OK
softkey.
Flow Sensor Test Check Flow Sensor is connected and drops count.
SENSOR TESTS
Door Frame Test Check door registers as open and closed. Flow Sensor Test
Safety Clamp Test Check Safety clamp detection registers clamp enabled Door Frame Test
or disabled. Safety Clamp Test
Sear Test Check Sear detection registers sear enabled or disabled. Sear Test
Air In Line Test Check Air In Line sensor detects fluid and air correctly. Air In Line Test
Run-In Mode Performs a continuous infusion for burn in testing.
Run-In Mode
Pumping Effic’y Test
Pumping Efficiency Test This test is used to confirm that the Pump is able to
generate sufficient pressure. Pump Finger Height
Pump Finger Height Allows the mechanism to be parked. SELECT WITH
or Parking Test* QUIT OK
* Test name has changed to Parking Test for latest software versions however the
procedure is the same.
Test
START to begin...
QUIT DETAILS START
Test
START to begin...
QUIT START
Clamp enabled
Test
Opto Tx En 0mV
Opto Tx Dis 0mV
START to begin...
QUIT START
Sear Test
1. Press the START softkey to begin.
2. Check Sear in/out is correctly indicated and press P softkey or press O softkey if
not correctly detected.
SEAR TEST
3. Press PASS softkey to confirm pass and exit.
Working
Sear in place
Test
START to begin...
QUIT DETAILS START
Downstream: VALID
Detecting
START to begin...
QUIT DETAILS START
Run-In Mode
1. Load an Infusion Set.
2. Set the rate required using the f keys and press the START softkey to
begin test.
RUN-IN MODE
3. Press STOP softkey when test is completed.
4. Press PASS softkey to confirm pass and exit.
Rate 125ml/h
CHANGE RATE
START to begin...
QUIT START
450 mm
Pressure Gauge ± 20 mm
3-way tap A a is
GP
150 mm ± 5 mm
Parked
START to begin...
QUIT START
COMMS Test
Select the required option using the f keys and the OK softkey.
IrDA Test Check IrDA operates correctly. COMMS TESTS
RS232 Loop Back Check RS232 operates correctly.
Nurse Call Test Check Nurse Call operates correctly. IrDA Test
RS232 Loop Back
IrDA Test requires specialist equipment.
Nurse Call Test
A For further details please contact CareFusion.
SELECT WITH
QUIT OK
Apply loopback by
connecting pins 2 & 3
QUIT START
Monitor
Test
START to begin...
QUIT DETAILS START
Occlusion Test
This test can be only done as part of the PVP Work Flow.
Use the Infusion Set ten times only and then replace. Record how many times the Infusion Set has been used.
Note: The Occlusion Pressure Test is carried out with fluid in the Infusion Set.
This test is used to confirm that the pressure sensor is correctly calibrated and able to detect an occlusion at the correct line pressure.
This is done by pumping into a calibrated pressure gauge and checking that an alarm occurs at the correct line pressure. The test set-up
is as per figure 3 - 1.
1. Put the fluid filled Infusion Set (60793) into the Pump.
2. Enter the PVP Work Flow and proceed to the Occlusion Pressure Test.
3. Open the 3-way tap to atmosphere then press the LEVEL softkey to adjust the alarm level to L5.
4. Configure the Calibrated Pressure Gauge to hold the Peak/MAX Pressure reading, in preparation for the test.
5. Press the START softkey to begin running the Pump at a rate of 125ml/h. Allow the Pump to run for 1 minute, so that the pressure
reading stabilises.
6. Turn the tap to occlude the Infusion Set into the pressure gauge.
7. The Pump will continue to infuse and it will be observed that the pressure reading increases. Eventually a high-pressure alarm will
occur and the Pump will stop infusing. Note the reading on the pressure gauge and confirm that it is 500mmHg ±100mmHg.
8. Press PASS softkey if Pump passes test at all levels.
If the pressure is outside of tolerance pressure calibration is required. Calibration should be performed as per
A procedure in Chapter 2 ‘Configuration and Calibration’. If the pump continues to fail the occlusion test then the
pressure sensors should be replaced and perform the calibration procedure again.
Volumetric Accuracy
This test can be done as part of the PVP Work Flow or in the calibration menu.
1. Load the Infusion Set (60793) into the Pump and set-up as shown in Figure 3-2
below and adjust the fluid level so that the meniscus is level with the zero mark.
VOLUMETRIC CALIBRATION
2. Press START to begin. Test will run and fluid will be delivered into the burette.
3. When Volume delivered! is displayed, check accumulated air in line value
is less than 100µl then enter the volume delivered into the burette using the Rate 125ml/h
f keys and the OK softkey. If accumulated air in line value is greater VTBI 20.0ml
than 100µl then repeat test. Cal Value 920
4. If no calibration is required then press PASS to confirm and exit. Acc’d Air 0µl
5. If the Calibration value is changed automatically then press VERIFY and repeat
steps 2 to 4.
6. If the pump still fails replace the Platen and Fingers then repeat the calibration
procedure.
START to begin...
QUIT DETAILS START
450 mm
± 20 mm
A aris
GP
CH3
Inspection Physical inspection and clean
Check all functions in PVP Work Flow
Enter access code 212 and go to PVP Work Flow
• Software Versions
• Date/Time
• Serial Number
• Door Frame
• Safety Clamp
• Sear
Self TestCH3
• Audio Test
• Chequerboard
• LED’s
• Keypad
• Nurse Call
• RS232 Loop Back
• Pumping Efficiency Test
-- Time taken = 2 minutes or less ______ minutes ______seconds
• Downstream Occlusion Pressure Test
-- Occlusion alarm = 500 ± 100 mmHg ______________mmHg
• Alarms Functionality
____________________
Verification
Performed
By ____________________________ ____________________________ _____________________
Sign Print Date
CHX indicates the chapter number in the Technical Service Manual (TSM) - 1000SM00013.
E.G. CH2 = Refer to TSM Chapter 2.
4 Troubleshooting
Log Downloads
For Alaris® GP Pumps (with Plus software) the event log is downloaded via the Alaris® Transfer Tool (1000SP01463), refer to the relevant
Directions For Use for further details.
Warning -
A At no time should the Event Log be downloaded while the pump is connected to a patient.
For pumps with software version v1.9.x and above also download the Presentation Style Sheet to enable the logs
A to be viewed (this file only needs to be downloaded once). Also the downloaded event log needs to be stored in the
same directory as the Presentation Style Sheet. To view the downloaded event log open file with Microsoft Excel and
select style sheet.
Introduction
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 table lists the error messages and describes what action to take to resolve the problem. A
general fault diagnosis checklist is also provided. For information on alarm procedures and messages, refer to the DFU.
Parts to Check/Test
Interface PCB
Mechanism
Control PCB
Display PCB
Mains Lead
Power PCB
Front Case
Rear Case
Battery
Fuses
Door
Dropped or damaged
Exposed to fluids
General Fault
No battery power
No AC mains power
Delivery rates out of
tolerance
5 Circuit Descriptions
Functional Module Block Diagram
CHASSIS
GP PRESSURE
PCB UPSTREAM
J15 PRESSURE INTERFACE PCB
MEASUREMENT
GP PRESSURE J16 MODULE
PCB DOWN
STREAM
J6 ENCODER
MOTOR
ENCODER PCB INTERFACE
J7 MODULE
FLUID DELIVERY DROP SENSOR
PROCESSOR MODULE J5
AIL/SAFETY
MODULE
CLAMP HOUSING AIR IN LINE
J3 MODULE
DOOR DETECT J2
FLEXIBLE PCB
J8
SAFETY
J4 PROCESSOR
MODULE
BOOT FLASH
SD RAM
J9 J3
MAIN COMMS PCB
SD MEMORY PROCESSOR J1 J6 (RS232 &
CARD J2 MODULE NURSE CALL)
MEMBRANE
J9 KEYPAD
POWER
REGULATION
MODULE
POWER
MANAGEMENT
MODULE CONTROL PCB
J13 J11
BATTERY PACK
GAS GAUGE
PCB POWER SUPPLY IEC MAINS
J2 PCB J1 INLET
BATTERY
CELLS
Control PCB
The Control PCB is broken into a number of functional blocks. A description of each block follows:
Display PCB
This is an ISTN negative mode graphics display with built in temperature compensation.
GP Pressure PCB
Two pressure boards are used, one above the pumping mechanism to measure upstream pressure and one below to measure down
stream pressure. The tubing is compressed against a force transducer. As pressure builds up in the line the tubing expands and hence
the force measured increases. Similarly as the pressure falls the tubing contracts and the force decreases. The software converts the
force into a relative pressure measurement. The pressure board contains a silicon bridge force sensor, an instrumentation amplifier and
diagnostic systems to check gain and the voltage across the force sensor.
Motor
A three phase stepper motor coupled to the cam shaft by a toothed drive belt. The motor does 5,689 microsteps per ml.
Interface PCB
The Interface PCB provides all the low level control and monitoring functionality of the system. It is broken into the following functional
blocks:
Battery Pack
The battery pack contains a smart gas gauge device that provides charge information to the charger and the status of the battery
(capacity, voltage, current and temperature) to the main processor. The pack also contains a thermal fuse and thermal cut out. The
battery will be charged when ever the unit is connected to the main supply.
Power Supply
A universal input switched mode power supply used to regulate the mains input voltage.
Membrane Keypad
The membrane keypad consists of fourteen keys and LED’s to indicate battery, mains, start and stop. The on / off key connects to the
main processor and the safety processor. The safety processor manages the power up sequence and the main processor power down.
6 Corrective Maintenance
Ensure the pump is disconnected from the AC power supply and switched off before attempting to service.
A V The pump contains static-sensitive components and therefore strict ESD precautions should be observed at all
times.
Batteries should be disposed of as outlined by the local country regulations. Do not send batteries back to the
manufacturer.
Only use CareFusion recommended spare parts.
This chapter contains procedures required to properly disassemble, repair and replace parts and then to reassemble the pump.
Following all spare part replacement and repair activities, testing must be performed in accordance with the Performance Verification
Procedure (PVP), see Chapter 3, ‘Preventative Maintenance’. Additional testing and calibration may be required after certain repairs are
completed, see table below for more information.
Repair/Replacement of
AIL/Safety Clamp
Pressure Sensors
Chassis / Pump
Interface PCB
Mechanism
Control PCB
Display PCB
Power PCB
Front Case
Rear Case
Housing
Battery
Door
Performance Verification
Procedure
Test/calibration to perform
Battery Calibration
Volumetric Verification /
Calibration
Zero Point Calibration
Pressure Calibration
= Required
Blank = Optional
Torque Guide
The torque levels established during the manufacturing process are outlined in this chapter, for example 40cNm. Torque levels selected
apply throughout product life.
Use the information as a guide to the ‘do not exceed’ torque levels when servicing the pump. When servicing, it is recommended that
torque is applied gradually until the component is secure. In any process do not exceed the stated levels.
If a torque driver is available for servicing this will help control the applied torque; otherwise, be aware that excess force may cause the
component to fail.
• Always use the correct torque level when performing an assembly stage.
• Take care with the torque applied when re-assembling parts.
• The head patterns of the fasteners are of the following types:
-- Torx T8
-- Torx T10
-- Allen key 2mm
-- Small flat blade
-- Hex 4.5mm
-- Hex 10mm
• Always select the correct tool and bit pattern for the fastener.
Access to Pump
Replacement Procedure
1. Remove the two case screws with integral flat washer in battery cover, remove cover and battery.
2. Remove the five case screws with integral flat washer .
3. Carefully separate case halves.
4. Remove screw holding earth cable to mechanism and disconnect four other cables.
5. Where necessary, remove the feet and/or seal.
6. Reassemble in reverse order.
A Battery pack
B Battery Cover
B or E Feet
C Screw/Washer x5 40cNm
F Case seal
C Screw 70cNm
E Feet x2
A PSU
B IrDA PCB
AF AC
A AC Mains Mains Inlet C Screw
and Bracket (x2) 40cNm
Inlet Gasket
E PE Stud
C Washer
D Magnet
C Nut B IrDA PCB bracket
150cNm
Pole Clamp
Replacement Procedure
1. R emove three pole clamp screws.
2. Reassemble in reverse order.
A Pole Clamp
B Bung
Rail Cam
Replacement Procedure
1. Remove screw from lever release.
2. emove screw from lever rail cam.
R
3. Remove spring from the lever rail cam.
4. Reassemble in reverse order.
B Screw 70cNm
B Screw 70cNm
C Screw/washer 40cNm
C Screw 40cNm
A Comms PCB C Screw (x2) 40cNm
B RS232
Connector cover
D Flow Sensor
Connector cover
A RS232 Socket
Screw (x2) 40cNm
Handle
Replacement Procedure
1. Remove two screw from handle block.
2. Remove handle block, handle spring and handle.
3. Reassemble in reverse order.
Refitting notes:
• Make sure that the handle spring is in front of the handle and not behind it.
C Handle block
B Handle spring
A Handle
A Membrane
B Door
C Door Lever
Chassis assembly
Replacement Procedure
1. isconnect four cables from the Interface PCB and one cable from the Control PCB.
D
2. Remove the two screws securing the roller mounting.
3. Remove the roller mounting and gasket.
4. Remove the snap rivet securing the door detector flexible circuit.
5. Remove the two screws securing the chassis.
6. Carefully withdraw the chassis.
7. Reassemble in reverse order.
B Snap rivet
A Gasket
A Roller mounting
bracket
A Motor Insulator
F Encoder PCB
C Seal (x4)
Platten
When replacing the pumping mechanism (1000SP01247) the platten must be replaced with the platten supplied in
A the kit.
A Interface PCB
C Screw (x3)
65cNm
B Control PCB
Pillar supports (x3)
Recommended when serviced: Replace the SD card (1000SP01299) for Alaris® GP Volumetric Pumps with serial
numbers between 802608618 and 802611376 that had not exhibited a DSC2 fault prior to June 2008.
Display PCB
Replacement Procedure
1. R emove the two fixing screws from display frame.
2. Remove Display Frame and Gasket as required.
3. Reassemble in reverse order.
A Display
B Display Frame
AIL/Safety Clamp Housing, Top Retainer & Door Sensor Flexible Circuit
Replacement Procedure
1. Remove the four fixing screws from AIL/Safety Clamp Housing.
2. Remove AIL/Safety Clamp Housing and remove seal as required.
3. Remove one screw securing coloured insert as required.
4. Remove one screw from Top Retainer.
5. Remove Top Retainer and remove O ring as required.
6. Remove Door Sensor Flexible Circuit as required.
7. Reassemble in reverse order.
Refitting notes:
• Door Sensor Flexible Circuit is retained using hot melt glue.
• The Screw F for the insert torque is 25cNm instead of the original 10cNm due to the new insert plastic which is more tolerant
and will not crack. Any cracked Inserts should be replaced by the kit part number 1000SP01417.
F Screw 25cNm
F Insert
C Screw (x4) 65cNm
A AIL/Safety
Clamp Housing
B Door Sensor
E Seal
D Top Retainer
A Keypad
C.1
C3
C.1
2 x T 1.25A
Made in U.K. 20 x 5 mm 250V
100 - 230V ~ 50 - 60Hz 60VA (Max.) Alaris® GP
B
C.3
7 Appendix
Electromagnetic Compatibility
Warning:
• The use of any accessory, transducer, or cable with the Pump other than those specified may result in increased emissions or
decreased immunity of the pump.
• The Pump should not be used adjacent to or stacked with other equipment, however if adjacent or stacked use is necessary, the
Pump should be observed to verify normal operation in the configuration in which it will be used.
Caution:
• The Pump is a CISPR 11 Group 1 Class B 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.
The Pump is intended for use in the electromagnetic environment specified below.
The customer or the user of the Pump should assure that it is used in such an environment.
Emissions Test Compliance Electromagnetic Environment – Guidance
CISPR 11 The pump uses RF energy only for its internal function in the normal product
Group 1 offering. Therefore, its RF emissions are very low and are not likely to cause
RF Emissions any interface in nearby electronic equipment.
CISPR 11
Class B
RF Emissions
The pump is suitable for use in all establishments, including domestic, and
EN 61000-3-2 those directly connected to the public low-voltage power supply network that
Class A
Harmonic Emissions supplies buildings used for domestic purposes.
EN 61000-3-3
Voltage Fluctuations, Complies
Flicker Emissions
The Pump is intended for use in the electromagnetic environment specified below.
The customer or the user of Pump should assure that it is used in such an environment.
Compliance Level
Immunity Test EN 60601-2-24 Electromagnetic Environment – Guidance
EN 60601-1-2
<5 % UT
(>95 % dip in UT)
for 0.5 cycle
<5 % UT
(>95 % dip in UT)
for 5 sec
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—CareFusion recommends using signal cables of less than 3 metres in length and this requirement is applicable only if signal
cables are 3 metres or more in length. (EN 60601-1-2:2002, Clause 36.202.4)
3.5
d = [-----] √P
EN 61000-4-6 10 V rms
V1
Conducted RF (Note 3)
12
d = [-----] √P 80 MHz to 800 MHz
V2
EN 61000-4-3 10 V/m
Radiated RF (Note 3)
12
d = [-----] √P 80 MHz to 2.5 GHz
E1
23
d = [-----] √P 800 MHz to 2.5 GHz
E1
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 metres (m).a
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.
The Pump is intended for use in an electromagnetic environment in which radiated RF disturbances
are controlled.
The user of the Pump can help prevent electromagnetic interference by maintaining a minimum distance between portable and
mobile RF communications equipment (transmitters) and the Pump as recommended below, according to the maximum output
power of the communications equipment.
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.
Disposal
Ensure the pump is disconnected from the AC power supply and switched off before attempting to service.
A VThe pump contains static-sensitive components and therefore strict ESD precautions should be observed at all
times.
Following all spare part replacement and repair activities, testing must be performed in accordance with the
Performance Verification Procedure (PVP), see Chapter 3 ‘Preventative Maintenance’.
Only use CareFusion recommended spare parts.
Battery Removal
Removal Procedure
Remove the two case screws with integral flat washer in battery cover, remove cover and battery.
Battery pack
Battery Cover
Individual Components
Part Number Description
0000ME00141 Stud PE Connector M6 Thread X 15
0000ME00770 Bussmann Fuse Gmd-1.25a
1000EL00605 Drop Sensor Cable
1000EL00606 RS232 Nurse Call Cable
1000EL00607 PSU Cable
1000ME00291 Asena GW, Assy, Cover Dust Drop Sensor
1000ME00630 Handle Spring Asena LVP
1000ME00632 Asena LVP Handle Retaining Block
1000ME01845 Asena LVP Overmould Handle
1000ME00636 Asena LVP Mains Inlet Bracket
1000ME00655 Fuse Cover
1000ME01303 Magnet IR Detect
1000ME01745 Cover RS-232
1000ME00649 Foot Front Asena LVP
1000ME01611 Seal Case Nickel/graphite
1000ME00667 Asena LVP Assembly Membrane
0000ME00767 V Seals Hinge Pins V5a-nbr
1000EL00643 Door Detect Flexible Circuit
1000ME00701 Asena LVP GP Top Retainer
0000ME00691 Seal O Ring 6id 1csdia silicon
0000ME00423 Pad Self Adhesive Double Sided 12x12mm
Software
Part Number Description
1000SP01412 Alaris LVP GP F/ware Upgrade V1.7.18 Kit
1000SP01430 GP G/R S/W V1.9.2 (PKG8.9.16) SPARES KIT
1000SP01529 GP Field Action Kit V2.1.14 (RA-2010-01)
1000CD00028 Alaris SMU
1000SP01310 Alaris GP Editor Software Kit
1000SP01389 G/Rails Editor V3.1 - Software kit
1000SP01390 G/Rails Editor V3.1 - Trans Tool S/W kit
1000SP01462 Editor & Transfer Tool kit (Plus)V4.2.14
1000SP01463 Transfer Tool Kit (Plus) v4.2
Test Equipment
Part Number Description
60793 GP Series Infusion Set, 2 Y
1000EL00979 Converter Cable -usb To Serial
1000EL00980 Converter Cable -usb To 4x Serial
1000SP01183 Cable RS232 Filtered
1000SP01422 GP Field and Prod Press. Cal Set
1000SP01247 Alaris GP Pumping Mech (Minus Motor) Kit Alaris GP Pumping Mech 1
Rivet Snap 03 6 5/7.5 Panel Thickness 1
V Seals Hinge Pins V5a-nbr 6
Screw M3x8 Button Head With Patch 4
Machined Platen 2.900 1
1000SP01248 Alaris GP Front Case Kit Case Front Moulded Asena LVP 1
Alaris GP Keypad Bom 1
Asena LVP Assembly Membrane 1
Seal O Ring 6id 1csdia Silicon 1
Asena LVP GP Top Retainer 1
Screw M3 X 8 Pan Washer Head With Patch 1
Foam Gasket Display Asena LVP 1
Door Detect Flexible Circuit 1
Rivet Snap 03 6 5/7.5 Panel Thickness 1
Foot Front Asena LVP 2
Seal Case Nickel/graphite 1
V Seals Hinge Pins V5a-nbr 2
Adhesive Hot Melt Stick 12mm White 1
1000SP01250 Alaris GP Rear Case Kit Case Rear Moulded Asena LVP 1
Seal Case Nickel/Graphite 1
Alaris GP Label Set Bom 1
Spacer Speaker Label 1
1000SP01251 Alaris GP Mains Inlet Kit Mains Inlet Schaffner Fn9260b Inc Cable 1
Asena LVP Gasket Mains Inlet 1
1000SP01256 Alaris GP Comms PCB Kit Asena LVP Rs232 Nurse Call 1
Screw Lock Rs232 4-40 Unc -4-40 Unc 2
Gasket,pvc Foam,597/8/9 Fso 1
Insulator Rs232 PCB Asena LVP 1
Plastic Snap Rivet 1
1000SP01298 Alaris GP Control PCB Kit Asena LVP Control Card PCB 1
Rivet Memory Crd 1
Spacer PCB Richco Pst- 6-01 2
Asena LVP PCB Clip 3
1000SP01303 Alaris GP Roller Mounting Bracket Kit Assembly Roller Mounting Bracket 1
Gasket Assembly Roller LVP 1
Screw M3x4 Cap Head Shoulder With Patch 2
1000SP01254 Alaris GP Pressure Sensor Kit Housing Upper Pressure Sensor Asena LVP 1
Actuator Pressure Sensor Asena LVP 1
Asena GP Pressure Sensor PCB 1
Housing Lower Pressure Sensor Asena LVP 1
Flexi Pressure Board to Interface Board 1
1000SP01417 Spares Kit (Orange Clip & Screw) Insert Coloured Housing Flowstop AIL 1
Screw M2, 5 X 8 Csk Head, With Patch 1
Service Contacts
For service, contact your local Affiliate Office or Distributor.
AE CN GB NZ
CareFusion, CareFusion, CareFusion, CareFusion,
PO Box 5527, Shanghai Representative Office, Suite The Crescent, Jays Close, 14B George Bourke Drive,
Dubai, United Arab Emirates. A, Floor 24, Basingstoke, Mt Wellington 1060,
Shanghai Times Square Office Building, Hampshire, RG22 4BS, PO Box 14-518,
No.500 Zhangyang Road, United Kingdom. Panmure 1741, Auckland,
Shanghai 200122, China. New Zealand
Tel: (971) 4 28 22 842 Tel: (86) 21 58368028 Tel: (44) 0800 917 8776 Tel: 09 270 2420
Freephone: 0508 422734
Fax: (971) 4 28 22 914 Fax: (86) 21 58368017 Fax: (44) 1256 330860 Fax: 09 270 6285
AU DE HU SE
CareFusion, CareFusion, CareFusion, CareFusion,
3/167 Prospect Highway, Pascalstr. 2, Döbrentei tér 1, Hammarbacken 4B,
PO Box 355 52499 Baesweiler, H-1013 Budapest, 191 46 Sollentuna,
Seven Hills, NSW 2147, Deutschland. Magyarország. Sverige.
Australia.
Tel: (61) 2 9838 0255 Tel: (49) 2401 604 0 Tel: (36) 14 88 0232 Tel: (46) 8 544 43 200
Tel: (36) 14 88 0233
Fax: (61) 2 9674 4444 Fax: (49) 2401 604 121 Fax: (36) 12 01 5987 Fax: (46) 8 544 43 225
BE DK IT US
CareFusion, CareFusion, CareFusion, CareFusion,
Leuvensesteenweg 248 D, Firskovvej 25 B, Via Ticino 4, 10020 Pacific Mesa Blvd.,
1800 Vilvoorde, 2800 Lyngby, 50019 Sesto Fiorentino, San Diego, CA 92121,
Belgium. Danmark. Firenze, Italia. USA.
Tel: (32) 2 267 38 99 Tlf. (45)70 20 30 74 Tél: (39) 055 30 33 93 00 Tel: (1) 800 854 7128
Fax: (32) 2 267 99 21 Fax. (45)70 20 30 98 Fax: (39) 055 34 00 24 Fax: (1) 858 458 6179
CA ES NL ZA
CareFusion, CareFusion, CareFusion, CareFusion,
235 Shields Court, Edificio Veganova, De Molen 8-10, Unit 2 Oude Molen Business Park,
Markham, Avenida de La Vega, nº1, 3994 DB Houten, Oude Molen Road, Ndabeni,
Ontario L3R 8V2, Bloque 1 - Planta 1, Nederland. Cape Town 7405, South Africa.
Canada. 28108 Alcobendas, Madrid,
España.
Tel: (1) 905-752-3333 Tel: (34) 902 555 660 Tel: (31) 30 228 97 11 Tel: (27) (0) 860 597 572
Tel: (27) 21 510 7562
Fax: (1) 905-752-3343 Fax: (34) 902 555 661 Fax: (31) 30 225 86 58 Fax: (27) 21 5107567
CH FR NO
CareFusion Switzerland 221 CareFusion, CareFusion,
Sàrl Parc d’affaire le Val Saint Quentin Solbråveien 10 A,
Critical Care 2, rue René Caudron 1383 ASKER,
A-One Business Centre 78960 Voisins le Bretonneux Norge.
Zone d’activitiés Vers-la-Pièce France
n° 10
1180 Rolle / Switzerland
Ph.: 0848 244 433 Tél: (33) 1 30 05 34 00 Tel: (47) 66 98 76 00
Fax: 0848 244 100 Fax: (33) 1 30 05 34 43 Fax: (47) 66 98 76 01
Document History
Issue Date CO No. Author Update Description
1 20/01/06 5999 Ian Tyler Initial release
New Tech mode section.
Spare Part Replacement Procedures chapter added.
2 December 06 7111 Ian Tyler Troubleshooting chapter added.
New Software features added.
Spare Parts Listing appendix added.
Introduce Calibration information.
Update Preventative Maintenance information.
3 September 08 8587 Ian Tyler
Add information on the Alaris® GP Guardrails® Volumetric Pump.
Update Corrective Maintenance information.
4 March 10 10254 Ian Tyler Rebrand TSM
[Link]