LIFEPAK 3312981-000_B Code Management Module Instruction Manual Product Information

June 1, 2024
LIFEPAK

3312981-000_B Code Management Module

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Product Information

Specifications

  • Manufacturer: Fluke Biomedical
  • Model: CodeManagement Module
  • Part Number: 3312981-000_B

Product Usage Instructions

Performance Inspection Procedures (PIP)

The Performance Inspection Procedures (PIP) are manual test
procedures used for evaluating the CodeManagement Module’s
operational performance. These tests are essential to ensure that
the module operates within the required specifications.

When to Perform PIP

Perform the PIP as part of a regularly scheduled preventive
maintenance routine and after any repair, replacement, or
calibration procedure.

Equipment Required for PIP

  • Safety Analyzer: Fluke Biomedical ESA612 (or
    equivalent)

  • Digital Pressure Meter: Fluke Biomedical
    DPM2Plus (or equivalent)

  • Alligator Clip: Fluke P/N AC220 (or
    equivalent)

  • Cable Assemblies:

    • 3 Lead ECG: 11110-000029
    • 5 Lead ECG: 11110-000066
    • QUIKCOMBO Therapy Cable: 11110-000040
    • QUIK-COMBO to Snap Termination Cable: 3009139-001

Personnel Requirements

Service personnel conducting the PIP must be familiar with the
operation of the LIFEPAK 20e defibrillator and CodeManagement
Module. They must meet specific requirements related to biomedical
electronics.

Test Equipment Verification

All test equipment used for the PIP must have a current
calibration label from a certified calibration facility.

Workstation Power

The workstation power must be connected to a grounded power
source for safe operation.

Frequently Asked Questions (FAQ)

Q: Why is it important to perform the PIP?

A: The PIP ensures that the CodeManagement Module operates
within the required specifications and helps detect any
malfunctions or out-of-tolerance conditions that need
correction.

Q: What should service personnel be familiar with?

A: Service personnel must be familiar with the operation of the
LIFEPAK 20e defibrillator and CodeManagement Module, and meet
specific requirements related to biomedical electronics.

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CodeManagement Module

Section Contents

Performance Inspection Procedures

6
The Performance Inspection Procedures (PIP) are a set of manual test procedures used for an operational closed-case evaluation of the CodeManagement Module.This section describes the test procedures you will perform to determine if the CodeManagement Module is operating within the required specifications. Investigate and correct any malfunctions or out- oftolerance test conditions detected during the PIP.

The PIP comprises safety and performance tests recommended by AHA/ASHE (American Hospital Association/American Society for Hospital Engineering) Maintenance Management for Medical Equipment and International Electrotechnical Commission (IEC) Technical Report 1288-2, Maintenance of Cardiac Defibrillators-Monitors.

Perform the PIP as part of a regularly scheduled preventive maintenance routine. Also, perform the PIP after any repair, replacement, or calibration procedure.

PIP/TCP ­ Scope and Applicability PIP/TCP ­ Resource Requirements

PIP/TCP ­ Test Equipment Requirements

PIP ­ Instructions

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TCP ­ CO2 Calibration

PIP ­ Checklist

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CodeManagement Module
PIP/TCP ­ Scope and Applicability

Performance Inspection Procedures

The PIP applies to the CodeManagement Module exclusively. To complete the PIP, you must perform the combination of manual tests outlined in the PIP ­ Instructions section of this electronic service manual. All PIP tests applicable to the CodeManagement Module configuration under test must be performed.
Refer to the PIP/TCP ­ Resource Requirements for a listing of the necessary qualifications for PIP equipment, test equipment verification, workstation power, and personnel.
Refer to the PIP/TCP ­ Test Equipment Requirements for a listing of test equipment, including specifications, required to complete the PIP/TCP.

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CodeManagement Module

Performance Inspection Procedures

PIP/TCP ­ Resource Requirements

This section describes the requirements for PIP/TCP equipment, test equipment verification, workstation power, and personnel.

Equipment

To perform the PIP, you must use the equipment listed in the PIP/TCP ­ Test Equipment Requirements table. Although the table lists specific test equipment by manufacturer, test equipment with equivalent specifications may be substituted.

Test Equipment Verification

All test equipment used to perform the PIP must have a current calibration label, issued by a certified calibration facility.

Workstation Power

The ac line power to the workstation used must be connected to a grounded power source.

Personnel
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Service personnel who perform the PIP must be thoroughly familiar with the operation of the LIFEPAK 20e defibrillator and CodeManagement Module and must meet at least one of the following requirements (or the equivalent):
­ Associate of Applied Science, in the field of electronic technology. ­ Certificate of Technical Training, in the field of electronic technology. ­ Equivalent electronics experience with a preferred emphasis in
biomedical electronics.

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CodeManagement Module

Performance Inspection Procedures

PIP/TCP ­ Test Equipment Requirements

The following is a list of test equipment required to conduct the PIP/TCP.

Equipment/Cable

Specifications

Manufacturer/Part Number/ Catalog Number

Safety Analyzer

110 or 220 Vac line voltage Current range: 0-1999 mA
Current accuracy: 5% of reading or 1 digit (whichever is greater) Resistance range: 0-1.000 Ohm

Fluke Biomedical ESA612 (or equivalent)

ESA612 adapter box

Provides additional ECG snap connections.

Fluke Biomedical model 1210

Digital Pressure Meter

+/- 1% of full scale. Used as a vacuum manometer.

Fluke Biomedical DPM2Plus (or equivalent)

Alligator Clip

Used to access to LIFEPAK 20e defibrillator/monitor Fluke P/N AC220 (or equivalent) ground stud for electrical safety testing.

Cable Assembly, 3 Lead, ECG

Standard accessory with the 3-Lead LIFEPAK 20e defibrillator/monitor.

11110-000029

Cable Assembly, 5 Lead, ECG LIFEPAK 20e defibrillator optional accessory.

11110-000066

Cable Assy-Therapy, QUIKCOMBO

11110-000040

Cable, QUIK-COMBO to Snap Termination

For use in electrical safety testing with QUIK-COMBO 3009139-001 therapy cable.

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CodeManagement Module

Performance Inspection Procedures

PIP/TCP ­ Test Equipment Requirements

Equipment/Cable

Specifications

Cable Assy, LP20 SPO2 Test

For use in electrical safety testing.

Paddle Assy-Detachable, LP20

LIFEPAK 20e defibrillator/monitor optional accessory.

Adapter – Test, Paddles Leakage, For use in electrical safety testing with standard

LP12 & LP20

paddles.

QUIK-COMBO Leakage Cable

For use in electrical safety testing with standard paddles.

Cable, Test, ECG Snap to Banana Plug

For use in electrical safety testing.

RS-232 (DB9 M/F) Cable

USB to Serial Adapter (as required)

Computer

OS, Windows XP, 7

Software, CodeManagement Module Computer Assisted Test

Wireless network (WPA/WPA2 enterprise or personal)

Required to test Wireless functionality.

LIFENET Device Agent Component (LDA)

Used to check and calibrate CO2.

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Manufacturer/Part Number/ Catalog Number
3201832 (Multiple REF) 3200936 (Multiple REF)
3206631
3207066
3305684
Commercial Commercial
Commercial 3313963
Commercial
21340-000836

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CodeManagement Module

Performance Inspection Procedures

PIP/TCP ­ Test Equipment Requirements

Equipment/Cable

Specifications

Manufacturer/Part Number/ Catalog Number

Paper clip, Large
LIFEPAK 20e defibrillator/monitor with CodeManagement Module compatible software Tubing Assy – CO2 Calibration Filterline H Set Adult/Pediatric Chemical – Gas, Mixture, Calibration, Aerosol Tubing Assy – Service, CO2 Male Luer
Self powered 1.1 Compliant USB device AC power cable, hospital grade (USA) Stopwatch

Used to access the CodeManagement Module reset button.
For use in CO2 calibration and calibration check. For use in CO2 calibration and calibration check. For use in CO2 calibration and calibration check.
For use in CO2 leak testing. Used to connect CO2 tubing assy to CO2 exhaust port. Used as part of the computer assisted test software, 3313963, to test the USB interface. International users – local hospital grade cable is an acceptable substitution.

Commercial
Physio-Control, Inc.
21330-000239 11996-000068 21300-001572
21330-000238 Value Plastics MTLL250
Belkin 4-Port Hub F5U021V (or equivalent) Physio-Control 11140-000015 Commercial

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP ­ General Instructions

This section lists the general instructions for performing the Performance Inspection Procedure (PIP).
· All required PIP tests applicable to the CodeManagement Module under test must be performed.
· The PIP Checklist is provided as an optional tool for the recording of test results.
· Throughout the body of this PIP, the LIFEPAK 20e defibrillator/monitor is referred to as the defibrillator.
· Throughout the body of this PIP, the CodeManagement Module is referred to as the Device Under Test or DUT.
· Unless specified in the test step, the DUT should have a battery installed and be connected to AC power.

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

Warnings

WARNING!
Shock hazard. The LIFEPAK 20e defibrillator/monitor discharges up to 360 J of electrical energy through the defibrillator cable. You must safely discharge this electrical energy. Do not attempt to perform this procedure unless you are thoroughly familiar with the operation of the LIFEPAK 20e defibrillator/monitor and CodeManagement Module.

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP ­ Exterior Physical Inspection

To perform an exterior physical inspection: 1. Inspect the DUT exterior for the following:
­ Damage ­ Excessive wear ­ Improper mechanical function ­ Damaged connectors
2. Pick up and turn over the DUT and listen for loose or rattling hardware. Locate any loose or rattling hardware and tighten or replace it.
3. Inspect the rubber feet on the underside of the DUT. Reinstall or replace rubber feet as necessary.
4. Inspect carrying strap and storage bags for damage (if equipped).

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP- Power Port and AC Mains LED

To test the Power Port and AC Mains LED: 1. Verify the DUT battery is installed. 2. Disconnect the AC power cable from the DUT to the power source. 3. Verify the DUT AC Mains LED is OFF. 4. Connect the AC power cable from the DUT to the power source. 5. Verify the DUT AC Mains LED is ON. 6. Verify the defibrillator AC Mains LED is ON. 7. Turn ON the defibrillator and verify the defibrillator turns ON. 8. Turn the defibrillator OFF.

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP- Reset Button

To test the Reset Button: 1. Press and hold the reset button for a minimum of 1 second and release. Note: Use the straightened end of a large paper clip to access the reset button.

Note: Upon initial release of the reset button, all LEDs will glow steadily. After ~30-60 seconds, the AC mains LED will flash and then glow steadily.
2. Verify the DUT AC mains LED flashes, then glows steadily.

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP- CO2 Leakage Test

Note: Perform the CO2 tests if the device is equipped with the CO2 option. Otherwise, skip to PIP – Computer Assisted Tests.
To test the CO2 monitoring system for leaks:
Note: Make sure the defibrillator is turned OFF and no tubing is connected to the device.
1. Open the hose clamp on the CO2 leak test kit and depress the syringe fully.
2. Connect the tubing to the front panel CO2 connector. 3. Use P/N MTLL250 to connect the tubing to the back panel CO2 gas outlet. 4. Secure the fittings that connect to the device to avoid leakage.
vacuum manometer

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to vacuum manometer

CO2 leak test kit REF 21330-000238

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use P/N MTLL250 to connect tubing to back-panel gas outlet
to front-panel CO2
connector

DUT
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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP- CO2 Leakage Test (continued)

5. Pull the syringe plunger out to induce a vacuum into the system. When the vacuum manometer indicates approximately -250 mmHg +/- 50 mmHg, close the tubing clamp firmly.
6. Wait a minimum of three (3) seconds after closing the tubing clamp, then obtain an intitial vacuum reading.
7. Verify that after 30 seconds, the change in vacuum reading is less than 15 mmHg (20 mBars).
8. Disconnect the tubing connection from the front panel CO2 connector to release the vacuum.
9. Disconnect the tubing connection from the back panel gas outlet and release the tubing clamp.

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP- CO2 Calibration Check

To check CO2 calibration: 1. Connect the RS-232 (DB9 M/F) cable from the DUT to the test computer. 2. Launch the LIFENET Device Agent (LDA) from the test computer. 3. Follow instructions as prompted by the LDA to check CO2 calibration.

CO2 calibration kit REF 21330-000239

Cut CO2 filter line REF 11996-000068 to ~18 inches in length

Remove luer Fitting

to front-panel DUT CO2 connector

Calibration gas REF 21300-001572

DUT

4. Verify that the measured gas concentration reads 5.0% ± 0.3%. If the measured value is incorrect, perform the TCP ­ CO2 Calibration.
5. Disconnect the CO2 filter line from the DUT.

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CodeManagement Module

Performance Inspection Procedures

PIP ­ Instructions

PIP – Computer Assisted Tests
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The CodeManagement Module Computer Assisted Test software automatically tests the serial communication to the defibrillator, the USB interface, battery power, battery I2C, Wireless and Wireless switch functionality.
1. Ensure that an operational wireless network (WPA/WPA2 enterprise or personal) signal is being broadcasted.

2. Launch the CodeManagement Module Test software P/N 3313963 from the test computer and follow instructions as prompted.

Note: Use a USB to Serial adapter as required to connect the DUT to the test computer.

Note: If the DUT does not communicate with the test computer, remove both the battery and AC power from the DUT. Wait ~ 1 minute. Reinstall both the battery and AC power. Try the test again as necessary.

3. Verify all tests PASS.

Note:
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If any difficulty is observed during communication between the PC and

the CodeManagement Module while using a USB to Serial adapter, in

particular during the Wireless communications test, it is possible that the

Serial to USB adapter is configured incorrectly, or is incompatible with

the PC and/or its operating system. Replace the Serial to USB adapter

with an alternate model as necessary.

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP – Computer Assisted Tests (continued)

Note: A wireless communications test failure could be the result of the wireless signal. Retry the test as necessary.
4. Turn off the defibrillator and disconnect the RS-232 cable from the DUT. 5. Press the reset button on the side of the DUT to reboot the DUT. Note: Ensure the DUT completes the reboot before continuing (~1 min).

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

Electrical Safety Tests

Perform leakage current testing in accordance to the following electrical safety standards:
· IEC (International Electrotechnical Commission) 62353 · IEC (International Electrotechnical Commission) 60601-1 and 60601-2-4

Warning
SHOCK HAZARD. Failure to properly perform these tests could result in a failure to detect excessive leakage current. Make sure you are familiar with your test equipment and these test performance procedures.

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Leakage ­ Current flow induced by the application of high voltage to a material or object with high dielectric strength.
Earth Ground ­ Third wire ground.
Normal Condition (N.C.) ­ AC voltage is applied in either normal or reversed polarity (that is, measurements made with the POLARITY switch in both NORMAL [NC] and REVERSED [RM] positions). The earth ground is intact during these measurements.
Single Fault Condition (S.F.C.) ­ AC voltage is applied in either normal or reversed polarity (that is, measurements made with the POLARITY switch in both NORMAL [NC] and REVERSED [RM] positions). The earth ground is NOT intact during these measurements.
Note: Ensure the RS-232 cable is not connected to the DUT during electrical safety testing.
Note: Safety analyzer setup instructions are specific to the Fluke Biomedical ESA612.

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CodeManagement Module

Performance Inspection Procedures

PIP ­ Instructions

PIP- Protective Earth Resistance LIFEPAK 20e Defibrillator Ground Stud

To test the Protective Earth Resistance from the defibrillator ground stud: 1. Turn the defibrillator OFF.
2. Set up the test as shown below.
Note: Use Alligator Clip P/N AC220 (or equivalent) to access the defibrillator ground stud through the DUT bridge opening for the DB15 port.

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3. Set the safety analyzer controls to measure Ohms by selecting the Ohm button on the safety analyzer.

4. Verify the measured protective earth resistance is less than 0.3 Ohms (120

and 240 Vac).
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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP- Protective Earth Resistance CodeManagement Module Ground Stud

To test the Protective Earth Resistance from the CodeManagement Module ground stud: 1. Turn the defibrillator OFF.
2. Set up the test as shown below.

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3. Set the safety analyzer controls to measure Ohms by selecting the Ohm button on the safety analyzer.

4. Verify that the measured protective earth resistance is less than 0.3 Ohms

(120 and 240 Vac).
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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP- Leakage Current Setup

To set up the remaining leakage current tests:
Note: Reference the figures below for test setup using QUIK-COMBO therapy cable and test setup using STANDARD PADDLES.
1. Connect a banana cable between the CodeManagement Module ground stud and the safety analyzer V/Ohm/A output.
2. Connect the customer ECG Lead (5-wire or 3-lead) cable between the defibrillator and the 1210 box.
3. Connect the 1210 box to the safety analyzer at RA snap with an ECG snap to banana plug cable.
4. Connect the Therapy cable (QUIK-COMBO or Standard Paddles) between the defibrillator and the safety analyzer at LL and LA snaps.
5. Connect the AC power from the CodeManagement Module to the safety analyzer AC output.
6. Connect the SpO2 Leakage cable (if equipped) between the defibrillator and the safety analyzer at RL snap.

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Warning

SHOCK HAZARD. Do not defibrillate when connected to the safety analyzer.

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CodeManagement Module
PIP ­ Instructions
PIP- Leakage Setup

Performance Inspection Procedures
QUIK-COMBO Therapy Setup

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CodeManagement Module
PIP ­ Instructions
PIP- Leakage Setup

Standard Paddles setup

Performance Inspection Procedures

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

Earth Leakage Test Setup

To perform the Earth Leakage test in accordance with IEC 60601, set up the safety analyzer as follows:
­ Press the SETUP button on the safety analyzer ­ Press the F4/MORE button ­ Press the F2/INSTRUMENT button ­ Press the F1/STANDARD button ­ Press the UP/DOWN arrows to select the 60601 standard ­ Press the DONE button

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP – Earth Leakage Test – Normal Condition (NC)

1. Turn the defibrillator ON. 2. Press the µA button on the safety analyzer.
3. Press the F1/EARTH button on the safety analyzer and set the safety analyzer controls as follows:

Neutral Closed

Polarity Normal/Reverse

Current Mode AC only

Note: Pause briefly between switching polarity to prevent damage to the defibrillator.
4. Verify the DUT AC Mains LED is ON.
5. Verify the defibrillator AC Mains LED is ON.
6. Verify the measured current is between 15 µA and 300 µA (120 Vac) or between 15 µA and 500 µA (240 Vac).

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

PIP – Earth Leakage Test – Single Fault Condisiont (SFC)

1. Verify the defibrillator is ON. 2. Press the µA button on the safety analyzer.
3. Press the F1/EARTH button on the safety analyzer and set the safety analyzer controls as follows:

Neutral Open

Polarity Normal/Reverse

Current Mode AC only

Note: Pause briefly between switching polarity to prevent damage to the defibrillator.
4. Verify the DUT AC Mains LED is OFF.
5. Verify the defibrillator AC Mains LED is OFF.
6. Verify the measured current is between 15 µA and 1000 µA (120 and 240 Vac).

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

Direct Equipment Leakage and Direct Applied Part Leakage Test Setup
PIP – Direct Equipment Leakage Test – Single Fault Condition (SFC)

To perform the Direct Equipment Leakage and Direct Applied Part Leakage tests in accordance with IEC 62353, set up the safety analyzer as follows:
­ Press the SETUP button on the safety analyzer ­ Press the F4/MORE button ­ Press the F2/INSTRUMENT button ­ Press the F1/STANDARD button ­ Press the UP/DOWN arrows to select the 62353 standard ­ Press the DONE button
1. Verify the defibrillator is ON.
2. Press the µA button on the safety analyzer.
3. Press the F1/DIRECT EQUIPMENT button on the safety analyzer and set the safety analyzer controls as follows:

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Earth Open

Polarity Normal/Reverse

Current Mode AC only

4. Verify the DUT and defibrillator AC Mains LEDs are ON.

5. Verify the measured current is between 15 µA and 300 µA (120 Vac) or between 15 µA and 500 µA (240 Vac).

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CodeManagement Module

Performance Inspection Procedures

PIP ­ Instructions

Direct Applied Part Leakage Test Setup
PIP – Direct Applied Part Leakage Test ECG

To set up the safety analyzer to measure Direct Applied Part Leakage: ­ Press the µA button on the safety analyzer ­ Press the F4/MORE button ­ Press the UP/DOWN arrows to select the appropriate A.P. groups ­ Press F1/SELECT then F1/Direct A.P.
1. Verify the defibrillator is ON.
2. Press the LEFT/RIGHT arrows to select the RA lead, and set the safety analyzer controls as follows:

Polarity Normal/Reverse

Lead
RA (ECG group from Fluke 1210 adapter)

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Warning

Shock Hazard. During Direct Applied Part Leakage tests, high voltage is present on the safety analyzer electrode snaps. Do not touch snaps or device connections during these tests.

3. Press the TEST button to measure the Direct Applied Part Leakage current.

4. Verify the DUT and defibrillator AC Mains LEDs are ON.

5. Verify the measured current is between 2 µA and 45 µA(120 and 240 Vac). 3312981-000_B

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

Direct Applied Part Leakage Test – Therapy

1. Verify the defibrillator is ON.
2. Press the LEFT/RIGHT arrows to select the LL and LA leads, and set the safety analyzer controls as follows:
Note: The A.P. group should be set up to measure the combined leakage of the LL and LA leads.

Polarity Normal/Reverse

Lead
LL-LA (Therapy group)

3. Press the TEST button to measure the Direct Applied Part Leakage current.

Warning
Shock Hazard. During Direct Applied Part Leakage tests, high voltage is present on the safety analyzer electrode snaps. Do not touch snaps or device connections during these tests.

4. Verify the DUT and defibrillator AC mains LEDs are ON.
5. Verify the measured current is between 2 µA and 5000 µA (120 and 240 Vac).

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CodeManagement Module
PIP ­ Instructions

Performance Inspection Procedures

Direct Applied Part Leakage Test – SpO2

Note: Execute this test if the LIFEPAK 20e defibrillator/monitor is equipped with SpO2.
1. Verify the defibrillator is ON.
2. Press the LEFT/RIGHT arrows to select the RL lead and set the safety analyzer controls as follows:

Polarity Normal/Reverse

Lead
RL (SpO2 group)

3. Press the TEST button to measure the Direct Applied Part Leakage current.

Warning
Shock Hazard. During Direct Applied Part Leakage tests, high voltage is present on the safety analyzer electrode snaps. Do not touch snaps or device connections during these tests.

4. Verify the DUT and defibrillator AC Mains LEDs are ON. 5. Verify the measured current is less than 5000 µA (120 and 240 Vac).

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CodeManagement Module
PIP – Leakage Current Test Limits

Performance Inspection Procedures

Leakage Current Test Limit Summary TABLE – IEC 62353 Leakage Test Limits

Leakage Test to be Performed

Test Conditions

Range at 120V, 60HZ Range at 240V, 50HZ

ECG Direct Applied Part

Normal Reversed

2 – 45 µA 2 – 45µA

2 – 45 µA 2 – 45µA

Therapy (Apex, Sternum) Direct Applied Part Normal Reversed

2 – 5000 µA 2 – 5000 µA

2 – 5000 µA 2 – 5000 µA

SPO2 Direct Applied Part

Normal Reversed

0 – 5000 µA 0 – 5000 µA

0 – 5000 µA 0 – 5000 µA

Direct Equipment Leakage

Normal, Open Earth Reversed, Open Earth

15 – 300 µA 15 – 300 µA

15 – 500 µA 15 – 500 µA

Protective Earth Resistance

Measured from CodeManagement Module ground stud

0.3 Ohms

0.3 Ohms

Protective Earth Resistance
TABLE – IEC 60601 Leakage Test Limits

Measured from LIFEPAK20/20e defibrillator ground stud

0.3 Ohms

0.3 Ohms

Leakage Test to be Performed

Test Conditions

Range at 120V, 60HZ Range at 240V,50HZ

Earth Leakage Current

Normal Condition

15 – 300 µA

Single Fault Condition 15 – 1000 µA

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15 – 500 µA 15 – 1000 µA

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CodeManagement Module

Test and Calibration Procedure

TCP ­ Scope and Applicability

Test and Calibration Procedure

This section contains the Test and Calibration Procedures (TCP). Perform this section as necessary after replacing components or to correct out- ofspecification conditions detected during the PIP.
Refer to the PIP/TCP ­ Resource Requirements for a listing of the necessary qualifications for PIP equipment, test equipment verification, workstation power, and personnel.
Refer to the PIP/TCP ­ Test Equipment Requirements for a listing of test equipment, including specifications, required to complete the PIP.
Throughout the body of this TCP, the CodeManagement Module is referred to as the Device Under Test or DUT.

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CodeManagement Module
TCP ­ Instructions

Test and Calibration Procedure

TCP ­ CO2 Calibration

Note: Perform this test only if PIP- CO2 Calibration Check fails or if required by the LIFENET Device Agent (LDA).
To calibrate CO2: 1. Connect the RS-232 (DB9 M/F) cable from the DUT to the test computer.
2. Launch the Lifenet Device Agent (LDA) from the test computer. 3. Follow instructions as prompted by the LDA to calibrate CO2.

CO2 calibration kit REF 21330-000239

Cut CO2 filter line REF 11996-000068 to ~18 inches in length

remove luer fitting

to front-panel DUT CO2 connector

Calibration gas REF 21300-001572
4. Verify that the CO2 calibration was successful.

DUT

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