Physio Control LIFEPAK 15 User manual

Title
LIFEPAK 15 Monitor Defibrillator CO2 Upgrade
Page
1 of 33
Doc Type
Service Process Document
Doc ID
3308217
Doc Rev
A
Doc State
Released
State Date
09/08/2011
Owner
Corporate
Attachments (Optional):
Qty
Pages
Page
Sequencing
Change Description
Create field service update of the LIFEPAK 15 Monitor/Defibrillator to add CO2 monitoring capability
This document is electronically signed in the Physio-Control, Inc. Product Lifecycle Management (PLM) System. Approvals can be
obtained from the PLM system which displays the selected approvers, their approval roles, and approval dates.
PROPRIETARY AND CONFIDENTIAL DOCUMENT FOR PHYSIO-CONTROL, INC. USE ONLY. This document is property of Physio-
Control and may not be used, reproduced, published or disclosed to others without authorization from Physio-Control.

Title
LIFEPAK 15 Monitor Defibrillator CO2 Upgrade
Page
2 of 33
Doc Type
Service Process Document
Doc ID
3308217
Doc Rev
A
Doc State
Released
State Date
09/08/2011
Purpose:
This instruction guides the Field Service Representative through the update process to add the CO2 feature to a LIFEPAK® 15
monitor/defibrillator.
Scope:
This upgrade is for 3206720-All (Version 1) and 3306272-All (Version 2) LIFEPAK 15 monitor/defibrillators that do not have the End-Tidal
Carbon Dioxide (CO2) monitoring feature installed.
These instructions are intended for authorized field service personnel who have reviewed the upgrade procedure and who are familiar with
the LIFEPAK 15 device.
Training:
As a prerequisite, only personnel that have completed LIFEPAK 15 monitor/defibrillator repair training are allowed to perform this upgrade
on a LIFEPAK 15 device. An individual will be considered fully trained when they meet the prerequisite, and read and understand this
document. Once this task is performed the individual has completed training. A documented training record will be retained.
Tools Required: (substitute of equivalent or better equipment allowed)
Computer –XP operating system
LIFEPAK 15 To PC Interconnect Cable 3009817-00 or 3009817-002
Torque Driver –Hand Operation, with an adjustable range of 5–12 in-lb.
Torque Driver –Hand Operation, with an adjustable range of 32–64 in-oz.
Driver Bits –P0 (2” minimum shaft), P1 (2” minimum shaft), P2 (5” minimum shaft), Torx, T-15 (2” minimum shaft)
Tools called out in the PIP - TCP sections of LIFEPAK 15 Monitor/Defibrillator PIP Test Procedure
All tools requiring calibration should be calibrated and within their calibration cycle dates.
Torque Driver conversions –2 lb-in = 32 in-oz = 22.5 cNm, 4 lb-in = 64 in-oz = 45 cNm, 6.8 lb-in = 77cNm, 10 lb-in = 113 cNm
Documentation Required:
Instructions –Installation, Software, Combined Loader P/N 3206073 revision N or greater
LIFEPAK 15 PIP/TCP Procedure P/N 3207841 revision D or greater
LIFEPAK 15 Service Manual, CD P/N 3208091-000 (V1) or 3309059-000 (V1/V2)
Work Instructions –CAPIP Test P/N 3301593.C or greater

Title
LIFEPAK 15 Monitor Defibrillator CO2 Upgrade
Page
3 of 33
Doc Type
Service Process Document
Doc ID
3308217
Doc Rev
A
Doc State
Released
State Date
09/08/2011
Materials Required:
Part Number
Description
Qty
3207813-XXX
Or
3305642-XXX
(V1) LABEL SET-(configured per kit)
(V2) LABEL SET-(configured per kit)
1
3012121-002
RETAINER-CO2 CONN
1
3012140-006
MODULE, CO2, MINI
1
202253-760
SCREW-M,PH,NYLOK,CS,4-40,.250L
4
3012397-01
CABLE ASSY-CO2, ADAPTER
1
3007997-01
SEAL-CO2 CONNECTOR
1
3012119-02
ADAPTER-CO2 CONNECTOR
1
3012140-008
FRS ASSEMBLY-CO2, MINI-MODULE, LP15
1
3206998-002
CABLE ASSY-CO2 MODULE, OEM PCB
1
3012140-002
EXHAUST TUBING-CO2
1
202253-732
SCREW-MACH,NYLOK,PNH,PHH,2-56X0.500,CS,ZN
4
3207337-312
SCREW-MACH,PNH,PHH,NYLOCK,4-40,0.312L,WSHR,CS,ZN
4
201407-069
SCREW,SELF-SEAL,SELF-LOCK,6-32 X 0.375
14
202253-760
SCREW-M,PH,NYLOK,CS,4-40,.250L
8
202253-761
SCREW-M,CS,Z,PH, NYLOCK, 4-40 X .312L 12
13
202253-763
SCREW,MACHINE,PANHEAD,NYLOK,4-40 X .437
2
3207361-375
SCREW-CAP,SCH,REC 15IP TORX PLUS,6-32,0.375L,SS
8
Warnings and Cautions:
LETHAL VOLTAGES MAY BE PRESENT INSIDE THIS DEVICE. THE STORAGE CAPACITOR MUST BE
DISCHARGED PRIOR TO PERFORMING ANY WORK WITHIN THE REAR CASE ASSEMBLY.
FAILURE TO DISCHARGE THE STORAGE CAPACITOR MAY RESULT IN INJURY OR DEATH.
General Requirements:
Unless specifically noted, all removed fasteners are to be discarded and new fasteners used for reassembly.
All removed parts with adhesive backing are to be discarded and new parts used for reassembly.
Unless specifically noted, all removed parts, except fasteners and adhesive backed parts, are to be kept with the device being
upgraded and re-used to reassemble the device.
Inspect all removed components for damage during disassembly and replace all damaged parts with new parts.

Title
LIFEPAK 15 Monitor Defibrillator CO2 Upgrade
Page
4 of 33
Doc Type
Service Process Document
Doc ID
3308217
Doc Rev
A
Doc State
Released
State Date
09/08/2011
Work Instruction Icon Definitions:
Work
Content
1
1st Person
Verify
Torque
!
Caution
Shock
Hazard
E
N
S
W
Orient
Clean
Work Content: The value add activity being done at the operation. Create a text box in this color to highlight the parts being
added.
1st Person Verify: Checking a person’s own work. This can be added as part of a pair of verifications driven from risk
assessment or can be called out by itself based upon some business need. Good verification practice
involves multiple senses (usually touch and look).
Torque: Use with any fastener that has a specific torque specification. Call out the specific torque requirement in
association with this symbol (measure and units). A fastener can be screws, bolts, nuts, or another
mechanical fastening device.
Caution: When a specific operation requires extra attention. It can be something that is challenging to perform, has a
higher likelihood of being performed incorrectly, or could present some level of risk to the person performing
the process.
Shock Hazard: When a person is exposed to something that contains electrical energy. Most likely during disassembly after
a unit has been energized.
Orient: When the orientation of the part matters and it could be assembled multiple ways. Making sure that labeling is
readable is the most common example.
Clean: For cosmetics or for adhesive preparation. The default cleaning material is chem-wipes. Call out if any
additional materials are to be used (such as alcohol) and the purpose of the cleaning.
1. Verify the Device Serial Number
Verify that device’s serial number label matches the serial number listed in the upgrade kit documentation.
2. Initial Power-Up Check
Install a fully charged battery onto the LIFEPAK 15 Monitor/Defibrillator. Press the ON key. Verify that the
device powers up with no service indicator light. If the service indicator light is illuminated, do not proceed
with this upgrade, and repair per the appropriate LIFEPAK 15 Monitor/Defibrillator repair process. If the
service indicator light is not illuminated, power off the device, remove the battery and continue with upgrade.
3. Downloading Device Data (Pre-Service Report Download)
FOR INTERNATIONAL, Use your normal service reporting process to document the service activity.
Open a service report and download the device data to the service report before proceeding with disassembly
of the device.
TORQUE
TORQUE
TORQUE
XX.X In-Lb

Title
LIFEPAK 15 Monitor Defibrillator CO2 Upgrade
Page
5 of 33
Doc Type
Service Process Document
Doc ID
3308217
Doc Rev
A
Doc State
Released
State Date
09/08/2011
4. Disassembling the Case
4.1 If applicable, remove carrying case.
4.2 Remove all cables and patient connections,
and then remove the batteries.
4.3 Remove the four front mounting screws
(3207361-375) from the bumpers. (Torx-15)
4.4 Remove the four rear mounting screws
(3207361-375) from the bumpers. (Torx-15)
4.5 Remove the bumpers (3207307-001 and
3206968-000) from the case and set aside.
Remove Screws
(4 places)
Remove Screws
(4 places)