Trademarks Stryker or its affiliates own, use, or have applied for the following trademarks or service marks: CODE-STAT, Code Summary, cprINSIGHT, DT EXPRESS, LIFENET, LIFEPAK, LIFEPAK FLEX, QUIK-COMBO, REDI-PAK, ProCare, SAS, Shock Advisory System, SideKick, STJ Insight, Stryker.
Replacements and adjustments must be made by qualified service personnel. To obtain service and maintenance for your device, contact your local Stryker service or sales representative. In the USA, call Stryker’s technical support at 1 800 STRYKER. Outside the USA, contact your local Stryker representative.
Operating Instructions. Recycling Information The LIFEPAK 35 device should be recycled at the end of its useful life. See below for details. Recycling assistance: The device and its accessories should be recycled according to national and local regulations. For instructions on disposing of this product or its accessories, contact your local Stryker representative, or see stryker.com/ec-recycling.
Stryker has no information regarding the performance or effectiveness of its LIFEPAK defibrillators if they are used in conjunction with defibrillation electrodes or other parts and supplies from other sources. If device failure is attributable to defibrillation electrodes or other parts or supplies not provided by Stryker, this may void the product warranty.
Some symbols may not be relevant to your device or used in every country. Additional symbols may be found in the LIFEPAK 35 monitor/defibrillator Visit ifu.stryker.com for additional information about symbols that are defined in standards Operating Instructions.
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Use By date shown: YYYY-MM-DD Keep electrodes away from direct sunlight and heat sources. Recommended storage temperatures of 15° to 35°C (59° to 95°F). See Specifications in the LIFEPAK 35 monitor/defibrillator Technical Manual for detailed shelf life/temperature information. Recommended storage atmospheric pressure range 50 to 106 kPa Do not reuse Do not dispose of this product in the unsorted municipal waste stream.
Caution: Hazards or unsafe practices that may result in minor personal injury, product damage, or property damage. General Dangers and Warnings The following are the general danger and warning statements. Keep them in mind when working with the LIFEPAK 35 monitor/defibrillator. Additional specific warnings and cautions appear throughout this service manual and in the LIFEPAK 35 monitor/defibrillator Operating Instructions.
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, Temp, IP, and NIBP cables that are specified for use with this device. Protection of the device against defibrillator discharge is dependent on the use of cables that are specified by Stryker. Refer to the LIFEPAK 35 monitor/defibrillator Operating Instructions.
CAUTION Possible skin injury. The LIFEPAK 35 monitor/defibrillator may become warm when used for an extended period of time. Prolonged contact between exposed skin and a warm device may cause skin irritation or burns. If a warm device is placed against a patient, the operator should ensure that the patient's skin is adequately protected.
3. Device Description LIFEPAK 35 monitor/defibrillator General Description The LIFEPAK 35 monitor/defibrillator (LP35) is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient management protocols. This section provides a high-level description of the LIFEPAK 35 device and basic specifications. For more operation and technical information, refer to the LIFEPAK 35 monitor/defibrillator Operating Instructions or the LIFEPAK 35 monitor/defibrillator Technical Manual.
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The device meets functional requirements during exposure to the following environments unless otherwise stated. For additional information about environmental specifications, refer to the LIFEPAK 35 monitor/defibrillator Technical Manual. See the LIFEPAK 35 monitor/defibrillator Operating Instructions for a list of compatible accessories.
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Cleaning • Stryker SideKick disinfecting wipes • Sodium hypochlorite (5.25%-6.15% bleach diluted 1:10) For additional information on cleaning, refer to the LIFEPAK 35 monitor/defibrillator Operating Instructions. Withstands 480 applications of the following: Chemical resistance • Ethyl or isopropyl alcohol (70-90%) •...
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Shock hazard. If you are monitoring a patient and using any of the peripheral connector ports, all equipment connected to the ports must be battery powered or electrically isolated from AC power according to IEC 60601-1. Use only accessories that are approved by Stryker with these ports. For more information, contact Technical Support.
Note: The following setup options are available for the readiness alert indicator: Alert when device is turned off and not connected to auxiliary power See setup options in the LIFEPAK 35 monitor/defibrillator Technical Manual for information about setup options. LIFEPAK ®...
Insert each battery until it clicks. To remove a battery, squeeze the device operating instructions. latch and remove battery from well. Symbol for “Defibrillation-proof type CF applied part.” Symbol for “Warning: Use only accessories approved by Stryker.” See safety information in section 2. LIFEPAK ®...
1. Press the release button on the therapy cable connector. 2. Slide the therapy cable out. Note: Therapy cables for use with LIFEPAK 15 and 20e devices are not compatible with the LIFEPAK 35 monitor/defibrillator. Use only the therapy cable specified above.
FOR MORE INFORMATION Access port. Connects to optional printer. Also connects to a PC See data management in the running Stryker applications that support transfer of device and device operating instructions. patient data, updates to setup options, and update software.
Figure 9 AC power adapter connector The LIFEPAK 35 AC power adapter plugs directly into the back of the device. To connect, push the plug firmly into the connector until it clicks. To disconnect, rotate the ring on the plug counterclockwise and pull.
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1. Squeeze the battery latch. 2. Remove the battery from the well. For additional information about battery maintenance, refer to the preventive maintenance section of this manual, or the Battery Maintenance section of the LIFEPAK 35 monitor/defibrillator Operating Instructions. LIFEPAK ®...
Masimo Medtronic SunTech Power, therapy, monitoring, and other accessories are available for the LIFEPAK 35. For more detail, refer to the LIFEPAK 35 monitor/defibrillator Operating Instructions. For ordering information, contact Stryker. System Block Diagram The mechanical assembly block diagram below shows, at a high level, the major hardware modules and subassemblies which make up the LIFEPAK 35 monitor/defibrillator.
Functional Descriptions The functional descriptions that follow provide a basic understanding of the LIFEPAK 35 device design and its major components. It is intended to assist the qualified service technician in troubleshooting to the subassembly level. Troubleshooting below the subassembly level, outside the factory is not recommended, nor is it within the scope of this service manual to provide the detail necessary to support such repairs.
4. Modes of Operation The LIFEPAK 35 monitor/defibrillator has a number of operating and non-operating modes. The figure below maps the various operating and non-operating modes and shows transition paths between modes. Figure 13 Operating and non-operating modes Off Mode In off mode, no power is applied to the device, and device functionality including the ability to perform auto test is not available.
PIP/TCP. You can transmit current and archived data from the LIFEPAK 35 monitor/defibrillator to the LIFENET system using a Wi-Fi or cellular connection to the internet.
Important! Customer should follow Wi-Fi Security Best Practices (specifications chapter). Unsecured data could lead to unidentified risks to patients, operators, or third parties. For more information, refer to the LIFEPAK 35 monitor/defibrillator Technical Manual or the LIFEPAK 35 monitor/defibrillator Product Security Information.
Transmissions to LIFENET are executed when the device is turned off, and when the user runs Check for Updates in setup mode or manually initiates transmission of records. For detailed information on Wi-Fi connection and data transmission, refer to the LIFEPAK 35 monitor/defibrillator Operating Instructions.
6. Troubleshooting This section contains information pertaining to troubleshooting methods for LIFEPAK 35, including error code usage, interpretation, and corrective action. General troubleshooting tips may be found in the LIFEPAK 35 monitor/defibrillator Operating Instructions. General Troubleshooting The table below describes general troubleshooting tips, including possible causes of problems, and associated corrective actions.
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Time is incorrectly set time setting. incorrect Change the time setting on the device. See “Changing the Date and Time” in the LIFEPAK 35 technical manual. Connect to LIFENET System to automatically update Date printed on report is Date is incorrectly set date setting.
To run PSST, start the application, and follow the on-screen instructions. Device Logs Logs containing LIFEPAK 35 device information are structured differently from past LIFEPAK devices. The prognostic log contains a variety of different types of information, including the following: Device data: Static, non-changing asset data for an individual device, such as serial numbers, manufacture date, and hardware and software part numbers.
A table of current active service codes can be retrieved from the device, using a PC-based Stryker service application. Service codes and service code history may also be found in the LIFENET device fault log for devices that are enrolled in LIFENET. This information is vital to troubleshooting issues and will be viewed by service providers during device maintenance and repair.
Troubleshooting section above for guidance on interpreting and correcting issues. Test results, and the resulting readiness status, are transmitted to LIFENET when a Wi-Fi or cellular connection exists. Test logs may also be printed if a printer is connected. See the LIFEPAK 35 monitor/defibrillator Operating Instructions for more detail. Device User Tests User-initiated tests should be run to ensure that internal electrical components and circuitry work properly and that the device is ready for operation.
After completing a scheduled maintenance, reset the maintenance prompt interval timer, via PSST, to clear the MAINTENANCE DUE message and begin the count for the next scheduled maintenance. Device Service Life The LIFEPAK 35 monitor/defibrillator has an 8-year expected service life under normal use conditions and with appropriate periodic maintenance. LIFEPAK ®...
Test and Calibration Procedure – TCP The TCP may be used to calibrate certain functions of the LIFEPAK 35 when a device has failed a test, or requires calibration after replacing certain parts or modules within the device. The TCP is defined in a separate document.
Flashing yellow: door open, out of paper, over/under temperature, or printer fault Off: printer off The printer stops automatically if the paper runs out or the printer door is open. Refer to the LIFEPAK 35 monitor/defibrillator Operating Instructions for detailed instructions on loading printer paper.
Battery fuel gauge indicates three or fewer LEDs (bars) after the battery completes a charge cycle. FAULT indication during charging or use (Fault/Unrecognized Battery symbol on LIFEPAK 35 device screen or flashing red LED on LIFEPAK FLEX battery charger) BATTERY AT END OF SERVICE LIFE indication on LIFEPAK 35 device screen.
Test all the anti-static parts of the work area (mat, straps, and cables) routinely. Tools List The suggested list of tools for the LIFEPAK 35 monitor/defibrillator replacement procedures is as follows: Static-dissipative mat and wrist strap. Anti-static rack and/or conductive bags.
Ensuring that electrical connections are made properly during device servicing is important. This section describes different types of connectors used throughout the LIFEPAK 35 device, and how to connect and disconnect them completely and securely and without damage to ensure that they function as intended.
If a device has had a repair which includes a PCBA replacement, setup options and software will need to be restored via LIFENET Device Agent service repair mode. Note that only Stryker authorized personnel may perform this type of repair.
7. Install kickstand as described in Installing the Kickstand. 8. Execute the LIFEPAK 35 PIP. Power Plug Replacement Note: The standard power plug is shown in the following procedures. For the blade style connector, follow the same process, except as noted in the procedure. Refer to the assembly diagrams in section 9 for more detail.
5. Remove adhesive liner from back side of label. 6. Apply label, pressing firmly in place. 7. Execute the LIFEPAK 35 PIP. Label (L05) Printer Replacement The printer is an optional, non-repairable accessory. If it is damaged or inoperable, it may be replaced. Refer to the printer instructions for use.
Installing the Parameter E27 NIBP module) Module. 5. Execute the LIFEPAK 35 PIP. Removing the Patient Parameter PCBA To perform many of the parameter module repair procedures, the patient parameter PCBA must first be removed. This section describes how to remove the patient parameter PCBA, and the subsequent section describes how to install the patient parameter PCBA.
4. Install the patient parameter PCBA as described in Installing the Patient Parameter PCBA. 5. Execute the LIFEPAK 35 PIP. 6.8 in-lb Screw (4X F04) Connector Replacement (Masimo) The parts listed in the following table will be required to complete this repair. Reference...
4. Install the patient parameter PCBA as described in Installing the Patient Parameter PCBA. Connect V1.1.1 5. Execute the LIFEPAK 35 PIP. pictured here Pump Hose (M39) V1.1.2 pictured here Patient Parameter PCBA Replacement The parts listed in the following table will be required to complete this repair. Reference...
Installing the Parameter Patient Parameter Board Module, if not already completed. (A04) 5. Execute the LIFEPAK 35 PIP. Module Replacement (Medtronic) The parts listed in the following table will be required to complete this repair. Reference Parameter Module Assembly (-002, without temp/IP).
Replacement, steps 19-29, omitting steps already completed. 22. Install the parameter module as described in Installing the Parameter Module, if not already completed. 23. Execute the LIFEPAK 35 TCP – CO calibration. 24. Execute the LIFEPAK 35 PIP. Exhaust Port Replacement The parts listed in the following table will be required to complete this repair.
Press firmly to adhere to housing, routing wire as shown. 4. Connect fan connector to interface PCBA P312. 5. Assemble the case as described in Adhesive liner Assembling the Case. 6. Execute the LIFEPAK 35 PIP. Connect Aligning pin locations Fan Assembly (E10) LIFEPAK ®...
6. Assemble the case as described in Assembling the Case. Routing Guide 7. Execute the LIFEPAK 35 PIP. Video Display Flex Replacement The parts listed in the following table will be required to complete this repair. Reference Front Housing Assembly.
PCBA J307. 6. Assemble the case as described Assembling the Case. 7. Execute the LIFEPAK 35 PIP. Routing Guide Rotary Switch Replacement The parts listed in the following table will be required to complete this repair. Reference Front Housing Assembly.
Rotary Knob (M02) Interface PCBA Replacement Note: This repair may be performed only by Stryker service technicians. The parts listed in the following table will be required to complete this repair. Reference Front Housing Assembly. service bom ref description notes...
18. Restore device software and settings using LIFENET Device Agent in Service Repair Mode. 19. Execute the LIFEPAK 35 PIP. Display Power Cable Replacement The parts listed in the following table will be required to complete this repair. Reference Front Housing Assembly.
7. Assemble the case as described in Assembling the Case. 8. Execute the LIFEPAK 35 PIP. Keypad Replacement Note that replacement of the keypad requires replacement of the readiness indicator beacon. The parts listed in the following table will be required to complete this repair. Reference Configuration Assembly.
3. Assemble the case as described in Assembling the Case. 4. Execute the LIFEPAK 35 PIP. Inductive Resistor (E04) Energy Storage Capacitor Replacement The parts listed in the following table will be required to complete this repair. Reference Defib Assembly.
System PCBA Replacement Note: This repair may be performed only by Stryker service technicians. The parts listed in the following table will be required to complete this repair. Reference Defib Assembly. SERVICE BOM REF DESCRIPTION NOTES KIT, REPAIR, SYSTEM PCBA, LP35...
Energy Delivery PCBA Replacement Note: This repair may be performed only by Stryker service technicians. The parts listed in the following table will be required to complete this repair. Reference Defib Assembly. SERVICE BOM REF DESCRIPTION NOTES KIT, REPAIR, ENERGY...
Installing the Inductive Resistor. 6. Assemble the case as described in Assembling the Case. 7. Execute the LIFEPAK 35 PIP. Access Port Flex Replacement The parts listed in the following table will be required to complete this repair. Reference Rear Housing Assembly.
9. Assembly Diagrams and Parts Lists Assembly Diagrams The exploded-view diagrams below show the parts that make up the LIFEPAK 35 device, and are presented in the various subassemblies, with the hierarchy of subassemblies generally following the product structure. Reference numbers in the tables below map to parts in service bill of materials (BOM), and/or parts within service repair kits.
PCBA Stack Assembly SERVICE BOM REF DESCRIPTION NOTES ASSY, PCBA STACK, LP35 ASSY, PCB, ENERGY Available only as part of DELIVERY, LIFEPAK 35 repair kit(s). HEADER, BOARD STACKER, .100 IN, 44 PIN HEADER, BOARD STACKER, .100 IN, 8 PIN GUIDE, BATTERY...
This information may be found on the serial label on the back of the device, or if the device is powered on, may be found on the touch screen via the menu under System, or via LIFENET Device Agent. Note that if the device rear housing is being replaced, a new serial label will need to be requested from Stryker service.
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LIFEPAK ® 35 monitor/defibrillator SERVICE MANUAL For further information, call Stryker at 1 800 STRYKER or visit stryker.com Stryker Emergency Care P.O. Box 97006 Redmond, WA 98073-9706 USA + 1 800 STRYKER + 1 800 787 9537 + 1 425 867 4000 stryker.com...
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