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General| Device Type | Defibrillator/Monitor |
|---|---|
| ECG Monitoring | Yes |
| Battery Type | Lithium-ion |
| Operating Temperature | 0°C to 50°C (32°F to 122°F) |
| Storage Temperature | -20°C to 60°C (-4°F to 140°F) |
| Altitude | Up to 15, 000 feet |
| Monitoring Parameters | ECG, SpO2, EtCO2 |
| Waveform | Biphasic Truncated Exponential (BTE) |
| Humidity | 5% to 95% (non-condensing) |
Lists registered trademarks and trademarks used in the manual, including company and software brands.
Instructions on how to view and use the bookmark pane for manual navigation.
Details on how to jump between topics and pages using links and footer navigation.
Specifies the required qualifications and familiarity for service personnel working with the device.
Defines key terms like Danger, Warning, Caution, and Note used for safety communication.
Provides essential safety warnings and cautions for handling the device and preventing hazards.
Lists and explains various safety symbols used on the device and in the manual.
Overview of the LIFEPAK 20 defibrillator/monitor as an acute cardiac care response system.
Details the physical components, controls, indicators, and connectors of the device.
Lists optional configurations, supplies, and accessories available for ordering with part numbers.
Explains the device's medical capabilities, therapeutic features, and monitoring functions.
Introduction to the operating instructions, familiarizing operators with device functions and controls.
Covers unpacking, controls, connectors, patient data entry, and setup options.
Details on monitoring the ECG and SpO2 parameters.
Information on therapy delivery, paddle accessory options, and cleaning guidelines.
Covers general maintenance, testing, service, repair, and product recycling information.
Explains how to configure device settings, including manual, AED, pacing, and monitoring menus.
Details on determining when to deliver a shock and configuring turn-on options in manual mode.
Describes automatic evaluation of patient rhythm and prompts for shock delivery in AED mode.
Explains how to configure operating defaults, save configurations, and create passcodes.
Details functions for qualified service personnel, including calibration routines and device tests.
Defines the applicability of PIP tests to the LIFEPAK 20 defibrillator/monitor.
Outlines requirements for PIP equipment, test equipment verification, workstation power, and personnel.
Lists all necessary test equipment and their specifications required to conduct the PIP.
Provides general instructions and detailed procedures for performing various PIP tests.
Summarizes leakage current specifications for various tests, detailing maximum allowable values.
Defines the scope of TCP procedures, applicable only to the LIFEPAK 20 defibrillator/monitor.
Lists requirements for TCP equipment, verification, workstation power, and personnel qualifications.
Lists all necessary test equipment and specifications required to conduct TCP procedures.
Describes the setup requirements for the LIFEPAK 20 defibrillator/monitor for TCP execution.
Details the procedure for performing defibrillator calibration, including analyzer connections and steps.
Explains how to verify the defibrillator's delivered energy output against specified acceptable limits.
Explains how error codes are logged, their causes, and the procedure for processing them.
Provides a guide to diagnose observed symptoms and suggests corrective actions for various areas.
Lists error codes, their descriptions, and recommended corrective actions for system issues.
Details how to access and use service/status screens for device data, logs, and counters.
Explains the data included in the Device Log, such as manufacturing date and operation counters.
Describes how to clear flash data management memory, including ECG data and patient reports.
Outlines the schedule for preventive maintenance activities, including inspections and cleaning.
Lists tools and materials for external and internal cleaning of the device.
Provides guidance on storing the device during long periods and recycling at the end of its life.
Describes the main backup battery and the coin battery, including their specifications and lifespan.
Explains the built-in high-current charger and the process for recharging the backup battery.
Provides criteria for identifying end-of-life batteries and guidelines for recycling them.
An index of detailed disassembly and reassembly procedures for various device components.
Highlights critical warnings and cautions related to servicing, handling capacitors, and reassembly.
Details precautions for handling electronic semiconductor devices susceptible to static discharge damage.
Instructions for constructing and using a tool to safely discharge the energy storage capacitor.
Procedures for saving device setup configuration via transfer or printout and restoring it later.
Illustrates the major assemblies of the device, including front, top, bottom, boardstack, power, and printer.
Information on software replacement and device upgrades, requiring authorized Medtronic personnel.
Details on checking configuration data integrity and identifying potential loss or corruption.
Explains how to identify and understand the device's part number and serial number for ordering.
Provides instructions for ordering parts, including contact information and required details.
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