LIFEPAK 1000 DEFIBRILLATOR ® OPERATING INSTRUCTIONS
® LIFEPAK 1000 DEFIBRILLATOR OPERATING INSTRUCTIONS
Important This instrument is to be used by authorized personnel only. !USA Rx Only !USA Device Tracking The U.S. Food and Drug Administration requires defibrillator manufacturers and distributors to track the location of their defibrillators.
TABLE OF CONTENTS 1 Preface About Defibrillation ....................................................................................................... vi Indications for Use ........................................................................................................ vi Defibrillation ............................................................................................................ vi ECG Monitoring.....................................................................................
Defibrillation in Manual Mode .................................................................................... 3-6 Analysis ................................................................................................................ 3-6 Troubleshooting Tips for Defibrillation ....................................................................... 3-7 ECG Monitoring (ECG Mode) .....................................................................................
PREFACE 1 This section provides information about defibrillation and an overview of the LIFEPAK® 1000 defibrillator. About Defibrillation page vi Indications for Use vi Operator Considerations vii About the LIFEPAK 1000 Defibrillator vii Text Conventions viii LIFEPAK 1000 Defibrillator Operating Instructions ©2006-2012 Physio-Control, Inc.
Preface ABOUT DEFIBRILLATION Defibrillation is a recognized means of terminating certain potentially fatal arrhythmias. A direct current defibrillator applies a brief, high-energy pulse of electricity to the heart muscle. The Physio-Control LIFEPAK® 1000 defibrillator is an automated external defibrillator (AED) that delivers this energy through disposable defibrillation electrodes applied to the patient's chest.
Preface OPERATOR CONSIDERATIONS The LIFEPAK 1000 defibrillator requires operator interaction to defibrillate the patient. The defibrillator is intended for use by personnel who are authorized by a physician or medical director and have, at a minimum, the following skills and training.
Preface cprMAX™ Technology The cprMAX technology is designed to allow resuscitation protocols to maximize the amount of CPR administered during treatment using the LIFEPAK 1000 defibrillator. When used with the factory default settings enabled, the defibrillator allows AED protocols to be consistent with the 2005 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care and European Resuscitation Council Guidelines for Resuscitation.
SAFETY 1 This section provides important information to help you operate the LIFEPAK 1000 defibrillator. Familiarize yourself with all of these terms, warnings, and symbols. Terms page 1-2 General Warnings and Cautions 1-2 Symbols 1-3 LIFEPAK 1000 Defibrillator Operating Instructions ©2006-2012 Physio-Control, Inc.
Safety TERMS The following terms are used either in this manual or on the LIFEPAK 1000 defibrillator. Danger: Immediate hazards that will result in serious personal injury or death. Warning: Hazards or unsafe practices that could result in serious personal injury or death. Caution: Hazards or unsafe practices that could result in minor personal injury, product damage, or property damage. GENERAL WARNINGS AND CAUTIONS The following section provides general warning and caution statements.
Safety WARNINGS! (CONTINUED) Possible device shutdown. Always have access to a spare, fully-charged, properly maintained battery. Replace the battery when the device displays a low battery warning. Possible improper device performance. Using other manufacturers’ cables, electrodes, or batteries may cause the device to perform improperly and invalidates the safety agency certification and may invalidate the warranty. Use only the accessories specified in these operating instructions.
Safety Service symbol OK Symbol indicating self-test completed successfully Use By or Install By date shown: yyyy-mm-dd or yyyy-mm This end up Fragile/breakable. Handle with care.
Safety Symbol indicating location of battery compartment Recommended storage temperature: 15° to 35°C (59° to 95°F). Storage at extreme temperatures of -30° and 60°C (-22° and 140°F) is limited to seven days. If storage at these temperatures exceeds one week, the electrode shelf-life will be reduced. Recommended shipping temperature: -20° to 50°C (-4° to 122°F).
Safety CAT Catalog number REF Reorder number SN Serial number Rx Only or Rx Only By prescription only IP55 1-6 Enclosure ingress protection code per IEC 60529 LIFEPAK 1000 Defibrillator Operating Instructions
CONTROLS AND INDICATORS 2 This section provides a description of each of the LIFEPAK 1000 defibrillator primary controls and indications. Controls and Indicators page 2-2 Battery Indicators 2-5 Battery Charger Indicators 2-6 LIFEPAK 1000 Defibrillator Operating Instructions ©2006-2012 Physio-Control, Inc.
Controls and Indicators CONTROLS AND INDICATORS This section introduces you to the controls and indicators on the LIFEPAK 1000 defibrillator. 1 10 9 8 9 (Left side) 2 7 3 6 (Left side) 4 5 Figure 2-1 Controls and Indicator Table 2-1 Controls and Indicators 1 Feature Description Readiness display The readiness display alerts you to the defibrillator’s readiness status. Three symbols ( , , ) allow you to determine whether the defibrillator is ready for use or needs attention.
Controls and Indicators Table 2-1 Controls and Indicators (Continued) Feature 3 ON Description Green ON/OFF button turns the power on or off. The button is lit whenever the defibrillator is on. ON/OFF button Pressing the SHOCK button (when flashing) delivers a shock to the patient. 4 SHOCK button 5 Used to select operating modes (Manual or AED) and enter information in Setup mode. MENU button 6 Battery compartment Accommodates a single battery.
Controls and Indicators Shock indicator Heart rate indicator Battery status symbol Message area Elapsed time ECG Prompts Enter Manual Mode? Softkey label YES NO Menu button Softkeys Figure 2-2 Defibrillator Screen Heart rate indicator. The heart rate indicator displays heart rates between 20 – 300 bpm. Indicator is present in Manual mode or when the 3-wire ECG cable is used. Battery status symbol.
Controls and Indicators BATTERY INDICATORS The LIFEPAK 1000 defibrillator can be powered by two types of batteries: • A nonrechargeable Lithium manganese dioxide battery • A rechargeable Lithium-ion battery Battery Charge Level Indicators Both battery types have a fuel gauge that indicates the approximate charge level of the battery when it is not installed in a defibrillator. Push the gray button below the battery symbol to check the battery’s charge level before installing it in the defibrillator.
Controls and Indicators least once every six months thereafter. When optimally maintained, a new fully-charged battery provides approximately ten hours on “ON time” or 261 discharges at 200 joules. Since all rechargeable batteries permanently lose battery capacity over time, and because battery capacity together with the level of battery charge determines how long a rechargeable battery will provide defibrillator power, you can expect that a fully-charged battery’s “ON time” will decrease with age.
HOW TO USE THE LIFEPAK 1000 DEFIBRILLATOR 3 This section provides an overview of information and instructions for using the LIFEPAK 1000 defibrillator. Modes of Operation page 3-2 Defibrillation in AED Mode 3-3 Defibrillation in Manual Mode 3-6 Troubleshooting Tips for Defibrillation 3-7 ECG Monitoring (ECG Mode) 3-9 LIFEPAK 1000 Defibrillator Operating Instructions ©2006-2012 Physio-Control, Inc.
How to Use the LIFEPAK 1000 Defibrillator MODES OF OPERATION You can use the LIFEPAK 1000 defibrillator for: • Automated external defibrillation (AED mode) • Manual defibrillation therapy (Manual mode) (Requires ECG display option) • ECG monitoring (ECG mode) (Requires ECG display option) Defibrillation Warnings and Cautions WARNINGS! Shock hazard. The defibrillator delivers up to 360 J of electrical energy. When discharging the defibrillator, do not touch the disposable therapy electrodes. Shock hazard.
How to Use the LIFEPAK 1000 Defibrillator DEFIBRILLATION IN AED MODE The LIFEPAK 1000 defibrillator uses the patented Physio-Control Shock Advisory System to evaluate the patient’s heart rhythm. The LIFEPAK 1000 defibrillator has an optional feature that displays the ECG waveform and Heart Rate Indicator in AED mode. The operation in AED mode remains the same whether or not the defibrillator displays the ECG waveform. When ECG DISPLAY is set to ON, the ECG appears with all of the AED messages and prompts.
How to Use the LIFEPAK 1000 Defibrillator 6 Connect the electrodes to the defibrillator (if they are not already connected). 7 Follow the screen messages and voice prompts provided by the defibrillator. Voice Prompts and Messages in AED Mode The following descriptions of voice prompts and messages are based on the default settings for AED mode. Changing the setup options may result in different AED behavior.
How to Use the LIFEPAK 1000 Defibrillator Special Situations for Electrode Placement When placing electrodes on the patient, be aware of special situations: Obese Patients or Patients with Large Breasts Apply the electrodes to a flat area on the chest, if possible. If skin folds or breast tissue prevent good adhesion, spread skin folds apart to create a flat surface. Thin Patients Follow the contour of the ribs and spaces when pressing the electrodes onto the torso.
How to Use the LIFEPAK 1000 Defibrillator DEFIBRILLATION IN MANUAL MODE The LIFEPAK 1000 defibrillator provides a Manual mode to override the AED features of the defibrillator. Manual mode provides operator-initiated analysis, charge, shock, and disarm functions. This mode is useful in a tiered response system when a provider trained in manual defibrillation and authorized to place the defibrillator in Manual mode takes over the scene from a BLS-AED trained provider.
How to Use the LIFEPAK 1000 Defibrillator TROUBLESHOOTING TIPS FOR DEFIBRILLATION This section explains problem conditions that you may encounter while using the defibrillator. Table 3-1 Troubleshooting Tips for Defibrillation Observation Possible Cause What To Do Screen blank and ON LED lit. Screen not functioning properly. • AED and therapy functions may still operate. If needed for therapy, follow voice prompts and continue to use device to treat patient.
How to Use the LIFEPAK 1000 Defibrillator Table 3-1 Troubleshooting Tips for Defibrillation (Continued) Observation Possible Cause MOTION DETECTED and STOP MOTION voice prompts are heard. Patient movement because of • Move patient to stable location, if location. possible. Patient movement because of breathing. • Check patient for normal breathing. CPR being performed during analysis. • Stop CPR during analysis. Vehicle motion. • Stop vehicle during analysis, if possible.
How to Use the LIFEPAK 1000 Defibrillator ECG MONITORING (ECG MODE) WARNING! Possible misinterpretation of ECG data. The frequency response of the screen is intended only for basic ECG rhythm identification; it does not provide the resolution required for pacemaker pulse visibility, accurate measurements, such as QRS duration, and ST segment interpretation. For such purposes, use ECG monitors with an appropriate frequency response. Possible delay in therapy.
How to Use the LIFEPAK 1000 Defibrillator Troubleshooting Tips for ECG Monitoring If problems occur while monitoring the ECG, check this list of observations for troubleshooting assistance. Table 3-2 Troubleshooting Tips for ECG Monitoring Observation Possible Cause What to Do Screen blank and ON LED lit. Screen not functioning properly. • Contact authorized service personnel. • AED and therapy functions may still operate. If needed for therapy, continue to use device to treat patient.
How to Use the LIFEPAK 1000 Defibrillator Table 3-2 Troubleshooting Tips for ECG Monitoring (Continued) Observation Possible Cause What to Do Poor ECG signal quality. Poor electrode-to-skin contact. • Reposition cable and/or lead wires to prevent electrodes from pulling away from patient. Secure cable clasp to patient’s clothing. • Clean, shave, and dry the patient’s skin as recommended on page 3-3. • Replace electrode(s). Outdated, corroded, or dried-out electrodes.
DATA MANAGEMENT 4 This section introduces data management for the LIFEPAK 1000 defibrillator. Managing Defibrillator Data LIFEPAK 1000 Defibrillator Operating Instructions ©2006-2012 Physio-Control, Inc.
Data Management MANAGING DEFIBRILLATOR DATA The LIFEPAK 1000 defibrillator provides an infrared method to transfer defibrillator data. Overview of Data Storage Every time you use the defibrillator, it digitally saves patient data that can be transferred to a PC. You can provide patient data to aid in case review for quality control, training, and research purposes. You should become familiar with local requirements for reporting a use of the LIFEPAK 1000 defibrillator and for providing use data.
Data Management Test and Service Data The LIFEPAK 1000 defibrillator stores a test log consisting of the most recent auto-tests, power cycles, and battery replacements. The test log lists the test results and any errors detected. The test log data is available only to authorized service personnel or to responders who are using the appropriate LIFENET system product. Event and Test Log Table 4-3 and Table 4-4 list the types of events that may be annotated on event and test log reports.
Data Management Note: The shaded cone in Figure 4-1 represents the approximate parameters for positioning the defibrillator’s IrDA port opposite the IrDA adapter. As the distance between the two increases, so does the possible range for aligning them. Distance: 1 meter (3.28 feet) Alignment Range: 30° IrDA Adapter/ Computer 15° Defibrillator 15° Figure 4-1 IrDA Connections You initiate and control transmission of device data at your computer using a LIFENET system product.
CARING FOR THE LIFEPAK 1000 DEFIBRILLATOR 5 This section explains how to help keep your LIFEPAK 1000 defibrillator in good working condition. Cared for properly, the defibrillator is built to give you many years of service.
Caring for the LIFEPAK 1000 MAINTENANCE AND TESTING SCHEDULE Use the following schedule in conjunction with the internal quality assurance program of the hospital, clinic, or emergency medical service where the defibrillator is used. On a regular basis, you should do the following: • Check the readiness display to determine the level of battery charge and that the OK symbol is visible. • Check the Use By date on the therapy electrode packet.
Caring for the LIFEPAK 1000 Auto Tests The defibrillator performs automatic self-tests daily and monthly at 0300 (3:00 a.m.) if not in use. During the automatic self-test, the defibrillator turns itself on (ON/OFF LED illuminates) briefly and completes the following tasks: • Performs a self-test • Stores the self-test results in the Test Log • Turns itself off If the defibrillator detects a problem during an auto test that requires service, it displays the service symbol.
Caring for the LIFEPAK 1000 CLEANING Clean the LIFEPAK 1000 defibrillator accessories as described in Table 5-3. Use only the cleaning agents listed in the table. CAUTION! Possible equipment damage. Do not clean any part of the defibrillator or accessories with bleach, bleach dilution, or phenolic compounds. Do not use abrasive or flammable cleaning agents. Do not steam, autoclave, or gas-sterilize the defibrillator or accessories.
Caring for the LIFEPAK 1000 LIFEPAK 1000 Defibrillator Nonrechargeable Battery The nonrechargeable battery never requires recharging. The approximate level of charge in the battery is indicated by the fuel gauge on the battery, on the readiness display when the defibrillator is off, or on the screen when the defibrillator is in use.
Caring for the LIFEPAK 1000 Any patient or training use of the defibrillator, including “ON” time and shocks, reduces the battery’s charge level. Battery charge also decreases while the battery is in the defibrillator because of the battery’s normal self-discharge rate and the energy used by the defibrillator auto tests.
Caring for the LIFEPAK 1000 WARNINGS! Possible loss of power and delay of therapy during patient care. • Using an improperly maintained battery to power a defibrillator may cause power failure without warning. Follow these instructions for proper care of the battery. • Stored batteries lose charge. Failure to charge a stored rechargeable battery before use may cause device power failure without warning. Always charge a stored rechargeable battery before placing it in active use.
Caring for the LIFEPAK 1000 PRODUCT RECYCLING INFORMATION All materials should be recycled according to national and local regulations. Contact your local Physio-Control representative for assistance or refer to www.physio-control.com/recycling for instructions on disposing of this product. Preparing for Disposal of Nonrechargeable Batteries Nonrechargeable batteries should be fully discharged before disposal.
Caring for the LIFEPAK 1000 Table 5-4 Supplies, Accessories, and Training Tools (Continued) Item Description 3-Wire Monitoring Cable (IEC) Quick Reference Card IrDA Adapter (attachment for a PC) CODE-STAT Data Review Software DT EXPRESS™ Data Transfer Software WARRANTY INFORMATION Refer to the product warranty statement included with your LIFEPAK 1000 defibrillator. For duplicate copies, contact your local Physio-Control representative.
APPENDIX A SPECIFICATIONS LIFEPAK 1000 Defibrillator Operating Instructions ©2006-2012 Physio-Control, Inc.
Specifications SPECIFICATIONS All specifications are at 20°C (68°F) unless otherwise stated. Defibrillator Waveform Biphasic Truncated Exponential with voltage and duration compensation for patient impedance. With Adult Pads: Patient Impedance Range: 10 – 300 ohms The following specifications apply from 25 to 175 ohms.
Specifications Waveshape and Measured Parameters: I1 T1 I2 I4 T2 I3 Patient Impedance () I1 (A) I2 (A) I3 (A) I4 (A) T1 (ms) T2 (ms) 25 50.3 20.1 19.7 10.7 5.9 3.9 50 28.2 14.6 14.5 9.3 7.5 5.0 75 19.8 11.7 11.7 8.2 8.7 5.8 100 15.5 10.0 9.9 7.3 9.7 6.5 125 12.9 8.7 8.7 6.6 10.4 7.0 150 11.1 7.8 7.7 6.2 11.1 7.4 175 9.8 7.1 7.1 5.7 11.7 7.8 Note: Table values are nominal for a 200-joule shock.
Specifications Waveform (continued) With Infant/Child pads: The following specifications apply from 25 to 175 ohms. Energy Accuracy (into 50 ohms): Selected energy 4 +/- 15%; 86 joules +/- 15% maximum Rated energy output is the nominal delivered energy based on the energy setting and patient impedance, as defined in the following chart.
Specifications Waveshape and Measured Parameters: I1 T1 I2 I4 T2 I3 Patient Impedance () I1 (A) I2 (A) I3 (A) I4 (A) T1 (ms) T2 (ms) 25 19.4 10.2 10.1 6.6 7.6 5.1 50 13.2 7.4 7.3 5.0 8.1 5.4 75 10.1 5.8 5.7 4.0 8.3 5.6 100 8.3 4.8 4.8 3.3 8.6 5.7 125 7.0 4.2 4.1 2.9 8.8 5.9 150 6.2 3.7 3.7 2.6 8.8 5.9 175 5.5 3.3 3.3 2.3 8.9 6.0 Note: Table values are nominal for a 50-joule shock (200 ÷ 4).
Specifications Electrical Protection: Input protected against high voltage defibrillator pulses per IEC 60601-1. See Figure A-1. Figure A-1 Defibrillation–protected, Type BF Patient Connection Safety Classification: Internally powered equipment. IEC 60601-1 AED Mode Shock Advisory System (SAS): ECG Analysis system that advises whether a shock is appropriate, meets rhythm recognition criteria specified in DF80 and IEC 60601-2-4.
Specifications Waveform Amplitude 1 cm/mV, nominal Display Range Differential: ±1.4 mV full scale, nominal Heart Rate 20 to 300 BPM digital display. Display "---" if heart rate is less than 20 BPM. Heart symbol flashes for each QRS detection Displayed ECG ECG information is received from therapy pads in anterior-lateral or anterior-posterior positions, or from the 3-wire ECG cable in Lead II.
Specifications Drop • 18-inch drop onto each surface, repeated 5 times each, 30 drops total • EN 1789 0.75 meter drop onto each surface, 6 drops total • MIL-STD-810F, 516.5 Procedure IV, 1 meter drop on each corner, edge, and surface Vibration MIL-STD-810F, Method 514.5, Category 20 Ground Vehicle: Random vibration test, 1 hour per axis, 3.15g rms EMC For EMC information, refer to the EMC tables Physical Characteristics Weight 3.2 kg (7.
Specifications Standby Life A new battery provides device power for 5 years. Low Battery Indicator At least 30 200-joule shocks or 75 minutes of operating time remain when low battery is first indicated. Rechargeable Batteries: A-8 Type Lithium-ion, 11.1 V, 4.8 amp hours Capacity Typically will provide 261 200-joule discharges or 608 minutes of operating time with a new fully-charged battery (247 200-joule shocks or 576 minutes of operating time at 0°C (32°F)). Battery Charging Time Within 4.
APPENDIX B SHOCK ADVISORY SYSTEM LIFEPAK 1000 Defibrillator Operating Instructions ©2006-2012 Physio-Control, Inc.
Shock Advisory System OVERVIEW OF THE SHOCK ADVISORY SYSTEM The Shock Advisory System (SAS) is an ECG analysis system built into the LIFEPAK 1000 defibrillator that advises the responder if it detects a shockable or nonshockable rhythm. This system makes it possible for individuals not trained to interpret ECG rhythms to provide potentially-lifesaving therapy to victims of ventricular fibrillation or pulseless ventricular tachycardia.
Shock Advisory System A number of activities can create motion, including CPR, rescuer movement, patient movement, vehicle movement, and some internal pacemakers. If variations in the transthoracic impedance signal exceed a maximum limit, the Shock Advisory System determines that patient motion of some kind is present. If motion is detected, the ECG analysis is inhibited. The operator is advised by a displayed message, a voice prompt, and an audible alert.
APPENDIX C cprMAX™ TECHNOLOGY LIFEPAK 1000 Defibrillator Operating Instructions ©2006-2012 Physio-Control, Inc.
cprMAX™ Technology ABOUT cprMAX TECHNOLOGY Physio-Control cprMAX technology is designed to allow resuscitation protocols to maximize the quantity of CPR administered during treatment with an AED, consistent with the 2005 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care 1 (AHA Guidelines) and the European Resuscitation Council Guidelines for Resuscitation 2005 2 (ERC Guidelines).
cprMAX™ Technology that a shock is needed, the AED will prompt, IF YOU WITNESSED THE ARREST, PUSH CANCEL, which provides the opportunity to end CPR early and proceed directly to delivering a shock. • The CPR FIRST setting prompts the user to perform CPR immediately after the defibrillator is powered on. The AED will also prompt, IF YOU WITNESSED THE ARREST, PUSH CANCEL, which provides the opportunity to end CPR early and proceed directly to analysis.
cprMAX™ Technology Pulse Check The PULSE CHECK option inserts prompting to check for a pulse or check the patient, depending on the PULSE PROMPT setting. The choices for PULSE CHECK are: ALWAYS, AFTER EVERY NSA, AFTER SECOND NSA, and NEVER. The default setting is NEVER.
APPENDIX D CHANGING SETUP OPTIONS LIFEPAK 1000 Defibrillator Operating Instructions ©2006-2012 Physio-Control, Inc.
Changing Setup Options CHANGING SETUP OPTIONS Setup options allow you to define operating features for your defibrillator, such as CPR intervals. Setup options are listed in tables beginning with Table D-1. To enter Setup mode: 1 Ensure that no electrodes or cables are connected to the defibrillator. 2 Press and hold both softkeys and press the ON/OFF button. The Enter Setup Mode screen appears.
Changing Setup Options Setup Set up general device options General... AED Mode... Manual Mode... Set Passcode... Service Mode... Labels Softkeys Next Select Menu button Figure D-2 Setup Mode Screen Setup Menu Options All setup options for your defibrillator are grouped under these top-level headings. • • • • • General AED Mode Manual Mode Set Passcode Service Mode Use the softkeys to navigate and make selections on the Setup screen.
Changing Setup Options Access the General Setup menu from Setup to view general purpose settings. The underlined bold options in Table D-2 are the factory default settings. Table D-2 General Setup Menu Menu Item Help Message Options DEVICE ID Set the device ID. User selectable, 0-9, A-Z, up to 20 characters. Default is SERIAL NUMBER. DATE/TIME Set current date and time. Default is PACIFIC TIME. AUDIO Set audio parameters. See Table D-3. DEVICE DATA Display device data.
Changing Setup Options Access Energy Protocols from the AED menu. The underlined bold options in Table D-5 are the factory default settings. Table D-5 AED Setup Menu—Energy Protocols Submenu Menu Item Help Message Options ENERGY 1 Select energy level for shock 1. 150, 175, 200, 225, 250, 275, 300, 325, 360* joules. ENERGY 2 Select energy equal to or greater than Energy 1. 150, 175, 200, 225, 250, 275, 300, 325, 360 Joules. ENERGY 3 Select energy equal to or greater than Energy 2.
Changing Setup Options Access Pulse Setup from the AED menu. The underlined bold options in Table D-7 are the factory default settings. Table D-7 AED Setup Menu—Pulse Setup Submenu Menu Item Help Message Options PULSE CHECK Enable pulse check prompt. NEVER: Never prompt for PULSE CHECK. AFTER SECOND NSA: After every NSA except for first analysis NSA result. AFTER EVERY NSA: Only after NO SHOCK ADVISED. ALWAYS: After every stack of shocks and every NSA finding.
Changing Setup Options Access the Set Passcode screen, shown in Figure D-3, from the top-level Setup menu. Setup / Set Passcode Set Setup Mode passcode Press button to set Increase Decrease Figure D-3 Set Passcode Screen Use the INCREASE and DECREASE softkeys and the MENU button to set the passcode. Be sure to record the new passcode—the passcode is required each time you enter Setup mode. Access Service mode, shown in Table D-9, from the top-level Setup menu.
Changing Setup Options How to Enter and Delete Device Information Figure D-4 shows the Device ID screen used to enter device information into the defibrillator. Softkeys Menu button Figure D-4 Device ID Screen To enter device information: 1 Use the softkeys under the clockwise and counterclockwise arrows to navigate to the character or number you want to enter. Note: Pressing the clockwise arrow moves the cursor forward one space at a time; the counterclockwise arrow moves it back one space at a time.
APPENDIX E USER’S CHECKLIST LIFEPAK 1000 Defibrillator Operating Instructions ©2006-2012 Physio-Control, Inc.
LIFEPAK® 1000 DEFIBRILLATOR USER’S CHECKLIST Unit Serial Number __________________________ Department/Location ________________________ Date Instruction 1 Recommended Corrective Action Initials Check readiness display for: WRENCH symbol Contact authorized service personnel. OK symbol None. Battery level Replace if low battery indicated. 2 Check Use By date on electrode packet. Replace electrode packet if date has passed. 3 Check additional supplies. Replenish as needed.
INDEX A About Defibrillation vi, 3-3, 3-6 LIFEPAK 1000 defibrillator vii Accessories 5-8 AED mode vi, 3-2, 3-3, A-5 AED Mode setup menu D-3 AED operation C-1 Alternate anterior-posterior electrode position 3-5 Audio setup submenu D-3 Auto Tests 5-3 Cleaning 5-4 General caution 1-3 General therapy 3-2 Nonrechargeable battery 5-5, 5-7 Checklist, User’s E-3 Cleaning 5-4 CODE-STAT software 4-3 Controls and indicators 2-2, A-6 CPR setup submenu D-4 cprMAX Technology viii B Batteries viii Battery charger 2-6 B
Index Heart rhythm analysis vii LIFEPAK 1000 defibrillator vii Readiness display viii G General setup menu D-3 H Heart Rate Indicator 2-4 Heart rhythm analysis vii, B-1 I Implanted pacemakers/ defibrillators 3-5 Indications for use vi Inspection 5-3 IrDA adapter 4-3 IrDA connections 4-3, 4-4 IrDA port 2-3 M Maintenance and testing schedule 5-2 Maintenance, battery 5-4 Manual mode 3-2, 3-6, A-5 Manual mode therapy 3-6 Manual setup menu D-5 Modes of operation 3-2 Monitoring in ECG mode 3-9 Motion Detected 3
Physio-Control, Inc. 11811 Willows Road NE Redmond, WA 98052 USA Telephone: 425.867.4000 Toll Free (USA only): 800.442.1142 Fax: 425.867.4121 www.physio-control.com Physio-Control, Inc., 11811 Willows Road NE, Redmond, WA 98052 USA Physio-Control Operations Netherlands, B.V.
