Medtronic Lifepak 20 Defibrillator, Heart Monitor, Ecg, Electrodes Included

US $827

  • Kennesaw, Georgia, United States
  • Jun 2nd
THIS LISTING INCLUDES ALL PICTURED PIECES. FOR PADDLES PLEASE MAKE OFFER +$300. THIS ITEM HAS BEEN CLEANED AND INSPECTED AND IS IN PERFECT WORKING CONDITION. 1 BOX OF 40 ELECTRODES ALSO INCLUDED. Thank you for giving me the opportunity to earn your business. MESSAGE ME FOR QUANTITY DISCOUNTS! RETURN POLICY If you are unhappy with this item for any reason, return it within 14 days of delivery for a full refund. Just pay return shipping. SPECIFICATIONS GENERAL The LIFEPAK 20 defibrillator/monitor has seven main operating modes: Manual Mode: Provides a normal operating capability for ALS users. Allows access to manual mode energy selections up to 360J, synchronous cardioversion and pacing. ECG waveform is displayed.  AED Mode: (Consistent with 2005 AHA Guidelines for CPR and ECC and ERC Guidelines for Resuscitation 2005.) Provides a normal operating capability for BLS users. All user features are available except manual defibrillation, synchronous cardioversion, pacing, and access to archived patient records. Provides shock energy defaults up to 360J. User selectable option to display ECG waveforms and/or visual AED prompts.  Setup Mode: Allows the operator to configure the device settings.  Service Mode: Allows the operator to execute diagnostic tests and calibrations, to display device module software and hardware versions, and to display and print the diagnostic code log.  Inservice Mode: Simulated waveforms are available for demonstration purposes. The waveforms consist of short segments of realistic data, which are repeated to form a continuous waveform.  Archive Mode: Provides operator the opportunity to access records of previous patients for review, transmission, printing, editing or deletion.  Auto Test Mode: Performs daily self tests.  Daily Auto Test: Each day at approximately 0300 (3:00 am), the 20 automatically completes the following tasks: • Turns itself on. • Performs self-tests. • Charges to a low energy level and then discharges through a test load. • Tests the pacing circuitry (if noninvasive pacing installed). • Turns itself off.  POWER  The device is an AC line operated device with an internal battery as backup. AC Powered: 90–132 VAC 50/60Hz, 198–264 VAC 50/60 Hz, total power draw less than 120 volt-amperes (VA).  Internal Battery Backup: NiMh. Batteries charge while device operates from AC Power.  Operating Time: A new fully charged internal backup battery will provide the following prior to shutdown                                                                                                  TOTAL      AFTER LOW BATTERY  Monitoring (minutes):                                                             120                             5 Monitoring in device without Pulse Oximeter (minutes):    135                             5 Defibrillation (360J discharges):                                             90                              3  Monitoring plus pacing (Minutes at 100 ma, 60 ppm):         70                              2  Typical Battery Charge Time: <2 hours when device is powered off and AC power is applied  Low Battery Indication and Message: When the device is unplugged from AC power, it switches to battery. When battery gets low, the battery detection icon is indicated with a low battery message in the status area, and a warning tone occurs.  Service Indicator: When error detected.  PHYSICAL CHARACTERISTICS  Weight: Fully featured defibrillator/monitor (pacing and SpO2) 5.58 kg (12.3 lbs)  QUIK-COMBO cable: .20 kg (.43 lbs)  Standard (hard) paddles: .88 kg (1.95 lbs)  Height: 21.3 cm (8.4 in)  Width: 26.2 cm (10.3 in)  Depth: 26.2 cm (10.3 in)  DISPLAY  Size (active viewing area): 115.18 mm (4.53 in) wide x 86.38 mm (3.4 in) high Resolution: 320 x 240 dot color active LCD.  Displays a minimum of 4 seconds of ECG and alphanumerics for values, device instructions or prompts.  Option to display one additional waveform.  Waveform display sweep speed: 25 mm/sec for ECG  DATA MANAGEMENT  The device can easily print a CODE SUMMARY™ report, including an introduction with patient information and critical event record. The summary report also includes event and vital signs log, and waveforms associated with certain events. The device can print archived patient records and has two data communication ports—infrared (IrDA) and a direct serial port, which supports a serial data cable.  COMMUNICATIONS  The device is capable of transferring data records by serial connection:  • EIA/TIA-232E compatible at 9600, 19200, 38400, 57600 and 115200 bps  MONITOR  ECG ECG can be monitored through 3-wire or 5-wire ECG cables. Standard paddles or therapy electrodes (QUIK-COMBO pacing/defibrillation/ECG electrodes or FAST-PATCH® disposable defibrillation/ECG electrodes) are used for paddles lead monitoring. Compatible with LIFEPAK 12 ECG and therapy cables.  Lead Selection:  • Leads I, II and III, (3-wire ECG cable)  • Leads I, II, III, AVR, AVL, and AVF, V (c) acquired simultaneously, (5-wire ECG cable)  ECG size: 4, 3, 2.5, 2, 1.5, 1, 0.5, 0.25 cm/mV  Heart Rate Display: 20–350 BPM digital display  Out of Range Indication: Display symbol “---” Heart symbol flash for each QRS detection.  Continuous Patient Surveillance System (CPSS): In AED mode, while Shock Advisory System is not active, CPSS monitors the patient, via QUIK-COMBO paddles or lead II ECG, for potentially shockable rhythms.  Voice Prompts: Used for selected warnings and alarms (Configurable On/Off)  Analog ECG Output: 1V/mV X 1.0 gain < 30 ms delay Common Mode Rejection: 90db at 50/60 Hz  SpO2  Masimo SET Sensors  Saturation Range: 1 to 100% Saturation Accuracy: (70–100%) (0–69% unspecified)  Adults/Pediatrics: +/- 2 digits (during no motion conditions) +/- 3 digits (during motion conditions)  Neonates: +/- 3 digits (during no motion conditions) +/- 3 digits (during motion conditions) Dynamic signal strength bar graph Pulse tone at the onset of the pleth waveform SpO2 Update  Averaging Rate: User selectable 4, 8, 12 or 16 seconds SpO2 Measurement: Functional SpO2 values are displayed and stored Pulse Rate Range: 25 to 240 pulses per minute Pulse Rate Accuracy: (Adults/Pediatrics/Neonates) +/- 3 digits (during no motion conditions) +/- 5 digits (during motion conditions) SpO2 waveform with autogain control    ALARMS  Quick Set: Activates alarms for all parameters  VF/VT Alarm: Activates continuous CPSS monitoring in Manual Mode PRINTER  Prints continuous strips of the displayed patient information  Paper size: 50 mm (2.0 in)  Print speed: Continuous ECG 25 mm/sec +/- 5% (measured in accordance with AAMI EC-11, 4.2.5.2)  Delay: 8 seconds  Autoprint: Waveform events print automatically (user configurable)  Print Speed for CODE SUMMARY Reports: 25 mm/sec  FREQUENCY RESPONSE  Diagnostic: 0.05 to 150 Hz or 0.05 to 40 Hz (user configurable)  Monitor: 0.67 to 40 Hz or 1 to 30 Hz (user configurable)  Paddles: 2.5 to 30 Hz Analog ECG Output: 0.67 to 32 Hz (except 2.5 to 30 Hz for paddles ECG)  DEFIBRILLATOR  Waveform: Biphasic Truncated Exponential.  The following specifications apply from 25 to 200 ohms, unless otherwise specified.  Energy Accuracy: ±1 joule or 10% of setting, whichever is greater, into 50 ohms ±2 joule or 15% of setting, whichever is greater, into any impedance from 25–100 ohms.  Voltage Compensation: Active when disposable therapy electrodes are attached.  Energy output within ± 5% or ± 1 joule, whichever is greater, of 50 ohm value, limited to the available energy which results in the delivery of 360 joules into 50 ohms.     Patient Impedance      Phase 1 Duration (ms)     Phase 2 Duration (ms)                                           Min.      Max.                    Min.      Max.                25                        5.1         6.0                       3.4         4.0               50                        6.8         7.9                       4.5         5.3               100                       8.7        10.6                      5.8         7.1               125                       9.5        11.2                      6.3         7.4  Paddle Options:  • QUIK-COMBO pacing/defibrillation/ECG electrodes (standard)  • Standard adult paddles with embedded pediatric paddles (optional)  • Internal handles with discharge control (optional)  • External sterilizable paddles (optional)  • FAST-PATCH disposable defibrillation/ECG electrodes (optional)  Cable length: 2.44 meter (8-foot) long QUIK-COMBO cable (not including electrode assembly)  MANUAL  Energy Select: 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 30, 50, 70, 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, and 360 joules and user configurable sequence of 100–360, 100–360, 100–360.  Charge time:  • Charge time to 200J <4 seconds with fully charged battery  • Charge time to 360J <7 seconds with fully charged battery  • Charge time to 360J <10 seconds while not in low battery operations  Synchronous Cardioversion:  • Energy transfer begins within 60 ms of the QRS peak  • Energy transfer begins within 25 ms of the External Sync Pulse  • External Sync Pulse; 0–5V (TTL Level) Pulse, active High, > 5 ms in duration, no closer than 200 ms apart and no further than 1 second apart  AED  Shock Advisory System (SAS) is an ECG analysis system that advises the operator if the algorithm detects a shockable or nonshockable ECG rhythm. SAS acquires ECG via therapy electrodes only.  Shock Ready Time: Using a fully charged battery at normal room temperature, the device is ready to shock within 16 seconds of power on, if initial rhythm finding is “Shock Advised.” The AED mode of the LIFEPAK 20 defibrillator/monitor is not intended for use on children less than 8 years of age.  cprMAX technology Setup Options (items marked with * are default settings):  • Stacked Shocks: Off*, On • Initial CPR: Off*, Analyze First, CPR First  • Preshock CPR: Off*, 15, 30 seconds  • Auto Analyze: Off*, After 1st Shock, On  • Pulse Check: Never*, After Second No Shock Advised, After Every No Shock Advised, Always  • CPR Time 1 & 2: 15, 30, 45, 60, 90, 120*, 180 seconds, 30 minutes  Users should refer to the LIFEPAK 20 defibrillator/ monitor operating instructions for details on how to customize the configuration of their devices to hospital protocols.  PACER  Pacing Mode: Demand or nondemand Rate and current defaults (user configurable)  Pacing Rate: 40 to 170 ppm Rate Accuracy: +/- 1.5% over entire range  Output Waveform: Monophasic, amplitude stable to +/- 5% relative to leading edge for currents greater than or equal to 40 mA, Duration 20 +/- 1 ms, Rise/Fall times <= 1 ms [10–90% levels]  Output Current: 0 to 200 mA  Pause: Pacing pulse frequency reduced by a factor of 4 when activated Refractory Period: 200 to 300 ms +/- 3% (function of rate)  ENVIRONMENTAL  Temperature, Operating: 5 to 45° C (41 to 113°F)  Temperature, Nonoperating: -20 to +60° C (-4 to +140° F) except therapy electrodes  Relative Humidity, Operating: 5 to 95%, noncondensing  Atmospheric Pressure, Operating: Ambient to 429 mmHg (0 to 4,572 meters) (0 to 15,000 feet)  Water Resistance, Operating (without accessories except for ECG Cable and hard paddles): IPX1 (spillage) per IEC 60601-1 clause 44.6 (1995)  Vibration: MIL-STD-810E Method 514.4, Cat1  Shock (Drop): 1 drop on each side from 457.2 mm (18 in.) onto a steel surface

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