Physio-Control LIFEPAK Express Defibrillator

Get Quote

The Physio-Control LIFEPAK Express Defibrillator (#80427-000134) is a first response defibrillator when responding to an SCA (Sudden Cardiac Arrest) patient. This Express Defibrillator is designed for any first responder to use, whether its a bystander or a coworker, and no emergency training is required. 

Warranty: 5 Years.

The Physio-Control LIFEPAK Express Defibrillator is a simplified defibrillator that can be operated by any untrained responder in a cardiac emergency. This device is equipped with both visual cues and voice prompts that guide the user through each step of defibrillation. It's a low-profile, simple design that won't cause any confusion as well as being light and compact.

The initial shock to a patient is set at 200 joules, with the ability to increase to 360 joules if needed for patients who need more intense  defibrillation. The device is also equipped with a readiness indicator so users know when this device is prepared for use or needs to be replaced.

Features

Physio-Control LIFEPAK Express Defibrillator Features

  • Simplified for use by untrained responders, such as co-workers or bystanders.
  • Includes electrodes and has a readiness indicator.
  • Capable of providing shocks measuring 20 joules to 360 joules.

Specifications

Physio-Control LIFEPAK Express Defibrillator Specifications

Physical Characteristics

  • Height: 4.2 in (10.7 cm).
  • Width: 8 in (20.3 cm).
  • Depth: 9.5 in (24.1 cm), excluding handle.
  • Weight: 4.5 lb (2 kg) with CHARGE-PAK battery charger and electrodes.

Defibrillator 

  • Waveform: Biphasic truncated exponential, with voltage and current duration compensation for patient impedance.
  • Output Energy Sequence: Multiple levels, configurable from 150 joules to 360 joules. Factory default settings of 200J, 300J, 360J.
  • Output Energy Accuracy: ±10% into 50 ohms, ±15% into 25 to 100 ohms.
  • Shock Advisory System: An ECG analysis system that advises whether a shock is appropriate; meets rhythm recognition criteria specified in DF39. The device charges for shock only when the Shock Advisory System advises defibrillation.
  • Device Capacity: Twenty (20) full discharges or 140 minutes of “on time” with a fully charged device.
  • Shock Charge Time: Charge times with a fully charged device: 200 joules in less than 9 seconds, 360 joules in less than 15 seconds.
  • System Recharge Times: Recharge times with a fully discharged device: able to deliver 6 shocks or provide 42 minutes of operating time after 24 hours of recharge time and 20 shocks or 140 minutes of operating time after 72 hours of recharge time with a new CHARGE-PAK battery charger at temperatures above 15°C (59°F).
  • Controls: Lid Release/ON-OFF - Controls device power. Shock button delivers defibrillation energy.
  • Electrical Protection: Input protected against high voltage defibrillator pulses per IEC60601-1/EN60601-1
  • Safety Classification: Internally powered equipment.IEC60601-1/EN60601-1.

User Interface

  • User Interface: The user interface includes voice prompts, audible tones and graphic prompts.
  • Readiness Display: The readiness display shows the device status.
  • OK Indicator: Shows “OK” when the last self-test was completed successfully. When the “OK” indicator is visible, all other indicators are not visible. The “OK” indicator is not displayed during device operation.
  • CHARGE-PAK Indicator: When displayed, replace the CHARGE-PAK™ battery charger.
  • Attention Indicator: When first displayed, at least six (6) discharges or 42 minutes of operating time remain.
  • Service Indicator: Service required when displayed.

Environmental

  • Operating Temperature: +32° to +122°F (0° to +50°C).
  • Storage Temperature: -40° to +158°F (-40° to +70°C) with CHARGE-PAK battery charger and electrodes, maximum exposure time limited to one week.
  • Atmospheric Pressure: 760 mmHg to 429 mmHg, 0 to 15,000 feet above sea level.
  • Relative Humidity: 5 to 95% (non-condensing).
  • Water Resistance: IEC60529/EN60529 IPX4 “Splash proof” with electrodes connected, CHARGE-PAK battery charger installed.
  • Shock: MIL-STD-810E, Method 516.4, Procedure 1, (40 g, 6-9 ms pulse, 1/2 sine each axis).
  • Vibration: MIL-STD-810E, Method 514.4, Helicopter - category 6 (3.75 Grms) and Ground Mobile - category 8 (2.85 Grms).

Default Settings

  • Energy Sequence: Energy sequence is set to 200J, 300J, 360J.
  • Motion Detection: The motion detection system is set to on during analysis.
  • Energy Protocol: The energy protocol is set to increase energy only after a lower energy shock was unsuccessful.
  • Stack Shocks: Stack shocks option is set to off.
  • Turn-On Prompt: The turn-on prompt is set to provide voice prompts upon power on.
  • CPR Time: The CPR Time is set to 120 seconds.
  • Voice Prompt Volume: The voice prompt volume is set to high.

Data Storage

  • Memory Type: Internal digital memory.
  • ECG Storage: Dual patient data storage. Minimum 20 minutes of ECG stored for the current patient, summarized data stored for the previous patient.
  • Report Types:
    • Continuous ECG – A continuous patient ECG report.
    • Continuous Summary report – A summary of critical resuscitation events and ECG waveform segments associated with these events.
    • Event Log report – A report of time stamped markers, which reflect operator and device activity.
    • Test Log report – A device self-test activity report.
  • Capacity: Minimum 200 time-stamped event log markers.
  • Communications: Wireless transfer to a personal computer.
  • Data Review: Physio-Control provides an array of tools to meet customer needs for data viewing and analysis.

Literature

Physio-Control LIFEPAK Express Defibrillator Literature

Stryker LIFEPAK Express Defibrillator Data Sheet

Physio-Control LIFEPAK CR Plus / LIFEPAK EXPRESS Defibrillator Operating Instructions

Physio-Control LIFEPAK CR Plus / LIFEPAK EXPRESS Defibrillators Accessories Brochure