The LIFEPAK 1000 ECG Display AED is a rugged, professional-grade automated external defibrillator designed for EMS, fire departments, hospitals, law enforcement, and other professional first-response environments. This configuration features an ECG display, allowing appropriately trained responders to view the patient’s ECG rhythm directly on the device while providing lifesaving defibrillation therapy.
Designed for demanding field use, the LIFEPAK 1000 combines semi-automatic defibrillation with advanced capabilities for professional responders. Its rugged construction, escalating energy capability, configurable protocols, and manual override functionality make it an excellent choice for organizations that require more advanced capabilities than a traditional public-access AED.
Key Features
ECG display for viewing the patient’s cardiac rhythm
Semi-automatic operation with user-initiated shock delivery
Escalating energy capability up to 360 joules
Manual override capability for appropriately trained responders
Rugged construction designed for professional first-response environments
Pre-connected electrode capability for rapid deployment
Configurable CPR and resuscitation protocols
Post-event rescue data recording
What’s Included (Typical Configuration)
LIFEPAK 1000 ECG Display AED
Adult defibrillation electrodes
Non-rechargeable lithium battery
Carrying case
Documentation and warranty
Applications
Emergency Medical Services (EMS)
Fire departments
Hospitals and healthcare facilities
Police and law enforcement
Professional first responders
Advanced AED programs
Condition
👉 Available New or Recertified
Recertified equipment is professionally inspected, tested, and prepared for deployment.
👉 Request a quote today for pricing, availability, and bundle packages.
Some equipment offered by Parrott Med is refurbished. Refurbished devices are inspected and tested to help ensure proper functionality; however, they may not be certified by the original manufacturer unless explicitly stated.
Parrott Med is an independent reseller and is not aAiliated with or authorized by all original equipment manufacturers unless otherwise specified.
FDA / Regulatory Disclaimer
Certain medical devices sold by Parrott Med may be subject to regulation by the U.S. Food and Drug Administration (FDA). It is the responsibility of the purchaser to ensure compliance with all applicable regulatory requirements, including device registration, use, and maintenance.
Parrott Med does not provide medical or regulatory advice. Buyers should consult appropriate regulatory authorities or qualified professionals regarding compliance requirements.
Limitation of Liability
All equipment is sold in accordance with the terms outlined at the time of sale. Parrott Med shall not be held liable for improper use, installation, or operation of any equipment after delivery.
Buyers are responsible for ensuring that all equipment is properly installed, maintained, and operated by qualified personnel.
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