The LIFEPAK 1000 Graphical Display AED is a rugged, professional-grade automated external defibrillator designed for EMS, fire departments, hospitals, law enforcement, and first-response environments. Its large graphical display provides clear visual and text-based rescue guidance alongside audible prompts, helping responders move quickly and confidently during sudden cardiac arrest emergencies.
Built for demanding professional use, the LIFEPAK 1000 combines semi-automatic defibrillation with configurable rescue protocols and manual override capability for appropriately trained responders. The device is designed to deliver dependable performance in high-pressure environments while supporting fast deployment, effective CPR response, and post-event data review.
Key Features
Graphical display with clear visual and text-based rescue guidance
Semi-automatic operation with user-initiated shock delivery
Escalating energy capability up to 360 joules
Manual override capability for trained responders
Rugged design for EMS and 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 Graphical 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
Public-access 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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