Stryker LUCAS 3 Chest Compression System (99576-000063)
SKU: 99576-000063
Product Description
The Stryker LUCAS® 3 Chest Compression System is an advanced automated CPR device designed to deliver consistent, high-quality chest compressions during cardiac arrest. Built for EMS, hospitals, and critical care transport, the LUCAS 3 ensures uninterrupted compressions while allowing providers to focus on advanced life-saving interventions.
As the next generation of mechanical CPR systems, the LUCAS 3 delivers guideline-consistent compressions at optimal rate and depth, improving circulation and patient outcomes in high-pressure environments. Its enhanced design includes improved handling, wireless data capabilities, and faster deployment for real-world emergency response.
Reduces provider fatigue during prolonged resuscitation
Battery-powered with external AC power capability
Lightweight, portable design for rapid deployment
Wireless connectivity for post-event data review
Designed for EMS, hospital, and transport environments
What’s Included (Typical Configuration)
LUCAS 3 Chest Compression Device
Rechargeable battery
AC power supply and cord
Carrying case
Back plate
Stabilization strap and accessories
Documentation and warranty
Applications
Emergency Medical Services (EMS)
Hospitals and emergency departments
Ambulance and transport teams
Cardiac arrest and resuscitation scenarios
Condition
Available new or recertified, inspected, and ready for deployment.
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LUCAS 3 Chest Compression System for Sale | Stryker CPR Device
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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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