The Stryker LIFEPAK® 15 Monitor Defibrillator V2 is a high-performance, field-proven cardiac monitoring and defibrillation system designed for advanced life support (ALS) teams in EMS, hospital, and critical care transport environments. Recognized as an industry standard, the LIFEPAK 15 delivers powerful defibrillation, advanced monitoring, and data-driven decision support in one rugged, reliable platform.
Built for high-acuity patient care, the Version 2 system integrates defibrillation, pacing, and comprehensive monitoring capabilities—including ECG, SpO2, NIBP, and EtCO2—into a single device designed to perform in the most demanding conditions.
Key Features
Biphasic defibrillation with escalating energy up to 360J
12-lead ECG monitoring with continuous analysis
Advanced parameters: SpO2, NIBP, EtCO2, and invasive pressures
Pacing and AED functionality for versatile patient care
SunVue™ high-visibility display for use in bright environments
Bluetooth and data connectivity for patient data transmission
Rugged, field-ready design built for EMS and transport use
Advanced Clinical Capabilities
The LIFEPAK 15 is designed to support real-time clinical decision-making with continuous monitoring and waveform analysis. Its integrated data capabilities allow providers to capture, review, and transmit patient data for improved coordination of care and post-event analysis.
Applications
Emergency Medical Services (EMS)
Hospitals and emergency departments
Ambulance and transport teams
Fire departments and first responders
Condition
Professionally refurbished, tested, and ready for deployment. Multiple configurations available based on monitoring and accessory requirements.
👉 Request a quote today for pricing, configurations, and available accessories.
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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