The Stryker LIFEPAK® 15 Carrying Case is a durable, field-ready transport solution designed to protect and organize LIFEPAK 15 monitor defibrillators in EMS, hospital, and critical care environments. Built to OEM specifications, this case provides secure storage and easy access to essential accessories during emergency response.
Designed for real-world use, the case includes integrated side pouches for organizing cables, electrodes, and monitoring accessories, allowing providers to keep critical equipment within reach at all times. Its rugged construction ensures protection against impact and wear during transport in demanding field conditions.
Key Features
OEM Stryker LIFEPAK 15 carrying case
Designed specifically for LIFEPAK 15 monitor defibrillators
Integrated right and left side pouches for accessory storage
Durable construction for EMS and field environments
Secure fit for safe transport and rapid deployment
Supports organized storage of cables, electrodes, and sensors
What’s Included
LIFEPAK 15 carrying case
Integrated side pouches
Mounting hardware (varies by configuration)
Shoulder strap may be included or sold separately depending on configuration.
Applications
Emergency Medical Services (EMS)
Hospitals and emergency departments
Ambulance and transport teams
Fire departments and first responders
Condition
Available new or refurbished. Fully inspected and ready for deployment.
👉 Contact us for bundle options including monitor systems, accessories, and full EMS configurations.
Stryker LIFEPAK 15 Carrying Case (OEM)
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Refurbished Equipment Disclaimer
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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