The Stryker SMRT Pak Stretcher Battery (6500-101-010) is a reliable power solution designed for use with Stryker Power-PRO XT ambulance stretcher systems. Built for demanding EMS and patient transport environments, this battery ensures consistent performance and dependable operation when it matters most.
Designed to support high-cycle usage in emergency medical settings, the SMRT Pak battery provides extended runtime and efficient power management. Its durable construction and compatibility with Stryker charging systems make it an essential component for maintaining operational readiness across ambulance fleets and hospital transport teams.
Key Features
Compatible with Stryker Power-PRO XT stretcher systems
Reliable power source for EMS and patient transport equipment
Designed for high-demand emergency environments
Durable construction for long-term use
Rechargeable battery with efficient charging capability
Supports consistent stretcher operation and performance
Ideal replacement for worn or depleted battery units
What’s Included (Typical Configuration)
Stryker SMRT Pak Stretcher Battery (6500-101-010)
Tested and verified battery unit
Ready for installation
Warranty and documentation
Applications
Emergency Medical Services (EMS)
Ambulance and transport teams
Hospital patient transport departments
Medical equipment service and maintenance teams
Condition
Available new or recertified, inspected, tested, and ready for deployment.
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Stryker SMRT Pak Stretcher Battery (6500-101-010)
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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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