AED Oversight & Program Management
Automated External Defibrillators (AEDs) are regulated by the Food & Drug Administration (FDA) and are classified as a Class III medical device. Almost all AEDs require the purchaser to obtain a prescription from a physician under FDA rules.
Most AED manufacturers in the US provide the initial prescription when a new device is purchased although the initial prescription does not satisfy the widely varying state laws regarding AED ownership and compliance. Ongoing maintenance checks, battery and pad expiration date management and CPR/AED two-year certification training are all highly regulated for each state in the US.
Protect It’s AED oversight program was designed by our team of AED Compliance Specialists and makes all state specific requirements and legislation easy and automatic. We do the heavy lifting to insure that your AEDs are functioning properly and your entire AED program is compliant so that the Good Samaritan Laws provide the maximum protection they were created to deliver.
Good Samaritan laws offer legal protection to anyone who gives reasonable assistance to those who are, or who they believe to be, injured, ill, in peril, or otherwise incapacitated.
Protect It’s AED Medical Direction & Program Management includes:
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Device set-up & registration
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Prescription & program oversight by licensed physician
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State and/or County EMS registration
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Device service checks
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Battery & Pad expiration tracking
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First Aid/CPR/AED training expiration tracking
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Post AED event data retrieval, reporting, reset and loaner program
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Archived and detailed history of Program in Protect It Cloud EHS Portal
AED Medical Oversight 3 Year
