Emergency Care

Find a Rep

Find a rep

Device registration

Register your device

The U.S. Food and Drug Administration classifies defibrillators as medical devices that require tracking (knowing where each device is). As such, federal regulations require that manufacturers maintain tracking information for each device distributed. We rely on our customers to provide accurate device location information. This tracking information provides the manufacturer the ability to locate the device and perform a product correction, should it ever be needed

Tracking information must specify the physical location of the device, not just the headquarters or receiving department’s shipping address. The tracking information required is:

  • Customer name and department name
  • Physical address (Please provide an actual physical location.
    For example: 123 Main Street, Third Floor, Suite A)
  • City, State and Zip Code
  • A contact name and telephone number
  • Device part number and serial number

The address to which this particular device was shipped is the current tracking location. If this device is located somewhere other than the shipping address, or you have purchased this device from someone other than Physio-Control, please either call the device tracking coordinator at (800) 426-4448, or complete the form below to update this vital information.

Physio-Control Privacy Policy

Fields marked with '*' are required.