MDR system

(redirected from Medical Device Reporting system)

MDR system

Medical Device Reporting system. A regulatory program requiring manufacturers and importers of medical devices to inform the FDA should they receive information suggesting that one of their devices may have caused or contributed to death or serious injury.

MDR system

Medical Device Reporting system FDA A program requiring manufacturers and importers of medical devices to inform the FDA should they receive information suggesting that one of their devices may have caused/contributed to death/serious injury. See Medical device.
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Food and Drug Administration (FDA) is close to pulling the trigger on an electronic medical device reporting system (eMDR) for post-market safety tracking of adverse events.

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