Class II Device Makers: UDI Mistakes You Can Avoid
Reed Tech has processed more than 100,000 UDI submissions for Class III devices and Class II implants, life-sustaining, and life-supporting devices marketed in the U.S.
If you market a Class II device in the U.S., you’ll need to report your Device Identifier by September 24, 2016.
To help, Gary’s noticed a distinct pattern between (a) applications that sail through FDA GUDID and (b) applications that get sent back.
Tune in. Trust me, the video and slides will save you a lot of time later.
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