Replay and slides available now; transcript to follow.

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.

BONUS! When you register below, you’ll get immediate access to five very popular presentations Gary made for the Medical Devices Group.

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