After the date September 24, 2016 for the registration of medical devices in the US Class II in the "Global UDI Data Base - GUDID it goes according to the plan of the FDA in the phase of the last group of Class I.
The new EU regulation for medical devices "Medical Device Regulation (MDR)" is now at the start as part of "UDI".
For information about the UDI implementation steps in accordance with the identification and registration requirements for UDI in USA and Europe and how manufacturers UDI manage, you can log in to the following event dates:
|26.of September 2016||IHK Darmstadt||German||to article...|
|28. of September 2016||Medical-Valley Erlangen/Forchheim||German||to article...|
|29. of November 2016||Medical-Mountain Tuttlingen||German||to article...|