Device Registration ‘is live’ for voluntary UDI data submission

by Innovit Corporate Affairs | October 12, 2021 | Blog

Last week, the European Commission announced the successful launch of its EUDAMED “Device Registration” and “NBs & Certificate” modules (Production release “v2.0 – September version” was deployed). 

The EUDAMED UDI/Device Registration and NBs & Certificates modules have been successfully deployed into the Production environment and are available for use as of 4th October 2021.  

You can find links to the EUDAMED restricted website and the public website below: 

Economic Operators and Notified Bodies can start entering data on a voluntary basis. It’s important to remember that each manufacturer should decide whether or not to use EUDAMED under this voluntary regime. 

Are you still deciding whether you should begin entering data on a voluntary basis?  What are the Pros & Cons of submitting now versus later? 

Innovit is here to help you prepare UDI and BUDI data for EUDAMED data compliance. 

Innovit’s – our cloud-based system that’s designed to validate your UDI regulatory data for EUDAMED compliance. is loaded with online tutorials and audio-visual training materials to help you get started right away – at no cost to you.  Yes, it includes a free online knowledge base and resource center!  

Get started today with preparing your  UDI and BUDI master data to meet EUDAMED Compliance!  Learn more!