Unique Device Identification (UDI) Final Rule was announced by the FDA on September 20, 2013. The rule was published in the Code of Federal Regulations as of September 24, 2013. Implementation for Class III device labeling is required in 2014. Implementation for other device Classes follow per a defined schedule.
Related Posts
News
Additive Manufacturing
Manufacturing
People and Culture
Cretex Medical Exhibits at MD&M West 2026
February 9, 2026
News
Press Release
Cretex Medical Signs Agreement to Acquire Atemisa Precision, S.A. in Costa Rica
October 15, 2025
News
Events
Blogs
People and Culture
Cretex Medical Sponsors Thumbs Up Annual 5K/10K Walk/Run/Bike Event
September 24, 2025