Cretex News & Events

UDI Rule Announced

Written by Cretex Medical | Sep 30, 2013 8:38:00 PM

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.