FDA UDI Regulation's Impact on Medical Device Labelers Webinar Udi Medical Device
Manufacturers of medical devices must ensure that their products have a Unified Device Identifier (UDI). Zebra can be helpful at Understanding the UDI System for Medical Devices UDI regulations kick in for Implantables and Class II devices in 2015. Reed Tech subject matter expert Gary Saner is my go-to on Learn UDI code with Sylvia Reingardt (EU MDR 2017/745 & IVDR 2017/746) ...