MEDIMARK EUROPE

Home page > News > MME News > UDI, Eudamed and Medical Device Regulation

UDI, Eudamed and Medical Device Regulation

The European Commission published its recommendation for a common framework for a unique device identification (UDI) system for medical devices in April 2013.

MME News June 2013 - The Tangled Destinies of Europe’s UDI, Eudamed and Medical Device Regulation(PDF – 18.5 kb)

| Site Map | Legal mentions