Preparing for EU UDI for Medical Devices – A Detailed Guide
As the result of the universal trend about application of medical devices’ UDI, The EU Commission has stated its requirements clearly regarding the use of the UDI (Unique Device Identification) System in the last publication of the new EU (MDR) Medical Device Regulation 2017/745 and (IVDR) In Vitro Diagnostic Medical Device Regulation 2017/746. Both were […]