While the European Commission proposal for a new type of unique device identification – the Master UDI – didn’t engender a high volume of responses, it did receive some enthusiastic feedback. AgencyIQ took a look at what people had to say: In brief, responses were about 50-50 in support of the idea, or in “strong” opposition.
Quick regulatory background on E.U. device regulation and UDI
Unique Device Identification (UDI) is an important part of the E.U. Medical Device and IVD regulations.
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