Following the lifecycle approach of the MDR, the identification system aims to enhance the effectiveness of the post-market safety-related activities. The system brings about two key obligations: ...
On 15 February 2021, the European Commission published guidance on the Management of legacy devices in EUDAMED. This guidance addresses the registration and identification of legacy devices in EUDAMED ...
The European Commission on Wednesday released eight documents related to the technical specifications for unique device identifiers (UDIs). Four of the documents are related to Basic UDI-DI, which ...
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