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 ...
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: ...
Dubai, United Arab Emirates – GS1 UAE recently hosted an exclusive Healthcare User Group UDI Stream focused on accelerating the implementation of Unique Device Identification (UDI) for medical devices ...
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