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: ...
VOORHEES, N.J., July 8, 2025 /PRNewswire/ -- Comar, a leader in healthcare packaging, has achieved CE certification under the EU Medical Device Regulation (EU MDR 2017/745), reaffirming its commitment ...
Building off guidance released in March, the European Commission this month unveiled five new guidance documents on the use of unique device identifiers (UDIs). The guidances deal with UDIs for ...
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