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    Full text of EU MDR (Medical Device Regulation)
    EU MDR Chapter 10 Article 121

    Article 121 – Evaluation

    By 27 May 2027, the Commission shall assess the application of this Regulation and produce an evaluation report on the progress towards achievement of the objectives contained herein including an assessment of the resources required to implement this Regulation. Special attention shall be given to the traceability of medical devices through the storage, pursuant to Article 27, of the UDI by economic operators, health institutions and health professionals.

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