Is it possible to continue selling medical devices that are already on the EU Market after the MDR/IVDR application deadlines?

Modified on Wed, 28 Aug at 8:12 PM

Yes, it is possible to continue selling products that today fall under the scope of the Medical devices directives provided that they are still covered by a valid certificate, until the end of the 4-year transition period, that is to say May 2025.
Please refer to article 120 of the EU Medical Devices Regulation for further details:https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02017R0745-20170505

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