The European Commission has recently released an informative Q&A document addressing the practical aspects concerning the implementation of Regulation (EU) 2023/607. This regulation brings amendments to Regulations (EU) 2017/745 and (EU) 2017/746, specifically focusing on the transitional provisions for specific medical devices and in vitro diagnostic medical devices. The published Q&A offers valuable insights and guidance on these matters.

🔗 Original Document:  https://health.ec.europa.eu/system/files/2023-03/mdr_proposal_extension-q-n-a_0.pdf