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Medical Device Market Approval & Certification

MDR Request For Service Registration

EU MDR (2017/745) covers medical device regulation in the EU. Regulation EU 2023/607 extends the transition period for products certified under MDD/AIMDD to adapt remain on the market under certain conditions.

EU MDR (2017/745) covers medical device regulation in the EU. Regulation EU 2023/607 extends the transition period for products certified under MDD/AIMDD to adapt remain on the market under certain conditions.

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