Transition MDD to MDR
Dear Madam, Dear Sir,
the EU Medical Device Regulation (MDR) was originally intended to come into force in a few weeks. We would like to inform you that (subject to the approval of the EU member states) that the EU Parliament has accepted the proposal provided by the EU Commission to delay MDR by one year. May 26th 2021 is going to be the new date of full MDR application.
For this reason, we can accept applications for new products or product changes from existing customers, which are submitted to us by 30.08.2020 together with the complete documentation.
As soon as we have further information, we will make it available to you.
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Besuchen Sie TÜV NORD auf
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This newsletter is carried out on behalf of TÜV NORD AG based in Hanover, Germany.
Am TÜV 1 30519 Hannover, Germany
Registration office: Hanover Local Court, HRB 200158 – VAT ID no. DE 234039777
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