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.

 

Yours sincerely,
Your Team
Medical Device International TUV NORD CERT
medical@tuev-nord.de

 
 
 
 

TÜV NORD CERT GmbH

Langemarckstr. 20
45141 Essen

Tel.: 0800 2457-457
(kostenlose Service-Hotline)

info.tncert@tuev-nord.de
www.tuev-nord-cert.de

 

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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