Customer Information MDR - the new EU Medical Device Regulation 2017 / 745 (MDR).

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We would like to inform you about the new EU Medical Device Regulation 2017 / 745 (MDR). Already today we, Hermann Bock GmbH, promise that every product placed on the market as of May 26, 2020 will be compliant with the new EU Medical Products Directive.

We would like to inform you about the new EU Medical Device Regulation 2017 / 745 (MDR).  Already today we, Hermann Bock GmbH, promise that every product placed on the market as of May 26, 2020 will be compliant with the new EU Medical Products Directive. All technical documents as well as the declaration of conformity will be changed over by the deadline mentioned above. Accordingly, we are already working on the necessary adjustments to our processes. 

Products lawfully placed on the market before May 26, 2020 in accordance with Directive 93/42/EEC may continue to be made available on the market or put into service until May 27, 2025 (cf. the transitional provisions pursuant to Article 120 of the MDR).

More detailed information about the MDR can be found here: https://eur-lex.europa.eu/legal-content/DE/TXT/?uri=CELEX%3A32017R0745

If you have any questions or require further information, please call us (+49) 5246 920 50 or write an email to infoNOSPAM@bock.net.


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