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EU’s decision to extend the Medical Device Regulation transition periods for legacy medical device directives products will be mirrored in the UK

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Susanna Al Halabi
Regulatory Lead

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Susanna Al Halabi
Regulatory Lead

The EU has taken steps to give manufacturers more time to get certain medical devices certified under the EU Medical Devices Regulation (EU MDR). 

These changes to the EU MDR apply automatically in Northern Ireland under the terms of the Northern Ireland Protocol. Certificates that have been extended will also be recognised as valid for placing CE marked devices on the GB market, for more information visit the link below.

The EU has taken steps to give manufacturers more time to get certain medical devices certified under the EU Medical Devices Regulation (EU MDR).
www.gov.uk/...

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mdr, medical

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Susanna Al Halabi
Regulatory Lead

Get in touch

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Susanna Al Halabi
Regulatory Lead

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