Medical Device Regulations 2017 Uk

These directives are transposed into uk law in the medical devices regulations 2002 si 2002 no 618 as amended uk mdr 2002.

Medical device regulations 2017 uk.

Regulation eu 2017 745 of the european parliament and of the council of 5 april 2017 on medical devices amending directive 2001 83 ec regulation ec no 178 2002 and regulation ec no 1223 2009 and repealing council directives 90 385 eec and 93 42 eec text with eea relevance. The new guide should prove useful for ce mark certificate holders has they prepare for full compliance with the medical devices regulation mdr 2017 745 and in vitro diagnostic regulation ivdr 2017 746. The adoption in april 2017 of regulation eu 2017 745 on medical devices mdr and regulation eu 2017 746 on in vitro diagnostic devices ivdr changed the european legal framework for medical devices introducing new responsibilities for ema and for national competent authorities. Regulation 2017 745 on medical devices eu mdr.

Added a link to guidance for manufacturers who don t design or manufacture devices but place their names. Although the united kingdom will have officially left the european union by the end of march 2019 the country is continuing to regulate medical devices using the mdr and ivdr regulations which were introduced in may 2017. A new interactive online guide from the uk mhra provides high level overviews of new european medical device and ivd regulations. Regulation eu 2017 745 of the european parliament and of the council show full title.

Both regulations entered into force in may 2017 and have a staggered transitional period. Medical devices regulations 238 kb pdf full document. Added a new section on covid 19 medical devices guidance. Entering into force on 25 may 2017 the three and five year transition periods also known as implementation are now underway.

Medical devices regulations 558 kb regulations are current to 2020 09 09 and last amended on 2019 12 16.