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Follow-up measures to ensure smooth functioning of medical device certification

On 19 May 2020, Commission Implementing Regulation (EU) No 2020/666 of 18 May 2020 amending Implementing Regulation (EU) No 920/2013 as regards the extension of the validity of the designation, supervision and monitoring of notified bodies was published in the Official Journal of the European Union (L 156).

These are follow-up measures to ensure the smooth functioning of certification of medical devices in the context of the postponement of the application of Regulation (EU) No 2017/745 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