Commission Implementing Decision (EU) 2020/1808 of 30 November 2020 amending Implementing Decision (EU) 2019/1698 as regards European standards for certain child care articles, children's furniture, stationary training equipment, and the ignition propensity of cigarettes
Edition 2020-11-30

Commission Implementing Decision (EU) 2021/1195 of 19 July 2021 on the harmonised standards for in vitro diagnostic medical devices drafted in support of Regulation (EU) 2017/746 of the European Parliament and of the Council
Edition 2021-07-19

Commission Implementing Decision (EU) 2022/622 of 7 April 2022 amending Implementing Decision (EU) 2019/1326 as regards the harmonised standards for electromagnetic compatibility of electricity metering equipment and circuit breakers for household and similar uses
Edition 2022-04-07

Commission Implementing Decision (EU) 2022/729 of 11 May 2022 amending Implementing Decision (EU) 2021/1195 as regards harmonised standards for quality management systems and for application of risk management to medical devices
Edition 2022-05-11

Commission Implementing Decision (EU) 2022/910 of 9 June 2022 amending Implementing Decision (EU) 2019/1326 as regards the harmonised standards for electromagnetic compatibility of low-voltage switches, disconnectors, switch-disconnectors and fuse-combination units, and for external power supply for mobile phones
Edition 2022-06-09

Commission Implementing Decision (EU) 2023/941 of 2 May 2023 on harmonised standards for personal protective equipment drafted in support of Regulation (EU) 2016/425 of the European Parliament and of the Council
Edition 2023-05-02

Corrigendum to Regulation (EU) 2022/112 of the European Parliament and of the Council of 25 January 2022 amending Regulation (EU) 2017/746 as regards transitional provisions for certain in vitro diagnostic medical devices and the deferred application of conditions for in-house devices
Edition 2022-02-03

Regulation (EU) 2022/112 of the European Parliament and of the Council of 25 January 2022 amending Regulation (EU) 2017/746 as regards transitional provisions for certain in vitro diagnostic medical devices and the deferred application of conditions for in-house devices
Edition 2022-01-25

Commission Delegated Regulation (EU) 2022/30 of 29 October 2021 supplementing Directive 2014/53/EU of the European Parliament and of the Council with regard to the application of the essential requirements referred to in Article 3(3), points (d), (e) and (f), of that Directive
Edition 2021-10-29

Commission Implementing Decision (EU) 2022/15 of 6 January 2022 amending Implementing Decision (EU) 2021/1195 as regards harmonised standards for sterilisation of health care products, aseptic processing of health care products, quality management systems, symbols to be used with information to be supplied by the manufacturer and requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
Edition 2022-01-06