# Commission Implementing Decision (EU) 2019/1729 of 15 October 2019 on the harmonised standard for conformity assessment drafted in support of Regulations (EC) No 765/2008 and (EC) No 1221/2009 of the European Parliament and of the Council, Directive 2006/42/EC of the European Parliament and of the Council and Union acts incorporating the reference provisions of Decision No 768/2008/EC of the European Parliament and of the Council (Text with EEA relevance), Division 25

Extent: E+W+S+N.I.

Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (OJ L 117, 5.5.2017, p. 176);

---
Source: https://www.legislation.gov.uk/eudn/2019/1729/annex/division/25 (the official version)
Page: https://openlegislation.uk/eu-decision-2019-1729/annex/division-25
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.