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. )
Modified by
Regulation (EU) 2024/1860 of the European Parliament and of the Council of 13 June 2024 amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards a gradual roll-out of Eudamed, the obligation to inform in case of interruption or discontinuation of supply, and transitional provisions for certain in vitro diagnostic medical devices (Text with EEA relevance)
January 10, 2025 article 10a Addition
July 9, 2024 article 123 paragraph 3 point (ea) Addition
July 9, 2024 article 123 paragraph 3 point (ec) Addition
July 9, 2024 article 120 paragraph 13 Addition
July 9, 2024 article 123 paragraph 3 point (d) unnumbered paragraph 1 indent Addition
July 9, 2024 article 123 paragraph 3 point (d) unnumbered paragraph 1 Text Replacement
July 9, 2024 article 34 paragraph 2 Replacement
July 9, 2024 article 34 paragraph 1 Replacement
July 9, 2024 article 122 unnumbered paragraph 1 indent 2 Replacement
July 9, 2024 article 123 paragraph 3 point (eb) Addition
July 9, 2024 article 78 paragraph 14 Replacement
July 9, 2024 article 122 unnumbered paragraph 1 indent 1 Replacement
July 9, 2024 article 123 paragraph 3 point (d) unnumbered paragraph 2 Replacement
July 9, 2024 article 123 paragraph 3 point (e) Replacement
July 9, 2024 article 120 paragraph 8 Deletion
July 9, 2024 article 123 paragraph 3 point (d) unnumbered paragraph 1 indent 14 Replacement
July 9, 2024 article 122 unnumbered paragraph 1 indent 3 Replacement
July 9, 2024 article 122 unnumbered paragraph 1 indent 4 Replacement
July 9, 2024 article 123 paragraph 3 point (h) Deletion