欧盟医疗器械法规英文版EU 20172185-2017.pdf

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欧盟医疗器械法规英文版EU 20172185-2017.pdf

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An official EU website Title and reference Commission Implementing Regulation (EU) 2017/2185 of 23 November 2017 on the list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notiﬁed bodies in the ﬁeld of medical devices under Regulation (EU) 2017/745 of the European Parliament and of the Council and in vitro diagnostic medical devices under Regulation (EU) 2017/746 of the European Parliament and of the Council (Text with EEA relevance. ) C/2017/7779 OJ L 309, 24.11.2017, p. 7–17 (BG, ES, CS, DA, DE, E T, EL, EN, FR, HR, I T, LV, LT, HU, M T, NL, PL, PT, RO, SK, SL, FI, SV) In force ELI: http://data.europa.eu/eli/reg_impl/2017/2185/oj Languages, formats and link to OJ BG ES CS DA DE ET EL EN FR GA HR IT LV LT HU MTNL PL PT RO SK SL FI SV HTML PDF Oﬃcial Journal Multilingual display English (en) Please choose Please choose Display Text 24.11.2017 EN Official Journal of the European Union L 309/7 COMMISSION IMPLEMENTING REGULATION (EU) 2017/2185 of 23 November 2017 on the list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of medical devices under Regulation (EU) 2017/745 of the European Parliament and of the Council and in vitro diagnostic medical devices under Regulation (EU) 2017/746 of the European Parliament and of the Council (Text with EEA relevance) THE EUROPEAN COMMISSION, Havi