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Full Description

EEC 2017/745/EC lays down rules concerning the placing on the market, making available on the market or putting into service of medical devices for human use and accessories for such devices in the Union. This Regulation also applies to clinical investigations concerning such medical devices and accessories conducted in the Union.

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. )
 

Document History

  1. EEC 2017/745/EC

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    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

    • Most Recent
  2. EEC 93/42/EEC


    Council Directive 93/42/EEC

    • Historical Version
  3. EEC 90/385/EEC


    Council Directive 90/385/EEC, Corrected by 1994 Corrigendum

    • Historical Version