The Medical Device Directive—Council Directive 93/42/EEC of 14 June 1993 concerning medical devices—is intended to harmonise the laws relating to medical devices within the European Union. The MD Directive is a 'New Approach' Directive and consequently in order for a manufacturer to legally place a medical device on the European market the requirements of the MD Directive have to be met. Manufacturers' products meeting 'harmonised standards'[1] have a presumption of conformity to the Directive. Products conforming with the MD Directive must have a CE mark applied. The Directive was most recently reviewed and amended by the 2007/47/EC and a number of changes were made. Compliance with the revised directive became mandatory on 21 March 2010.[citation needed]
European Union directive | |
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Title | Council Directive concerning medical devices |
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Made by | Council |
Made under | Art. 100a TEEC |
Journal reference | [31993L0042 L169, 12 July 1993 pp. 1-43] |
History | |
Date made | 1993-06-14 |
Entry into force | 1993-07-12 |
Implementation date | 1994-07-01 |
Other legislation | |
Replaces | Directive 76/764/EEC |
Amends | Directive 84/539/EEC, Directive 90/385/EEC |
Replaced by | Directive EU 2017/745 |
Repealed |
The Medical Devices Directive is being repealed and replaced by the 2017 EU Medical Device Regulation (EU 2017/745),[2] effective on 26 May 2021.[3]
See also
editReferences
edit- ^ Harmonised Standards under the MDD
- ^ 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
- ^ "Date of application of the Medical Devices Regulation postponed until May 2021".