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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 (Text with EEA relevance. )

    Legal status of the documentIn force

    CELEX number:
    32017R0745
    Form:
    Regulation
    Author:
    European Parliament, Council of the European Union
    Date of document:
    05/04/2017; Date of signature
    Number of pages:
    175

    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 (Text with EEA relevance. )

    Legal status of the documentIn force

    CELEX number:
    32017R0746
    Form:
    Regulation
    Author:
    European Parliament, Council of the European Union
    Date of document:
    05/04/2017; Date of signature
    Number of pages:
    157

    COMMISSION STAFF WORKING DOCUMENT Accompanying the document Report from the Commission to the European Parliament and the Council Implementation of the third programme of EU action in the field of health in 2017

    SWD/2020/52 final

    CELEX number:
    52020SC0052
    Form:
    Staff working document
    Author:
    European Commission, Directorate-General for Health and Food Safety
    Date of document:
    10/03/2020

    Decision of the EEA Joint Committee No 301/2019 of 13 December 2019 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2020/319]

    Legal status of the documentIn force

    CELEX number:
    22020D0319
    Form:
    Decision adopted by bodies created by international agreements
    Author:
    EEA Joint Committee
    Date of document:
    13/12/2019; Date of adoption
    Number of pages:
    2

    P7_TA(2014)0267 In vitro diagnostic medical devices ***I European Parliament legislative resolution of 2 April 2014 on the proposal for a regulation of the European Parliament and of the Council on in vitro diagnostic medical devices (COM(2012)0541 — C7-0317/2012 — 2012/0267(COD)) P7_TC1-COD(2012)0267 Position of the European Parliament adopted at first reading on 2 April 2014 with a view to the adoption of Regulation (EU) No …/2014 of the European Parliament and of the Council on in vitro diagnostic medical devicesText with EEA relevance.

    CELEX number:
    52014AP0267
    Form:
    Legislative resolution
    Author:
    European Parliament, Committee on Employment and Social Affairs, Committee on Industry, Research and Energy, Committee on International Trade, Committee on the Environment, Public Health and Food Safety, Committee on the Internal Market and Consumer Protection
    Date of document:
    02/04/2014; Date of vote
    Number of pages:
    140

    P7_TA(2014)0266 Medical devices ***I European Parliament legislative resolution of 2 April 2014 on the proposal for a regulation of the European Parliament and of the Council on medical devices, and amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 (COM(2012)0542 — C7-0318/2012 — 2012/0266(COD)) P7_TC1-COD(2012)0266 Position of the European Parliament adopted at first reading on 2 April 2014 with a view to the adoption of Regulation (EU) No …/2014 of the European Parliament and of the Council on medical devices, and amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009Text with EEA relevance.

    CELEX number:
    52014AP0266
    Form:
    Legislative resolution
    Author:
    European Parliament, Committee on Employment and Social Affairs, Committee on Industry, Research and Energy, Committee on International Trade, Committee on the Environment, Public Health and Food Safety, Committee on the Internal Market and Consumer Protection
    Date of document:
    02/04/2014; Date of vote
    Number of pages:
    154

    Position (EU) No 3/2017 of the Council at first reading with a view to the adoption of a Regulation of the European Parliament and of the Council on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU Adopted by the Council on 7 March 2017 (Text with EEA relevance. )

    CELEX number:
    52017AG0003(01)
    Form:
    Position
    Author:
    Council of the European Union
    Date of document:
    07/03/2017; Date of adoption
    Number of pages:
    154

    Position (EU) No 2/2017 of the Council at first reading with a view to the adoption of a Regulation of the European Parliament and of the Council 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 Adopted by the Council on 7 March 2017 (Text with EEA relevance)

    CELEX number:
    52017AG0002(01)
    Form:
    Position
    Author:
    Council of the European Union
    Date of document:
    07/03/2017; Date of adoption
    Number of pages:
    196

    Amendments adopted by the European Parliament on 22 October 2013 on the proposal for a regulation of the European Parliament and of the Council on medical devices, and amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 (COM(2012)0542 — C7-0318/2012 — 2012/0266(COD))

    CELEX number:
    52013AP0428
    Form:
    Legislative resolution
    Author:
    European Parliament, Committee on Employment and Social Affairs, Committee on Industry, Research and Energy, Committee on International Trade, Committee on the Environment, Public Health and Food Safety, Committee on the Internal Market and Consumer Protection
    Date of document:
    22/10/2013; Date of vote
    Number of pages:
    164
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    Domain: All, Documents mentioning: 32010D0227, Search language: English