Language:
    • Available Formats
    •  
    • Availability
    • Priced From ( in USD )
    • Printed Edition
    • Ships in 1-2 business days
    • $61.00
    • Add to Cart

Customers Who Bought This Also Bought

 

About This Item

 

Full Description

Sets general requirements & requirements relating to the design & construction of medical devices. Applies to all medical devices, except for active implantable medical devices.
 

Document History

  1. EEC 2017/745/EC


    Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices (Consolidated 2020), 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

    👀currently
    viewing


    Council Directive 93/42/EEC

    • Historical Version
  3. EEC 90/385/EEC


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

    • Historical Version
 

Amendments, rulings, supplements, and errata

  1. EEC 2001/104/EC


    Regulation (EC) No. 1882/2003 of the European Parliament and of the Council of 29 September 2003 adapting to the Council Decision 1999/468/EC the provisions relating to committees which assist the Commisssion in the exercise of its implementing powers

  2. EEC 2001/104/EC


    Directive 2001/104/EC of the European Parliament and of the Council of 7 December 2001 amending Council Directive 93/42/EEC concerning medical devices

  3. EEC 2007/47/EC


    Council Directive 2007/47/EC amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical

  4. EEC 98/79/EC


    Council Directive 98/79/EC

  5. EEC 2000/70/EC


    Parliament and Council Directive 2000/70/EC