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2005/50/EG
Commission Directive 2005/50/EC of 11 August 2005 on the reclassification of hip, knee and shoulder joint replacements in the framework of Council Directive 93/42/EEC concerning medical devices
Edition
2005-08-11
EUV 2017/746
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
Edition
2017-04-05
EUV 2017/745
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
Edition
2017-04-05
EUV 722/2012
Commission Regulation (EU) No 722/2012 of 8 August 2012 concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin
Edition
2012-08-08
Bestellformular GEFMA-Richtlinien (en)
order form
Edition
2015-01
Preisliste 2024
Price list - DIN Standards, draft DIN Standards and other technical rules
Edition
2024-05
Preisliste (VDE) 2024
Price list - DIN Standards, draft DIN Standards with "K" price group classification (VDE)
Edition
2024-05