Gesetz zur Änderung medizinprodukterechtlicher Vorschriften
Edition 2009-07-29

Allgemeine Verwaltungsvorschrift zur Durchführung des Medizinproduktegesetzes (Medizinprodukte-Durchführungsvorschrift - MPGVwV)
Edition 2012-05-18

Bekanntmachung der Fundstellen von Normen gemäß § 3 Nummer 18 des Medizinproduktegesetzes (MPG)
Edition 2015-04-20

Commission Implementing Regulation (EU) No 920/2013 of 24 September 2013 on the designation and the supervision of notified bodies under Council Directive 90/385/EEC on active implantable medical devices and Council Directive 93/42/EEC on medical devices
Edition 2013-09-24

Commission Recommendation of 24 September 2013 on the audits and assessments performed by notified bodies in the field of medical devices
Edition 2013-09-24

Bekanntmachung der Fundstellen von Normen gemäß § 3 Nummer 18 des Medizinproduktegesetzes (MPG)
Edition 2014-02-06

Commission Implementing Decision (EU) 2021/1195 of 19 July 2021 on the harmonised standards for in vitro diagnostic medical devices drafted in support of Regulation (EU) 2017/746 of the European Parliament and of the Council
Edition 2021-07-19

Commission Implementing Decision (EU) 2022/729 of 11 May 2022 amending Implementing Decision (EU) 2021/1195 as regards harmonised standards for quality management systems and for application of risk management to medical devices
Edition 2022-05-11

Corrigendum to Regulation (EU) 2022/112 of the European Parliament and of the Council of 25 January 2022 amending Regulation (EU) 2017/746 as regards transitional provisions for certain in vitro diagnostic medical devices and the deferred application of conditions for in-house devices
Edition 2022-02-03

Commission Delegated Regulation (EU) 2023/503 of 1 December 2022 amending Regulation (EU) 2017/746 of the European Parliament and of the Council as regards the frequency of complete re-assessments of notified bodies
Edition 2022-12-01