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  6. Factsheet - 32013R0920

Factsheet - 32013R0920

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
Proposed act with possible EEA relevance
Act under scrutiny by EEA EFTA
Draft Joint Committee Decision (JCD) under consideration
Entry into force of Joint Committee Decision (JCD) pending
Incorporated into the EEA Agreement and in force
Incorporated into the EEA Agreement but no longer in force
Legal status
EU legal act incorporated into the EEA Agreement by a Joint Committee Decision (JCD)
Area (EEA Agreement)
II Technical Regulations, Standards, Testing and Certification
II.XXX Medical Devices
Joint committee decision (JCD)
218/2015
In force in the EEA
Yes
Legal Documents
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
Joint Committee Decision in English: OJ L 85, 30.3.2017, p. 39
Legal act in EU languages: OJ L 253, 25.9.2013, p. 8
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) nr. 920/2013 frá 24. september 2013 um tilnefningu tilkynntra aðila og eftirlit með þeim samkvæmt tilskipun ráðsins 90/385/EBE um virk, ígræðanleg lækningatæki og tilskipun ráðsins 93/42/EBE um lækningatæki
Legal act in Icelandic: EEA Suppl. No 63, 15.10.2015, p. 1776-1787
Joint Committee Decision in Icelandic: EEA Supplement No 19, 30.3.2017, p. 38
Durchführungsverordnung (EU) Nr. 920/2013 der Kommission vom 24. September 2013 über die Benennung und Beaufsichtigung benannter Stellen gemäß der Richtlinie 90/385/EWG des Rates über aktive implantierbare medizinische Geräte und der Richtlinie 93/42/EWG des Rates über Medizinprodukte
Joint Committee Decision in German: OJ L 85, 30.3.2017, p. 39
Legal act in German: OJ L 253, 25.9.2013, p. 8
Kommisjonens gjennomføringsforordning (EU) nr. 920/2013 av 24. september 2013 om utpeking av og tilsyn med meldte organer i henhold til rådsdirektiv 90/385/EØF om aktivt implanterbart medisinsk utstyr og rådsdirektiv 93/42/EØF om medisinsk utstyr
Legal act in Norwegian: EEA Suppl. No 57, 27.8.2020, p. 1205-1216
Joint Committee Decision in Norwegian: EEA Supplement No 19, 30.3.2017, p. 38
History
26.09.2015 Adopted JCD confirmed entry into force date
26.09.2015 Compliance date in the EEA
25.09.2015 Adoption of Joint Commitee Decision (JCD) incorporating the act into the EEA Agreement
Joint Committee Decision in English: OJ L 85, 30.3.2017, p. 39
Joint Committee Decision in Icelandic: EEA Supplement No 19, 30.3.2017, p. 38
Joint Committee Decision in German: OJ L 85, 30.3.2017, p. 39
Joint Committee Decision in Norwegian: EEA Supplement No 19, 30.3.2017, p. 38
27.03.2015 Draft Joint Commitee Decision (JCD) incorporating the act into the EEA Agreement sent to Commission
15.10.2013 Compliance date in the EU
24.09.2013 Adoption date in the EU
Legal act in EU languages: EUR-LEX 0920
Legal act in German: EUR-LEX 0920

Disclaimer: EEA-Lex is provided for information purposes only. The information is not guaranteed or promised to be current or complete and is not intended to replace any applicable legal sources.

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