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Version · Medical Devices Regulation

Version in force

Made by Regulation (EU) 2023/502 32023R0502 on EUR-Lex (external, EUR-Lex)

Commission Delegated Regulation (EU) 2023/502 of 1 December 2022 amending Regulation (EU) 2017/745 of the European Parliament and of the Council as regards the frequency of complete re-assessments of notified bodies (Text with EEA relevance)

Version 3 of 8 recorded for Medical Devices Regulation.

First seen by emendrix on , when it first read this version; that is not a legal date.

1 change in this version

  • 1 without an explanation

What these mean

Consolidated versions 02017R0745-20200424 → 02017R0745-20230311. v1 is the previous version, v2 this one.

Everything Regulation (EU) 2023/502 changed

What changed

Art. 44 Monitoring and re-assessment of notified bodies, Modified

+1,160 −58 characters · Applies from: not readable (the text changed beyond its dates, so no date that moved can be read as the application date) why

dates added to the text: 2023-03-11

Twin in IVDR: Art. 40(10)(1), textually similar (0.985), paired on this act's text of 19 July 2026 and the IVDR text of 10 January 2025. The record holds no IVDR version made by the same amending act. See where the two texts differ.

No explanation shipped — ModelAPIError: Connection error..

Text from EUR-Lex, before and after

Previous version, in force 24 April 2020 02017R0745-20200424 → this version, in force 11 March 2023 02017R0745-20230311

Article 44 Monitoring and re-assessment of notified bodies 1. Notified bodies shall, without delay, and at the latest within 15 days, inform the authority responsible for notified bodies of relevant changes which may affect their compliance with the requirements set out in … 553 unchanged words … in Article 45. 9. The authority responsible for notified bodies shall document and record any findings regarding non-compliance of the notified body with the requirements set out in Annex VII and shall monitor the timely implementation of corrective and preventive actions. 10. Three 5 years after notification of a notified body, and again every fourth year 5 years thereafter, a complete re-assessment to determine whether the notified body still satisfies the requirements set out in Annex VII shall be conducted by the authority responsible for notified bodies of the Member State in which the body is established and by a joint assessment team appointed for the purpose of in accordance with the procedure described in Articles 38 Article 39. The authority responsible for notified bodies of the Member State in which the notified body is established may conduct a complete re-assessment prior to the dates referred to in the first subparagraph, upon request by the notified body or where, based on the results of the annual assessments conducted in accordance with paragraph 4 of this Article, it has concerns regarding the continued fulfilment by the notified body of the requirements set out in Annex VII. Complete re-assessments that have already started prior to 11 March 2023 shall continue to be conducted, unless the authority responsible for notified bodies of the Member State in which the notified body is established decides to suspend or terminate the ongoing complete re-assessment, taking into account its own resources and 39. the resources of the notified body already spent on the re-assessment, as well as the results of the annual assessments conducted in accordance with paragraph 4 of this Article. Before suspending or terminating an ongoing complete re-assessment, the authority responsible for notified bodies shall hear the notified body concerned. 11. The Commission is empowered to adopt delegated acts in accordance with Article 115 in order to amend paragraph 10 to modify the frequency at which the complete re-assessment referred to in that paragraph is to be carried out. 12. The Member States shall report to the Commission and to the MDCG, at least once a year, on their monitoring and on-site assessment activities regarding notified bodies and, where applicable, subsidiaries and subcontractors. The report shall provide details of the outcome of those activities, including activities pursuant to paragraph 7, and shall be treated as confidential by the MDCG and the Commission; however it shall contain a summary which shall be made publicly available. The summary of the report shall be uploaded to the electronic system referred to in Article 57.

The full entry is committed at eu/32017R0745/CHANGELOG.md.