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Unofficial consolidated textConsolidated 2026-01-01English

Article 92

Reproduced from official EUR-Lex 1/1/2026.

Official catalogue · non-binding

Related guidance (14)

Current English catalogue entries that refer to Article 92. Guidance is non-binding and kept separate from the regulation text.

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MDCG 2021-1 rev.1Guidance on harmonised administrative practices and alternative technical solutions until EUDAMED is fully functionalMay 2021
MDCG 2022-16Guidance on Authorised Representatives Regulation (EU) 2017/745 and Regulation (EU) 2017/746October 2022
MDCG 2019-16 rev.1Guidance on cybersecurity for medical devicesJuly 2020
MDCG 2024-6Preliminary re-assessment review (PRAR) form template (MDR)May 2024
MDCG 2024-7 rev.1 MDCG 2021-15/MDCG 2024-7 AnnexPreliminary assessment review (PAR) form template (MDR) Annex to Application Form & PAR Template MDR (List of documents)January 2025
MDCG 2021-15 rev.1 MDCG 2021-15/MDCG 2024-7 AnnexApplication form to be submitted by a conformity assessment body when applying for designation as notified body under the medical devices regulation (MDR)Annex to Application Form & PAR Template MDR (List of documents)January 2025
MDCG 2020-14Guidance for notified bodies on the use of MDSAP audit reports in the context of surveillance audits carried out under the Medical Devices Regulation (MDR)/In Vitro Diagnostic medical devices Regulation (IVDR)August 2020
MDCG 2024-1Device Specific Vigilance Guidance (DSVG) TemplateJanuary 2024
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MDCG 2024-1-1DSVG 01 on Cardiac ablationJanuary 2024
MDCG 2024-1-2DSVG 02 on Coronary stentsJanuary 2024
MDCG 2024-1-3DSVG 03 on Cardiac implantable electronic devices (CIEDs)January 2024
MDCG 2024-1-4DSVG 04 on Breast implantsJanuary 2024
MDCG 2024-1-5DSVG 05 on Urogynaecological Surgical Mesh Implants used for Pelvic Organ Prolapse repair and Stress Urinary IncontinenceJune 2024
MDCG 2023-3 rev.2Questions and Answers on vigilance terms and concepts as outlined in the Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746January 2025

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