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🇬🇧 United Kingdom · Hawarden, Deeside CH5 3US Withdrawn

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Designations

MDR Medical devices · Regulation (EU) 2017/745 Withdrawn

Conformity assessment annexesAnnex IV, Annex V, Annex II, Annex III, Annex VI

Designated since2006-04-09

Full scope text from the register

Annexes

Annex IV, Annex V, Annex II, Annex III, Annex VI

Procedures

EC verification, Production quality assurance, Product quality assurance, EC type-examination, Full quality assurance system

Products

All active medical devices

Source: EU Single Market Compliance Space (SMCS), retrieved 2026-06-23.
https://webgate.ec.europa.eu/single-market-compliance-space/notified-bodies/free-search?text=0518

This page is an informational mirror of the official register. It is not affiliated with the European Commission. Always verify the current designation and scope against the official SMCS record before relying on it.