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Designations

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

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

Designated since2006-04-09

Full scope text from the register

Annexes

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

Procedures

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

Products

All medical devices

LVD Low voltage electrical equipment · Directive 2014/35/EU Active

Conformity assessment annexesArticle 8, Article 9

Designated since2006-04-09

Full scope text from the register

Annexes

Article 8, Article 9

Procedures

Opinion on a safeguard action (Art 9), Report consequent on a challenge (Art 8)

Products

Electrical equipment designed for use within certain voltage limits

LVD Low voltage electrical equipment · Directive 2014/35/EU Active

Conformity assessment annexesArticle 8, Article 9

Designated since2006-04-09

Full scope text from the register

Annexes

Article 8, Article 9

Procedures

Opinion on a safeguard action (Art 9), Report consequent on a challenge (Art 8)

Products

Electrical equipment designed for use within certain voltage limits

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=1509

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.