GMED SAS

🇫🇷 France · PARIS Active

lne-gmed.com/fr

Designations

IVDR In vitro diagnostic medical devices · Regulation (EU) 2017/746 Active

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

Designated since2006-05-30

Full scope text from the register

Annexes

Annex VII, Annex VI, Annex IV, Annex V, Annex III

Procedures

EC declaration of conformity, EC type-examination, EC verification, Production quality assurance, Full quality assurance system

Products

In vitro diagnostic 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=0459

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.