Finder EU notified body intelligence
0297

DQS Medizinprodukte GmbH

🇩🇪 Germany · FRANKFURT AM MAIN Active

www.dqsglobal.com/de-de/zertifizieren/verordnung-mdr-eu-2017-745

Designations

MDR Medical devices · Regulation (EU) 2017/745 Active
Conformity assessment annexesAnnex VI, Annex II, Annex V
Designated since2008-07-08
Full scope text from the register
Annexes
  • Annex VI, Annex II, Annex V
Procedures
  • Product quality assurance, Full quality assurance system, Production quality assurance
Products
  • Non-active medical devices
  • Active medical devices, except
  • Medical devices covered by directive 2003/32/EC
  • hyperthermy 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=0297

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.