Finder EU notified body intelligence
0646

UNITED REGISTRAR OF SYSTEMS (INSPECTORATE) Ltd

🇬🇧 United Kingdom · 2AR SOMERSET Withdrawn

Designations

MDR Medical devices · Regulation (EU) 2017/745 Withdrawn
Conformity assessment annexesAnnex V, Annex II, Annex VI
Designated since2006-04-09
Full scope text from the register
Annexes
  • Annex V, Annex II, Annex VI
Procedures
  • Production quality assurance, Product quality assurance, Full quality assurance system
Products
  • Cardiovascular function analysis equipment
  • dental materials
  • Operating theatre equipment
  • Examination and care instruments (non sterile)
  • All Class I sterile devices
  • Surgical instruments (non sterile)
  • General electro / mechanical equipment
  • Anaesthetic and life support equipment
  • Respiratory analysis equipment
  • Dental instruments (non sterile) equipment
  • Infusion / syringe pumps
  • Resuscitation equipment (includes defibrillators)
  • Vital signs monitoring equipment
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=0646

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.