URZAD REJESTRACJI PRODUKTOW LECZNICZYCH, WYROBOW MEDYCZNYCH I PRODUKTOW

🇵🇱 Poland · 00 725 WARSZAWA Withdrawn

Designations

MDR Medical devices · Regulation (EU) 2017/745 Withdrawn

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

Designated since2006-04-09

Full scope text from the register

Annexes

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

Procedures

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

Products

All 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=1474

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.