AMTAC CERTIFICATION SERVICES LTD

🇬🇧 United Kingdom · Keynes MK5 8NL Active

www.intertek.com

Designations

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

Conformity assessment annexesAnnex II, Annex V, Annex VI

Designated since2007-04-19

Full scope text from the register

Annexes

Annex II, Annex V, Annex VI

Procedures

Full quality assurance system, Product quality assurance, Production quality assurance

Products

Devices manufactured utilising animal tissue covered by Directive 2003/32/EC are included

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=0473

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.