ZDH-ZERT [RECHTSNACHFOLGER IS DIE MDC MEDICAL DEVICE CERTIFICATION GMBH, KENN-NR 0483, STUTTGART]

🇩🇪 Germany · STUTTGART Withdrawn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MDR Medical devices · Regulation (EU) 2017/745 Withdrawn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

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

Products

orthopaedic implants
surgical devices and aids, except for lithotripsy devices
dental equipment
ventilators and oxygen therapy apparatus, except for devices for hyperbaric therapy
patient storage and transport equipment
reusable non-active medical instruments
rehabilitation devices and active prostheses
dental equipment and instruments
electrical stimulation and acupuncture devices, hydro electric bath
short waves and devices for treatment using heat
Active medical devices
high frequency surgery equipment
disposable products
devices to monitor and determine vital signs
hearing aids and audiometers
Non-active 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=0538

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.