DE/CA23
Competent authority · Germany · Darmstadt
A national competent authority for medical devices under the EU MDR/IVDR — market surveillance, vigilance and EUDAMED registration oversight.
A national body that oversees the application of EU medical-device regulation in its country — market surveillance, vigilance, economic-operator validation and EUDAMED registration oversight, under MDR Articles 101–108.
Explore every authority and economic operator registered in Germany.
A national body that oversees the application of EU medical-device regulation in its country — surveillance, vigilance, and registration oversight.
No — that's a notified body. A competent authority supervises the market; it does not issue device certificates.
Sourced directly from EUDAMED. This record was last updated Jun 25, 2026.
Operators whose registration was validated by this authority.
| Operator | Role | SRN | Country |
|---|---|---|---|
| ABAXIS Europe GmbH | Importer | DE-IM-000017366 | DE |
| ABAXIS Europe GmbH | Authorised representative | DE-AR-000017984 | DE |
| Abaxis, Inc. | Manufacturer | US-MF-000021651 | US |
| Achim Ruthner GmbH | Manufacturer | DE-MF-000016101 | DE |
| Acousticon Hörsysteme GmbH | Manufacturer | DE-MF-000013831 | DE |
| Acticore AG | Manufacturer | CH-MF-000016974 | CH |