DE/CA37, Regierungspräsidium Stuttgart
Competent authority · Germany · Stuttgart
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 29, 2026.
Operators whose registration was validated by this authority.
| Operator | Role | SRN | Country |
|---|---|---|---|
| 3a-diagnostics GmbH | Manufacturer | DE-MF-000030014 | DE |
| 4S Information Systems Ltd | Manufacturer | UK-MF-000044727 | GB |
| Aacurat GmbH | Manufacturer | DE-MF-000019560 | DE |
| ABW Automatisierung + Bildverarbeitung Dr. Wolf GmbH | Manufacturer | DE-MF-000033572 | DE |
| ACTIMI GmbH | Manufacturer | DE-MF-000024271 | DE |
| ACTIMI GmbH | System / procedure pack producer | DE-PR-000034383 | DE |