Zeisberg GmbH
DE-MF-000024273 · Germany · Metzingen
Zeisberg GmbH is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: T2401, T2402, Typ2102.
Among these devices, 7 are declared active.
Devices declared under this manufacturer
- CA350
- CA350ta
- CA350tb
- CA450
- Merlin
- VertiGuard D
- VertiGuard RT
Catalogue references include FP006.AR01, FP010.AR01, FP028.AR01, FP028.AR02, FP028.AR03, FP028.AR04.
European nomenclature codes declared: Z121401, Z12140401, Z12120124.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Zeisberg GmbH was not found in either the U.S. or the Canadian register.