Greggersen Gasetechnik GmbH
DE-MF-000006442 · Germany · Hamburg
Greggersen Gasetechnik GmbH is registered in the European database on medical devices as a manufacturer, with 307 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 307 |
|---|
Most frequent device types declared: Entnahmestelle, Flowmeter, Röhrenflowmeter, Ventilkasten.
Among these devices, 307 are declared active.
Devices declared under this manufacturer
- AGFS Forano
- Fink
- Forano
- Kolibri 2
- Ventus evo 2
Showing 12 of 307 declared devices.
Catalogue references include 505607, 506024, 506060, 903132, 903343, 905146.
European nomenclature codes declared: Z120309.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 307 |
| 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 | 307 |
|---|---|
| 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. Greggersen Gasetechnik GmbH was not found in either the U.S. or the Canadian register.