Gello GmbH Geltechnik
DE-MF-000010607 · Germany · Ahaus
Gello GmbH Geltechnik is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 27 |
|---|
Devices declared under this manufacturer
- Kalt-Warm-Kompresse
- Kältesofortkompresse
- Ultraschallgel
Showing 12 of 27 declared devices.
Catalogue references include 1500115110116216, 4000800570116021, 4000850570116021, L04900000, L04900001, L12291101.
European nomenclature codes declared: M9001, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| 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 | 27 |
|---|---|
| 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. Gello GmbH Geltechnik was not found in either the U.S. or the Canadian register.