Trebin Group B.V.
NL-MF-000053856 · Netherlands · Bunschoten-Spakenburg
Trebin Group B.V. is registered in the European database on medical devices as a manufacturer, with 57 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 57 |
|---|
Most frequent device types declared: 2001, 2219, 2284, 2306, 3040.
Devices declared under this manufacturer
- Trebin Duimbrace
- Trebin Elleboogbrace met Gelpad
- Trebin Enkelbandage
- Trebin Enkelbrace
- Trebin Heupbrace
- Trebin Houdingcorrector
- Trebin Inlegzolen 415
- Trebin Kniebandage
- Trebin Kniebrace met Gel
- Trebin Kuitbrace
- Trebin Patella Pees Brace
- Trebin Polsbrace met Spalk
Showing 12 of 57 declared devices.
Catalogue references include 2001, 2219, 2284-S, 3040-BEIGE, 3040-BLACK, 4003.
European nomenclature codes declared: Y061203, Y060612, Y06120601, Y060615, Y061209, Y060307.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 57 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 57 |
|---|---|
| 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. Trebin Group B.V. was not found in either the U.S. or the Canadian register.