Vermeiren Group
BE-MF-000019750 · Belgium · Kalmthout
Vermeiren Group is registered in the European database on medical devices as a manufacturer, with 222 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 222 |
|---|
Most frequent device types declared: 2219E, 268, 385, 9062, 9062 XXL.
Among these devices, 60 are declared active.
Devices declared under this manufacturer
- 2219E
- 268
- 385
- 9062
- 9062 XXL
- Alois
- Eclips X2 Kids
- Express VB
- Forest 3
- Goliat
- Plego
- Pluo
Showing 12 of 222 declared devices.
Catalogue references include 4015869, 4017195, 4019911, 5143701, 5145583, 6502325.
European nomenclature codes declared: Y122106, Y122127, Y122124, Y122103, Y120606, Y180918.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 222 |
| Country of registration | Belgium |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 222 |
|---|---|
| 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. Vermeiren Group was not found in either the U.S. or the Canadian register.