M.Ex.T. Belgium
BE-MF-000022927 · Belgium · Roeselare
M.Ex.T. Belgium is registered in the European database on medical devices as a manufacturer, with 52 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 52 |
|---|
Most frequent device types declared: Bandages, Plasters, Wound dressings.
Devices declared under this manufacturer
- Adhesive plaster blue, 0,02x5m
- Duoskin bleu, 10x8cm
- Duoskin, 10x6cm
- ECV5, 5cm x 4m
- Elwo Mix
- Finbo Large
- Hechtpleister zijde, 0,0125x5m
- Ideaalwindsel, 0,08x5m
- Pansement cohésif, 0,08x4m
- Pansement cohésif, 2,5cmx4m
- Pflasterstrip (7,2x1,9cm)
- Pleisterset 24 stuks
Showing 12 of 52 declared devices.
Catalogue references include 0010.013, 0010.024, 0010.025, 0010.026, 0020.011, 0020.014.
European nomenclature codes declared: M04010101, M03030103, M04010102, M030402020101, M04010202, M0303010101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 52 |
| 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 | 52 |
|---|---|
| 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. M.Ex.T. Belgium was not found in either the U.S. or the Canadian register.