Medilon Braces
NL-MF-000047759 · Netherlands · Beek en Donk
Medilon Braces is registered in the European database on medical devices as a manufacturer, with 78 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 78 |
|---|
Most frequent device types declared: Medilon Anti Snurk Set, Medilon Carpostab Pro Polsbrace Maat S Links, Medilon Corestab Buikband Maat S, Medilon Genustab Kniebrace, Medilon Lumbastab.
Devices declared under this manufacturer
- Medilon
- Medilon Braces
Showing 12 of 78 declared devices.
Catalogue references include MB1226, MB2304, MB3404, MB3404-3, MB5223, MB6346.
European nomenclature codes declared: M030405, Y060308, Y060403, Y061209, Y060612, Y061217.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 78 |
| 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 | 78 |
|---|---|
| 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. Medilon Braces was not found in either the U.S. or the Canadian register.