Oscimed SA
CH-MF-000009605 · Switzerland · La Chaux-de-Fonds
Oscimed SA is registered in the European database on medical devices as a manufacturer, with 75 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 75 |
|---|
Most frequent device types declared: Anti snoring devices, Anti-snoring belt, Bruxism devices, Cast cutter saw, Cast cutter vacuum cleaner.
Among these devices, 64 are declared active.
Authorised representative in the Union: OSCIMED EUROPE SAS.
Devices declared under this manufacturer
- Bande Somnofit
- Blades OSCIMED
- Blades Oscimed
- ClipAir nasal dilator medium size
- OSCIMED 2000
- OSCIMED ERGO II
- OSCIMED PSV II
- Polyester filter, d=23 cm, H=18 cm
- SANABRUX
- SOMNOFIT Mandibular advancement device
- SOMNOFIT-S Mandibular advancement device
- Somnofit-Pro
Showing 12 of 75 declared devices.
Catalogue references include BS-65, OSC 206-V00, OSC 206-V00-UK, OSC 400-US, S-02, S-03.
European nomenclature codes declared: Z12139099, Z12139005, Q03010299.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | OSCIMED SA (CH) · FDA 9614473 |
| Devices in EUDAMED | 75 |
| Country of registration | Switzerland |
Device-level evidence
| Devices with a numeric GTIN | 75 |
|---|---|
| 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: United States only. Oscimed SA is registered in the United States but was not found in the Canadian register.