OBA AG
CH-MF-000037383 · Switzerland · Basel
OBA AG is registered in the European database on medical devices as a manufacturer, with 637 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 637 |
|---|
Authorised representative in the Union: ANNIE BAUER CONFORT.
Devices declared under this manufacturer
- Anti Dekubitus Matratze 1T
- Anti Dekubitus Matratze Airsoft Duo
- Anti Dekubitus Matratze EvoSoft
- Anti Dekubitus Matratze Evoba
- Anti Dekubitus Matratze Hospisoft
- Anti Dekubitus Matratze Memoba
- Anti Dekubitus Matratze Motus
- Hospiseat Duro
- Hospiseat Standard
- Jimmy
- MOC
- OBA 600
Showing 12 of 637 declared devices.
Catalogue references include 3020.120, 3020.212, 3020.230, 3020.336, 3060.302, 5001.123.
European nomenclature codes declared: V080702, V080302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 637 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 637 |
|---|---|
| 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. OBA AG was not found in either the U.S. or the Canadian register.