AD SWISS MEDTECH SA
CH-MF-000037918 · Switzerland · Gravesano
AD SWISS MEDTECH SA is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Most frequent device types declared: DP001 Vibra 3.0, DP002 Vibra GO, DP003 MERT, DP005 PONOS, DP006 MONOS.
Among these devices, 5 are declared active.
Authorised representative in the Union: DO WELL TECHNOLOGIES DI BUCCI CLAUDIA.
Devices declared under this manufacturer
- MERT
- MONOS
- Vibra 3.0
- Vibra GO
Catalogue references include DP001, DP002, DP003, DP005, DP006.
European nomenclature codes declared: Z12062899.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. AD SWISS MEDTECH SA was not found in either the U.S. or the Canadian register.