Diaswiss SA
CH-MF-000012042 · Switzerland · Nyon
Diaswiss SA is registered in the European database on medical devices as a manufacturer, with 1 797 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 1 797 |
|---|
Most frequent device types declared: FG diamond standard, FG diamond coarse, FG diamond fine, FG diamond supercoarse, FG diamond superfine.
Authorised representative in the Union: DE-AR-000008273.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | DIASWISS S.A. (CH) · FDA 8031011 |
| Devices in EUDAMED | 1 797 |
| Country of registration | Switzerland |
⚠️ A similar name exists in the FDA register. We do not assert that it is the same company — the two registers share no common identifier, and a name alone is not proof. This entry needs a human check.