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: Carbide bur Diacarb FG, Diaceram 2-step, Diacomp, Diaprophy prophylaxis polishers cup;un, FG Swiss Goldie coarse.
Authorised representative in the Union: DFS-Diamon GmbH.
Devices declared under this manufacturer
- DIASWISS Bone Cutter
- DIASWISS Diamond CA
- DIASWISS Diamond FG
- Dental Polisher for Prophylaxis
- Diacarb
- Diaceram 2-Step
- Diaceram 3-Step
- Diacomp
- Endodontic Guttapercha Separator
- Perio Diamond
- Swiss Goldie
- rootEX Pilot Drill
Showing 12 of 1 797 declared devices.
Catalogue references include 103RA-0, 271UM, 313SG379.023, 314001.023, 314007.008, 314805.014.
European nomenclature codes declared: Z12110102, Q01010403, Q010399, Q010501.
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; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 1 797 |
|---|---|
| Found in the U.S. device database | 1 732 |
| Share | 96.4 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.