GaDia SA
CH-MF-000031123 · Switzerland · Monthey
GaDia SA is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: SCH-025.
Authorised representative in the Union: ER Egészségügyi, Kereskedelmi és Szolgáltató Kft..
Devices declared under this manufacturer
- CandiDia-Antibody
- FungaDia-Aspergillus ELISA
- FungaDia-Aspergillus Rapid Test
- KarbaDia Rapid Test
- PapilloDia Rapid Test
- SchistoDia Antibody
Catalogue references include ASP-025, ASPE-096, CAN-025, CER-020, KAR-025, SCH-025.
European nomenclature codes declared: W0105060301, W0104080506, W0105060302, W0105050206, W0102030399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. GaDia SA was not found in either the U.S. or the Canadian register.