DYONMED SA
GR-MF-000033588 · Greece · GLYKA NERA PAIANIA
DYONMED SA is registered in the European database on medical devices as a manufacturer, with 29 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: DyonCovid19-S (neutro), DyonHpAb triple, n-AbCovid19.
Devices declared under this manufacturer
- DyonCDA
- DyonCalpro
- DyonCalpro double (50/200)
- DyonCardiac 3 in 1
- DyonCovid19
- DyonCovid19-S (neutro)
- DyonMicroalbumin
- DyonMono
- DyoniFOB
- DyoniFOB Combo T
- FluCov2
- GynoLab (10 tests/box)
Showing 12 of 29 declared devices.
Catalogue references include DMAMFL322-20, DNAT708, DNBSCVNAF, DNCT102, DNCT105, DNCV19 MG.
European nomenclature codes declared: W0105040619, W0101060499, W0105090102, W0102039013, W0299, W0105011801.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 29 |
| Country of registration | Greece |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 29 |
|---|---|
| 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. DYONMED SA was not found in either the U.S. or the Canadian register.