STERGIOULAS VASILEIOS & Co L.P.
GR-MF-000018251 · Greece · THESSALONIKI
STERGIOULAS VASILEIOS & Co L.P. is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: ATHOMER SEAWATER NASAL SPRAYS.
Among these devices, 7 are declared sterile.
Devices declared under this manufacturer
- ATHOMER HYPERTONIC SEAWATER KIDS & ADULTS MIST SPRAY 100ml
- ATHOMER ISOTONIC SEAWATER BABIES & ADULTS MIST SPRAY 100ml
- ATHOMER ISOTONIC SEAWATER MINT & EUCALYPTUS KIDS & ADULTS MIST SPRAY 1
- ATHOMER ISOTONIC SEAWATER PROPOLIS BABIES & ADULTS MIST SPRAY 100ml
- ATHOMER MINI ISOTONIC SEAWATER MINT & EUCALYPTUS SPRAY 35ml
- ATHOMER MINI ISOTONIC SEAWATER PROPOLIS 35ml
- ATHOMER MINI ISOTONIC SEAWATER SPRAY 35ML
Catalogue references include 86203, 86204, 86205, 86206, 86207, 86208.
European nomenclature codes declared: Q030103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| 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 | 7 |
|---|---|
| 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. STERGIOULAS VASILEIOS & Co L.P. was not found in either the U.S. or the Canadian register.