Golias d.o.o.
SI-MF-000006917 · Slovenia · Kranj
Golias d.o.o. is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: PO100, Petrijevka fi 90mm K, Posodica 80ml zaskočni pokrov, Posodica za vzorec s pokrovom 120ml, Posodica za vzorec z žličko.
Devices declared under this manufacturer
- Epruveta 11 x 70mm
- Epruveta 12 x 75mm
- Epruveta 16 x 105mm z navojnim zamaškom PP z graduacijo
- Epruveta 16 x 120mm z navojem prozorna
- Epruveta za določanje sedimentacije
- Epruveta za določanje sedimentacije z zamaškom
- Petri dish fi 90mm ster. A
- Petrijevka fi 70mm
- Petrijevka fi 90mm K
- Petrijevka fi 90mm z 2 prekati
- Posodica za vzorec s pokrovom
- Posodica za vzorec s pokrovom 120ml bel zamašek zaprta
Showing 12 of 27 declared devices.
Catalogue references include EP103, EP45, PE01K, PE02, PE19, PE22A.
European nomenclature codes declared: W050301020102, W0503030101, W050180, W05010203, W05010202, W05019001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| Country of registration | Slovenia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 27 |
|---|---|
| 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. Golias d.o.o. was not found in either the U.S. or the Canadian register.