GVS S.p.A.
IT-MF-000028147 · Italy · Zola Predosa (Bologna)
GVS S.p.A. is registered in the European database on medical devices as a manufacturer, with 152 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 152 |
|---|
Among these devices, 146 are declared sterile.
Devices declared under this manufacturer
- 4058272BF119Y
- AQUALINE RCA
- AQUALINE S
- AQUASPIKE 2
- E3001OD
- E3002OD5
- E3005OD
- EPE1016AU
- HI-FLO IV Extension Set
- HI-FLO IV Set
- HT0250UVEVA
- HT0500EVA2
Showing 12 of 152 declared devices.
Catalogue references include 1500014406, 5030010216, GIS003B01S, GSS011A02S, GSS014A02S, GSS016B02S.
European nomenclature codes declared: A03020101, A080102, A03010102, A04010101, F020199, A088099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 152 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 152 |
|---|---|
| Found in the U.S. device database | 11 |
| Share | 7.2 % |
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. GVS S.p.A. was not found in either the U.S. or the Canadian register.