CFS ITALIA SRL
IT-MF-000045084 · Italy · SAN BIAGIO DI CALLALTA
CFS ITALIA SRL is registered in the European database on medical devices as a manufacturer, with 356 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 356 |
|---|
Most frequent device types declared: Aste flebo, Barelle, Carrelli biancheria, Carrelli da reparto, Carrelli sala operatoria.
Among these devices, 49 are declared active.
Devices declared under this manufacturer
- 100011
- ALFA 23/V
- ALV600610
- ALV900220
- BREEZE
- CFS 03F
- CLEAN SMALL
- MINI FILE
- R1
- SENIOR S/J
- STORM PEDIATRICO
- TORNADO LARGE ISO EMERGENZA
Showing 12 of 356 declared devices.
Catalogue references include 1050, 1077, 3055, 60182, 6058-1, 60805/V.
European nomenclature codes declared: V0899, Y122103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 356 |
| 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 | 356 |
|---|---|
| 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. CFS ITALIA SRL was not found in either the U.S. or the Canadian register.