Centrofarc S.p.A
IT-MF-000047697 · Italy · MONTERONI D'ARBIA
Centrofarc S.p.A is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Devices declared under this manufacturer
- GUANTO NITRILE BLU POWDERFREE mis.L
- GUANTO NITRILE BLU POWDERFREE mis.M
- GUANTO NITRILE BLU POWDERFREE mis.S
- GUANTO NITRILE BLU POWDERFREE mis.XL
- GUANTO NITRILE NERO POWDERFREE mis.L
- GUANTO NITRILE NERO POWDERFREE mis.M
- GUANTO NITRILE NERO POWDERFREE mis.S
- GUANTO NITRILE NERO POWDERFREE mis.XL
- GUANTO VINILE POWDERFREE mis. L
- GUANTO VINILE POWDERFREE mis. M
- GUANTO VINILE POWDERFREE mis. S
- GUANTO VINILE POWDERFREE mis. XL
Catalogue references include 4503, 4507, 4508, 4516, 4517, 4522.
European nomenclature codes declared: T01020204, T01020201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| 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 | 12 |
|---|---|
| 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. Centrofarc S.p.A was not found in either the U.S. or the Canadian register.