UNIFARCO SpA
IT-MF-000013304 · Italy · Santa Giustina
UNIFARCO SpA is registered in the European database on medical devices as a manufacturer, with 43 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 43 |
|---|
Devices declared under this manufacturer
- CREMA BETA COMPLEX
- Ceramol - Beta Complex Cream
- Ceramol - Beta Complex Crema
- Ceramol - Cream 311
- Ceramol - Crema 311
- Ceramol - Crema Beta Complex
- Ceramol - Lipocrema 311
- Ceramol Cream 311
- Ceramol Psor - Crema
- EUPILEN
- Gel Afta Repair
- PROCTOcrème
Showing 12 of 43 declared devices.
Catalogue references include 8029408107113, 8029408112513, 8029408149137, 8029408149229, 8029408161894, 8029408185364.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 43 |
| 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 | 15 |
|---|---|
| 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. UNIFARCO SpA was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
0425-MDR-030156-00 | issued | 2030-11-09 |