MORFEUS S.p.A.
IT-MF-000046753 · Italy · Tavoleto
MORFEUS S.p.A. is registered in the European database on medical devices as a manufacturer, with 279 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 279 |
|---|
Most frequent device types declared: ASTRA, ATHENA, CLAIRE, DREAM FIRM, IRIS.
Devices declared under this manufacturer
- Febal Casa
- Morfeus
- Parma Reti
- Stilfar Italia
Showing 12 of 279 declared devices.
Catalogue references include 6711, 6712, 7022, 7033, 7113, 7167.
European nomenclature codes declared: V080702, V0899.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 279 |
| 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 | 279 |
|---|---|
| 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. MORFEUS S.p.A. was not found in either the U.S. or the Canadian register.