Farmaceutici Damor S.p.A.
IT-MF-000023738 · Italy · Naples
Farmaceutici Damor S.p.A. is registered in the European database on medical devices as a manufacturer, with 36 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 36 |
|---|
Devices declared under this manufacturer
- Damorline garze
- Damorline garze advance
- Dermatix
- Fito gauzes
- Fitogauzes
- Fitogauzes advance
- Fitohydro jel
- Fitostimoline Idrogel
- Fitostimoline plus crema
- Fitostimoline plus spray
- Fitostimoline spray
- Foille
Showing 12 of 36 declared devices.
Catalogue references include MDR/02, MDR/03, MDR/04, MDR/05.
European nomenclature codes declared: M040499, M02030201, M9002.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 36 |
| 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 | 36 |
|---|---|
| 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. Farmaceutici Damor S.p.A. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
0425-MDR-030193-01 | supplemented | 2031-05-25 |