FISIOPRESS srl
IT-MF-000026366 · Italy · PORTO SAN GIORGIO (FM)
FISIOPRESS srl is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 23 |
|---|
Among these devices, 17 are declared active.
Devices declared under this manufacturer
- COPPIA GAMBALETTI PLURITERAPIA 4 SETTORI
- COPPIA GAMBALETTI PLURITERAPIA PIEDE POLPACCIO
- PPRESSOTERAPIA SEQUENTIAL 6 SETTORI
- PRESSOTERAPIA FP1000 DIGITAL
- PRESSOTERAPIA FP250 DIGITAL
- PRESSOTERAPIA FP4
- PRESSOTERAPIA FP4 FXX
- PRESSOTERAPIA FP4 MEDIPRESS
- PRESSOTERAPIA FP4 MINI
- PRESSOTERAPIA FP4 PENNY
- PRESSOTERAPIA FP4 PROFLOW
- PRESSOTERAPIA FP4 SSP DIGITAL
Showing 12 of 23 declared devices.
Catalogue references include FP1000 DIGITAL, FP4, FP4 FXX, FP4 MINI, FP4 SSP DIGITAL, PROGC2P.
European nomenclature codes declared: Z120607, Z12069080.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 23 |
| 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 | 23 |
|---|---|
| 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. FISIOPRESS srl was not found in either the U.S. or the Canadian register.