TECHNOGEL ITALIA SRL
IT-MF-000034169 · Italy · Pozzoleone
TECHNOGEL ITALIA SRL is registered in the European database on medical devices as a manufacturer, with 171 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 171 |
|---|
Most frequent device types declared: Guanciale, Materasso antidecubito.
Devices declared under this manufacturer
- GUANCIALE LAB CPAP 9 CE
- GUANCIALE ORIGINAL ANATOMIC CURVE 7 CE PCE
- GUANCIALE ORIGINAL CONVEXO 7 CE
- GUANCIALE ORIGINAL DELUXE 7 CE OBI
- MATERASSO ARMONIA 160X195 CE
- MATERASSO ESTASI 110X200 CE
- MATERASSO ESTASI 120X195 CE
- MATERASSO ESTASI 180X200 CE
- MATERASSO ESTASI 180X210 CE
- MATERASSO FAVOLA 100X210 CE
- MATERASSO FAVOLA 120X190 CE
- MATERASSO FAVOLA/FAVOLA 160X200 CE
Showing 12 of 171 declared devices.
Catalogue references include QE7120195EUCE, QE7180200EUCE, QF7100210EUCE, QF7120190EUCE, QFF160200EUCE, QFF180210EUCE.
European nomenclature codes declared: V080702, V080399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 171 |
| 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 | 171 |
|---|---|
| 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. TECHNOGEL ITALIA SRL was not found in either the U.S. or the Canadian register.