Manifatture dell’Adriatico S.r.l.s.
IT-MF-000055811 · Italy · Nereto
Manifatture dell’Adriatico S.r.l.s. is registered in the European database on medical devices as a manufacturer, with 40 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 40 |
|---|
Most frequent device types declared: CLASSIC MEMORY, DINAMIC, ELITE GREEN, EVOLUTION, FORM.
Devices declared under this manufacturer
- CLASSIC MEMORY
- DIAMANTE
- DINAMIC
- ELITE 1600
- ELITE BONNEL
Showing 12 of 40 declared devices.
Catalogue references include 04, 04 FUORI MISURA, 05, 07 FUORI MISURA, 13 - FUORI MISURA, 15.
European nomenclature codes declared: V080702, V0880.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 40 |
| 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 | 40 |
|---|---|
| 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. Manifatture dell’Adriatico S.r.l.s. was not found in either the U.S. or the Canadian register.