IDI EVOLUTION S.r.l.
IT-MF-000005920 · Italy · MONZA
IDI EVOLUTION S.r.l. is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 27 |
|---|
Most frequent device types declared: FDC, TMM3.
Among these devices, 6 are declared reusable, 2 active.
Devices declared under this manufacturer
- Cacciavite polivalente mini gold
- Contenitore e piastra frese carotatrici
- Contenitore e piastra set frese calibrate
- Contenitore e piastra set protesico
- FRESA 2DG START DLC
- Piastra 2DG B1ONE
- Piastra B1ONE
- Piastra Smart 2DG
- Piastra Smart 2DG TMM3
- Piastra Smart TMM3
- Piastra frese carotatrici
- Piastra set frese calibrate
Showing 12 of 27 declared devices.
Catalogue references include 515902, 600708, 905021, 905023, 905950, 909007.
European nomenclature codes declared: S0199, L159099, Q010399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| 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 | 27 |
|---|---|
| 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. IDI EVOLUTION S.r.l. was not found in either the U.S. or the Canadian register.