Neatech.it
IT-MF-000031601 · Italy · Cercola
Neatech.it is registered in the European database on medical devices as a manufacturer, with 31 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 31 |
|---|
Most frequent device types declared: A001ST, S042, S107, S211, S219.
Among these devices, 8 are declared active.
Devices declared under this manufacturer
- BEK HYBRID
- CAVIGLIERA
- DYNA 45
- DYNAMIC
- EVO3 RWD WITHOUT LIFT
- FURIOUS
- JOB WALKER
- NEATECH
- PEEZY
- PEEZY LIGHT
- STEADY
- TALLY MANUAL
Showing 12 of 31 declared devices.
Catalogue references include A001ST, S042, S107, S211, S304, S307.
European nomenclature codes declared: Y180939, Y122127, Y050202, Y122103, Y120609, Y122406.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 31 |
| 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 | 31 |
|---|---|
| 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. Neatech.it was not found in either the U.S. or the Canadian register.