NOI DELLA NOTTE SRL
IT-MF-000048624 · Italy · TORRITA DI SIENA
NOI DELLA NOTTE SRL is registered in the European database on medical devices as a manufacturer, with 101 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 101 |
|---|
Most frequent device types declared: ACTIVA MATRIMONIALE, CYBER-REST, GALAXY FISSA PIAZZA E MEZZO, GALAXY MANUALE PIAZZA E MEZZO, LOGIC ULTRA DOPPIA CULLA.
Among these devices, 12 are declared active.
Devices declared under this manufacturer
- ACTIVA
- BIONICA PLUS
- CYBER-REST
- GALAXY FISSA
- GALAXY MANUALE
- LOGIC ULTRA DOPPIA CULLA
- LOGIC ULTRA MOTORE
- MEDICAL
- PRO SPA
- PRO SPA MOTORE
- STARK 19
- SYN-ACTION
Showing 12 of 101 declared devices.
Catalogue references include 26PFRECYB-MT, 26PFRELGU - FS (diviso), 26PFREPRO - FS, 26PFRESTR - FS, 26PFRESYN - MT, 26PFREWD2 - MT.
European nomenclature codes declared: V080699, V08060199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 101 |
| 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 | 101 |
|---|---|
| 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. NOI DELLA NOTTE SRL was not found in either the U.S. or the Canadian register.