Movi S.p.A.
IT-MF-000032062 · Italy · Milano
Movi S.p.A. is registered in the European database on medical devices as a manufacturer, with 388 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 388 |
|---|
Most frequent device types declared: AUSILI DI PROTEZIONE ANTIDECUBITO PER TALLONE, GOMITO E GINOCCHIO, Carrozzine a spinta, Carrozzine ad Autospinta Posteriore, Compressori e Materassi per Sistemi Antidecubito, Cuscini Antidecubito non attivi.
Among these devices, 55 are declared active.
Devices declared under this manufacturer
- CARR. EVOLUX 18” (46cm) ROSSO
- CARR. EVOLUX 19” (48cm) ROSSO
- CARR. LIGHT PLUS 17\
- CARR. REVOLUX 20” (50cm) ROSSO
- CARR. SLIM PLUS-2 16\
- CUSCINO SEAT-DUO 51x41x7 cm
- EASY-WHEEL TRANSIT 20' /50cm BLU
- LETTO ELETTRICO TAMI
- ROLLATOR ASCELLARE CON TAVOLINO
- SEDIA COMODA IN PVC
- SEGGIOLONE POLIFUNZIONALE CONCEPT II RUOTE POST.16\
- TALLONIERA FIBRA CAVA SILIC.
Showing 12 of 388 declared devices.
Catalogue references include 15000013/N, 15302020, 15372018, 15501059, 15544510, 15555510.
European nomenclature codes declared: Y122106, Y122103, V08030102, Y120606, V08060101, Y122127.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 388 |
| 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 | 388 |
|---|---|
| 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. Movi S.p.A. was not found in either the U.S. or the Canadian register.