mo-vis bv
BE-MF-000000729 · Belgium · Deinze
mo-vis bv is registered in the European database on medical devices as a manufacturer, with 108 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 108 |
|---|
Most frequent device types declared: M013, P010, P011, P012, P014.
Among these devices, 55 are declared active.
Devices declared under this manufacturer
- Actuator Keypad PRO Paddle Rnet CJSM1
- All-round Joystick R-net Light
- Dual Isolated USB Charger, 3A, R-net
- Foot Control LiNX
- Head Control Omni Proportional Short
- IDM-MS
- MICRO-R
- Multi Joystick LiNX
- Multi Swing 2G Motor Unit
- Scoot Control R-net
- Scoot Control SUBD9
- Twister Bended Tube, (1500mm), Black
Showing 12 of 108 declared devices.
Catalogue references include P002-76, P005-50, P010-52, P015-61, P015-81, P021-53.
European nomenclature codes declared: Y122403, Y122499.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MO-VIS BV (BE) · FDA 3011795161 |
| Devices in EUDAMED | 108 |
| Country of registration | Belgium |
Device-level evidence
| Devices with a numeric GTIN | 108 |
|---|---|
| Found in the U.S. device database | 107 |
| Share | 99.1 % |
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: United States only. mo-vis bv is registered in the United States but was not found in the Canadian register.