Handi-Move NV
BE-MF-000016949 · Belgium · Ninove
Handi-Move NV is registered in the European database on medical devices as a manufacturer, with 244 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 244 |
|---|
Among these devices, 35 are declared active.
Devices declared under this manufacturer
- Amputationsling (1 leg) Large
- Amputationsling (2 legs) Daylite Fabric Custom Made
- Bathing Sling with integrated head support Small
- HM Daylite Sling Extra Large
- Mobile foldable hoist 1635, spreaderbar, battery powered
- Portable Motor 2845
- Sling, net, Medium
- Sling, net, Medium, custom made
- Sling; children ; Dino ; Small ; patient matched
- Sling; children ; Dragon ; XS ; patient matched
- Sling; children ; version dragon ; Extra Small
- Sling; net; moonshaped head support; Small; custom made
Showing 12 of 244 declared devices.
Catalogue references include 3415L 90000001, 3415S 90000001, 3418S 00000001, 3445XL 00000001, 3484M 00000001, 3484M 90000001.
European nomenclature codes declared: V0805038002, V08050302, V0805030102, V0805038001, V0805030101.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | HANDI-MOVE (BE) · FDA 3003063250 |
| Devices in EUDAMED | 244 |
| Country of registration | Belgium |
Device-level evidence
| Devices with a numeric GTIN | 244 |
|---|---|
| Found in the U.S. device database | 238 |
| Share | 97.5 % |
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. Handi-Move NV is registered in the United States but was not found in the Canadian register.