MoveUp
BE-MF-000011309 · Belgium · Brussels
MoveUp is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: 2.0.0 MDR, 2.2.0 MDR, 2.4.0 MDD, 2.5.0 MDD, 2.5.0 MDR.
Among these devices, 5 are declared active.
Devices declared under this manufacturer
- moveUP
- moveUP MD
- moveUP MDR
Catalogue references include 2.0.0 MDR, 2.2.0, 2.5.0, 2.5.0 MDD, V2.1.0, moveUP 2.4.0 MDD.
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MOVEUP (BE) · FDA 3023739055 |
| Devices in EUDAMED | 6 |
| Country of registration | Belgium |
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. MoveUp is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
20M00002SUP02 | supplemented | 2030-09-11 |