MOVE-UP
FR-MF-000000412 · France · Alixan
MOVE-UP is registered in the European database on medical devices as a manufacturer, with 574 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 376 |
|---|---|
| Class I | 197 |
| Class IIb | 1 |
Most frequent device types declared: isaonlay™, isastemless™.
Among these devices, 198 are declared sterile, 198 implantable, 350 reusable, 1 active.
Devices declared under this manufacturer
- Surgical instruments for isa™ prosthesis
- Surgical instruments for isa™ total and partial shoulder prosthesis
- Tray isaonlay™ 1
- isafracture™
- isahead™
- isahybrid+™
- isahybrid™
- isainlay™
- isaliner™
- isareverse™
- isareverse™+
- isarevision™
Showing 12 of 574 declared devices.
Catalogue references include 0009I4315, 0015I3902, 0032A1315, 0046A0000, 0066A4335, 0090A0053.
European nomenclature codes declared: L091104, L091102, P0901040202, P09010399, P090104010101, L091201.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MOVEUP (BE) · FDA 3023739055 |
| Devices in EUDAMED | 574 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 574 |
|---|---|
| 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: United States only. MOVE-UP is registered in the United States but was not found in the Canadian register.