movmedix
FR-MF-000000914 · France · ARC-SUR-TILLE
movmedix is registered in the European database on medical devices as a manufacturer, with 185 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 143 |
|---|---|
| Class IIb | 42 |
Among these devices, 42 are declared sterile, 42 implantable, 143 reusable.
Devices declared under this manufacturer
- Artificial ligament - AC 120 2BR
- Artificial ligament - AC 50 DB
- Artificial ligament - R06x400/V
- Cannulated drill bit diameter 9x250mm internal diameter 3,2mm
- Drift
- Drill bit diameter 4x150mm
- Drill bit diameter 5x150mm
- Hexagonal screwdriver diameter 3.5 mm, length 250 mm
- K-wire diameter 2,5x330mm - 2 trocar ends
- Reamer with blade L 13mm diameter 11mm
- Sterile Ti screw diameter 6x25mm
- Stopper for drill bit diameter 11 mm
Showing 12 of 185 declared devices.
Catalogue references include FST110625, L020505, L021202, L130605D, U01020, U01109.
European nomenclature codes declared: L0999, L0922, P0910, P09120605, P091299, L090999.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | Movmedix S.A.S (FR) · FDA 1000422168 |
| Devices in EUDAMED | 185 |
| Country of registration | France |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 185 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | MOVMEDIX |
What it holds in Canada
| Licences on record | 9 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 6 |
| Class 3 devices | 3 |
| First licensed | 2002-02-12 |
Licence types: Device Family (9).
Licensed under: MECHES LARS, LIGAMENT ARTIFICIEL, BROCHES, PASSEUR SOUS CORACOIDIEN, BOUCLES METALLIQUES, BROCHE A CHAS.