NEURO FRANCE Implants
FR-MF-000002210 · France · La ville aux Clercs
NEURO FRANCE Implants is registered in the European database on medical devices as a manufacturer, with 395 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 395 |
|---|
Most frequent device types declared: Vis G2S canulée polyaxiale Ø5,5mm L30mm, Vis G2S Ø8,5mm L40mm REVISION, Vis G2S® canulée polyaxiale Ø6,5mm L50mm, Vis KM Bébé polyaxiale de révision Ø4mm L20mm, Vis KM monoaxiale Ø4,5mm L35mm.
Among these devices, 1 are declared sterile, 393 implantable, 1 with a measuring function.
Devices declared under this manufacturer
- CTJ
- G2S
- KM
- STABILAR®
- TRIONIX®
- TRIONYX®
- ThoRib®
Showing 12 of 395 declared devices.
Catalogue references include 114014, 144014, 154020, 204535, 226555, 254010.
European nomenclature codes declared: P09070399, P09070305, P090799, P9099.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | NEURO FRANCE IMPLANTS (FR) · FDA 3007385214 |
| Devices in EUDAMED | 395 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 395 |
|---|---|
| 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. NEURO FRANCE Implants is registered in the United States but was not found in the Canadian register.