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: Crochet cervical gauche CTJ, Vis cervicale STABILAR® étoile Ø4mm L14mm, Vis G2S polyaxiale spondylo Ø7,5mm L45mm, Vis monoaxiale CTJ PLUS Ø5,5mm L26mm, Vis KM polyaxiale Ø6,5mm L35mm percutanée.
Among these devices, 1 are declared sterile, 393 implantable, 1 with a measuring function.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
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 |