COBLENTZ MEDICAL BLADES INDUSTRY
FR-MF-000010361 · France · ALLONNES
COBLENTZ MEDICAL BLADES INDUSTRY is registered in the European database on medical devices as a manufacturer, with 48 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 48 |
|---|
Most frequent device types declared: LAMES DE GOUGE.
Among these devices, 48 are declared sterile.
Devices declared under this manufacturer
- BASIC
- BEST BLADE
- BESTBLADE
- FIRST BLADES
- KOMET
- LA GOUGE BOX
- PODIATECH
- WICTOR
Showing 12 of 48 declared devices.
Catalogue references include 3760245971233, 3760245971431, 3760245971462, 3760245971875, 3760245971929, 3760245972001.
European nomenclature codes declared: V010302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 48 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 48 |
|---|---|
| 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: Neither register. COBLENTZ MEDICAL BLADES INDUSTRY was not found in either the U.S. or the Canadian register.