NICHROMINOX
FR-MF-000000181 · France · SAINT BONNET DE MURE
NICHROMINOX is registered in the European database on medical devices as a manufacturer, with 2 935 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 2 935 |
|---|
Most frequent device types declared: ALUMINIUM HOLDER FOR ROTATING INSTRUMENTS, ALUMINIUM INSTRUMENT HOLDERS, COMPRESSE OROPHARYNGÉE, INSTRUMENTATION, INTRA-ORAL PHOTOGRAPHY ACCESSORIES.
Devices declared under this manufacturer
- NICHROMINOX
Showing 12 of 2 935 declared devices.
Catalogue references include PN182703-5, PN182910-4, PN182953-11, PN182956-9, PN183712-2, PN183733-4.
European nomenclature codes declared: L15900699, Q010280, S010499, L150201, L160201, H9099.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | NICHROMINOX (FR) · FDA 3008519369 |
| Devices in EUDAMED | 2 935 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 2 935 |
|---|---|
| Found in the U.S. device database | 4 |
| Share | 0.1 % |
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. NICHROMINOX is registered in the United States but was not found in the Canadian register.