idmat
FR-MF-000040882 · France · PORNICHET
idmat is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: Embout Stabicane, STABICANE FANTAISIE BOIS, STABICANE FANTAISIE SATIN, STABICANE STANDARD, STABICANE VERNI.
Devices declared under this manufacturer
- STABICANE
- idmat
Showing 12 of 20 declared devices.
Catalogue references include CBSTABK03-BLP, CBSTABK03-FU, CBSTABK03-GN, CFB-STABK03-3, CFS-STABK03-KSH, ESTABK03-15.
European nomenclature codes declared: Y120380.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| 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 | 20 |
|---|---|
| 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. idmat was not found in either the U.S. or the Canadian register.