La Brosse et Dupont
FR-MF-000004610 · France · VILLEPINTE
La Brosse et Dupont is registered in the European database on medical devices as a manufacturer, with 43 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 43 |
|---|
Most frequent device types declared: Bandes, Coussin chaud-froid, Sparadraps, Support ajustable.
Devices declared under this manufacturer
- BANDE COHESIVE
- BANDE DE CONTENTION DOIGTS/ORTEILS
- BANDE KINESIOLOGIQUE
- BANDE À DÉCOUPER UNIVERSELLE
- BANDES A DECOUPER EXTENSIBLES
- BANDES A DECOUPER UNIVERSELLES
- BANDES ANTI FRICTION
- BANDES DE CRÊPE
- BANDES EXTENSIBLES
- BANDES KINESIOLOGIQUES
- Pompe Anti-venin
- SPARADRAP PEAU SENSIBLE
Showing 12 of 43 declared devices.
Catalogue references include 311212, 311223, 312006, 312013, 312101, 312102.
European nomenclature codes declared: M04010102, M03030203, M030102, M050101, M03040299, M030402010103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 43 |
| 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 | 43 |
|---|---|
| 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. La Brosse et Dupont was not found in either the U.S. or the Canadian register.