Laboratoires Chaix et Du Marais
FR-MF-000001185 · France · Paris
Laboratoires Chaix et Du Marais is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 4 |
|---|---|
| Class I | 4 |
Among these devices, 8 are declared sterile.
Devices declared under this manufacturer
- Chlorure de Sodium 0.9 % Stérile Lavoisier en ampoules verre 10 ml
- Chlorure de Sodium 0.9% Stérile Lavoisier en ampoules verre 20 ml
- Eau Stérile Lavoisier ampoules verre 10 ml
- Eau Stérile Lavoisier ampoules verre 20 ml
European nomenclature codes declared: M9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. Laboratoires Chaix et Du Marais was not found in either the U.S. or the Canadian register.