France Reval
FR-MF-000011523 · France · Sainte Soulle
France Reval is registered in the European database on medical devices as a manufacturer, with 123 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 123 |
|---|
Most frequent device types declared: BAGHEERA, BRANCARD DE DOUCHE ET D'HABILLAGE, BRANCARD ET TABLE D'HABILLAGE A HAUTEUR VARIABLE, CALECHE, CAPRICE.
Devices declared under this manufacturer
- BAGHEERA
- BRANCARD DE DOUCHE MOBILE A HAUTEUR VARIABLE
- BRANCARD DE DOUCHE MURAL A HAUTEUR VARIABLE ELECTRIQUE
- CALECHE
- CALECHE COMPACT
- CAPRICE
- CRYSTAL ELECTRIQUE
- CRYSTAL HYDRAULIQUE
- EASY-UP
- LITOO
- PUPITRE DE DOUCHE OPALE SENSE
- PUPITRE DE MASSAGE SOUS EAU
Showing 12 of 123 declared devices.
Catalogue references include 3011.01, 3700.00, 4502.10, 4502.20, 6012.00, 7100.1DS71.
European nomenclature codes declared: Y093399, Z12069099, Z12069080, V08050399, V0805030102, Y093312.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 123 |
| 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 | 123 |
|---|---|
| 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. France Reval was not found in either the U.S. or the Canadian register.