BENOIT SYSTEMES
FR-MF-000004445 · France · BILLY LES CHANCEAUX
BENOIT SYSTEMES is registered in the European database on medical devices as a manufacturer, with 38 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 38 |
|---|
Among these devices, 28 are declared active.
Devices declared under this manufacturer
- Acti'tab enfant gauche
- Acti'tab large gauche
- Acti'tab standard droit
- Acti'tab standard gauche
- KITCOOL MINI SANS TÊTIERE
- KITCOOL MINI STANDARD
- KITCOOL SANS TÊTIERE
- MOBILI KIT
- Minotor 3 Chassis fixe
- Minotor 3 Chassis fixe tierce personne
- Minotor 3 Rnet
- POUSSEUR 2.1 CARONY 16
Showing 12 of 38 declared devices.
Catalogue references include 81MIRN30, KCM, KCMST, KCSST, M11-000, T12-000.
European nomenclature codes declared: Y122410, Y122499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 38 |
| 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 | 38 |
|---|---|
| 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. BENOIT SYSTEMES was not found in either the U.S. or the Canadian register.