RTS CHAPUIS
FR-MF-000001550 · France · SAINT BONNET DE MURE
RTS CHAPUIS is registered in the European database on medical devices as a manufacturer, with 36 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 36 |
|---|
Most frequent device types declared: BRANCARD BARIATRIQUE, BRANCARD BI-BLOC, BRANCARD DE SECOURS, BRANCARD MONOBLOC SERIE 400, BRANCARD PEDIATRIQUE.
Devices declared under this manufacturer
- CABBRI
- RTS CHAPUIS
Showing 12 of 36 declared devices.
Catalogue references include 230 CF M, 240 CA, 340 CF, 350 CA, 400 PED PLUS, 400 PED SEUL.
European nomenclature codes declared: V080202, V08020199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 36 |
| 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 | 36 |
|---|---|
| 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. RTS CHAPUIS was not found in either the U.S. or the Canadian register.