BMB MEDICAL
FR-MF-000011270 · France · TREVOUX
BMB MEDICAL is registered in the European database on medical devices as a manufacturer, with 44 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 44 |
|---|
Most frequent device types declared: CARVI, CLAVIA FCD, CLAVIA LSA, CLAVIA LSA CHIR, DIVIA.
Among these devices, 25 are declared active.
Devices declared under this manufacturer
- CARVI 60CM
- CARVI 70CM
- CLAVIA FCD 75
- CLAVIA LSA 65
- CLAVIA LSA CHIR 65
- CLAVIA LSA CHIR 75
- DIVIA 65
- DIVIA 75
- DIVIA MIXTE 75
- I CARE U AMBULATORY 70
- I-CARE EMERGENCY 70
- I-CARE EZ-GO AMBULATORY 70
Showing 12 of 44 declared devices.
Catalogue references include CRCO7, DVM8, ERGOLYS, EZTRS, FCD8, FPV.
European nomenclature codes declared: V08050199, V08020101, V08060101, V08050103, Y122127, V080502.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | BMB MEDICAL (FR) · FDA 3014923086 |
| Devices in EUDAMED | 44 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 44 |
|---|---|
| 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: United States only. BMB MEDICAL is registered in the United States but was not found in the Canadian register.