Rovipharm
FR-MF-000000673 · France · Val-Revermont
Rovipharm is registered in the European database on medical devices as a manufacturer, with 501 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 501 |
|---|
Most frequent device types declared: CUILLERE, EVO1PF, EVO2ORP, EVO3PF, EVOTH5PF, EVOC10PF, ADV1 BF30, ADV1 BF90, ADV, GOB60.5 ; GOB30 ; GOB13, REG1.7.
Among these devices, 496 are declared with a measuring function.
Devices declared under this manufacturer
- PIBA PF PP28 TP CE + tube ENS MP
- PIBA PF PP28 plastic CE
- Réglette Bronchodermine BL CE
- réducteur PF PP28 glass CE
- réducteur PF PP28 glass CE ENS
Showing 12 of 501 declared devices.
Catalogue references include 26635541, 26650201, 26709891, 26709971, 26720391, 26960121.
European nomenclature codes declared: V0399, V0380.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ROVIPHARM (FR) · FDA 3005724348 |
| Devices in EUDAMED | 501 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 501 |
|---|---|
| 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. Rovipharm is registered in the United States but was not found in the Canadian register.