MEDIPREMA
FR-MF-000011274 · France · TAUXIGNY
MEDIPREMA is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 1 |
|---|---|
| Class IIa | 5 |
Most frequent device types declared: 1950L, 3600, 5035.
Among these devices, 2 are declared active, 1 with a measuring function.
Devices declared under this manufacturer
- BERCEAU DE SOINS
- BERCEAU GIGOGNE
- BERCEAU PRESTIGE
- Medirunner
- O'BLOO Leds
- SATIS +
Catalogue references include 1016, 1020, 1030, 1950, 3600, 5035.
European nomenclature codes declared: V0299, Z1208040301, Z12080401, V08050199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 5 |
|---|---|
| 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. MEDIPREMA was not found in either the U.S. or the Canadian register.