Eurobio Scientific
FR-MF-000011745 · France · Les Ulis
Eurobio Scientific is registered in the European database on medical devices as a manufacturer, with 109 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: EBX-042.
Devices declared under this manufacturer
- EurobioPlex BK Virus
- EurobioPlex Bartonella
- EurobioPlex Bordetella pertussis et parapertussis
- EurobioPlex Coxiella Burnetii
- EurobioPlex DNA QC Control of DNA extraction and amplification
- EurobioPlex HHV6-HHV8
- EurobioPlex Méningite bactérienne communautaire
- EurobioPlex Méningite bactérienne materno-foetale
- Milieu Essentiel Minimum De Eagle modifié Par Dulbecco
- Milieu Essentiel Minimum de Eagle
- Milieu L15 de Leibovitz
- Solution saline équilibrée de Earle
Showing 12 of 109 declared devices.
Catalogue references include CM1DME60-01, EBX-001-UN, EBX-013-48, EBX-015, EBX-017-24, EBX-020-09.
European nomenclature codes declared: W0101070304, W02039005, W0105070502, W0105070304, W0105070505, W01019099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 109 |
| 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 | 51 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | EUROBIO SCIENTIFIC GMBH |
What it holds in Canada
| Licences on record | 1 |
|---|---|
| Currently active | 0 |
| Class 3 devices | 1 |
| First licensed | 2020-08-21 |
Licence types: Test Kit (1).
Licensed under: ENDOPREDICT QS.
North American profile: Canada only. Eurobio Scientific holds a Canadian licence but was not found in the U.S. register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
40590 | issued | 2031-07-26 |