Groupe Servibio
FR-MF-000001714 · France · Les Ulis
Groupe Servibio is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: Easy Para.
Devices declared under this manufacturer
- Easy Para Bailenger
- Easy Para Check
- Easy Para Servisol
- Echantillon Easy Para Bailenger
- Echantillon Easy Para Servisol
Catalogue references include DSE-CQ, DSE4200BAI, DSE4200BAIU, DSE4200SER, DSE4200SERU.
European nomenclature codes declared: W0104050101, W01040699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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. Groupe Servibio was not found in either the U.S. or the Canadian register.