Institut de Biotechnologies Jacques Boy
FR-MF-000004609 · France · REIMS
Institut de Biotechnologies Jacques Boy is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: Coffret K-Matic, 5 flacons, Coffret K-Matic, 8 flacons.
Catalogue references include 152210263, 152210363, 152220463, 152250263, 157240163, 901080134.
European nomenclature codes declared: W0103030202, W0103030101, W0103010399, W0103030401, W0299, W0103030501.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| 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 | 20 |
|---|---|
| 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. Institut de Biotechnologies Jacques Boy was not found in either the U.S. or the Canadian register.