ETABLISSEMENT FRANCAIS DU SANG
FR-MF-000013221 · France · SAINT DENIS
ETABLISSEMENT FRANCAIS DU SANG 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: RedQal.
Devices declared under this manufacturer
- CQI ABO-D - Rh.K - Contrôle Qualité Interne pour la détermination des
- NatQal B19-L
- NatQal B19-M
- NatQal HAV
- NatQal HBV
- NatQal HCV
- NatQal HEV
- NatQal HIV
- SeroQal ALINI 6
- SeroQal ARCHI 7
- SeroQal COB 6
- Trousse NG-Mix Multiloci
Showing 12 of 20 declared devices.
Catalogue references include 190011, 242623, 247841, 247842, 247900, 270428.
European nomenclature codes declared: W0105080808, W0103030999, W01030403.
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. ETABLISSEMENT FRANCAIS DU SANG was not found in either the U.S. or the Canadian register.