AFI Centrifuge
FR-MF-000001636 · France · Château-Gontier Bazouges
AFI Centrifuge is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: ELLA Ventilated centrifuge, 230V IVD.
Devices declared under this manufacturer
- AFI
- ISA Refrigerated 230V
- ISA VENTILATED 230V
Showing 12 of 24 declared devices.
Catalogue references include AFI-C1200R-E-QBD/IVD, AFI-C200R/IVD, AFI-C200V-E/IVD, AFI-C300R-E/IVD, AFI-C300RF/IVD, AFI-CI060R-E/IVD.
European nomenclature codes declared: W02069005, W02069003.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 24 |
| 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 | 24 |
|---|---|
| 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. AFI Centrifuge was not found in either the U.S. or the Canadian register.