Genexpath
FR-MF-000029325 · France · Rouen
Genexpath is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: LymphoSign 16U, LymphoSign 24U, LymphoSign 48U, LymphoSign 8U, RT-MIS.
Devices declared under this manufacturer
- Genexpath
Catalogue references include GEP-LS08, GEP-LS16, GEP-LS24, GEP-LS48, GEP-SF08, GEP-SF16.
European nomenclature codes declared: W01060299, W02050192.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| 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 | 9 |
|---|---|
| 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. Genexpath was not found in either the U.S. or the Canadian register.