GENOTROPY
FR-MF-000026152 · France · ROUEN
GENOTROPY is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- AIO-RHD FETAL DNA KIT
Catalogue references include GNPY #010-004, GNPY #010-005, GNPY #010-006, GNPY #010-008, GNPY #010-009, GNPY #010-010.
European nomenclature codes declared: W0103030201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| 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 | 10 |
|---|---|
| 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. GENOTROPY was not found in either the U.S. or the Canadian register.