- Role
- Country
- Date of registration
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Data from EUDAMED, last updated Jun 11, 2026
B-069749699816601 reference
B-06974969981660European Medical Device Nomenclature — the EU product classifications carried across this device family's references.
W0102050106Progesterone1 reference
| Trade name | Reference / catalog number | UDI-DI code | Quantity | Status |
|---|---|---|---|---|
| Progesterone(P)Detection Kit(Magnetic Solid Phase Chemiluminescent Immunoassay) | 100 Tests/kit(DR1029-2) | 06974969981660 | 1 | On the market |