Data from EUDAMED, last updated Jun 11, 2026

Progesterone Rapid Test Kit (Fluorescence Immunochromatographic Assay)

B-06974464591555

1 reference

IVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk category: IVDD — General
Manufacturer: Guangzhou Decheng Biotechnology Co., Ltd.

Device family identification

Device name: Progesterone Rapid Test Kit (Fluorescence Immunochromatographic Assay)
Basic UDI-DI: B-06974464591555
Issuing agency: EUDAMED
Version date: May 13, 2026

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk category: IVDD — General
Status: On the market

ReagentProfessional testingAnimal tissues / cells

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

References

1 reference

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Progesterone Rapid Test Kit (Fluorescence Immunochromatographic Assay)	`5044C4X024`	`06974464591555`	1	On the market