Data from EUDAMED, last updated Jun 11, 2026

Beta-subunit of Human Chorionic Gonadotropin Test (Fluorescence Immunoassay)

B-06979878281122

1 reference

IVDD — General

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

Device family identification

Device name: Beta-subunit of Human Chorionic Gonadotropin Test (Fluorescence Immunoassay)
Basic UDI-DI: B-06979878281122
Issuing agency: EUDAMED
Version date: May 19, 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
1001048	`1001048`	`06979878281122`	1	On the market