Data from EUDAMED, last updated Jun 11, 2026

Progesterone Chemiluminescence Immunoassay Kit

B-06972719606559

1 reference

IVDD — General

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

Device family identification

Device name: Progesterone Chemiluminescence Immunoassay Kit
Basic UDI-DI: B-06972719606559
Device model: Reagents（include Calibrator 1x1mL/bottle and Control 1x1mL/bottle )50tests/kit
Issuing agency: EUDAMED
Version date: May 21, 2026

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

Reagent

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
50tests/kit	`50tests/kit`	`06972719606559`	1	On the market