Data from EUDAMED, last updated Jun 11, 2026

C-Reactive Protein (CRP) Test Kit (Homogeneous Chemiluminescence Immunoassay)

B-06974524061523

1 reference

IVDD — General

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

Device family identification

Device name: C-Reactive Protein (CRP) Test Kit (Homogeneous Chemiluminescence Immunoassay)
Basic UDI-DI: B-06974524061523
Device model: 25 tests/kit
Issuing agency: EUDAMED
Version date: May 14, 2026

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

ReagentProfessional testing

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
C-Reactive Protein (CRP) Test Kit (Homogeneous Chemiluminescence Immunoassay)	`HCLIA15101`	`06974524061523`	1	On the market