C-Reactive Protein Assay (C-Reactive Protein Assay ) - India CDSCO Medical Device Registration

C-Reactive Protein Assay (C-Reactive Protein Assay ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000383_4b638ce6a30c66ffd3e804843adcfd0f_614f97b5d525d975abd1bdbd808dfab4. This device is marketed under the brand name Immunofluorescence. The license holder is BIODX HEALTHCARE, and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered

Class Class C

C-Reactive Protein Assay (C-Reactive Protein Assay )

UID: IMP/IVD/2020/000383_4b638ce6a30c66ffd3e804843adcfd0f_614f97b5d525d975abd1bdbd808dfab4

Brand Name

Immunofluorescence

License Holder

BIODX HEALTHCARE

Device Class

Class C

Approving Authority

CDSCO

Product Information

The kit is used for the quantitative in vitro detection of C-Reactive Protein (Immunofluorescence) in human serum, plasma or whole blood samples

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