Test for C- Reactive Protein - India CDSCO Medical Device Registration

Test for C- Reactive Protein is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000203_374d9d3528bfebe06ef9774ccf9c947e_e64e96809cc55646a3dca57b5e68b0aa. This device is marketed under the brand name QDx Instacheck™ AFP. The license holder is DiaSys Diagnostics India Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered

Class Class C

Test for C- Reactive Protein

UID: IMP/MD/2018/000203_374d9d3528bfebe06ef9774ccf9c947e_e64e96809cc55646a3dca57b5e68b0aa

Brand Name

QDx Instacheck™ AFP

License Holder

DiaSys Diagnostics India Private Limited

Device Class

Class C

Approving Authority

CDSCO

Product Information

QDx Instacheck™ hsCRP - All in one along with QDx Instacheck™ Reader is a fluorescence immunoassay for quantitative determination of C-reactive protein (QDx Instacheck™ AFP) in human serum, plasma, or whole blood. The test is used as an aid to predict future cardiovascular diseases (QDx Instacheck™ AFP) as well as to see infection inflammation

Class C

Dengue IgG/IgM

Brand: QDx Instacheck™ AFP

DiaSys Diagnostics India Private Limited

Class C

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Test for C- Reactive Protein - India CDSCO Medical Device Registration

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Approving Authority

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