Dengue IgG/IgM - India CDSCO Medical Device Registration

Dengue IgG/IgM is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000203_13f95ef30fdeba669c96f2a354f4c8a8_657fb7755842422f52f250fdf71e74bc. 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

Dengue IgG/IgM

UID: IMP/MD/2018/000203_13f95ef30fdeba669c96f2a354f4c8a8_657fb7755842422f52f250fdf71e74bc

Brand Name

QDx Instacheck™ AFP

License Holder

DiaSys Diagnostics India Private Limited

Device Class

Class C

Approving Authority

CDSCO

Product Information

QDx Instacheck™ Dengue IgG/IgM is a fluorescence Immunoassay (QDx Instacheck™ AFP) for the qualitative determination of IgG/IgM antibodies against dengue virus in human whole blood/serum/plasma. It is useful as an aid in screening of Dengue virus infection. For in vitro diagnostic use only.,iFOB Neo(QDx Instacheck™ AFP)-QDx Instacheck™ iFOB Neo is a fluorescence Immunoassay (QDx Instacheck™ AFP) for the quantitative determination of hemoglobin in human feces. It is useful as an aid in management and monitoring of colorectal cancer. For in vitro diagnostic use only

Class C

Test for C- Reactive Protein

Brand: QDx Instacheck™ AFP

DiaSys Diagnostics India Private Limited

Class C

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Dengue IgG/IgM - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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