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Dengue IgG Antibody ELISA test Kit - India CDSCO Medical Device Registration

Dengue IgG Antibody ELISA test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000060_c1d40cbe498064b46a32ece62bee8277_42d4f64003a75652a7c441cb4425431b. The license holder is Genomix Molecular Diagnostics Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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CDSCO Registered
Class Class B
Dengue IgG Antibody ELISA test Kit
UID: MFG/IVD/2020/000060_c1d40cbe498064b46a32ece62bee8277_42d4f64003a75652a7c441cb4425431b

Device Class

Class B

Approving Authority

Telangana

Product Information

For in-vitro qualitative detection of Dengue IgG antibodies in human serum or plasma

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