Dengue IgG /lgM Antibody Rapid Test - India CDSCO Medical Device Registration

Dengue IgG /lgM Antibody Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000059_adcfdf9e61f065bd813a7914066ca37a_070d1a08d8681f612355f2ed0b7249f5. This device is marketed under the brand name Typhoid IgG/IgM Rapid Test. The license holder is Dygnova Healthcare Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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CDSCO Registered

Class Class B

Dengue IgG /lgM Antibody Rapid Test

UID: MFG/IVD/2023/000059_adcfdf9e61f065bd813a7914066ca37a_070d1a08d8681f612355f2ed0b7249f5

Brand Name

Typhoid IgG/IgM Rapid Test

License Holder

Dygnova Healthcare Pvt. Ltd

Device Class

Class B

Approving Authority

Kokan Division

Product Information

The Dengue IgG/IgM Rapid Test Cassette is a lateral flow immunoassay for the qualitative detection of IgG and IgM antibodies to Dengue virus in human whole blood, serum or plasma