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Dengue IgG/IgM Rapid Test - India CDSCO Medical Device Registration

Dengue IgG/IgM Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000071_1b7c799a223f84d606c111737f26e671_22446ef8c519e05f319394864ca94f14. The license holder is LABGENE BIO-TECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Gujarat.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
Dengue IgG/IgM Rapid Test
UID: MFG/IVD/2022/000071_1b7c799a223f84d606c111737f26e671_22446ef8c519e05f319394864ca94f14

Device Class

Class B

Approving Authority

Gujarat

Product Information

The Dengue IgG/IgM Rapid Test is a rapid immunochromatographic assay intended for the qualitative determination of IgG and/or IgM antibodies against Dengue Virus in human whole blood, serum and plasma samples

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