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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/2023/000106_1b7c799a223f84d606c111737f26e671_8e289505de0e5c64ff2c7ae259e0f23e. The license holder is Medlera Healthcare, 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/2023/000106_1b7c799a223f84d606c111737f26e671_8e289505de0e5c64ff2c7ae259e0f23e

License Holder

Medlera Healthcare

Device Class

Class B

Approving Authority

Gujarat

Product Information

The Dengue IgG/IgM Rapid test kit is a rapid immunochromatography assay for the qualitative detection and differentiation of the IgG and IgM antibodies against the Dengue virus in human whole blood, serum or plasma samples

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