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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/2022/000078_1b7c799a223f84d606c111737f26e671_39ed97fb37a5c70d3150dac7fa47dcbb. The license holder is Dia Sure Immunodiagnostic LLP, and it is classified as Device Class Class B. The approving authority is South Delhi Division.

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/2022/000078_1b7c799a223f84d606c111737f26e671_39ed97fb37a5c70d3150dac7fa47dcbb

Device Class

Class B

Approving Authority

South Delhi Division

Product Information

Dengue IgG/IgM Rapid test is an immunochromatographic rapid test for qualitative detection of IgG and IgM antibodies against dengue virus in human serum and plasma. It is for professional use only

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