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Dengue IgG/IgM test - India CDSCO Medical Device Registration

Dengue IgG/IgM test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000135_c5d6f33fc481c7d590e8b09278e278b1_8eb465475be09ea7181e935f7e848b62. The license holder is Seloi Healthcare Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Greater Mumbai 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 test
UID: MFG/IVD/2022/000135_c5d6f33fc481c7d590e8b09278e278b1_8eb465475be09ea7181e935f7e848b62

Device Class

Class B

Approving Authority

Greater Mumbai Division

Product Information

Dengue IgG/IgM device is rapid and qualitative test for the detection of IgG and IgM against all serotypes of Dengue in serum and plasma from human.

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