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Dengue Combo Rapid Test - India CDSCO Medical Device Registration

Dengue Combo Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000056_0a9affbfde75dc7d47edac99152ebeff_06028c1195b9ec7e7785dc10efea7488. The license holder is Biotrol Laboratories Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

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 C
Dengue Combo Rapid Test
UID: MFG/IVD/2022/000056_0a9affbfde75dc7d47edac99152ebeff_06028c1195b9ec7e7785dc10efea7488

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Dengue NS1 Ag-IgG/IgM Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of NS1 Antigen and IgG/IgM Antibodies of Dengue Virus in human whole blood, serum and plasma

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