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HIV 1+2 Triline Ab Test - India CDSCO Medical Device Registration

HIV 1+2 Triline Ab Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000139_e34d9e689939b163f5ceb4a51960208c_af47252056427bcad57c931f1dc5d2c3. The license holder is LABGENE BIO-TECH PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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 D
HIV 1+2 Triline Ab Test
UID: MFG/IVD/2022/000139_e34d9e689939b163f5ceb4a51960208c_af47252056427bcad57c931f1dc5d2c3

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

The HIV 1+2 Triline Rapid test kit is a rapid immunochromatography assay for the qualitative detection of antibodies against human immunodeficiency virus ##PLACEHOLDER_0## and/or HIV-2 in human whole blood samples, serum, or plasma samples

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