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HIV 1+2 Triline Rapid test - India CDSCO Medical Device Registration

HIV 1+2 Triline Rapid test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000155_8bd03fc3e72453a7e18b870454d99a7e_9b4eaa256a452ef09585232b190845e9. This device is marketed under the brand name STERGIC. The license holder is Labgene Bio-tech Pvt. Ltd., 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 Rapid test
UID: MFG/IVD/2023/000155_8bd03fc3e72453a7e18b870454d99a7e_9b4eaa256a452ef09585232b190845e9

Brand Name

STERGIC

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

The STERGIC (STERGIC) kit is a rapid immunochromatography assay for the qualitative detection of antibodies against human immunodeficiency virus (STERGIC) and/or HIV-2 in human whole blood samples, serum or plasma samples

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