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HIV-1 Quantitative RT-PCR Detection Kit - India CDSCO Medical Device Registration

HIV-1 Quantitative RT-PCR Detection Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000150_8ad46ec9da3d65151516a46b39c62147_5185669fcc006ed51c5661f6a764f390. This device is marketed under the brand name HBV. The license holder is NeoDx Biotech Labs Pvt Ltd, and it is classified as Device Class Class D. The approving authority is Sub Zonal Bangalore.

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 Quantitative RT-PCR Detection Kit
UID: MFG/IVD/2020/000150_8ad46ec9da3d65151516a46b39c62147_5185669fcc006ed51c5661f6a764f390

Brand Name

HBV

Device Class

Class D

Approving Authority

Sub Zonal Bangalore

Product Information

HIV-1 Quantitative Kit is an in-vitro Real-time PCR assay for the specific quantitation of HIV-1 in human plasma, serum, and whole blood. HIV-1 primer and probe sets are designed for the detection and quantitation of HIV-1 gene along with internal control ฮฒ-actin in a single tube multiplex assay

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