CDSCO UID MFG/IVD/2020/000150_9dc2a1b28293b5dc8435cbda346ba90b_6b1ebde11d7241c1bfd79ee18a201909

HCV Qualitative RT-PCR Detection Kit

NeoDx Biotech Labs Pvt Ltd·Device Class Class D·India CDSCO·Brand: HBV
Registration details
UID
MFG/IVD/2020/000150_9dc2a1b28293b5dc8435cbda346ba90b_6b1ebde11d7241c1bfd79ee18a201909
Device class
Class D
Brand name
HBV
Approving authority
Sub Zonal Bangalore
Product information
HCV Qualitative detection Kit is an in-vitro Real-time PCR assay for the specific detection of HCV in human plasma, serum, and whole blood. HCV primer and probe sets are designed for the detection of HCV gene along with internal control β-actin in a single tube multiplex assay
Similar products (3)
Other products with the same name or brand
HCV Quantitative RT-PCR Detection Kit
Brand: HBV
NeoDx Biotech Labs Pvt Ltd
Class D
HIV-1 Quantitative RT-PCR Detection Kit
Brand: HBV
NeoDx Biotech Labs Pvt Ltd
Class D
HIV-1 Qualitative RT-PCR Detection Kit
Brand: HBV
NeoDx Biotech Labs Pvt Ltd
Class D
Other products from NeoDx Biotech Labs Pvt Ltd
Products from the same license holder (10 products)
Molecular Transport Medium Sample Collection Kit
Brand: VTM
Class A
Dried Blood Spot Sample Collection Kit
Brand: VTM
Class A
:Viral Transport Medium Sample Collection Kit
Brand: VTM
Class A
CoviDx DirectPlex SARS-CoV-2 RT-PCR Detection Kit
Brand: Nil
Class C
RT-PCR Covid 19 Kit
Brand: NeoDx
Class C
RT-PCR Covid 19 Kit
Brand: NeoDx
Class C
HLA-B27 RT-PCR Detection Kit for Exon 2 & 3
Brand: NeoDx
Class D
JAK2 V617F Mutation RT-PCR Detection Kit
Brand: NeoDx
Class C
HCV Quantitative RT-PCR Detection Kit
Brand: HBV
Class D
BCR-ABL Qualitative RT-PCR Kit - Major, Minor, Micro
Class C
About this record

HCV Qualitative RT-PCR Detection Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000150_9dc2a1b28293b5dc8435cbda346ba90b_6b1ebde11d7241c1bfd79ee18a201909. 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.