HIV-1 Qualitative RT-PCR Detection Kit - India CDSCO Medical Device Registration
HIV-1 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_0d09102431a231fe3e15a6b7e6cfd5e7_23cc94a0d1dc1c43380d2977a12f13b4. 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.
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Brand Name
HBV
License Holder
NeoDx Biotech Labs Pvt LtdDevice Class
Approving Authority
Sub Zonal Bangalore
Product Information
HIV-1 Qualitative detection Kit is an in-vitro Real-time PCR assay for the specific detection of HIV-1 in human plasma, serum, and whole blood. HIV-1 primer and probe sets are designed for the detection of HIV-1 gene along with internal control ฮฒ-actin in a single tube multiplex assay
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