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CDSCO UID IMP/IVD/2021/000395_e2155b08104291a6af4a602972eadd3d_8d10665aad3c0dc9860bd297f0c21a77

LH Rapid Quantitative Test

M/s Vishat Diagnostic Pvt Ltd.·Device Class Class B·India CDSCO·Brand: Biotime
Registration details
UID
IMP/IVD/2021/000395_e2155b08104291a6af4a602972eadd3d_8d10665aad3c0dc9860bd297f0c21a77
Device class
Class B
Brand name
Biotime
License holder
M/s Vishat Diagnostic Pvt Ltd.
Approving authority
CDSCO
Product information
The Biotime LH Rapid Quantitative Test is intended to quantify the concentration of LH in human serum on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an aid detection of infertility
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About this record

LH Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000395_e2155b08104291a6af4a602972eadd3d_8d10665aad3c0dc9860bd297f0c21a77. This device is marketed under the brand name Biotime . The license holder is M/s Vishat Diagnostic Pvt Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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