LH Rapid Quantitative Test - India CDSCO Medical Device Registration
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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Brand Name
Biotime
License Holder
M/s Vishat Diagnostic Pvt Ltd.Device Class
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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