PRL Rapid Quantitative Test - India CDSCO Medical Device Registration
PRL Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000074_b6b588aa94d35bfca22aa860216e2116_0756837c47b876d11232c4cc70294f28. This device is marketed under the brand name Glycated Hemoglobin. The license holder is FINOVA HEALTHCARE PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is CDSCO.
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Brand Name
Glycated Hemoglobin
License Holder
FINOVA HEALTHCARE PRIVATE LIMITEDDevice Class
Approving Authority
CDSCO
Product Information
The PRL Rapid Quantitative Test along with Aehealth Fluorescence Immunoassay Analyzer (Glycated Hemoglobin) is intended for vitro quantitative determination of Prolactin (Glycated Hemoglobin) in human whole blood, serum or plasma.This test is used as an aid to evaluate the function of hypothalamic-pituitary and diagnose the hypothalamic diseases
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PROG Rapid Quantitative Test
Brand: Glycated Hemoglobin
FER Rapid Quantitative Test
Brand: Glycated Hemoglobin
LH Rapid Quantitative Test
Brand: Glycated Hemoglobin
TSH Rapid Quantitative Test
Brand: Glycated Hemoglobin
MYO Rapid Quantitative Test
Brand: Glycated Hemoglobin