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/2022/000074_c271250174a347e97511d75fd8da758b_11545d038466454d50eab9e250378280. 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 LH Rapid Quantitative Test along with Aehealth FIA Meter is intended for vitro quantitative determination of Luteinizing Hormone๏ผ LH๏ผ in human whole blood, serum or plasma. This test is used as an aid to diagnose the ovulation cycle, premature ovarian failure and gonadal hypoplasia
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Brand: Glycated Hemoglobin
MYO Rapid Quantitative Test
Brand: Glycated Hemoglobin