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CDSCO UID IMP/IVD/2022/000074_c271250174a347e97511d75fd8da758b_11545d038466454d50eab9e250378280

LH Rapid Quantitative Test

FINOVA HEALTHCARE PRIVATE LIMITED·Device Class Class B·India CDSCO·Brand: Glycated Hemoglobin
Registration details
UID
IMP/IVD/2022/000074_c271250174a347e97511d75fd8da758b_11545d038466454d50eab9e250378280
Device class
Class B
Brand name
Glycated Hemoglobin
License holder
FINOVA HEALTHCARE PRIVATE LIMITED
Approving authority
CDSCO
Product information
The LH Rapid Quantitative Test along with Aehealth FIA Meter is intended for vitro quantitative determination of Luteinizing Hormone（ LH） 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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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/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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