CDSCO UID IMP/IVD/2020/000278_f3105fc20b7f21d4d7b756f4d6fc9a23_b7adcf8f12466a8f52e990fb2e8bdd02

Estradiol Rapid Quantitative Test

RAPID DIAGNOSTIC PVT. LTD.·Device Class Class B·India CDSCO·Brand: LH

Registration details

UID: IMP/IVD/2020/000278_f3105fc20b7f21d4d7b756f4d6fc9a23_b7adcf8f12466a8f52e990fb2e8bdd02
Device class: Class B
Brand name: LH
License holder: RAPID DIAGNOSTIC PVT. LTD.
Approving authority: CDSCO
Product information: The Finecare Estradiol (LH) Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare FIA Meters (LH) is for quantitative measurement of Estradiol (LH) in human whole blood, serum or plasma. The test is used as an aid to the evaluation of ovarian diseases

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About this record

Estradiol Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000278_f3105fc20b7f21d4d7b756f4d6fc9a23_b7adcf8f12466a8f52e990fb2e8bdd02. This device is marketed under the brand name LH. The license holder is RAPID DIAGNOSTIC PVT. LTD., and it is classified as Device Class Class B. The approving authority is CDSCO.

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