Estradiol Rapid Quantitative Test - India CDSCO Medical Device Registration

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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CDSCO Registered

Class Class B

Estradiol Rapid Quantitative Test

UID: IMP/IVD/2020/000278_f3105fc20b7f21d4d7b756f4d6fc9a23_b7adcf8f12466a8f52e990fb2e8bdd02

Brand Name

License Holder

RAPID DIAGNOSTIC PVT. LTD.

Device Class

Class B

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

Class B

Urine Test Strip (URISelf Pro )

Brand: LH

PATHKITS HEALTHCARE PRIVATE LIMITED

Class B

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Estradiol Rapid Quantitative Test - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

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