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CDSCO UID IMP/IVD/2019/000191_69f1ba576334d901011e3c2f9347e29a_2aee097b7da964bdf4937c82407f6c92

E2 Test(Estradiol Rapid Quantitative Test)

Matrix Labs·Device Class Class B·India CDSCO·Brand: Testosterone Rapid Quantitative Test
Registration details
UID
IMP/IVD/2019/000191_69f1ba576334d901011e3c2f9347e29a_2aee097b7da964bdf4937c82407f6c92
Device class
Class B
Brand name
Testosterone Rapid Quantitative Test
License holder
Matrix Labs
Approving authority
CDSCO
Product information
The FinecareTM Estradiol (Testosterone Rapid Quantitative Test) Rapid Quantitative Test is a fluorescence immunoassay used along with FinecareTM FIA Meters (Testosterone Rapid Quantitative Test) is for quantitative measurement of Estradiol (Testosterone Rapid Quantitative Test) 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

E2 Test(Estradiol Rapid Quantitative Test) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000191_69f1ba576334d901011e3c2f9347e29a_2aee097b7da964bdf4937c82407f6c92. This device is marketed under the brand name Testosterone Rapid Quantitative Test. The license holder is Matrix Labs, and it is classified as Device Class Class B. The approving authority is CDSCO.

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