Prolactin Rapid Quantitative Test - India CDSCO Medical Device Registration

Prolactin Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000164_95d60e068d518a986c8b005c10fc72e2_ca4ca5e454d4647d3b7c70d6cfb86b52. This device is marketed under the brand name E2. The license holder is M/s Avantor Performance Materials India Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

Prolactin Rapid Quantitative Test

UID: IMP/IVD/2022/000164_95d60e068d518a986c8b005c10fc72e2_ca4ca5e454d4647d3b7c70d6cfb86b52

Brand Name

License Holder

M/s Avantor Performance Materials India Ltd

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Prolactin Rapid Quantitative Test is a fluorescence immunoassay used along with FIA Meters (E2) for quantitative measurement of Prolactin (E2) in human whole blood, serum or plasma. The test is used as an aid to the evaluation of pituitary endocrine function. For in vitro diagnostic use only. For professional use only