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FSH Rapid Quantitative Test - India CDSCO Medical Device Registration

FSH Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000278_6672cf907eb8bbdebf59f0bf17003c04_3139bab0be1270d344e431bcbdb0d00b. The license holder is RAPID DIAGNOSTIC PVT. LTD., and it is classified as Device Class Class B. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
FSH Rapid Quantitative Test
UID: IMP/IVD/2020/000278_6672cf907eb8bbdebf59f0bf17003c04_3139bab0be1270d344e431bcbdb0d00b

Device Class

Class B

Approving Authority

CDSCO

Product Information

Intended for quantitative measurement of Follicle-stimulating hormone ##PLACEHOLDER_0## in human whole blood, serum or plasma. This test used as an aid to evaluate the ovarian functions in clinical.,fT3 Rapid Quantitative Test-The Finecare TM fT3 Rapid Quantitative Test is a fluorescence immunoassay for quantitative measurement of free triiodothyronine ##PLACEHOLDER_0## in human whole blood, serum and plasma

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