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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/2019/000039_6672cf907eb8bbdebf59f0bf17003c04_06894d7a72b2aba70848fc9afb642d43. This device is marketed under the brand name Finecare . 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.

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/2019/000039_6672cf907eb8bbdebf59f0bf17003c04_06894d7a72b2aba70848fc9afb642d43

Brand Name

Finecare

Device Class

Class B

Approving Authority

CDSCO

Product Information

Intended for quantitative measurement of Follicle-stimulating hormone (Finecare ) in human whole blood or plasma

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