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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/2022/000074_87e76d9f26b0752527bf2c6ddc6700e3_95120b5145f5a1c83e042f87f3e2b074. This device is marketed under the brand name Glycated Hemoglobin. The license holder is FINOVA HEALTHCARE PRIVATE LIMITED, 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/2022/000074_87e76d9f26b0752527bf2c6ddc6700e3_95120b5145f5a1c83e042f87f3e2b074

Brand Name

Glycated Hemoglobin

Device Class

Class B

Approving Authority

CDSCO

Product Information

The FSH Rapid Quantitative Test along with Aehealth FIA Meter is intended for vitro quantitative determination of Follicle-stimulating hormone๏ผˆ FSH๏ผ‰ in human whole blood, serum or plasma.This test used as an aid to evaluate the ovarian functions in clinical

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