Pure Global

Test for Follicle Stimulating Hormone - India CDSCO Medical Device Registration

Test for Follicle Stimulating Hormone is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000074_8fd58e9177689b84c16e993768645c6a_673b3c5513fe24b4add78d01151dbda2. This device is marketed under the brand name ichroma™ T4. The license holder is Inkarp Instruments 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Test for Follicle Stimulating Hormone
UID: IMP/IVD/2019/000074_8fd58e9177689b84c16e993768645c6a_673b3c5513fe24b4add78d01151dbda2

Brand Name

ichroma™ T4

Device Class

Class B

Approving Authority

CDSCO

Product Information

ichroma™ FSH is a fluorescence Immunoassay (ichroma™ T4) for the quantitative determination of follicle stimulating hormone(ichroma™ T4) in human serum/ plasma. It is useful as an aid in management and monitoring of concentration of FSH

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing