Pure Global

FSH Test System - India CDSCO Medical Device Registration

FSH Test System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000404_ebd645d5749da63dbf3bfc1896d4e74f_0c0d53124c6c9f14c2cdb78d724f468e. This device is marketed under the brand name ELISA Kit. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
FSH Test System
UID: IMP/IVD/2019/000404_ebd645d5749da63dbf3bfc1896d4e74f_0c0d53124c6c9f14c2cdb78d724f468e

Brand Name

ELISA Kit

Device Class

Class B

Approving Authority

CDSCO

Product Information

Used Quantitative Determination of Follicle Stimulating Hormone in Human Serum

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing