Pure Global

Alpha Feto Protein - India CDSCO Medical Device Registration

Alpha Feto Protein is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000203_960a998a6aa2380d7f8bbcd4538fa040_0121f973ad83b28181edcc29d223c71c. This device is marketed under the brand name QDx Instacheck™ AFP. The license holder is DiaSys Diagnostics India Private Limited, and it is classified as Device Class Class C. 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 C
Alpha Feto Protein
UID: IMP/MD/2018/000203_960a998a6aa2380d7f8bbcd4538fa040_0121f973ad83b28181edcc29d223c71c

Brand Name

QDx Instacheck™ AFP

Device Class

Class C

Approving Authority

CDSCO

Product Information

QDx Instacheck™ AFP is a fluorescence immunoassay (QDx Instacheck™ AFP) for the quantitative determination of Alpha Feto Protein (QDx Instacheck™ AFP) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of primary hepatocellular carcinoma and non seminomatous testicular cancer. For in vitro diagnostic use only

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing