Pure Global

Anti Deamidated Gliadin Peptide IgA - India CDSCO Medical Device Registration

Anti Deamidated Gliadin Peptide IgA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000078_c96ad3eb48db7e1ded54d39c661ab3de_75e56f5fc3892111bce0c601b9c34de9. This device is marketed under the brand name p-ANCA. The license holder is M/s Vishat Diagnostic 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
Anti Deamidated Gliadin Peptide IgA
UID: IMP/IVD/2020/000078_c96ad3eb48db7e1ded54d39c661ab3de_75e56f5fc3892111bce0c601b9c34de9

Brand Name

p-ANCA

Device Class

Class B

Approving Authority

CDSCO

Product Information

Solid phase enzyme immunometric assay (p-ANCA) designed for the quantitative measurement of IgA class antibodies directed against deamidated Gliadin peptides (p-ANCA) in human serum or plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing