Pure Global

Chikungunya virus IgM Antibody ELISA test Kit - India CDSCO Medical Device Registration

Chikungunya virus IgM Antibody ELISA test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000060_ef3af018843a5c0a16c9579d34f2fd44_1a2573fbcf565fe3b685ef25a359caf1. The license holder is Genomix Molecular Diagnostics Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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
Chikungunya virus IgM Antibody ELISA test Kit
UID: MFG/IVD/2020/000060_ef3af018843a5c0a16c9579d34f2fd44_1a2573fbcf565fe3b685ef25a359caf1

Device Class

Class B

Approving Authority

Telangana

Product Information

For the detection of Chikungunya specific IgM antibodies in human serum or plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing