Pure Global

Dengue IgG/IgM Rapid Test - India CDSCO Medical Device Registration

Dengue IgG/IgM Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000082_1b7c799a223f84d606c111737f26e671_35e66c755aeb2872a1323450f342c470. The license holder is Biogenix Inc. Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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
Dengue IgG/IgM Rapid Test
UID: MFG/IVD/2020/000082_1b7c799a223f84d606c111737f26e671_35e66c755aeb2872a1323450f342c470

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

For detection of Dengue IgG/IgM virus in human serum and plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing