Pure Global

Chikungunya IgM Rapid Card Test - India CDSCO Medical Device Registration

Chikungunya IgM Rapid Card Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000003_27b881efd76b466061803bb37f8704d3_fd5383168960d3440a9b5e3c720250bb. This device is marketed under the brand name 3 Part Differential. The license holder is Avantor Performance Materials India Limited, and it is classified as Device Class Class B. The approving authority is Uttarakhand.

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 IgM Rapid Card Test
UID: MFG/IVD/2020/000003_27b881efd76b466061803bb37f8704d3_fd5383168960d3440a9b5e3c720250bb

Brand Name

3 Part Differential

Device Class

Class B

Approving Authority

Uttarakhand

Product Information

Qualitative Immunochromatographic test (3 Part Differential) for the detection of IgM antibodies specific to Chikungunya virus in human serum or plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing