Pure Global

Chikungunya IgM Ab ELISA Kit - India CDSCO Medical Device Registration

Chikungunya IgM Ab ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000082_f7b151f7415cdee51cc272a362cd6a53_e5b9ac2a53aa47d5c7c5710a69879546. This device is marketed under the brand name BIOGENIX. 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
Chikungunya IgM Ab ELISA Kit
UID: MFG/IVD/2020/000082_f7b151f7415cdee51cc272a362cd6a53_e5b9ac2a53aa47d5c7c5710a69879546

Brand Name

BIOGENIX

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

Chikungunya IgM ELISA is designed for in vitro qualitative detection of Chikungunya IgM in human serum or plasma of collected blood samples suspected for Chikungunya

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing