Pure Global

Syphilis (MAGLUMI® Syphilis ) - India CDSCO Medical Device Registration

Syphilis (MAGLUMI® Syphilis ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000036_ed6c759c66759810a1338570ea427bf2_0cd0a3b86c3ea1c3c750c316e42a9939. This device is marketed under the brand name CLIA. The license holder is SNIBE DIAGNOSTIC (India) Private Limited., and it is classified as Device Class Class D. 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 D
Syphilis (MAGLUMI® Syphilis )
UID: IMP/IVD/2023/000036_ed6c759c66759810a1338570ea427bf2_0cd0a3b86c3ea1c3c750c316e42a9939

Brand Name

CLIA

Device Class

Class D

Approving Authority

CDSCO

Product Information

The kit is an in vitro chemiluminescent immunoassay for the qualitative determination of total antibodies against Treponema pallidum (CLIA) in human serum and plasma.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing