Pure Global

Syphilis Antibody Test - India CDSCO Medical Device Registration

Syphilis Antibody Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000021_b06699a2c47d9765a702c206ca43b2f6_f4823a764caa60ecbf5cad8cf59c37cc. This device is marketed under the brand name PathoCatchTM. The license holder is Mylab Discovery S0lutions Pvt. Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

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 Antibody Test
UID: MFG/IVD/2020/000021_b06699a2c47d9765a702c206ca43b2f6_f4823a764caa60ecbf5cad8cf59c37cc

Brand Name

PathoCatchTM

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Syphilis Antibody test (PathoCatchTM) is an immunoassay for the rapid and visual detection of antibodies to Treponema pallidum in human serum or plasma or whole blood to aid in the diagnosis and screening of Syphilis. This kit is intended for professional and self testing.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing