Pure Global

SYPHILIS TEST DEVICE - India CDSCO Medical Device Registration

SYPHILIS TEST DEVICE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000035_465d950a02ac66aacb8f3970c6b823aa_5c88ac69985578dd38191a33657891ee. This device is marketed under the brand name TP. The license holder is Recombigen Laboratories Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

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 C
SYPHILIS TEST DEVICE
UID: MFG/MD/2018/000035_465d950a02ac66aacb8f3970c6b823aa_5c88ac69985578dd38191a33657891ee

Brand Name

TP

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

This is a rapid, in vitro, qualitative lateral flow immunoassay for the detection of antibodies to Treponema Pallidum in serum, plasma and whole blood samples

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing