Pure Global

One Step Syphilis Antibodies to Treponema Pallidum Test Device - India CDSCO Medical Device Registration

One Step Syphilis Antibodies to Treponema Pallidum Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000085_7af85881b225a8c740f6a41882abe15f_9a8173b28c6982c0a3f26afa6f4c784a. This device is marketed under the brand name Pratham. The license holder is M/s ASTAM DIAGNOSTICS PVT. LTD., and it is classified as Device Class Class D. 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 D
One Step Syphilis Antibodies to Treponema Pallidum Test Device
UID: MFG/IVD/2021/000085_7af85881b225a8c740f6a41882abe15f_9a8173b28c6982c0a3f26afa6f4c784a

Brand Name

Pratham

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Syphilis Test is a lateral flow through immunochromatographic test for the qualitative detection of antibodies to Treponema pallidum (Pratham) in human whole blood/serum/plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing