Pure Global

SD BIOLINE Syphilis Fast 3.0 - India CDSCO Medical Device Registration

SD BIOLINE Syphilis Fast 3.0 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_aede523f638edf6f14dbde8169e7bd0f_1313326c81f32cb742a9f4eaf3b54669. This device is marketed under the brand name SD BIOLINE Syphilis Fast 3.0. The license holder is Abbott Diagnostics Medical 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
SD BIOLINE Syphilis Fast 3.0
UID: IMP/MD/2018/000156_aede523f638edf6f14dbde8169e7bd0f_1313326c81f32cb742a9f4eaf3b54669

Brand Name

SD BIOLINE Syphilis Fast 3.0

Device Class

Class D

Approving Authority

CDSCO

Product Information

SD BIOLINE Syphilis Fast 3.0 test is a solid phase immunochromatographic assay for the qualitative detection of antibodies of all isotypes(SD BIOLINE Syphilis Fast 3.0) against Treponema pallidum (SD BIOLINE Syphilis Fast 3.0). This test is intended for professional use as an aid on the diagnosis of syphilis

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing