Syphilis Ab ELISA Kit - India CDSCO Medical Device Registration

Syphilis Ab ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000053_f029dbb7ffab61c47e9b8d7f1e926ea0_72f708664f0770e49a88121f1f589ccb. This device is marketed under the brand name HBsAg ELISA Kit, Labsystems Diagnostics . The license holder is Trivitron Healthcare Pvt. Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standard Control Organisation, South 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

CDSCO Registered

Class Class D

Syphilis Ab ELISA Kit

UID: MFG/IVD/2020/000053_f029dbb7ffab61c47e9b8d7f1e926ea0_72f708664f0770e49a88121f1f589ccb

Brand Name

HBsAg ELISA Kit, Labsystems Diagnostics

License Holder

Trivitron Healthcare Pvt. Ltd

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

The Syphilis Ab ELISA KIT is an in vitro diagnostics qualitative immunoassay for the detection of Antibodies to Treponema pallidum in human serum or plasma. The kit is basically intended to screen blood samples for clinical diagnostic testing