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Syphilis Test Card - India CDSCO Medical Device Registration

Syphilis Test Card is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000014_642357f15500d4d1be2bd48a7ef7235c_c23464c4f47148f1805b826b653f1ec1. This device is marketed under the brand name ERBA LISA. The license holder is M/s.Transasia Bio-Medicals 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.

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CDSCO Registered
Class Class D
Syphilis Test Card
UID: MFG/IVD/2020/000014_642357f15500d4d1be2bd48a7ef7235c_c23464c4f47148f1805b826b653f1ec1

Brand Name

ERBA LISA

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

ErbaQik Syphilis test is a quyalitative screening, in-vitro diagnostic Immunochromatographic assay designed for qualitative determination of antibodies (ERBA LISA) against Treponema pallidum (ERBA LISA) in human serum/plasma and Whole blood

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