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HIV 1+2 Test Card - India CDSCO Medical Device Registration

HIV 1+2 Test Card is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000014_ec67f9d7d044fc915255406e6943bcab_214084dc541d714015f2976b141675b7. 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
HIV 1+2 Test Card
UID: MFG/IVD/2020/000014_ec67f9d7d044fc915255406e6943bcab_214084dc541d714015f2976b141675b7

Brand Name

ERBA LISA

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

ErbaQik HIV 1+2 test is a qualitative screening, in-vitro diagnostic immunochromatographic assay for detection of antibodies specific to HIV-1 and HIV-2 in human serum/plasma or whole blood

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