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EbraQik COVID-19 Antigen Test Card - India CDSCO Medical Device Registration

EbraQik COVID-19 Antigen Test Card is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000014_39ff1364d8019dacf360ccce6ffa887a_5a06c28b348e16a5c1008f7d7e63d624. This device is marketed under the brand name ERBAQIK Dengue Alpha NS1Ag. The license holder is M/s.Transasia Bio-Medicals Ltd., and it is classified as Device Class Class C. 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 C
EbraQik COVID-19 Antigen Test Card
UID: MFG/IVD/2020/000014_39ff1364d8019dacf360ccce6ffa887a_5a06c28b348e16a5c1008f7d7e63d624

Brand Name

ERBAQIK Dengue Alpha NS1Ag

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Detection of Covid-19 Antigen in human Nasopharyngeal sample

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