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AviSure Syphilis Rapid Test - India CDSCO Medical Device Registration

AviSure Syphilis Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000082_cf5dbb73524ed48096698dd103864f1f_a450af8523d98199883f995504d31834. The license holder is Avience Biomedicals Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is CDSCO -North Zone, Ghaziabad.

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
AviSure Syphilis Rapid Test
UID: MFG/IVD/2021/000082_cf5dbb73524ed48096698dd103864f1f_a450af8523d98199883f995504d31834

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Detection of antibodies to Treponema pallidum in human serum, plasma or whole blood

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