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Vibrio Cholera Ag Rapid Test - India CDSCO Medical Device Registration

Vibrio Cholera Ag Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000056_a75f4f5a6b084902ee165be3e1031957_34d9a775d2330e9931c1eba9c8412c7d. The license holder is Biotrol Laboratories Pvt. Ltd., and it is classified as Device Class Class C. 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 C
Vibrio Cholera Ag Rapid Test
UID: MFG/IVD/2022/000056_a75f4f5a6b084902ee165be3e1031957_34d9a775d2330e9931c1eba9c8412c7d

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Cholera Ag Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of Vibrio Cholerae O139 antigen and O1 antigen in human fecal specimen.

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