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Dengue NS1 Antigen Rapid Card Test - India CDSCO Medical Device Registration

Dengue NS1 Antigen Rapid Card Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000133_dd9e83c7936bd1be513a9fc663d7f3b8_4af172a48983aa93dca162db3d3aeda1. This device is marketed under the brand name BeneSphera. The license holder is M/s Avantor Performance Materials India Private Limited, 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
Dengue NS1 Antigen Rapid Card Test
UID: MFG/IVD/2023/000133_dd9e83c7936bd1be513a9fc663d7f3b8_4af172a48983aa93dca162db3d3aeda1

Brand Name

BeneSphera

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Rapid card test (BeneSphera) for detection of dengue NS1 Antigen in human serum,plasma and whole blood

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