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Dengue IgG/IgM Rapid Card Test - India CDSCO Medical Device Registration

Dengue IgG/IgM Rapid Card Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000133_23bdaf10487b395fc9e0cf0fd722d5a6_186ec64d444fe3d7c23b7d50e9723c3a. 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 IgG/IgM Rapid Card Test
UID: MFG/IVD/2023/000133_23bdaf10487b395fc9e0cf0fd722d5a6_186ec64d444fe3d7c23b7d50e9723c3a

Brand Name

BeneSphera

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Rapid card test (BeneSphera) for detection of IgG & IgM Antibodies to dengue virus in human serum, plasma and whole blood

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