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Dengue NS1 and IgG/IgM Rapid Card Test - India CDSCO Medical Device Registration

Dengue NS1 and IgG/IgM Rapid Card Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000002_f9c89982639a8a5f0425103dd97fea4a_6bb370b8a2d34c1797fa9865856fffff. This device is marketed under the brand name Lateral Flow. The license holder is Avantor Performance Materials India 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 and IgG/IgM Rapid Card Test
UID: MFG/IVD/2020/000002_f9c89982639a8a5f0425103dd97fea4a_6bb370b8a2d34c1797fa9865856fffff

Brand Name

Lateral Flow

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Rapid cards test (Lateral Flow) for detection of dengue NS1 antigen, IgG/IgM antibodies to dengue virus in human serum , plasma or whole Blood

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