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Chikungunya IgM Rapid Card Test - India CDSCO Medical Device Registration

Chikungunya IgM Rapid Card Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000133_27b881efd76b466061803bb37f8704d3_5050ef38eb2f4b4fc9a0dc728bb25b35. This device is marketed under the brand name Lateral Flow. The license holder is M/s Avantor Performance Materials India Private Limited, 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
Chikungunya IgM Rapid Card Test
UID: MFG/IVD/2023/000133_27b881efd76b466061803bb37f8704d3_5050ef38eb2f4b4fc9a0dc728bb25b35

Brand Name

Lateral Flow

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Qualitative Immunochromatographic test (Lateral Flow) for the detection of IgM antibodies specific to Chikungunya virus in human serum or plasma

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