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

Rapid Dengue IgM/IgG Antibody Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000111_9631373c977bf8953bd56a276d2af32a_d71ed4e709227b39eae08a735316bb9f. This device is marketed under the brand name Mediline-SA. The license holder is S.A-MEDLINE 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
Rapid Dengue IgM/IgG Antibody Test
UID: MFG/IVD/2023/000111_9631373c977bf8953bd56a276d2af32a_d71ed4e709227b39eae08a735316bb9f

Brand Name

Mediline-SA

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Rapid Dengue IgM/IgG test is an immunochromatographic assay for the qualitative Detection of Dengue specific IgM/IgG antibodies in human serum/plasma

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