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BIOLINE Dengue Duo - India CDSCO Medical Device Registration

BIOLINE Dengue Duo is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_511769165e96d12daa0aee48cbe3d20b_00df6667ad52e0289725397bbb8be053. This device is marketed under the brand name SD BIOLINE Influenza Antigen. The license holder is Abbott Diagnostics Medical Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO.

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
BIOLINE Dengue Duo
UID: IMP/MD/2018/000156_511769165e96d12daa0aee48cbe3d20b_00df6667ad52e0289725397bbb8be053

Brand Name

SD BIOLINE Influenza Antigen

Device Class

Class C

Approving Authority

CDSCO

Product Information

The SD BIOLINE Dengue Duo Rapid Test is an in vitro immunochromatographic, one step assay designed to detect dengue virus NS1 antigen, IgG and IgM antibodies to dengue virus in human serum, plasma or whole blood

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