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Dengue IgG Capture ELISA - India CDSCO Medical Device Registration

Dengue IgG Capture ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_20200012445cce9e08e3e105a771bcc7_d6c0c89e96b1b310cc3640ac20b412de. This device is marketed under the brand name SD BIOLINE Dengue IgG/IgM WB. The license holder is Abbott Diagnostics Medical Private Limited, and it is classified as Device Class Class B. 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 B
Dengue IgG Capture ELISA
UID: IMP/MD/2018/000156_20200012445cce9e08e3e105a771bcc7_d6c0c89e96b1b310cc3640ac20b412de

Brand Name

SD BIOLINE Dengue IgG/IgM WB

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Dengue IgG Capture ELISA kit is an enzyme-linked immunosorbent assay for the qualitative detection of IgG antibodies specific to Dengue virus in human serum

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