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SD Chikungunya IgM ELISA - India CDSCO Medical Device Registration

SD Chikungunya IgM ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_18480c2c0aeda877d0531016e9fe9ffa_354e7570fee00f90a3f79edccd6e6bd3. 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
SD Chikungunya IgM ELISA
UID: IMP/MD/2018/000156_18480c2c0aeda877d0531016e9fe9ffa_354e7570fee00f90a3f79edccd6e6bd3

Brand Name

SD BIOLINE Dengue IgG/IgM WB

Device Class

Class B

Approving Authority

CDSCO

Product Information

The SD Chikungunya IgM ELISA is indirect sandwich ELISA for the qualitative detection of IgM antibodies against Chikungunya virus

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