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Dengue NS1 Ag ELISA - India CDSCO Medical Device Registration

Dengue NS1 Ag ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_3dc5315728bfd893dcf73fa886b01ca7_eb4a35cade03b92bb1c938da95eea5e9. 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
Dengue NS1 Ag ELISA
UID: IMP/MD/2018/000156_3dc5315728bfd893dcf73fa886b01ca7_eb4a35cade03b92bb1c938da95eea5e9

Brand Name

SD BIOLINE Influenza Antigen

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Dengue NS1 Ag ELISA kit is an enzymeโ€“linked immunosorbent assay for the qualitative detection of Dengue NS1 antigens in human serum

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