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SD BIOLINE AFP - India CDSCO Medical Device Registration

SD BIOLINE AFP is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_87b44a17975978eb073e2ddba04c7f68_e7c87839c8f3ea0698a34255ab4c8ff1. 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
SD BIOLINE AFP
UID: IMP/MD/2018/000156_87b44a17975978eb073e2ddba04c7f68_e7c87839c8f3ea0698a34255ab4c8ff1

Brand Name

SD BIOLINE Influenza Antigen

Device Class

Class C

Approving Authority

CDSCO

Product Information

The SD BIOLINE AFP test is an immunochromatographic, one-step assay designed for the qualitative determination of AFP in human serum or plasma

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