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SD BIOLINE CEA - India CDSCO Medical Device Registration

SD BIOLINE CEA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_58f3f95cefbf239f2ecd96b190ec89c6_99a8132b354865cd6c2315abb794da10. 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 CEA
UID: IMP/MD/2018/000156_58f3f95cefbf239f2ecd96b190ec89c6_99a8132b354865cd6c2315abb794da10

Brand Name

SD BIOLINE Influenza Antigen

Device Class

Class C

Approving Authority

CDSCO

Product Information

SD BIOLINE CEA kit is a rapid, qualitative test for the detection of CEA (SD BIOLINE Influenza Antigen) in human serum or plasma

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