BIOLINE Dengue NS1 Ag
- UID
- IMP/MD/2018/000156_aa1dc07597231743440052c0ef626a2d_02840ae9bfd0d3ff1640bb3663f27984
- Device class
- Class C
- Brand name
- SD BIOLINE Influenza Antigen
- License holder
- Abbott Diagnostics Medical Private Limited
- Approving authority
- CDSCO
- Product information
- The SD BIOLINE Dengue NS1 Ag Rapid Test is an in vitro immunochromatographic, one step assay designed to detect dengue virus NS1 antigen in human serum, plasma or whole blood
BIOLINE Dengue NS1 Ag is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_aa1dc07597231743440052c0ef626a2d_02840ae9bfd0d3ff1640bb3663f27984. 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.