SD BIOLINE H.Pylori
- UID
- IMP/MD/2018/000156_2ac917debedc1f09b54245aec261f812_4b7104a16a25daefa5f2e082cf94ea1d
- Device class
- Class B
- Brand name
- SD BIOLINE Dengue IgG/IgM WB
- License holder
- Abbott Diagnostics Medical Private Limited
- Approving authority
- CDSCO
- Product information
- The SD BIOLINE H. pylori kit is a rapid, qualitative test for the detection of antibodies to Helicobacter pylori in human serum and plasma. The SD BIOLINE H. pylori kit is intended only for an initial screening test and reactive samples should be confirmed by a supplemental assay such as ELISA (SD BIOLINE Dengue IgG/IgM WB)
SD BIOLINE H.Pylori is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_2ac917debedc1f09b54245aec261f812_4b7104a16a25daefa5f2e082cf94ea1d. 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.