Syphilis Ab ELISA Kit
- UID
- MFG/IVD/2020/000053_f029dbb7ffab61c47e9b8d7f1e926ea0_72f708664f0770e49a88121f1f589ccb
- Device class
- Class D
- Brand name
- HBsAg ELISA Kit, Labsystems Diagnostics
- License holder
- Trivitron Healthcare Pvt. Ltd
- Approving authority
- Central Drug Standard Control Organisation, South Zone
- Product information
- The Syphilis Ab ELISA KIT is an in vitro diagnostics qualitative immunoassay for the detection of Antibodies to Treponema pallidum in human serum or plasma. The kit is basically intended to screen blood samples for clinical diagnostic testing
Syphilis Ab ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000053_f029dbb7ffab61c47e9b8d7f1e926ea0_72f708664f0770e49a88121f1f589ccb. This device is marketed under the brand name HBsAg ELISA Kit, Labsystems Diagnostics . The license holder is Trivitron Healthcare Pvt. Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standard Control Organisation, South Zone.
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