Leishmania Ab Rapid Test
- UID
- MFG/IVD/2022/000088_99594fc3515a04388b5c9638d81ee02c_435e67ce258d03c1e53c20aa1c27b813
- Device class
- Class B
- Brand name
- HaemNest Sheath Fluid
- License holder
- Genenest Biotech Pvt. Ltd.
- Approving authority
- Uttar Pradesh
- Product information
- The Leishmania Ab Rapid Test (HaemNest Sheath Fluid) is a rapidchromatographic immunoassay for thequalitative detection of igG and igMantibodies to Leishmania in human's wholeblood, serum or plasma
Leishmania Ab Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000088_99594fc3515a04388b5c9638d81ee02c_435e67ce258d03c1e53c20aa1c27b813. This device is marketed under the brand name HaemNest Sheath Fluid. The license holder is Genenest Biotech Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.
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