CDSCO UID MFG/IVD/2022/000078_99594fc3515a04388b5c9638d81ee02c_fc21d4ad87c660a1a4c1a5da4033bf3e
Leishmania Ab Rapid Test
Dia Sure Immunodiagnostic LLP·Device Class Class B·India CDSCO
Registration details
- UID
- MFG/IVD/2022/000078_99594fc3515a04388b5c9638d81ee02c_fc21d4ad87c660a1a4c1a5da4033bf3e
- Device class
- Class B
- License holder
- Dia Sure Immunodiagnostic LLP
- Approving authority
- South Delhi Division
- Product information
- Leishmania Ab Rapid Test is an immunochromatographic rapid test for qualitative detection of antibodies against Leishmania in human serum and plasma. It is for professional use only
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About this record
Leishmania Ab Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000078_99594fc3515a04388b5c9638d81ee02c_fc21d4ad87c660a1a4c1a5da4033bf3e. The license holder is Dia Sure Immunodiagnostic LLP, and it is classified as Device Class Class B. The approving authority is South Delhi Division.
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