Leishmania Ab Rapid Test - India CDSCO Medical Device Registration
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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License Holder
Dia Sure Immunodiagnostic LLPDevice Class
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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