Syphilis Antibody Rapid Test kit - India CDSCO Medical Device Registration
Syphilis Antibody Rapid Test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000109_52260464ef102e34065d11c96ad554f9_73a267147fb21fd7e5f39481a80fe67d. The license holder is Levram Lifesciences Private Limited, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.
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License Holder
Levram Lifesciences Private LimitedDevice Class
Approving Authority
Central Drug Standards Control Organization, West Zone
Product Information
The Syphilis antibody rapid test kit ##PLACEHOLDER_0## is a rapid chromatographic immunoassay for the qualitative detection of antibodies ##PLACEHOLDER_0## to Treponema Pallidum ##PLACEHOLDER_0## in the whole blood, Serum or Plasma to aid in the diagnosis of syphilis
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Brand: Pf. HRP-2