CDSCO UID MFG/IVD/2020/000014_4baa3e7bb1ef72a9850d7834399bacfc_acdd722f5a103543dddecd0c84aaf456Erba Lisa® Syphilis
- UID
- MFG/IVD/2020/000014_4baa3e7bb1ef72a9850d7834399bacfc_acdd722f5a103543dddecd0c84aaf456
- Device class
- Class D
- Brand name
- ERBA LISA
- License holder
- M/s.Transasia Bio-Medicals Ltd.
- Approving authority
- Central Drug Standards Control Organization, West Zone
- Product information
- Qualitative determination of total antibodies (ERBA LISA) to Treponema pallidum in human serum/plasma
Erba Lisa® Syphilis is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000014_4baa3e7bb1ef72a9850d7834399bacfc_acdd722f5a103543dddecd0c84aaf456. This device is marketed under the brand name ERBA LISA. The license holder is M/s.Transasia Bio-Medicals Ltd., and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.
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