RPR test for qualitative detection of Antibody to syphilis in Human Serum/plasma.
- UID
- MFG/IVD/2022/000085_9e368e2d444245ed492f1ae6447a2dcd_47f6b7cbd5f1711a2bdc856c58cab0e3
- Device class
- Class D
- Brand name
- Rapid Plasma Reagin
- License holder
- Voxtur Bio Ltd
- Approving authority
- Central Drug Standards Control Organization, West Zone
- Product information
- The RPR slide test is used for rapid visual test for the qualitative detection for the presence or absence of reagin antibodies in human serum/plasma
RPR test for qualitative detection of Antibody to syphilis in Human Serum/plasma. is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_9e368e2d444245ed492f1ae6447a2dcd_47f6b7cbd5f1711a2bdc856c58cab0e3. This device is marketed under the brand name Rapid Plasma Reagin. The license holder is Voxtur Bio 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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