Rapid test for detection of Antibodies to Syphilis in Human Serum/ Plasma/ Whole Blood
- UID
- MFG/IVD/2022/000085_c52d2642c69a8f47e616cde955b7ba03_c52d2642c69a8f47e616cde955b7ba03
- 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
- Rapid test for detection of Antibodies to Syphilis in Human Serum/ Plasma/ Whole Blood
Rapid test for detection of Antibodies to Syphilis in Human Serum/ Plasma/ Whole Blood is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_c52d2642c69a8f47e616cde955b7ba03_c52d2642c69a8f47e616cde955b7ba03. 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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