Rapid Test for Syphilis-WB (SYPHICHECK WB )
- UID
- MFG/IVD/2020/000130_e3e76cc8237016fb084a67abfd32fbc7_9cf59b751b69375c19b1f68d07257087
- Device class
- Class C
- Brand name
- Paracheck Pf Device
- Approving authority
- CDSCO -North Zone, Ghaziabad
- Product information
- Syphicheck-WB (Paracheck Pf Device) is a modified TPHA, which qualitatively detects the presence of IgM and IgG class of Treponema specific antibodies during syphilis in whole blood, serum or plasma specimens
Rapid Test for Syphilis-WB (SYPHICHECK WB ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000130_e3e76cc8237016fb084a67abfd32fbc7_9cf59b751b69375c19b1f68d07257087. This device is marketed under the brand name Paracheck Pf Device. The license holder is VIOLA DIAGNOSTIC SYSTEMS - A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED,, and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.
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