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Rapid Test for Syphilis (SYPHICHECK ) - India CDSCO Medical Device Registration

Rapid Test for Syphilis (SYPHICHECK ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000130_e494f333348140b4828a270450c7413c_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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CDSCO Registered
Class Class C
Rapid Test for Syphilis (SYPHICHECK )
UID: MFG/IVD/2020/000130_e494f333348140b4828a270450c7413c_9cf59b751b69375c19b1f68d07257087

Brand Name

Paracheck Pf Device

Device Class

Class C

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

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