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CDSCO UID MFG/IVD/2021/000104_a6c5387441afc0eb06e6ac88c95c0bd6_3f056ac05da32c3e44bef32915d85b26

Syphilis Rapid Card Test

Helico International·Device Class Class D·India CDSCO·Brand: HI-QUIK
Registration details
UID
MFG/IVD/2021/000104_a6c5387441afc0eb06e6ac88c95c0bd6_3f056ac05da32c3e44bef32915d85b26
Device class
Class D
Brand name
HI-QUIK
License holder
Helico International
Approving authority
Sub Zonal Bangalore
Product information
The HI-Quik Syphilis Rapid Test Card is a rapid chromatographic immunoassay for the qualitative detection of antibodies (HI-QUIK) to Treponema Pallidum (HI-QUIK) in serum or plasma to aid in the diagnosis of Syphilis.
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About this record

Syphilis Rapid Card Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000104_a6c5387441afc0eb06e6ac88c95c0bd6_3f056ac05da32c3e44bef32915d85b26. This device is marketed under the brand name HI-QUIK. The license holder is Helico International, and it is classified as Device Class Class D. The approving authority is Sub Zonal Bangalore.

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