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Syphilis Dipstick Rapid Test - India CDSCO Medical Device Registration

Syphilis Dipstick Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000104_ec4db3ce2e5ad189f65d26f9846817e8_826f00ff4fd11970617e47a1960b5967. 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.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class D
Syphilis Dipstick Rapid Test
UID: MFG/IVD/2021/000104_ec4db3ce2e5ad189f65d26f9846817e8_826f00ff4fd11970617e47a1960b5967

Brand Name

HI-QUIK

License Holder

Helico International

Device Class

Class D

Approving Authority

Sub Zonal Bangalore

Product Information

The HI-Quik Syphilis Rapid Test Dipstick (HI-QUIK) 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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