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Rheumatoid Factor Rapid Test - India CDSCO Medical Device Registration

Rheumatoid Factor Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000009_629b8f27642f1d413b60f5a74f04a896_b34d4142cfe5d13efb95576d3d5303e6. This device is marketed under the brand name HI-QUIK. The license holder is Helico International, and it is classified as Device Class Class B. The approving authority is Karnataka.

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 B
Rheumatoid Factor Rapid Test
UID: MFG/IVD/2019/000009_629b8f27642f1d413b60f5a74f04a896_b34d4142cfe5d13efb95576d3d5303e6

Brand Name

HI-QUIK

License Holder

Helico International

Device Class

Class B

Approving Authority

Karnataka

Product Information

Qualitative detection of rheumatoid factor in human serum or plasma

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