Pure Global

Scrub Typhus Rapid test - India CDSCO Medical Device Registration

Scrub Typhus Rapid test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000009_c6d8f90de388d8f5b6dbd104fd99bb50_9d645569d747e4273682dba2be06ed61. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Scrub Typhus Rapid test
UID: MFG/IVD/2019/000009_c6d8f90de388d8f5b6dbd104fd99bb50_9d645569d747e4273682dba2be06ed61

Brand Name

HI-QUIK

License Holder

Helico International

Device Class

Class B

Approving Authority

Karnataka

Product Information

qualitative detection of antibodies against Orientia tsutsugamushi in the patientโ€™s plasma, serum or blood

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing