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IL-6 Rapid Quantitative Test - India CDSCO Medical Device Registration

IL-6 Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000191_86a63e60da2b55b0e474ea08b2fd0b1a_2ee555e620db8a66c65e39575cc2e3af. This device is marketed under the brand name Testosterone Rapid Quantitative Test. The license holder is Matrix Labs, and it is classified as Device Class Class B. The approving authority is CDSCO.

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
IL-6 Rapid Quantitative Test
UID: IMP/IVD/2019/000191_86a63e60da2b55b0e474ea08b2fd0b1a_2ee555e620db8a66c65e39575cc2e3af

Brand Name

Testosterone Rapid Quantitative Test

License Holder

Matrix Labs

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Finecareโ„ข IL-6 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecareโ„ข FIA System (Testosterone Rapid Quantitative Test) for quantitative determination of Interleukin-6 (Testosterone Rapid Quantitative Test) in human whole blood, serum or plasma.

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