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Diagnostic Kit for T4 - India CDSCO Medical Device Registration

Diagnostic Kit for T4 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000169_b49c06892e8c5d64f954e62bee1956ad_a89ca713d226ae62280c47fcd298cfb3. This device is marketed under the brand name Time-resolved Fluorescence Immunochromatographic Assay. The license holder is Arkray Healthcare Pvt., Ltd.,, 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
Diagnostic Kit for T4
UID: IMP/IVD/2023/000169_b49c06892e8c5d64f954e62bee1956ad_a89ca713d226ae62280c47fcd298cfb3

Brand Name

Time-resolved Fluorescence Immunochromatographic Assay

Device Class

Class B

Approving Authority

CDSCO

Product Information

This kit uses competitive principle and fluorescence immunochromatography analysis technology to quantitatively detect the concentration of T4 in human serum, plasma, and whole blood samples

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