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Diagnostic Kit for Beta-HCG - India CDSCO Medical Device Registration

Diagnostic Kit for Beta-HCG is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000169_a4c14b302056880a1c50bb47f77bf32a_59ce07161ccf24ee70fdceb323606d7c. This device is marketed under the brand name cTnI. The license holder is Arkray Healthcare Pvt., Ltd.,, and it is classified as Device Class Class C. 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 C
Diagnostic Kit for Beta-HCG
UID: IMP/IVD/2023/000169_a4c14b302056880a1c50bb47f77bf32a_59ce07161ccf24ee70fdceb323606d7c

Brand Name

cTnI

Device Class

Class C

Approving Authority

CDSCO

Product Information

This kit uses double antibody sandwich method principle and fluorescence immunochromatography analysis technology to quantitatively detect the concentration of ฮฒ-HCG in human serum, plasma, and whole blood samples

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