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Diagnostic Kit for D-Dimer - India CDSCO Medical Device Registration

Diagnostic Kit for D-Dimer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000169_69db9c216a19b8f515bc6bad365a5a50_9c01b8ee5a17c71467d90bc6058790d6. 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 D-Dimer
UID: IMP/IVD/2023/000169_69db9c216a19b8f515bc6bad365a5a50_9c01b8ee5a17c71467d90bc6058790d6

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 D-Dimer in human plasma and whole blood samples

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