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Fully automated coagulation analyser - India CDSCO Medical Device Registration

Fully automated coagulation analyser is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_8570c1bd717d0987fbbc1132657226e9_ab2eb6742c8403088da854e5ae7e9629. This device is marketed under the brand name HumaCLIA 150 . The license holder is M/s Stedman Pharmaceuticals Pvt. Ltd., and it is classified as Device Class Class A. 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 A
Fully automated coagulation analyser
UID: IMP/IVD/2019/000206_8570c1bd717d0987fbbc1132657226e9_ab2eb6742c8403088da854e5ae7e9629

Brand Name

HumaCLIA 150

Device Class

Class A

Approving Authority

CDSCO

Product Information

The HumaClot Pro is an automated coagulation analyser for the photo-optical determination of various parameters in human citrate plasma. In combination with HUMANยดs hemostasis reagents it may be used as an aid to diagnosis or monitoring of a range of blood clotting disorders, depending on the used rea-gent. For laboratory professional use only

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