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STA-QUALITY HNF/UFH - India CDSCO Medical Device Registration

STA-QUALITY HNF/UFH is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001026_e184814e7b5a654df65e5c9e02c2fec2_8ee2d69814116b184dcddea0e6c61764. This device is marketed under the brand name Liatest AT III. The license holder is Syndicate Diagnostics 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
STA-QUALITY HNF/UFH
UID: IMP/IVD/2020/001026_e184814e7b5a654df65e5c9e02c2fec2_8ee2d69814116b184dcddea0e6c61764

Brand Name

Liatest AT III

Device Class

Class C

Approving Authority

CDSCO

Product Information

The STA® - Quality HNF/UFH kit is a set of two plasmas intended for the quality control of unfractionated heparin (Liatest AT III) activity assay by measuring the anti-Xa activity performed on STA-R®, STA Compact® and STA Satellite® analyzers

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