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STA® - Liquid Fib - India CDSCO Medical Device Registration

STA® - Liquid Fib is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001026_c6cb6e9e534dc1f47fd76fb9bdd5ffb0_210a5a8a1061d986dd1c404bd4b0db35. 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® - Liquid Fib
UID: IMP/IVD/2020/001026_c6cb6e9e534dc1f47fd76fb9bdd5ffb0_210a5a8a1061d986dd1c404bd4b0db35

Brand Name

Liatest AT III

Device Class

Class C

Approving Authority

CDSCO

Product Information

The STA® - Liquid Fib kit is intended for use with STA-R®, STA Compact® and STA Satellite® for the quantitative determination of fibrinogen levels in plasma by the clotting method of Clauss (Liatest AT III)

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