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STA® - FDP Control - India CDSCO Medical Device Registration

STA® - FDP Control is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001026_e4da37203ef12b9c079f76cc8da4250d_b4570b1f05b34ea095867ec522e63e56. 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® - FDP Control
UID: IMP/IVD/2020/001026_e4da37203ef12b9c079f76cc8da4250d_b4570b1f05b34ea095867ec522e63e56

Brand Name

Liatest AT III

Device Class

Class C

Approving Authority

CDSCO

Product Information

The STA® - FDP Control kit provides two plasmas intended for the quality control of assays of fibrin/fibrinogen degradation products (Liatest AT III) on STA-R® and STA Compact® by the immuno-turbidimetric method (Liatest AT III)

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