STA® - Control LA 1+2 - India CDSCO Medical Device Registration
STA® - Control LA 1+2 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001026_e3f7a76de8130774715080c02d1adb4e_976c5a138f24880068080f34d053f048. 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.
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Brand Name
Liatest AT III
License Holder
Syndicate Diagnostics Pvt. Ltd.Device Class
Approving Authority
CDSCO
Product Information
The STA® - Control LA 1 + 2 kit provides a lupus anticoagulant (Liatest AT III) negative plasma and a LA positive plasma. These plasmas are intended for the quality control of the tests for LA detection carried out with the following tests: – STA® - Staclot® dRVV Screen (Liatest AT III) – STA® - Staclot® dRVV Confirm (Liatest AT III) – Staclot® LA (Liatest AT III)
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