ASSERACHROM® HPIA - India CDSCO Medical Device Registration
ASSERACHROM® HPIA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001026_f2cd6f247a8c71fa94a297cc803f1cf8_299d1a5381c1e484f651be1e1786ff2b. 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 Asserachrom® HPIA kit is intended for the qualitative detection in plasma or serum of the anti-heparin-platelet factor 4 (Liatest AT III) antibodies generated during the type II heparin-induced thrombocytopenias (Liatest AT III) by ELISA (Liatest AT III)
STA® - RIVAROXABAN CALIBRATOR
Brand: Liatest AT III
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Brand: Liatest AT III
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Weilland C. on STA
Brand: Liatest AT III
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Brand: Liatest AT III
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Brand: Liatest AT III
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Brand: Liatest AT III
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Brand: Liatest AT III
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Brand: Liatest AT III
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Brand: Liatest AT III
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Brand: Liatest AT III
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Brand: Liatest AT III
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Brand: Liatest AT III
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Brand: Liatest AT III