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CDSCO UID IMP/IVD/2020/001026_f2cd6f247a8c71fa94a297cc803f1cf8_299d1a5381c1e484f651be1e1786ff2b

ASSERACHROM® HPIA

Syndicate Diagnostics Pvt. Ltd.·Device Class Class C·India CDSCO·Brand: Liatest AT III
Registration details
UID
IMP/IVD/2020/001026_f2cd6f247a8c71fa94a297cc803f1cf8_299d1a5381c1e484f651be1e1786ff2b
Device class
Class C
Brand name
Liatest AT III
License holder
Syndicate Diagnostics Pvt. Ltd.
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)
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About this record

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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