CREATINE KINASE REAGENT - India CDSCO Medical Device Registration

CREATINE KINASE REAGENT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000042_e441bf9db319e8436253773cb725cd0d_d5f5fb13bb2df84d3e99e112d826944b. This device is marketed under the brand name LIQUIXX -M- URIC ACID. The license holder is Transasia Bio-Medicals Limited, and it is classified as Device Class Class B. The approving authority is Solan(BBN).

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CDSCO Registered

Class Class B

CREATINE KINASE REAGENT

UID: MFG/IVD/2022/000042_e441bf9db319e8436253773cb725cd0d_d5f5fb13bb2df84d3e99e112d826944b

Brand Name

LIQUIXX -M- URIC ACID

License Holder

Transasia Bio-Medicals Limited

Device Class

Class B

Approving Authority

Solan(BBN)

Product Information

CK reagent, when used in conjunction with XL Systems 300/600/Semi-Auto and XL multi calibrator and Fixed factor intended for the quantitative determination of Creatine Kinase activity in human serum or plasma