ALKALINE PHOSPHATASE REAGENT - India CDSCO Medical Device Registration

ALKALINE PHOSPHATASE REAGENT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000042_eaeca618b2532a3cc964e4d98278534c_fb6f8b3e19c6fda05f12bf726a3addc1. 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

ALKALINE PHOSPHATASE REAGENT

UID: MFG/IVD/2022/000042_eaeca618b2532a3cc964e4d98278534c_fb6f8b3e19c6fda05f12bf726a3addc1

Brand Name

LIQUIXX -M- URIC ACID

License Holder

Transasia Bio-Medicals Limited

Device Class

Class B

Approving Authority

Solan(BBN)

Product Information

Alkaline Phosphatasee reagent, in conjunction with XL Systems/Semi Automated and XL multi calibrator/Fixed Factor is intended for the quantitative determination of total Alkaline Phosphatase activity in human serum, plasma or urine