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_d1a268ee026a7b6d1a1d1f850e1f478d. 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_d1a268ee026a7b6d1a1d1f850e1f478d

Brand Name

LIQUIXX -M- URIC ACID

License Holder

Transasia Bio-Medicals Limited

Device Class

Class B

Approving Authority

Solan(BBN)

Product Information

This reagent is intended for in vitro quantitative determination of ALP in human serum or plasma

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