URIC ACID liquicolor plus - India CDSCO Medical Device Registration
URIC ACID liquicolor plus is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_e5005ac66d6076461ddcdbdfc46fd1e4_66ec4cc4109f7837ea76d1e95544debf. The license holder is Stedman Pharmaceuticals Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.
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License Holder
Stedman Pharmaceuticals Pvt. Ltd.Device Class
Approving Authority
CDSCO
Product Information
The Uric Acid liquicolor plus is a PAP-Method Enzymatic Colorimetric Test ##PLACEHOLDER_0## and has been designed for the quantitative determination of uric acid in human serum and plasma
