QUANTILAB Uric Acid - Indonesia BPOM Medical Device Registration
QUANTILAB Uric Acid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101123079. The device is manufactured by INSTRUMENTATION LABORATORY SPA, from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEXA ARFINDO PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INSTRUMENTATION LABORATORY SPA,Country of Origin
Italy
Authorized Representative
PT. DEXA ARFINDO PRATAMAAR Address
Jl. Dr. Ir. H. Soekarno 407 RT 1 RW 9
Registration Date
Dec 27, 2024
Expiry Date
Sep 23, 2029
Product Type
Clinical Chemistry Test System
Uric acid test system (kit & cair)
Invitro Diagnostics
QUANTILAB Phosphorus
QUANTILAB TOTAL PROTEIN
QUANTILAB AST/GOT Liquid
QUANTILAB Magnesium
QUANTILAB ReferrIL G Diluent
QUANTILAB AMYLASE
QUANTILAB ReferrIL HDL-LDL
QUANTILAB Total Bilirubin
QUANTILAB Triglycerides
QUANTILAB ALT/GPT LIQUID
QUANTILAB Phosphorus
INSTRUMENTATION LABORATORY SPA,
QUANTILAB AST/GOT Liquid
INSTRUMENTATION LABORATORY SPA,
QUANTILAB TOTAL PROTEIN
INSTRUMENTATION LABORATORY SPA,
QUANTILAB Iron
INSTRUMENTATION LABORATORY SPA.
QUANTILAB Magnesium
INSTRUMENTATION LABORATORY SPA,
QUANTILAB Cholesterol
INSTRUMENTATION LABORATORY SPA.
QUANTILAB ReferrIL G Diluent
INSTRUMENTATION LABORATORY SPA,
QUANTILAB TIBC
INSTRUMENTATION LABORATORY SPA.
QUANTILAB ฮณ-GT Liquid
INSTRUMENTATION LABORATORY SPA.
QUANTILAB Creatinine
INSTRUMENTATION LABORATORY SPA.,

