QUANTILAB ฮณ-GT Liquid - Indonesia BPOM Medical Device Registration
QUANTILAB ฮณ-GT Liquid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101122345. 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 24, 2024
Expiry Date
Sep 23, 2029
Product Type
Clinical Chemistry Test System
Gamma-glutamyl transpeptidase and isoenzymes test system (kit & cair)
Invitro Diagnostics
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