WIENER γ-G-Test Kinetic AA Liquid - Indonesia BPOM Medical Device Registration
WIENER γ-G-Test Kinetic AA Liquid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101020604. The device is manufactured by WIENER LABORATORIOS S. A. I. C. from Argentina, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRATAMINDO MITRA RIZKY.
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WIENER γ-G-Test Cinetica AA Liquida
Risk Classification
Product Class
Kelas : 2
Manufacturer
WIENER LABORATORIOS S. A. I. C.Country of Origin
Argentina
Authorized Representative
PT. PRATAMINDO MITRA RIZKYAR Address
Perumahan Bogorami Indah Regency, Jl. Bulak Setro Indah II Blok B 51-52, Surabaya
Registration Date
Apr 07, 2022
Expiry Date
Mar 31, 2025
Product Type
Clinical Chemistry Test System
Gamma-glutamyl transpeptidase and isoenzymes test system (kit & cair)
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