GREINER Uric Acid Mono - Indonesia BPOM Medical Device Registration
GREINER Uric Acid Mono is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101815182. The device is manufactured by GREINER DIAGNOSTIC GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RAJAWALI NUSINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GREINER DIAGNOSTIC GMBH.Country of Origin
Germany
Authorized Representative
PT. RAJAWALI NUSINDOAR Address
Gedung RNI Jl. Denpasar Raya Kav DIII Kuningan Jakarta Selatan
Registration Date
Jan 18, 2022
Expiry Date
Nov 11, 2026
Product Type
Clinical Chemistry Test System
Uric acid test system (kit & cair)
Invitro Diagnostics
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