SANYMED URIC ACID LR MONO - Indonesia BPOM Medical Device Registration
SANYMED URIC ACID LR MONO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101915854. The device is manufactured by SANYMED S.A.S from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PERFECT MEDILAB INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SANYMED S.A.SCountry of Origin
Italy
Authorized Representative
PT. PERFECT MEDILAB INDONESIAAR Address
jl.Bunga Wijaya Kesuma Psr.IV No.11 Titi Rante
Registration Date
Mar 18, 2024
Expiry Date
Jan 10, 2029
Product Type
Clinical Chemistry Test System
Uric acid test system (kit & cair)
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