EASYRA Uric Acid Reagent Kit - Indonesia BPOM Medical Device Registration
EASYRA Uric Acid Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101914914. The device is manufactured by MEDICA CORPORATION. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SABA INDOMEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDICA CORPORATION.Country of Origin
United States
Authorized Representative
SABA INDOMEDIKAAR Address
Ruko Kedoya Elok Plaza DB-33 Jl. Panjang No.7-9
Registration Date
Oct 05, 2023
Expiry Date
May 03, 2028
Product Type
Clinical Chemistry Test System
Uric acid test system (kit & cair)
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