AIM URI TEST 3 - Indonesia BPOM Medical Device Registration
AIM URI TEST 3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101126597. The device is manufactured by BIOWAY BIOLOGICAL TECHNOLOGY CO.,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ACCURATE INTAN MADYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOWAY BIOLOGICAL TECHNOLOGY CO.,LTDCountry of Origin
China
Authorized Representative
PT. ACCURATE INTAN MADYAAR Address
KOMPLEK DUTA MERLIN, BLOK. F5 & F6, JL. GAJAH MADA NO. 3-5
Registration Date
Jun 04, 2024
Expiry Date
Jun 02, 2027
Product Type
Clinical Chemistry Test System
Multi parameter clinical chemistry test system
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