LABScan 3D ™ - Indonesia BPOM Medical Device Registration
LABScan 3D ™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102120487. The device is manufactured by LUMINEX CORPORATION. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SETIA GUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUMINEX CORPORATION.Country of Origin
United States
Authorized Representative
PT. SETIA GUNA MEDIKAAR Address
KOMPLEK TAMAN KEBUN JERUK BLOK AA IV NO. 39-40, KEBUN JERUK, JAKARTA BARAT
Registration Date
Dec 15, 2021
Expiry Date
Dec 31, 2024
Product Type
Clinical Laboratory Equipment
Instrumentation for clinical multiplex test systems.
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