LABScan 3D Performance Verification Kit - Indonesia BPOM Medical Device Registration
LABScan 3D Performance Verification Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322556. The device is manufactured by LUMINEX CORP from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SETIA GUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUMINEX CORPCountry of Origin
United States
Authorized Representative
SETIA GUNA MEDIKAAR Address
KOMPLEK TAMAN KEBUN JERUK BLOK AA IV NO. 39-40, KEBUN JERUK, JAKARTA BARAT
Registration Date
Feb 09, 2023
Expiry Date
Dec 31, 2024
Product Type
Clinical Chemistry Test System
Calibrator (cair)
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