LABScan 3D Verification Kit - Indonesia BPOM Medical Device Registration
LABScan 3D Verification Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101520199. 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. SEGMED DISTRIBUTION INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUMINEX CORPORATIONCountry of Origin
United States
Authorized Representative
PT. SEGMED DISTRIBUTION INDONESIAAR Address
SEGMED DISTRIBUSI INDONESIA
Registration Date
Jan 24, 2025
Expiry Date
Dec 31, 2027
Product Type
Clinical Chemistry Test System
Calibrator (cair)
Invitro Diagnostics
LABScan 3D Calibration Kit
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FLEXMAP 3D Performance Verification Kit
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LUMINEX 100/200 Performance Verification Kit
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