SwiftMR A22-OP - Indonesia BPOM Medical Device Registration
SwiftMR A22-OP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321025. The device is manufactured by AIRS MEDICAL INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ASIA ACTUAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AIRS MEDICAL INC.Country of Origin
Korea
Authorized Representative
PT. ASIA ACTUAL INDONESIAAR Address
PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN
Registration Date
Dec 13, 2023
Expiry Date
Apr 28, 2028
Product Type
Diagnostic Radiology Equipment
Medical image management and processing system.
Non Radiation Electromedics
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