Rapid ME - Indonesia BPOM Medical Device Registration
Rapid ME is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420536. The device is manufactured by ISCHEMAVIEW, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ASIA ACTUAL INDONESIA.
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Rapid ICH
Risk Classification
Product Class
Kelas : 2
Manufacturer
ISCHEMAVIEW, INC.Country of Origin
United States
Authorized Representative
ASIA ACTUAL INDONESIAAR Address
PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN
Registration Date
Aug 19, 2024
Expiry Date
May 06, 2029
Product Type
Diagnostic Radiology Equipment
Radiological computer aided triage and notification software
Non Radiation Electromedics
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