FUJIFILM Whole Body X-ray CT System Scenaria View - Indonesia BPOM Medical Device Registration
FUJIFILM Whole Body X-ray CT System Scenaria View is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321001. The device is manufactured by FUJIFILM HEALTHCARE CORPORATION MEDICAL SYSTEM OPERATIONS GROUP, KASHIWA from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FUJIFILM INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Japan
Authorized Representative
PT. FUJIFILM INDONESIAAR Address
: EightyEight@Kasablanka Office Tower A, Lantai 36 Jl. Casablanca Raya Kav. 88, Desa/Kelurahan Menteng Dalam, Kec. Tebet, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12870 No Telp: 021-21282182
Registration Date
Jun 04, 2023
Expiry Date
Jun 30, 2026
Product Type
Diagnostic Radiology Equipment
Computed tomography x-ray system.
Electromedic Radiation
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