AMULET Bellus II - Indonesia BPOM Medical Device Registration
AMULET Bellus II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420840. The device is manufactured by FUJIFILM HEALTHCARE MANUFACTURING CORPORATION HANAMAKI OFFICE from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FUJIFILM INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Japan
Authorized Representative
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
Nov 22, 2024
Expiry Date
Jun 30, 2029
Product Type
Diagnostic Radiology Equipment
Medical image management and processing system.
Non Radiation Electromedics
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FUJI DRI-CHEM SLIDE NH3 – W II
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