FUJIFILM Diagnostic X-Ray System FDR SMART - Indonesia BPOM Medical Device Registration
FUJIFILM Diagnostic X-Ray System FDR SMART is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501816084. The device is manufactured by DRGEM CORPORATION from Korea, 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
Manufacturer
DRGEM CORPORATIONCountry of Origin
Korea
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
Apr 18, 2024
Expiry Date
Feb 07, 2029
Product Type
Diagnostic Radiology Equipment
Stationary x-ray system.
Electromedic Radiation
FUJIFILM Digital Radiography System FDR SMART X
FUJIFILM Diagnostic X-Ray System FDR SMART
FUJIFILM Digital Radiography System FDR SMART X
FUJIFILM Digital Radiography System FDR SMART X
FUJIFILM Digital Radiography System FDR SMART X
FUJIFILM Digital Radiography System FDR Smart X
FUJIFILM Digital Radiography System FDR Smart X
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