FUJI Medical Dry Laser Imager - Indonesia BPOM Medical Device Registration
FUJI Medical Dry Laser Imager is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501719219. The device is manufactured by FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FUJIFILM INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.Country of Origin
China
Authorized Representative
FUJIFILM INDONESIAAR Address
Eightyeight@Kasablanka Office Tower Lantai 36, Unit A, B dan C, Jl. Casablanca Kav. 88
Registration Date
Apr 16, 2021
Expiry Date
Apr 15, 2026
Product Type
Diagnostic Radiology Equipment
Medical image digitizer.
Non Radiation Electromedics
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COLENTA DX Easy Imaging CR Retrofit Kit HighCap XLr
AMULET Bellus II
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FUJI DRI-CHEM NX700i and Accessories
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FUJI DRI-CHEM NX600 and Accessories
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FUJI DRI-CHEM NX700 and Accessories
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FUJI DRI-CHEM NX600i and Accessories
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FUJI DRI-CHEM SLIDE NH3 – W II
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FUJIFILM Digital Mammography System AMULET Sophinity
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FUJI DRI-CHEM SLIDE Mg - P III
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FUJI DRI-CHEM SLIDE LIP - P
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FUJI DRI-CHEM Slide HDL-C-PIII D
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