FUJI MEDICAL Dry Laser Imager Drypix Edge - Indonesia BPOM Medical Device Registration
FUJI MEDICAL Dry Laser Imager Drypix Edge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501814770. 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 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 21, 2024
Expiry Date
Jun 30, 2028
Product Type
Diagnostic Radiology Equipment
Medical image digitizer.
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