FUJIFILM FDR D-EVO II - Indonesia BPOM Medical Device Registration
FUJIFILM FDR D-EVO II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501817505. The device is manufactured by FUJIFILM HEALTHCARE MANUFACTURING CORPORATION HANAMAKI OFFICE from Japan, and is classified as Risk Class Kelas Resiko : B. 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 Lantai 36, Unit A, B dan C, Jl. Casablanca Kav. 88
Registration Date
Nov 28, 2022
Expiry Date
May 19, 2026
Product Type
Diagnostic Radiology Equipment
Solid State X-Ray Imager (Flat Panel/Digital Imager)
Non Radiation Electromedics
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FUJIFILM FDR SE Console
FUJIFILM Console Advance
FUJIFILM Digital Mammography System AMULET Sophinity
FUJIFILM FDR D-EVO II Medical Digital Radiography
FUJIFILM FDR D-EVO II
FUJIFILM Whole Body X-ray CT System Scenaria View Plus
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FUJIFILM Whole Body X-ray CT System Scenaria View (84 kW)
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FUJIFILM Diagnostic Ultrasound System
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FUJIFILM MR Imaging System ECHELON Synergy
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FUJIFILM FDR D-EVO GL
FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION ANALYTICAL SYSTEM KASHIWA FACTORY
AIRIS Vento MR Imaging System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE.
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE
FUJIFILM Diagnostic Ultrasound System
FUJIFILM HEALTHCARE MANUFACTURING CORPORATION KASHIWA OFFICE