Japanese data is current through August 2018. All of the data comes from the Japanese Pharmaceuticals and Medical Devices Agency, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Japan.
(1) stationary analog type general-purpose X-ray diagnostic apparatus (2) non-electric type patient table for general purpose X-ray diagnostic apparatus (3) non-motorized patient table for general purpose X-