Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
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During dicom export of plan level images with a non square exported field of view (fov) an anomoly in the process of squaring the plan level image may cause the image to shift with respect to roi's and dose. when the anomoly occurs the magnitude of the image shift can be a full iec-x voxel a full iec-z voxel or full voxels in both iec-x and iec-z.