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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When an roi with material override overlaps a fixation or support roi the material used for dose calculation in the overlapping region may not be as intended. also when a support or fixation roi overlaps the patient outline (external roi) in a dose grid voxel along the outer surface of the patient outline the density used for dose calculation in that voxel may not be as intended.