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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Certain treatment techniques require that the couch be rotated to a position where the gantry is moving in a trajectory that could strike the couch and / or the patient who is positioned on the couch. particular care should be observed during automated treatment that includes couch rotation.