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 more than one beam is defined on the same isocenter center beam in field (cbf) affects all beams in a way that the user may not expect. after using cbf the resulting fields are clearly displayed in raystation/rayplan for review and approval. however one mistreatment incident using the cbf functionality has been reported where the user failed to review the resulting beam apertures before treatment delivery.