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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Elekta has become aware of the potential for incorrect dicom mapping of the exported collimator or couch angles from ergo which would lead to incorrect rotation of the collimator or couch when using a mlc device for planning.