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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The tumorloc application has the capability to generate intensity projection datasets from respiratory gated data. philips healthcare has become aware of a circumstance where these generated datasets are flipped and incorrectly labeled left to right when they are saved to disk.