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 annotated numberic roi values on a batched perfusion map are incorrect when created using the auto batching function with the auto roi templates enabled which could result in incorrect diagnosis or treatment when evaluating brain perfusion conditions such as stroke.