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 displaying fused images using high zoom a shift could occur between ct and pet portions of the images which could lead to misdiagnosis if used as a stand-alone exam for staging the location of tumours.