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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Oes imaging has discovered during internal testing that images or graphics included in the patient clinical files and reports could be wrong when two image series are opened and reviewed simultaneously with the 3d module of the stereos workstation.