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 instructions for use are being updated to contain tolerances of generator parameters of the mobilediagnost wdr as required by iec 60601-1-3 chapter 6.4.3. these required parameters are not present in the current instruction for use of the mobilediagnost wdr.