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 rf tag on the white protection sheet of the media stack is incorrect. after reading one of these rf tags and due to the inconsistency between rf tagthe material and the imager the drystar imager will generate an error code and print a warning sheet.