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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Eos imaging has discovered that "print true size" print requests from the eos acquisition station or the stereos image station may be affected by a different enlargement factor during printing. therefore measurements taken manually could be incorrect if the dimensions are not converted according to the scale used on the printed image.