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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Two issues affecting the monaco device: 1) when ct images are created this latter way and imported in monaco the image is displayed correctly but the electron densities are incorrecly flipped in both the right-left and superior-inferior directions. 2) when using multiple prescription and the first prescription has forced densities these forced densities are not being maintained with the second prescription.