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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Due to an incorrect algorithm the air kerma (ak) and air kerma rate values are not displayed correctly. the displayed ak is using an incorrect point of reference. this is a non-compliance per the radiation emitting devices act (r.S.C. 1985 section 6).