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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When a respiratory gated 40 ct scan is performed with the bellows pulmonary gating device in some circumstances the ct images might be reconstructed at a single phase while the annotations on the images incorrectly indicate that the reconstruction is from the requested specific phases (0% to 90%).