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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During regular testing at siemens it was found that incorrect measurements in multi-planar reformattings (mprs) of a volume were acquired with a ct scanner with a titled gantry. in this situation the "4d" tabcard will incorrectly display length measurements that are too small if the measurement has been performed at the upper right mpr in a 2x2 layout.