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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Siemens has identified a potential malfunction when using syngo.Via version va11a_hf02 and higher. this malfunction occurs only with static and wholebody nuclear medicine images. in this case it can happen that the orientation lables at the segment borders are in conflict with the view name in the image text which has been entered by the user.