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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A potential issue may arise when using syngo imaging xs version va70a or higher in combination with other dicom nodes not supporting presentations states (pr). it may occur that images get corrupted when sending them to other dicom nodes which are configured as a non-pr supported network partner.