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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Images might be lost and corresponding acquisitions have to be repeated under the following circumstances: -during an image recovery process on systems with portable detectors (max wi-d max mini) the connection of the portable detector is sporadically not re-established. -if either the "undo" button on the rad subtask card or the "previous series" button on the image subtask card are pressed during image readout. -sporadically during an automatic or a manual ris update. this may cause the deletion of the currently used study and all acquired images within this study.