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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This issue happens for rf projection images [the 12 dicom sop classes]. if user measures on rf image "cal" (calibration) is not displayed and measurement is not correct. the "cal" label is not displayed on the projection images after calibration is performed which should be present if the measurement is presented based on pixel spacing.