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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The ecg waveform trace may be missing in retro recon from scan data where the r-peak coincides with x-ray on signal resulting in captured data for an extra r-peak. as a result the ecg waveform trace will not display and retrospective reconstruction is not possible for that series.