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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When the system configuration of the clinical workstation is set to averaging ecg as the start-view the area showing averaging ecg is not re-drawn until new valid data is received. this field can then contain data from a previous patient.