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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Cardiac output values are being incorrectly transmitted from the sc 7000 sc 9000 or sc 9000xl patient monitor to cathcor when the dialogue language is set to french or german. this update will correct this.