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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Cdi system 500 monitor displaying the "h/s disconnect at cuvette" error message when the cdi h/s cuvette does not make a proper connection to the cdi h/s probe. in this situation blood parameter values for hct hgb and so2 do not display.