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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Vitek 2 7.01 software introduced a feature (enable - convention for highest reportable mic) that can be used to modify the reporting convention when an ast result is within the highest reportable mic range. advanced expert system (aes) parameter sets are configurable in the vitek 2 software to allow users to select mic breakpoint interpretation as well as aes functionality related to recommended guidelines. when "enabled - convention for highest reportable mic configuration option modifies the highest reportable mic value for each specific antimicrobial to half its doubling dilution and displays the value with a "greater than" symbol.