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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Reagent mixing information described in the method sheet that was not provided in the tas/tasu of the cobas integra 400/800 for benzodiazepines ii may have an impact on calibration stability.