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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An incorrect warning message occurs during calibrating of the fl4 time delay. the message appears at the bottom of the bd facscomp setup report (below the histograms) even when the results pass and there is no.