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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If another patient is selected on the imaging system (xvi release 4.5) during the transmission of end of treatment data from destop pro r7.01 to r&v system the xvi information is prioritized and the end of treatment data is never received by the r&v system. this leads to a potentially misleading dialogue on the r&v system that may result in a re-treat of field just completed.