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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After performing a snap verification that is a monoscopic intra-fraction x-ray monitoring using only one x-ray tube in combination with implanted markers the exactrac 6.0 x-ray monitoring tab might display an incorrect hint icon and result text.