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 anomaly exists in eclipse software whereby swapping id's of planning fields can produce inconsistencies between the dose matrix and field parameters. inconsistencies can occur related to various field parameters such as field size blocks or wedges.