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 has been identified with the optical guidance platform (ogp) software v2.6 and v2.6.1. this defect causes lat error of 0.8mm - 1mm for datasets arriving to optical guidance platform (ogp) from eclipse and other planning systems in the left side first orientation. this issue is only applicable to sites using direct eclipse or other non fastplan 3rd party treatment planning software that send data in true dicom format. this issue afects body array frameless array and frameless array srs.