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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Potential risk of interference when using brainlab m3 on a varian linear accelerator with the internal varian multileaf collimator not in park mode during treatment: the internal varian f-collimator could interfeere with the intended conformal fields of the brainlab m3 during patient treatment. this may cause a critical under-dosage of the target region.