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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The issue is caused by the measured source paths for the following applicators: ring applicator sets ring ct/mr applicator sets interstitial ct/mr rings vienna ct/mr rings and advanced gynecological applicator - venezia with lunar-shaped ovoids which have a source step size of 2.5 mm for the microselectron afterloader. if you use such an applicator model to create a plan while the default step size of the afterloader is 5.0 the step size in the ring or lunar-shaped ovoids will be incorrect. they will be shown as 2.5 mm while the afterloader will deliver at 5.0 mm if the error is not detected during plan approval.
Model Catalog: 170.730 (Lot serial: Version 4.5.2); Model Catalog: 170.730 (Lot serial: Version 4.5.1); Model Catalog: 170.730 (Lot serial: Version 4.5)