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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Brainlab has detected an unexpected phenomenon for exactrac v.6.X that could occur within an unusual workflow when using the exactrac cone beam ct (cbct) module in combination with actively re-reconstructed cbct images of a subvolume from the original cbct volume. for a re-reconstructed cbct subvolume the acquisition position of the original cbct is not regarded by the brainlab exactrac cbct module. therefore the position of such a cbct subvolume may not be correcly imported by exactrac.
Model Catalog: 49971 (Lot serial: Version 6.0.5); Model Catalog: 49971 (Lot serial: Version 6.0.4); Model Catalog: 49971 (Lot serial: Version 6.0.3); Model Catalog: 49971 (Lot serial: Version 6.1.0); Model Catalog: 49971 (Lot serial: Version 6.0.2); Model Catalog: 49971 (Lot serial: Version 6.0.1); Model Catalog: 49971 (Lot serial: Version 6.0.0)