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 was discovered in which a second or subsequent user can access a patient record which is already open at another workstation and if they ignore the warning the message that the record is being edited by another user and proceed to edit the plan and save the record a corrupted but usable patient plan record may result. errors can include but are not limited to incorrect mu incorrect beam modifiers incorrect gantry angles incorrect field sizes etc.
Model Catalog: V.6.5 (Lot serial: manufacturer.); Model Catalog: V.6.5 (Lot serial: >10 units. Contact); Model Catalog: VERSION 6.5 (Lot serial: >10 units. Contact); Model Catalog: VERSION 6.5 (Lot serial: manufacturer.)