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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Ct transcatheter aortic valve implantation (ct tavi) planning applicationsupplied as an option to intellispace portal software version 6 may display incorrect measurements of cardiac and aortic anatomy. clinicians use this information to plan tavi procedures and to select and size the transcatheter heart valve (thv) to be used in the procedures.Reliance on incorrect information could contribute to an unsuccessful thv implantation procedure.