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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Intuitive urgical system uses a sterile adapter as the interface between the (sterile) instrument and the (non-sterile) system. for the is2000 and is3000 system models. the sterile adapter is integrated into the instrument arm drape. intuitive surgical is implementing a voluntary action to provide users of the da vinci s si and si-e systems with additional information regarding sterile adapter engagement and instrument installation.