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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Veinviewer 1.1 gs (model no. p00800-l) has the potential to tip over if the device is not moved properly as outlined in the user guide. the device may tip over if the user pulls on the head or the arm when the arm/head is fully extended to the furthest and highest position or if the user attempts to lift the device to move it.