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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These lite wands were originally classified as class i however upon further discussion it was determined that this device could be exposed to fat and blood and is therefore considered invasive and should therefore be class ii per rule 1(1) subject to subrules (2) and (3) all surgically invasive devices are classified as class ii.