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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The instructions for use (ifu) sent with the product prior to 2004 indicates the allowed number of sterilization cycles is 100. the current version of the ifu indicates that the allowed number of sterilization is 25 and is the accurate limit for the flexible probe with a blocking washer gm11002420 usage.