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 current iol master 700 software version 1.14.84 sometimes shows an unexpected behavior during toric iol power calculation with the haigis suite: in some cases of low cylinder power with a theoretically ideal iol below the delivery range of the selected toric iol model the device suggests a toric iol with significant remaining cylinder refraction.