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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Pupil centroid shift compensation is not functioning as intended in the iris registration (ir) software versions 5.00 through 5.30. as a result the center of the ablation pattern may not be optimally aligned. this may in some cases result in visual disturbances or reduced best corrected visual acuity.