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.
데이터 추가 비고
원인
When used in a clinical environment the curix opthos h film described above "flipped" or "reversed" loaded in an curix opthos h asymmetric screens and cassette and exposed as normal may be viewed to have slightly different image quality than the expected normal curix opthos h image quality.