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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Unexpected behavior can occur when the user selects patient studies for display. a relevant prior study can unexpectedly display instead of the study selected. if a prior study must be retrieved (because "relevance" is selected and the prior study is not readily available locally) and the retrieval of the prior study completes before the selected study is available for display then the prior study will display instead of the selected (current) study.
Model Catalog: 6.6 (Lot serial: software version 6.6.1); Model Catalog: 6.5 (Lot serial: software version 6.6.1); Model Catalog: 6.6 (Lot serial: software version 6.5.5); Model Catalog: 6.5 (Lot serial: software version 6.5.5)