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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If the end-user requests to move a report into a study that currently has a report associated with it the system will allow the move however the result is that there is no indication that the moved report exists when viewing the study through the user interface.
Model Catalog: 60+00007791 (Lot serial: SOFTWARE VERSION 1.00.26); Model Catalog: 60+00007791 (Lot serial: SOFTWARE VERSION CV7.4.SU3); Model Catalog: 60+00007791 (Lot serial: SOFTWARE VERSION CV7.8); Model Catalog: 60+00007791 (Lot serial: SOFTWARE VERSION 1.00.27)