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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Siemens has confirmed that version (v1.0) of the data management software (dms) cd was packaged with some xprecia stride coagulation analyzers. the version of the dms cd should have been v1.1 as this will match the version of firmware pre-loaded on the analyzer. these two versions must match in order to provide full functionality to the analyzer.