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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An error message e705 could be displayed caused by an internal communication error with the measurement module for the software version 3.00.00. when this situation would occur it would be impossible to carry out any measurements and no result could be generated from the instrument.