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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Pq-series scanners provide information to the pinnacle3 rtp software to enable the absolute marking feature of the acqsim3 simulation application. the software interpretation of this info can be inconsistent.