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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When interfaced via a 9015 cable to an external data collection device a 9004 monitor configured with ccap 1.13 software will not communicate reliably through either channel 3 or 4. this issue only occurs when the monitor's analog output is set to external.