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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The channel configuration in the ep amplifier is not always fully restored when returning to the waveform display. intermittently the effected channel (s) becomes disconnected from the ep amplifier input pins leaving the input signal floating. the results in no curve displayed or the displayed curve (s) becoming distorted (noisy unstable).