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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Beckman coulter has identified that the fluorescence photo-multiplier tube (pmt) gain settings displayed in the cytometer control dialog box may not reflect the actual pmt gain settings on the navios flow cytometer. if a change to the fluorescence gain is made at any time to any protocol and saved (or not saved) all subsequently loaded protocols will apply the previously set gain parameters regardless of what the cytometer control dialog is showing. therefore any subsequent protocol may not reflect the actual system gain in the cytometer control dialog box.