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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Radiometer has been made aware that the aqure system may display the sample type as "blank" if the sample type is not specified by the user. as multiple result values for the same patient and the same parameter can be displayed side by side on the screen there is a potential risk of misinterpretation of results the user may confuse the blank/unspecified sample type with the content of a specified sample type field.