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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Siemens has identified a mismatch between orientation labels and displayed anatomy (e.G. in the 3d task card) within the software version syngo e11p for biograph mmr. this will lead to a wrong attenuation correction of the pet data.