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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Bruker released updates to the maldi biotyper msp database where organism naming changes have been implemented. bd was unaware of these changes and consequently did not implement corresponding changes to the bd epicenter database if a maldi biotyper msp database was updated after the initial interfacing to bd epicenter inconsistent organism naming may be observed between the bd epicenter and bruker maldi biotyper software for a very limited number of organisms.