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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Sigma has become aware of an unintended use of the example drug library. some customers have used the example drug library to create their own facility drug library for use on patients or transmitted to a pump. sigma provided the example drug library solely as an example of how user can apply the functions of a drug library to ensure safe and effective pump use.