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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Immage igg lot m610132a parameter card barcode does not include the "a" suffix encoded in the barcode. the reagent cartridge barcode needed to pair with the parameter card includes the "a" suffix. lot number mismatch causes a "parameters not found" error upon reagent cartridge barcode read. input of parameters and reagent load is by barcode only. system is not capable of manual entry.