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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The entire breast image or a portion of the breast image as sent from the ge senographe 2000d the senographe ds or the senographe essential may not be displayed in the monitor region(s).
Model Catalog: K2022PJ (Lot serial: HIGHER); Model Catalog: K2022PF (Lot serial: SOFTWARE VERSION 2.1.X.X AND); Model Catalog: K2022PJ (Lot serial: SOFTWARE VERSION 2.1.X.X AND); Model Catalog: K2022PF (Lot serial: HIGHER)