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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During a recent internal review of medical devices it was discovered that two ivd antibodies from lab vision were loaded into our system as class i medical device which is sold and classified in the united states as class i.The lab vision antibodies which are classified as ivd (in vitro diagnosis) are classified as medical device class ii in canada. since it was downloaded from the us system as class i medical device it was not being verified against health canada medical device licensing at the time.