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.
데이터 추가 비고
원인
On the abl800 series analyzers the sample type "cord blood" has been changed into the two sample types "cord blood arterial" and "cord blood venous". the selected sample type is displayed correctly on the analyzer itself. however irrespectively of the sample type selected on the analyzer during sample processing the analyzer will transmit the less specific sample type "cord blood" to a his/lis or middleware system.