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
While imaging with a transesophageal (tee) transducer (z6ms v5ms or v7m) the operator may lose the ability to control the color region of interest the pulsed wave or continuous wave doppler gate or cursor the m-mode cursor the 2d field of view or the res region of interest with the trackball.