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 the development process on a research product platform sonosite discovered a data (ratio) display anomaly for a specific calculation within the extended ob/gyn calculation software package. the anomaly exists on the noted m-turbo and micromaxx ultrasound systems when enabled with the extended ob/gyn calculation package. while performing a systolic/diastolic (s/d) ratio measurement if the systolic caliper is repositioned after setting the diastolic cursor the s/d ratio shown at the bottom of the display screen is not updated to reflect the new ratio value (but the correct s/d ratio is printed on patient reports).