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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There is a performance issue during initializing of application that could lead to the unavailability of the follow c-arc function. as a consequence the function cannot be used but this will not impact patient safety.
Model Catalog: ALLURA XPER FD20/10 (Lot serial: ); Model Catalog: ALLURA XPER FD10/10 (Lot serial: N/A FOR ALL); Model Catalog: ALLURA XPER FD20 (Lot serial: ); Model Catalog: ALLURA XPER FD20/20 (Lot serial: ); Model Catalog: ALLURA XPER FD10 (Lot serial: )