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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The wedge mu is correct after the first treatment at the non-varian machine however after treatment varis may prompt to save and the wedge mu is reset to null for sebsequent sessions.
Model Catalog: (Lot serial: H859003); Model Catalog: (Lot serial: H859040); Model Catalog: (Lot serial: H850284); Model Catalog: (Lot serial: H859017); Model Catalog: (Lot serial: H850315)