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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Some digital accelerators have increased electron applicator auto-tracking setting settings in the field to values greater than the factory-set defaults. increasing auto-tracking values from factory set defaults can result in the system becoming non-compliant with iec standards in particular with the safety standard iec 60601-2-1.
Model Catalog: XRT 0101 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: MRT 6011 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: MRT 6001 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: MRT 3041 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: MRT 2161 (Lot serial: ALL SERIAL NUMBERS)