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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It is possible to have incorrect label information displayed when viewing multiple hamamatsu.Ndpi (brightfield) and .Ndpis (fluorescent) images with imagescope software. slides which do not use the .Ndpi file format are not affected.
Model Catalog: 23ESLIDEMGR1-IVD (Lot serial: Software Version 12.2.2); Model Catalog: 23ESLIDEMAN-PERP1-IVD (Lot serial: Software Version 12.2.2); Model Catalog: 23S+2-IVD (Lot serial: Software Version 12.2.2); Model Catalog: 23ESLIDEMGR1-IVD (Lot serial: Software Version 12.2.1); Model Catalog: 23S+2-IVD (Lot serial: Software Version 12.3); Model Catalog: 23S+2-IVD (Lot serial: Software Version 12.2.1); Model Catalog: 23ESLIDEMGR1-IVD (Lot serial: Software Version 12.3); Model Catalog: 23ESLIDEMAN-PERP1-IVD (Lot serial: Software Version 12.3); Model Catalog: 23ESLIDEMAN-PERP1-IVD (Lot serial: Software Version 12.2.1)