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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When the observa system is interfaced to a laboratory information management system (lis) some error conditions may cause a delay in reporting positive cultures to the lis.
Model Catalog: R02.00.17 (Lot serial: VERSION R01.0016); Model Catalog: R01.00.16 (Lot serial: VERSION R01.0016); Model Catalog: R02.01.05 (Lot serial: VERSION R02.01.05); Model Catalog: R02.00.17 (Lot serial: VERSION R02.01.05); Model Catalog: R02.01.05 (Lot serial: VERSION R01.0016); Model Catalog: R02.01.05 (Lot serial: VERSION R02.00.17); Model Catalog: R02.00.17 (Lot serial: VERSION R02.00.17); Model Catalog: R01.00.16 (Lot serial: VERSION R02.00.17); Model Catalog: R01.00.16 (Lot serial: VERSION R02.01.05)