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.
데이터 추가 비고
원인
Philips has become aware of the following seven software issues: 1.Sagittal result shortened for axial scans 2.Single series displayed in console viewer when creating mpr's. 3.Scan length changes with a change in field of view 4.Different ctdi values with doseright 5.Scan length changes on subsequent axial results 6. surview scan lengths near 135mm or 184mm may result in unexpected scan start positions and 7.Reconstruction length does not equal scan length.
Model Catalog: 728311 (Lot serial: all lots); Model Catalog: 4550 110 09021 (Lot serial: all lots); Model Catalog: 728326 (Lot serial: all lots); Model Catalog: 728323 (Lot serial: all lots); Model Catalog: 728306 (Lot serial: all lots)
제품 설명
BRILLIANCE ICT SP SYSTEM - MAIN;BRILLIANCE 40/64 SLICE CT SYSTEM;INGENUITY CT SYSTEM;BRILLIANCE ICT SYSTEM - SYSTEM