Avis De Sécurité sur cordis smart flex vascular stent system, sizes 5x200mm and 6x200mm, catalog numbers sf05200mv, sf05200sv, sf06200mv and sf06200sv

Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, 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 Poland.