French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), 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 France.
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Sedat informed AFSSAPS of a reminder it issued on 11 April 2003 concerning Dolphin inflation systems for balloon catheters. Sedat sent the attached mail (05/05/2003) (136 KB) on April 11 to the 17 user centers and 2 vending companies, for the attention of pharmacy services.