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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The Afssaps was informed on 06/07/10 of the implementation of a security action carried out by the Siemens company. The users of the reagent on the Dimension Vista 500 system received the attached mail (19 / 07/2010) (97 KB)