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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Lot G22512 of the reagent called Microtrak II Chlamydia EIA - reference 8H709 of the company DADE BEHRING SA is withdrawn from the market following a possible invalidation of the controls in 3% of the kits, resulting in invalidation of the results.