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 company J2L ELITECH withdraws from the market batches 758532 (per 31.05.03) and 828571 (per 31.12.03) of the in vitro diagnostic medical device called IMAGEN INFLUENZA A and B - reference 0404-DK6105, following the possible presence high background noise preventing playback.