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 RADIOMETER withdraws from the market the KA-03 batch of the medical device called PICO 70 - syringe with needle for arterial sampling - reference 956-547, following the possibility of defective individual packaging for certain syringes of this lot.