Greek data is current through July 2018. All of the data comes from the National Organization for Medicines, 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 Greece.
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Recall of batches of medical device "400mm pointed tip"
Call for batch 2014085 and 2014480 of the medical device: 400 mm long pointed wire and a wire with a sharp end and a cap of 400 mm; (No. 10.23.370) Draht mit Bajonettspitze, 400 mm lang und Draht mit Bajonettspitze.u.Stopper 400 mm; 10.23.370 Manufacturer