PadPro and R2 multifunction electrodes 를 위한 안전성 경고 / 현장 안전성 서한

Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.

Philips Healthcare has made changes to the design of the connection between electrodes and the defibrillator so some Conmed electrodes are no longer compatible.This MDA is for information only and no product needs to be returned to Conmed.The labelling on new electrodes has been updated to show compatibility.