I. Introduction
SINCE the mid-1990s the risk of electromagnetic interference (EMI) due to the increasing number of medical electrical equipment (MEE) in the professional healthcare facility environment has been continuously reported [1]. Despite manufacturers' efforts to enhance the MEE conformity, new challenges are introduced to the electromagnetic compatibility (EMC) based on the newest health technologies [2], [3]. The trend is to define the MEE regulations directly at manufacturers to ensure conformity and EMC. On the other hand, the risk management processes [4] in professional healthcare facility environments ensure patient safety when using the MEE.