The company I work for manufactures audio/visual medical devices (monitors, cameras, etc) and we have followed the various medical device regulations and testing requirements. Recently we have begun developing various types of modems and scalers. During the design review discussions we started to question whether these new products should even be considered medical devices. I am now trying to determine the correct European regulatory pathway. I believe they may be considered IT equipment. I looked on the European commission website and downloaded the EMC directive, which I will start looking at today. Where can I go to determine exactly what types of equipment these products are and the correct EU directive?