Medical device testing for radio compliance - Requirements of RED

As medical devices become increasingly complex, many manufacturers are now turning to radio technologies such as RFID, Bluetooth, WLAN and cellular. Even implants in the patient are configured and controlled via radio interface.

Medical devices with integrated radio technologies are classed as radio equipment and fall under the scope of the Radio Equipment Directive (RED) 2014/53/EU.

What are the requirements introduced by the RED and how to address them?

This webinar gives an overview of the essential requirements of the RED. What do manufacturers have to consider when choosing radio modules? What obligations do they have to fulfil? What is required for a declaration of conformity? Which laboratory tests are required and how do they work?

The webinar also presents the situation regarding certification by the Federal Communications Commission (FCC). Which requirements apply to the integration of radio modules and which tests are required for market access?


Date and time: Tuesday, 18 May 2021, 11.30 am (CEST)

Your speakers: Matthias Stumpe, Team Manager Radio Test Lab


Registration »