Information on the new EU Medical Device Regulation

Medical Device Regulation (MDR)

We support you with implementing the MDR

The new EU Medical Device Regulation (MDR) came into force in May 2021 and brings changes for many players in the healthcare sector. Therefore, our safety officer for Stiegelmeyer and his colleague for Burmeier have already completed the implementation of the MDR for all products long before the deadline.

This means planning security for our partners who trade in our beds in purchasing associations and medical supply stores. Our Person Responsible for Regulatory Compliance (PRRC) will continue to closely monitor all processes that the MDR will entail in the coming years. If you have any questions on the subject, please use the contact form on this page.

You can find more information on the MDR on our topic page