Building on the role of the medical device product safety manager for healthcare facilities (Para. 6 of the Medical Device Regulations) manufacturers, suppliers and customers now have a central point of contact for the following matters:

  • reporting risks related to medical devices
  • support in deploying necessary corrective measures and product recalls
  • assistance with reporting and collaboration obligations in respect of users and operators

It is also possible to receive targeted notifications via the functional e-mail address, containing information about new product developments and changes, as well as medical devices that are no longer available, thereby enabling us to communicate with relevant departments.

Medical Devices

Product Manager Medical Technology
Helena Bosch
Phone: +49 5925 991-138

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