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.

medizintechnik@was-vehicles.com