Since 1 January 2012, the Code of Medical Devices is in force. The code provides rules for suppliers of medical devices and healthcare professionals.
The rules of conduct laid down in the Code are intended to – in addition to the applicable legislation – further substance to a careful, transparent and responsible dealings between suppliers of medical devices and the parties involved in deciding on the purchase and / or the application, regardless of the setting in which they work.
The Code of Conduct covers on one hand expressions on medical resources in the broadest sense. On the other hand the Conduct gives norms for responsible interactions between providers and health care professionals.