The MEDDEV Guidelines are non-legally binding guidelines drawn up by the European Commission to concretise the guidelines of the Medical Device Directive (MDD). They were developed by authorities, Notified Bodies, the Commission, committees, and stakeholders. With the introduction of the Medical Device Regulation (MDR), the Medical Device Coordination Group (MDCG) was established to perform similar functions to the MEDDEV guidelines.
If you are unsure whether a particular MEDDEV document is still valid or whether it has become obsolete due to the new regulations, we are happy to help. You can contact us via chat, contact form, email, or phone.
