Medical Device Directive
/ˈmɛdɪkəl dɪˈvaɪs dɪˈrɛktɪv/
Definitions
- (n.) A European Union directive regulating the safety and performance of medical devices to ensure they meet legal standards before marketing.
The manufacturer ensured compliance with the Medical Device Directive before launching the new implant in the EU market.
Forms
- medical device directive
- medical device directives
Related terms
See also
Commentary
The Medical Device Directive (MDD) was replaced by the Medical Device Regulation (MDR) in 2017; however, references to the MDD remain relevant for products certified before the MDR's full application.
This glossary is for general informational and educational purposes only. Definitions are jurisdiction-agnostic but reflect terminology and concepts primarily drawn from English and American legal traditions. Nothing herein constitutes legal advice or creates a lawyer-client relationship. Users should consult qualified counsel for advice on specific matters or jurisdictions.