| Date | Guidance No | About the guidance |
|---|---|---|
| 20 Apr 2026 | MDCG 2021-24 Rev.1 | Guidance on classification of medical devices The purpose of this chapter is to provide a general overview on the impact of the classification of medical devices on different aspects of the device compliance with the legal requirements. The explanations provide some simplified concepts and are not exhaustive. For details see the MDR and related additional guidance. The revisions to the document are detailed on page 3. |
Pharmavibes
medicines-medical devices-regulatory affairs