meddev-eu-mdr
Provide actionable guidance for software under EU MDR, focusing on classification (Rule 11), technical documentation expectations, UDI for software, PMS/PMCF needs, and alignment with MDCG guidance. Use when working on eu mdr in medical device software.
- Version
- 1.0.0
- License
- MIT
Pinned to revision 74dbf9c3aa13, so it is the text this page describes rather than whatever the author pushed since.
Files
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