Artifakt Compass — EU MDR pathfinder for medical device startups

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ARTIFAKTCOMPASS

A free preliminary EU MDR pathfinder for medical devices across every risk class (I–III) — part of Artifakt, a living MedTech compliance system.

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How it works

Artifakt

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Compass output is preliminary, derived from the inputs you provide, and requires human regulatory-affairs review before any submission. It is not regulatory advice and does not guarantee any classification or conformity outcome. EU MDR is Regulation (EU) 2017/745.