Legal
Regulatory
How meda is classified under the MDR and the AI Act. For practice IT, data protection officers and management.
01Intended purpose
meda produces structured documentation from the consultation and proposes billing codes under EBM, GOÄ and HzV, each with the supporting passage. The physician decides, and nothing enters your practice management system (PVS) without their release.
02Not a medical device
meda is not a medical device within Regulation (EU) 2017/745. meda makes no diagnosis and gives no treatment recommendation. Our classification assessment is available on request.
03AI Act
meda is not a high-risk AI system under Regulation (EU) 2024/1689. meda is the provider, your practice the deployer. Training material on AI literacy (Art. 4) for your team is available on request.
Questions: support@mymeda.ai · Last updated: 07.10.2026