Under the new MDR (Medical Device Regulation) 2017/745, QRMA devices that claim "risk assessment" may need Class IIa certification. The latest update for EU markets includes a "Wellness Mode" that disables specific disease-related terms (e.g., "tumor" is replaced with "cellular stress").
: Basic health (36 reports), gender-specific (male/female), children's reports, and comparison reports to track health changes over time. Language Support quantum resonance magnetic analyzer update