EU Medical Devices Regulation (MDR 2017/745)vsEU Digital Markets Act
See exactly how EU Medical Devices Regulation (MDR 2017/745) controls map to EU Digital Markets Act. Pre-computed mappings, identified gaps, and coverage analysis.
According to the TheArtOfService Compliance Knowledge Graph:
EU Medical Devices Regulation (MDR 2017/745) maps to EU Digital Markets Act with 40% coverage across 8 directly mapped controls. Analysis of 20 EU Medical Devices Regulation (MDR 2017/745) controls identifies 12 compliance gaps — primarily concentrated in Annex I — General Safety and Performance Requirements.
Source: TheArtOfService Knowledge Graph | 20 controls analysed | 693 frameworks | 819K+ cross-framework mappings
Control Mappings
Showing 11 of 11 mapped controls across 4 domains. Sign up to explore all 819K+ mappings across 693 frameworks.
Annex I — General Safety and Performance Requirements(1 mappings)
Chapter II — Device Classification and Conformity(3 mappings)
Chapter III — Economic Operators(4 mappings)
Chapter VII — Post-Market Surveillance(3 mappings)
Related Comparisons
Other EU Medical Devices Regulation (MDR 2017/745) comparisons
Other EU Digital Markets Act comparisons
Stop Paying Consultants to Read Spreadsheets
AI-powered compliance intelligence across 693 frameworks — at a fraction of consulting costs.
Free
- ✓ 693 framework browser
- ✓ Cross-framework mappings (819K+)
- ✓ 824 compliance assessments
- ✓ 3 AI queries & searches per day
Professional
- ✓ Unlimited AI Compliance Advisory
- ✓ Unlimited full-text search
- ✓ Framework self-assessment
- ✓ PDF, Excel & CSV exports
What are the key differences between EU Medical Devices Regulation (MDR 2017/745) and EU Digital Markets Act?
EU Medical Devices Regulation (MDR 2017/745) has 20 controls across its framework, while EU Digital Markets Act covers 61 controls. Direct mapping analysis identifies 8 overlapping controls (40% coverage). The frameworks diverge most significantly in Annex I — General Safety and Performance Requirements, where 5 EU Medical Devices Regulation (MDR 2017/745) controls have no direct EU Digital Markets Act equivalent.
How many controls map between EU Medical Devices Regulation (MDR 2017/745) and EU Digital Markets Act?
Of 20 total EU Medical Devices Regulation (MDR 2017/745) controls, 8 map directly to EU Digital Markets Act controls — representing 40% coverage. The remaining 12 controls represent compliance gaps requiring additional documentation or compensating controls to satisfy both frameworks simultaneously.
What are the compliance gaps when mapping EU Medical Devices Regulation (MDR 2017/745) to EU Digital Markets Act?
12 EU Medical Devices Regulation (MDR 2017/745) controls have no direct equivalent in EU Digital Markets Act. The highest concentration of gaps is in Annex I — General Safety and Performance Requirements with 5 unmapped controls. These gaps represent areas where additional controls, policies, or documentation must be created to achieve compliance with both frameworks.
Which control domains have the most gaps between EU Medical Devices Regulation (MDR 2017/745) and EU Digital Markets Act?
The domain with the highest gap count is Annex I — General Safety and Performance Requirements (5 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.
Related Resources
This platform provides educational compliance tools, not legal, regulatory, or professional compliance advice. Cross-framework mappings are AI-assisted interpretations and do not reproduce or replace official standards. Framework names and trademarks belong to their respective owners. Consult qualified professionals for your specific compliance requirements. See our Terms of Service.