INTEGRITY GOVERNANCE FOR AUTONOMOUS SYSTEMS · SOFTWARE-ONLY · ZERO HARDWARE CHANGES
david@olikonste.com
Full technical briefing available under NDA
Medical Exoskeleton Platform
EU Medical Exoskeleton Deployment
EU regulatory deadlines create binding evidence obligations for this platform category. EXOS-LINK adds runtime integrity monitoring and tamper-evident compliance evidence — zero hardware changes required.
ON REQUEST
COMMERCIAL TERMS
EU MDR
PRIMARY REGULATION
DEPLOYABLE TODAY
6 DEPLOYABLE MODULES
▸ REGULATORY CONTEXT — WHY THIS MATTERS NOW
⚠
REGULATORY DEADLINE
EU MDR + Machinery Reg Annex III. Your platform in EU rehabilitation requires per-session sensor integrity evidence. EXOS-LINK supports this evidence workflow.

Your platform's bio-electrical signal detection is unique — EXOS-LINK sits above your existing sensing layer and produces the EU MDR and Machinery Reg evidence record that EU market access increasingly requires, with zero modification to your current sensor or control architecture.
▸ LIVE DEMO — BUILT FOR YOUR PLATFORM
▶ Exoskeleton — Gait Assistance Integrity Demo
SCENARIO BUILT FOR MEDICAL EXOSKELETON
Full-body gait assistance cycle. Per-joint health monitoring across hip, knee, ankle, foot. Progressive fault scenario showing healthy → supervised → guarded → safe stop. EU Machinery Regulation Annex III and EU MDR pathway evidence log.
▶ LAUNCH DEMO — NO INSTALL REQUIRED
BODY MODEL INTEGRITY REGULATORY EVIDENCE GENERATOR SIGNAL INTEGRITY LAYER TRUST-STATE GOVERNOR DISTRIBUTED TIMING INTEGRITY NOISE SUPPRESSION
▸ REGULATORY COVERAGE — WHAT THIS ADDRESSES
EU MDR
SUPPORTS EVIDENCE
Supports evidence and record-keeping obligations for EU MDR. Final conformity assessment depends on system classification, intended use, and integrator. Tamper-evident audit log generated on each integration run.
Machinery Reg Annex III
SUPPORTS EVIDENCE
Supports evidence and record-keeping obligations for Machinery Reg Annex III. Final conformity assessment depends on system classification, intended use, and integrator. Tamper-evident audit log generated on each integration run.
AI Act Arts. 9/12/13/14/15/17
SUPPORTS EVIDENCE
Supports evidence for Arts. 9, 12, 13, 14, 15, and 17 (high-risk provider obligations). Tamper-evident audit log generated on each integration run.
Ready to discuss a pilot?
Pilot scope and timeline available on request.
REST / ROS2 / file tail — same schema. Output: signed compliance evidence on each integration run.
Medical exoskeleton dual evidence pathway.
✉ REQUEST 20-MIN CALL
All company names, product names, and trademarks referenced on this page are the property of their respective owners. Olikonste Systems AB is not affiliated with, endorsed by, or in partnership with any of the companies named. This page is an independent technical overview prepared for informational purposes only. Nothing on this page constitutes legal advice or a conformity assessment. Final regulatory classification, conformity assessment, and compliance determination depend on system classification, intended use, and the responsible integrator or manufacturer.