Providing the world's clinics with validated surgical access solutions — designed under Finnish quality control and CE-marked under MDR (EU) 2017/745.
Motion Medical gives procurement teams one accountable partner for CE-marked interventional devices — with tender-ready documentation, traceable manufacturing, and EU-adjacent dispatch.
Our Finnish team owns design control, the technical file, post-market surveillance, and Notified Body interface. Our Ankara facility handles clean-room production, EO sterilisation, and global dispatch. One quality system. Every device accountable end-to-end.
Two clinical pillars. Five product families. Every device validated under the same Helsinki-owned quality system.
Every product is CE-marked under MDR (EU) 2017/745 and manufactured under ISO 13485:2016.
Burst-rated manifolds, 0–30 atm indeflators and colour-coded pressure gauges — calibrated for the procedure.
Ergonomic bodies, secure Luer-lock connections and EO-sterilised single-use delivery for patient safety.
Two clinical pillars and a dedicated bone cement line.
Our team responds to procurement and technical inquiries within one business day.
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