Helsinki HQ +358 40 3290538 MDR (EU) 2017/745·ISO 13485:2016
Motion Medical · Helsinki, Finland

Nordic integrity —
interventional excellence.

Providing the world's clinics with validated surgical access solutions — designed under Finnish quality control and CE-marked under MDR (EU) 2017/745.

CE-Certified MDR Trusted in 50+ Countries 100,000+ procedures
Motion Medical 20 cc balloon inflator — macro detail
Trusted across Europe and the Mediterranean
The Finnish Connection

A bridge between Nordic quality and high-capacity manufacturing.

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.

Regulatory HQ
Helsinki, Finland
Quality system · MDR file · PMS
Manufacturing
Ankara, Türkiye
ISO 13485 facility · EO sterile
Logistics
Ex-Works Ankara
Container & air freight ready

Built for the cath-lab and the spine theatre

Two clinical pillars. Five product families. Every device validated under the same Helsinki-owned quality system.

MDR & ISO certified

Every product is CE-marked under MDR (EU) 2017/745 and manufactured under ISO 13485:2016.

Precision at 1 200 PSI

Burst-rated manifolds, 0–30 atm indeflators and colour-coded pressure gauges — calibrated for the procedure.

Atraumatic by design

Ergonomic bodies, secure Luer-lock connections and EO-sterilised single-use delivery for patient safety.

Our product range

Two clinical pillars and a dedicated bone cement line.

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Need a quote or a sample?

Our team responds to procurement and technical inquiries within one business day.

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