Key Milestone: Kossel’s Overseas Peripheral Portfolio Accelerates Global Expansion via EU CE‑MDR Certification

Kossel is pleased to announce a major regulatory milestone. Its peripheral interventional device portfolio has obtained EU CE‑MDR certification, granting official European market access and marking a key step in the company’s global expansion. All four newly‑certified devices are independently developed in‑house by Kossel: Falspeed® PTA Balloon Dilatation Catheter, Falexpand® HP PTA Balloon Dilatation Catheter, […]