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Xeltis announces FDA Breakthrough Device Designation for aXessTM and first patient treated in US pivotal trial - PressReach

Summary by pressreach.com
Designation recognizes aXess has the potential of providing a more effective vascular access option for dialysis patients, bringing significant advantages over current therapies First patient treated in US pivotal trial, marking significant clinical milestone EINDHOVEN, The Netherlands, Nov. 14, 2024 /PRNewswire/ — Xeltis, a leading developer of transformative implants that enable the natural creation of living and long-lasting vessels, today a…
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