Instructions for Use
To view aXess™ documentation please select your role as a Healthcare Professional or a Patient.
Healthcare Professionals
aXess™ Instructions for Use and other relevant documentation for professionals.
Regulatory status
The aXess™ Hemodialysis Conduit is CE marked in accordance with EU Medical Device Regulation 2017/745. In the United States it is an investigational device, limited by federal law to investigational use only, and not yet approved for commercial distribution.
