Aran provides comprehensive medical device development services in accordance with regulatory guidelines (FDA, CE), from inception to product market launch – including research, design input, early risk management, system engineering, concepts, detailed design, V&V and transfer to production.
Our creative teams of experts – designers and biomedical, mechanical and electrical engineers – successfully develop cardiovascular devices, In-Vitro Diagnostics, surgical instruments, medical robots and more.
We lead and manage the highest standards of regulatory processes. Our comprehensive service extends to manufacture in our ISO 13485 certified class 7 cleanroom and supporting preclinical and clinical trials.

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