Safety and Clinical Performance Study of the ARTUS® Artificial Urinary Sphincter (AUS)

Inclusion Criteria: 1. Male subject between 18 and 80 years (inclusive) of age at the time of consent signature 2. Subject with persistent urinary incontinence, defined as \>12 months 3. Subject with severe Stress Urinary Incontinence, defined as a mean value of 3 consecutive 24-hour Pad Weight Test \> 75 grams 4. Subject willing and able to provide written informed consent 5. Subject willing and able to comply with all clinical study requirements, including the ability to independently operate the device remote control 6. Subject willing and able to comply with follow-up visits 7. Subject having understood and accepted to be unable to proceed to an MRI examination after the surgical procedure due to the non-MRI compatibility of the device 8. Subject having signed the informed consent Exclusion Criteria: 1. Subject with documented neurological bladder or history of neurological disease liable to interfere with urinary symptoms 2. Subject with history of Artificial Urinary Sphincter or male sling implantation 3. Subject with history of pelvic radiotherapy 4. Subject with history of Artificial Urinary Sphincter-related urethral erosion 5. Subject with history of urethral fistula 6. Subject with history of bladder tumour 7. Subject with severe urethral stenosis 8. Subject with urge incontinence due to hyperactive bladder not adequately controlled by drug therapy 9. Subject with severe congenital or acquired haemorrhagic disease, haemophilia, or another coagulopathy 10. Subject under anti-coagulation or anti-platelet medication that cannot be discontinued at least 5 days prior to surgery and restarted at least 5 days after surgery 11. Subject with currently active infection, including urinary tract infection 12. Subject with severe renal failure or obstructive pathologies of the upper urinary tract with severe renal failure 13. Subject with a current vesicourethral reflux 14. Subject with congenital or acquired immunodeficiency, including those who are immunocompromised or immunosuppressed 15. Subject with bladder or urethral foreign body or calculus 16. Subject with allergy to any components of the device 17. Subject deprived of liberty by administrative or judicial decision or under legal guardianship 18. Subject having a Body Mass Index (BMI) \> 40 19. Subject with post void residual volume greater than 200 mL, within the past 6 months 20. Subject with uncontrolled diabetes, defined as HbA1c \> 9.0%, within the past 6 months 21. Subject with history of recurrent bladder stones or history of failed bladder stone treatment within the past 12 months 22. Subject currently enrolled or plans to participate in another investigational study of a drug, biologic, or medical device from the point of enrolment through the 12 months post device activation period 23. Subject who underwent any surgical procedure in the last 3 months, or with planned surgical procedure within the next 3 months 24. Subject who is unwilling or deemed by the Investigator to be unwilling to comply with the Clinical Investigation Plan, or subject with a history of non-compliance 25. Subject unable to understand and sign the ICF in absence of legal representative 26. Subject with a lack of capacity to consent 27. Subject unable to read and write 28. Subject in emergency situation