Clinical Trial With Artiflex Presbyopic (Artiplus)

Inclusion Criteria: * Presbyopic adult * Potential for binocular vision * Subject wishes to be spectacle independent for near and far vision * Refractive error that can be corrected with correction at PIOL plane from +2.0 to -15.0 D * Subject requiring a presbyopic correction Patients with reading glasses of minimum +1D. * Stable refraction (±0.75 D), as expressed by manifest refraction spherical equivalent (MRSE) for a minimum of 12 months prior to surgery, verified by consecutive refractions and/or medical records or prescription history * Expected best corrected visual acuity of 0.2 logMAR (0.63 Snellen decimal) or better after lens implantation * Current contact lens wearer should demonstrate a stable refraction (± 0.5 D), expressed as subjective refraction spherical equivalent, on two consecutive examination dates performed at least 7 days apart. Before the first refraction, the contact lens wearer should not have worn lenses for at least 2 weeks in case of rigid and toric contact lenses, or 3 days for spherical soft contact lenses. * Any subject, who is expected to have a residual postoperative cylindrical refractive error of below 0.75 D * Ability to give informed consent * Availability, willingness and sufficient cognitive awareness and physical ability to comply with examination procedures throughout the entire duration of the study Exclusion Criteria: Pre-existing pathology or physiology which may be aggravated by the implant or where the implant may interfere wi…