Clareon™ Vivity™ Extended Vision Hydrophobic IOL. - ARCSA Registration 708899548680f41319821c6ee2466760
Access comprehensive regulatory information for Clareon™ Vivity™ Extended Vision Hydrophobic IOL. in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 708899548680f41319821c6ee2466760 and manufactured by ALCON LABORATORIES IRELAND LTD.. The device was registered on September 17, 2021.
This page provides complete registration details including product type (Invasive), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.
THE CLAREON VIVITY™ LIO IS INTENDED TO BE PLACED IN THE CAPSULAR SAC OF THE POSTERIOR CHAMBER OF THE EYE, REPLACING THE NATURAL LENS. THIS POSITION ALLOWS THE LIO TO FUNCTION AS A REFRACTIVE MEDIUM IN THE CORRECTION OF APHAKIA. THE BICONVEX ASPHERICAL OPTIC COMPENSATES FOR THE POSITIVE SPHERICAL ABERRATION OF THE CORNEA COMPARED TO A STANDARD SPHERICAL OPTIC.