FIELD: medical engineering. SUBSTANCE: device has optic part designed as lens from flexible optically transparent hydrogel material and its rest plate is produced from porous collagen copolymer with water-soluble monomers belonging to acryl and vinyl rows containing collagen in the amount of 0.5-10% by mass and sizes vary from 0.1 to 10 mcm. The number of postoperative complications reduces due to concentrated proliferation of porous rest part of the prosthesis with leukoma tissue and absent outflow of fluid from the conjunctival cavity taking place. EFFECT: better biocompatibility properties; low risk of postoperative adverse effects. 2 tbl
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