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Clinical Evaluation 1 to 3 months Follow Up Report SeeLens HP Intraocular Lens

SeeLens HP - Clinical Evaluation Report 11/03/2012 - Hanita Lenses

SeeLens HP - Clinical Evaluation Report 11/03/2012 - Hanita Lenses

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Page 10 of 11Ver. 1Graph 3: Refraction predictability (dSE)As can be seen in graph 3, 100% of the eyes implanted by Dr. Yatziv were found with dSEless than 0.5D. 100% of the eyes implanted by Prof. Assia were found with dSE less than 1D.Table 1 summaries the dSE results:dSE valueDr. Yatziv 0.08±0.28Prof. Assia -0.24±0.68Total -0.08±0.535.4 IOL PerformanceAll implantations were reported successful as the lens handling, folding and implantationwere easy and smooth.Dr. Yatziv reported of a few IOLs with glistening found one week post op, which was foundstable in the later follow ups, with no effect on visual acuity. Prof. Assia had also reported oftwo IOLs with glistening two <strong>months</strong> post op, again with no effect on the visual acuity.5.5 Adverse Events as defined by ISO 11979-7 2001No adverse events were reported by the surgeons. Thus, it can be concluded that the <strong>See<strong>Lens</strong></strong><strong>HP</strong> safety is fully in accordance <strong>to</strong> the ISO 11979-7 2001Hanita <strong>Lens</strong>es <strong>Intraocular</strong> & Contact <strong>Lens</strong>esעדשות חניתהעדשות מגע ועדשות השתלה תוך-עינית•קיבוץ חניתה • 88222 www.hanitalenses.com Kibbutz Hanita 22885 Israel • Tel. 972-4-9950 700• Fax: 972-4-9950 755 •

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