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SeeLens MF Intraocular Lens

SeeLens MF Intraocular Lens 4 August 2011 - Hanita Lenses

SeeLens MF Intraocular Lens 4 August 2011 - Hanita Lenses

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Page 19 of 21Secondary surgicalintervention 50.1% 4.2% 2 0% 0 PassPersistent (total number of occurrences at 3 months postoperative):Corneal stroma oedema 0.1% 3.0% 1 0% 0 PassCystoid macular oedema 0.1% 4.2% 2 2.5% 0 PassIritis 0.1% 3.0% 1 0% 0 PassRaised IOP req. treatment 0.1% 4.2% 2 0% 0 PassTABLE 7: ADVERSE EVENTS AS DEFINED BY ISO 11979-7 2006:As shown in table 7, 100% of 37 implanted eyes were not reported with any adverse events.Thus, it can be concluded that safety of <strong>See<strong>Lens</strong></strong> <strong>MF</strong> is in accordance to the ISO 11979-7 2006.11. CONCLUSIONS:3 months resultsThe detailed data from the current study on 37 eyes shows the following benefits of the <strong>See<strong>Lens</strong></strong><strong>MF</strong> IOL:Optical performance is in accordance to ISO 11979-7 2006 requirements. The IOL A constant using IOL MASTER and SRK/T is set at 118.6.Very good safety profile as reflected by a very low rate of intra- and post-operativecomplications at 3 months.5 Excludes posterior capsulotomies.

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