Created by: Leoneska
Number of Blossarys: 1
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En intraokulær linse (IOL) er en indopererede linse i øjet, som regel erstatter den eksisterende krystallinske linse, fordi det har været overskygget af en grå stær eller som en form for refraktiv kirurgi til at ændre øjets optiske effekt. Det består normalt af en lille plastic linse med plast side stivere, kaldet haptics, for at holde linsen på plads inden for den kapsulær taske inde i øjet.[redigér] IOLs var traditionelt lavet af et stift materiale (PMMA), selv om dette er stort set blevet afløst af brugen af fleksible materialer. De fleste IOLs monteret i dag er fast Monofokal linser passer til afstand vision. Men andre typer er tilgængelige, såsom multifokal IOLs, hvilket giver patienten med flere-fokuserede vision på langt og læse afstand og adaptive IOLs, hvilket giver patienten med begrænset visuel overnatning.
An intraocular lens (IOL) is an implanted lens in the eye, usually replacing the existing crystalline lens because it has been clouded over by a cataract, or as a form of refractive surgery to change the eye's optical power. It usually consists of a small plastic lens with plastic side struts, called haptics, to hold the lens in place within the capsular bag inside the eye.[citation needed] IOLs were traditionally made of an inflexible material (PMMA), although this has largely been superseded by the use of flexible materials. Most IOLs fitted today are fixed monofocal lenses matched to distance vision. However, other types are available, such as multifocal IOLs which provide the patient with multiple-focused vision at far and reading distance, and adaptive IOLs which provide the patient with limited visual accommodation.
Beskrivelse en erklæring præsentere noget i ord, fra verbet beskrive
description a statement presenting something in words, from verb describe
brugsanvisning
"a manual usually accompanying a technical device and explaining how to install or operate it" Essential Requirements - Medical Device Directive 93/42/EEC - Annex I, 13.1: Each device must be accompanied by the information needed to use it safely and to identify the manufacturer, taking account of the training and knowledge of the potential user. This information comprises the details on the label and the data in the instructions for use. As far as practicable and appropriate, the information needed to use the device safely must be set out on the device itself and/or on the packaging of each unit. If not practicable, the information must be set out in the leaflet supplied with one or more devices. Instructions for use must be included in the packaging for every device. By way of exception, no such instruction leaflet is needed for devices in Class I or Class IIa if they can be used completely safely without any such instructions.
