Suggestion of serious incidents in medical devices used in anterior segment surgery. Proposing ideas (II).

R Lorente-Moore, J Mendicute Del Barrio, M V Rojas Silva, A Macarro-Merino, E Larra Mateos, J C Pastor
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Abstract

The entry into force of the regulation on medical devices obliges ophthalmologists to identify and report possible serious incidents arising from their use. Faced with the doubts that may arise about what can or cannot be considered a serious incident, a working group of members of the Spanish Society of Refractive and Implant Eye Surgery (SECOIR) and the ophthalmology and vision sciences cluster (Cluster4Eye), have prepared a consensus document that aims to guide ophthalmologists on some of the incidents that, in the experience of the work team, are not common or can cause serious damage to the patient's function in relation to the use of medical devices. Incidents related to the use of viscoelastics, anterior capsule dyes, intraocular lenses, and other items used in anterior segment surgery have been addressed.

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关于前段手术中使用的医疗器械严重事故的建议。提出想法 (II)。
随着医疗器械法规的生效,眼科医生有义务识别和报告在使用过程中可能出现的严重事故。面对可能出现的关于什么可以或不可以被视为严重事故的疑虑,由西班牙屈光和植入眼科手术协会(SECOIR)和眼科与视觉科学组(Cluster4Eye)成员组成的工作小组编写了一份共识文件,旨在指导眼科医生了解根据工作小组的经验,与使用医疗器械有关的一些并不常见或可能对患者功能造成严重损害的事故。本文件讨论了与使用粘弹剂、前囊染料、眼内镜片和前段手术中使用的其他物品有关的事故。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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