发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22
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本标准规定了半导体激光光动力治疗机的术语和定义、产品组成、基本参数、技术要求、试验方法和检验规则等要求。 本标准适用于半导体激光光动力治疗机(以下简称治疗机),该治疗机采用特定波长的激光与光敏剂产生光化学作用,供临床单位进行光动力治疗
Laser therapeutic equipment.Diode laser equipment for photodynamic therapy
本标准规定了脉冲二氧化碳激光治疗机的基本参数和产品组成、技术要求、试验方法以及标志标签、包装等内容,本标准为脉冲二氧化碳激光治疗机制造商制定医疗器械注册产品标准提供技术规范。 本标准适用于只含有脉冲运行方式的脉冲二氧化碳激光治疗机和同时含有连续波运行方式、脉冲运行方式的二氧化碳激光治疗机中的脉冲
Laser therapeutic equipment.Pulsed carbon dioxide laser treating instrument
本标准规定了准分子激光角膜屈光治疗机的术语和定义、结构和基本参数、要求、试验方法、检验规则、标志、包装、运输、贮存。本标准适用于准分子激光角膜屈光治疗机(以下简称治疗机),治疗机采用193 nm准分子激光去除角膜组织来改变角膜形状从而改善视力,主要用于屈光性角膜切削术(PRK)、原位角膜磨镶术
Therapeutic laser equipment.Excimer laser cornea ametropia cure system
本标准规定了掺钬钇铝石榴石激光治疗机的要求、试验方法、标志、包装、运输及贮存、使用说明书。 本标准适用于以掺Cr、Tm、Ho离子的钇铝石榴石(YAG)为工作介质,发射的激光波长在2.1μm附近的激光治疗机(以下简称治疗机)。 治疗机可用于人体组织的切割、汽化、凝固以及体内碎石等
Laser therapeutic equipment.Ho:YAG laser equipment
Laser therapeutic equipment—Pulsed carbon dioxide laser treating instrument
本文件规定了眼科激光光凝仪的术语和定义、产品组成、要求、试验方法等内容。本文件适用于临床上进行眼底激光光凝治疗的设备
本标准规定了Q开关掺钕钇铝石榴石激光治疗机的基本参数和产品组成、技术要求、试验方法以及标志标签、包装等要求。 本标准适用于波长为1 064 nm或倍频532 nm的Q开关(采用调Q技术)掺钕钇铝石榴石激光治疗机(以下简称治疗机)。本治疗机利用激光与生物体组织的选择性吸收机理,进行微爆破达到治疗目的
Laser therapeutic equipment.Q-Switched Nd:YAG laser equipment
本标准规定了紫外治疗设备的术语和定义、分类、要求、试验方法、检验规则、标志及使用说明书、包装、运输及贮存。本标准适用于3.1所定义的医疗实践中使用的紫外治疗设备(以下简称设备)的要求。本标准不适用于下列设备:——仅用于照射器械和材料的紫外消毒或杀菌设备;——光固化机;——紫外激光设备;——紫外光敏
Ultraviolet therapy equipment
Addition:This Particular Standard specifies requirements applicable to INFANT PHOTOTHERAPY EQUIPMENT (as defined in 2.1.101) which by means of visible
Medical electrical equipment - Part 2-50: Particular requirements for the safety of infant phototherapy equipment
Medical electrical equipment - Part 2-50: Particular requirements for the safety of infant phototherapy equipment
Medical electrical equipment - Part 2-50 : particular requirements for the safety of infant phototherapy equipment.
This Particular Standard specifies requirements applicable to INFANT PHOTOTHERAPY EQUIPMENT (as defined in 2.1.101) which by means of visible
Medical electrical equipment - Part 2-50: Particular requirements for the safety of infant phototherapy equipment
This Standard contains basic requirements for products covered by Underwriters Laboratories Inc. (UL) under its Follow-Up Service for this category
Appareils 閘ectrom閐icaux ?Partie 2-50: R鑗les particuli鑢es de s閏urit?des appareils de phototh閞apie pour nouveau-n閟 Premi鑢e Edition,
Medical electrical equipment ?Part 2-50: Particular requirements for the safety of infant phototherapy equipment First Edition
Medical electrical equipment ?Part 2-50: Particular requirements for the safety of infant phototherapy equipment First Edition
Medical electrical equipment—Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipment
Medical Electrical Equipment Part 2-50: Particular Requirements for the Safety of Infant Phototherapy Equipment IEC 60601-2-50: 2000 + Corrigendum March 2001
To be read in conjunction with BS EN 60601-1
Medical electrical equipment - Particular requirements for safety - Particular requirements for the safety of infant phototherapy equipment
Safety of laser equipment for medical applications classified as a Class 3B or Class 4 laser product
Medical electrical equipment - Particular requirements for safety - Specification for diagnostic and therapeutic laser equipment
本专用标准适用于2.1.111条定义的,按照GB 7247-1995中 3.12和 3.13分类为 3B类或4类激光产品的医用激光设备,以下简称激光设备。 注:分类为 1类、2类和 3A类激光产品的医用激光设备,应符合GB 9706.l和GB 7247
Medical electrical equipment Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment
Medical electrical equipment—Part 2-75: Particular requirements for the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment
Zpracovatel: Medipo EM, spole?nost s r. o., I?O 18510931, Ing. Vladimír Vejrosta Technická normaliza?ní komise: TNK 81 Zdravotnické elektrické p
Medical electrical equipment.Part 2:Particular requirements for the safety of diagnostic and therapeutic laser equipment
Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment (IEC 60601-2-22:1995); German version EN 60601-2-22:1996