
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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Diagnostic and therapeutic laser equipment - Safety requirements
Laser therapeutic equipment—Carbon dioxide laser 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
Laser therapeutic equipment—Pulsed carbon dioxide laser treating instrument
Medical electrical equipment. Part 2. Particular requirements for the safety of diagnostic and therapeutic laser equipment
Replacement: This International Standard applies to BASIC SAFETY and ESSENTIAL PERFORMANCE of equipment incorporating one or more sources of OPTICAL
Medical electrical equipment. Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use
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
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
Medical electrical equipment - Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use
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
Diagnostic and therapeutic laser equipment - Safety requirements
Laser therapeutic equipment—Carbon dioxide laser 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
Laser therapeutic equipment—Pulsed carbon dioxide laser treating instrument
Medical electrical equipment. Part 2. Particular requirements for the safety of diagnostic and therapeutic laser equipment
Replacement: This International Standard applies to BASIC SAFETY and ESSENTIAL PERFORMANCE of equipment incorporating one or more sources of OPTICAL
Medical electrical equipment. Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use
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
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
Medical electrical equipment - Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use
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








