11.040.60 治疗设备 标准查询与下载
共找到 661 条与 治疗设备 相关的标准，共 45 页
This document specifies general requirements for the basic safety and essential performance of electro- acupuncture (EA) stimulators. It is not applicable to acupuncture needles, transcutaneous electrical nerve stimulators or electrical nerve and muscle stimulators.
Traditional Chinese medicine — General requirements for the basic safety and essential performance of electro-acupuncture stimulators
- ICS
- 11.040.60
- CCS
- 发布
- 2022-06-07
- 实施
1 Scope This document is applicable to ultrasonic equipment designed for physiotherapy containing an ultrasonic transducer generating continuous or quasi-continuous (e.g. tone burst) wave ultrasound in the frequency range 0,5 MHz to 5 MHz. This document only relates to ultrasonic physiotherapy equipment employing a single plane non-focusing circular transducer per treatment head , producing static beams perpendicular to the face of the treatment head . This document specifies: • methods of measurement and characterization of the output of ultrasonic physiotherapy equipment based on reference testing methods; • characteristics to be specified by manufacturers of ultrasonic physiotherapy equipment based on reference testing methods; • guidelines for safety of the ultrasonic field generated by ultrasonic physiotherapy equipment ; • methods of measurement and characterization of the output of ultrasonic physiotherapy equipment based on routine testing methods; • acceptance criteria for aspects of...
Ultrasonics. Physiotherapy systems. Field specifications and methods of measurement in the frequency range 0,5 MHz to 5 MHz
- ICS
- 11.040.60
- CCS
- 发布
- 2022-05-31
- 实施
- 2022-05-31
工作条件、能量稳定性、能流密度、穿透深度、频率、定时器或计数器、脉宽、手柄疲劳寿命、治疗头种类及尺寸、治疗头疲劳寿命、生物相容性、功能、安全要求等。
Electromagnetic Shock Wave Therapy Devices
- ICS
- 11.040.60
- CCS
- C131
- 发布
- 2022-05-25
- 实施
- 2022-05-25
Laser treatment equipment Nd-doped yttrium aluminum garnet laser treatment machine
- ICS
- 11.040.60
- CCS
- 发布
- 2022-05-18
- 实施
- 2025-06-01
Medical electrical equipment Part 2-68: X-ray image guides for electron accelerators, light ion beam therapy equipment and radionuclide beam therapy equipment
- ICS
- 11.040.60
- CCS
- 发布
- 2022-05-18
- 实施
- 2025-06-01
IEC TR 63183:2019 provides guidance on the usage and form of error or warning messages written for software used in RADIOTHERAPY. It does not replace any requirements existing in the safety standards but is meant to be used as a supplement to existing standards on usability by providing specific examples in the field of RADIOTHERAPY. The two main goals of this document are 1) to present in a concise manner the best practices and design guidelines for good message dialogs, and 2) to illustrate these design guidelines with specific examples from the field of radiation oncology. This document is intended to be read by the following MANUFACTURERS’ employees and representatives: – engineering department members including: software engineers, RISK managers, quality assurance engineers, technical writers, etc.; – usability and human factors engineers; – marketing representatives (product marketing, product managers, business analysts). Throughout this document, unless specifically called out, these guidelines apply to all categories of messages summarily called error or warning messages (e.g. critical error, warning, system status, informational, routine interlock messages).
Guidance on error and warning messages for software used in radiotherapy
- ICS
- 11.040.60
- CCS
- 发布
- 2022-05-12
- 实施
Ultrasonics - Physiotherapy systems - Field specifications and methods of measurement in the frequency range 0,5 MHz to 5 MHz
- ICS
- 11.040.60
- CCS
- 发布
- 2022-03-08
- 实施
Ultrasonics - Physiotherapy systems - Field specifications and methods of measurement in the frequency range 0,5 MHz to 5 MHz
- ICS
- 11.040.60
- CCS
- 发布
- 2022-03-08
- 实施
本文件规定了超设计使用医用氧舱检验的要求、检验项目和检测方法等内容。 本文件适用于TSG 24规定的山西省内超设计使用医用氧舱的检验。
Technical Specifications for Inspection of Medical Oxygen Chamber Part 1: Examination for Use Beyond Design
- ICS
- 11.040.60
- CCS
- C 42
- 发布
- 2021-12-31
- 实施
- 2022-03-31
本文件规定了医用氧舱电气系统检验的具体内容和要求。 本文件适用于山西省内医用氧舱安装监督检验和定期检验中电气系统的检验。
Technical Specifications for Inspection of Medical Oxygen Chamber Part 2: Electrical System Inspection
- ICS
- 11.040.60
- CCS
- C 42
- 发布
- 2021-12-31
- 实施
- 2022-03-31
Medical electrical equipment－Part 2-5：Particular requirements for the basic safety and essential performance of ultrasonic physiotherapy equipment
- ICS
- 11.040.60
- CCS
- 发布
- 20211208
- 实施
- 20211208
本文件规定了医用电子直线加速器的技术要求和试验方法。 本文件适用于医疗机构使用的医用电子直线加速器。 本文件适用于能产生X辐射和电子辐射的医用电子加速器，其标称能量为1MeV～50MeV。
Taishan Quality-Medical electron linear accelerator
- ICS
- 11.040.60
- CCS
- Q841
- 发布
- 2021-11-01
- 实施
- 2021-12-25
This International Standard is applicable to: – therapy equipment using extracorporeally induced non-focused or weakly focused pressure pulses; – therapy equipment producing extracorporeally induced non-focused or weakly focused mechanical energy; where the pressure pulses are re
Ultrasonics - Non-focusing short pressure pulse sources including ballistic pressure pulse sources - Characteristics of fields (IEC 63045:2020); German version EN IEC 63045:2020
- ICS
- 11.040.60
- CCS
- 发布
- 2021-11-00
- 实施
- 2021-11-01
3 术语和定义 3.1 检定分度值 4 型式 5 技术要求 5.1 环境要求 5.2 外观与结构 5.3 尺寸 5.4 计量性能 5.5 功能要求 5.6 噪声 5.7 电气安全 5.8 电磁兼容性 5.9 环境适应性 5.10 外壳防护 5.11 限用物质 6 试验方法 6.1 试验环境条件 6.2 外观及结构 6.3 尺寸 6.4 计量性能检查 6.5 功能 6.6 噪声 6.7 电气安全 6.8 电磁兼容性 6.9 环境适应性 6.10 外壳防护 6.11 限用物质 7 检验规则 7.1 检验分类 7.2 出厂检验 7.3 型式检验 7.4 判定规则 8 标志、包装、运输、贮存 8.1 标志 8.2 包装 8.3 运输 8.4 贮存
Technical specification for flow feedback devices for microdialysis systems
- ICS
- 11.040.60
- CCS
- C358
- 发布
- 2021-10-27
- 实施
- 2021-10-27
Paints and varnishes - Oils and waxes for timber surfaces - Terms and definitions with classifications
- ICS
- 11.040.60
- CCS
- 发布
- 2021-10-01
- 实施
- 2021-10-01
This document specifies requirements for therapeutic couch and serves as a german base of particular standard related to DIN EN 60601-1-series.
Medical electrical equipment - Part 2-52-2: Particular requirements for basic safety and essential performance of couches
- ICS
- 11.040.60
- CCS
- 发布
- 2021-10-00
- 实施
- 2021-10-01
Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment (IEC 60601-2-50:2020)
- ICS
- 11.040.60
- CCS
- 发布
- 2021-09-30
- 实施
- 2021-09-30
LST EN IEC 60601-2-1:2021 医用电气设备 第 2-1 部分：1 MeV 至 50 MeV 范围内电子加速器的基本安全和基本性能的特殊要求（IEC 60601-2-1:2020）
Medical electrical equipment - Part 2-1: Particular requirements for the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV (IEC 60601-2-1:2020)
- ICS
- 11.040.60
- CCS
- 发布
- 2021-09-30
- 实施
- 2021-09-30
Medical electrical equipment. Particular requirements for the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV
- ICS
- 11.040.60
- CCS
- 发布
- 2021-08-13
- 实施
- 2021-08-13
Medical electrical equipment. Particular requirements for the basic safety and essential performance of infant phototherapy equipment
- ICS
- 11.040.60
- CCS
- 发布
- 2021-08-13
- 实施
- 2021-08-13
