C43 医用射线设备 标准查询与下载
共找到 1065 条与 医用射线设备 相关的标准，共 71 页
本标准规定了医用诊断X射线管组件(以下简称管组件)泄漏辐射测试的术语和定义、测试方法。本标准适用于非电容放电式高压发生装置中管组件加载状态下泄漏辐射的测试。
Methods for the measurement of leakage radiation of medical diagnostic X-ray tube assemblies
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2013-10-21
- 实施
- 2014-10-01
本标准规定了放射治疗设备中X射线图像引导装置的成像剂量试验方法和对随机文件的要求。本标准适用于放射治疗设备中X射线图像引导装置。
Imaging dose of X-ray image-guided devices used in radiotherapy equipment
- ICS
- 11.040.60
- CCS
- C43
- 发布
- 2013-10-21
- 实施
- 2014-10-01
本标准适用于放射治疗计划系统(以下简称RTPS)的设计、制造、安装和使用等方面;--应用于医学实践中放射治疗的治疗计划设计;--输入的数据既可通过操作者输入,也可直接从其他设备获取;--输出数据既可打印文图阅览,也可直接输出到其他设备;--并预期:•在适当的许可或合格人员的授权下,由具备所需技能和培训的操作者正常使用;•按照使用说明书中推荐的方法维护,并;•在技术说明书中所规定的环境和供电条件使用。
Medical electrical equipment.Requirements for the safety of radiotherapy treatment planning systems
- ICS
- 11.040.60
- CCS
- C43
- 发布
- 2013-10-21
- 实施
- 2014-10-01
本标准规定了放射治疗计划系统(以下简称RTPS)调试中典型的外照射治疗技术的测试方法。本标准适用于RTPS在投入临床使用前对外照射高能光子束治疗技术的调试测试。
Commissioning of radiotherapy treatment planning systems.testing for typical externai Beam treatment techniques
- ICS
- 11.040.60
- CCS
- C43
- 发布
- 2013-10-21
- 实施
- 2014-10-01
本标准规定了医用诊断X射线影像增强器(以下简称增强器)的要求、试验方法、检验规则、标志、使用说明书、包装、运输和贮存。本标准适用于标称入射视野为 15 cm(6 in)、23 cm(9 in)、30 cm(12 in)、33 cm (13 in)和 40 cm(16 in)的装有图像缩小型X射线影像增强管的增强器,包括单视野及多重视野。该类产品主要用于与医用诊断X射线设备的配套使用,实现图像的转换。本标准不适用于平板型或其他类型的增强器。
Medical diagnostic X-ray image intensifier
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2013-10-21
- 实施
- 2014-10-01
本标准规定了放射性粒籽植入治疗计划系统(以下简称治疗计划系统)的剂量计算要求和试验方法。本标准适用于放射性粒籽植入治疗计划系统的剂量计算。
Radioactive seeds implantation treatment planning system.Requirements for dose calculations and test methods
- ICS
- 11.040.60
- CCS
- C43
- 发布
- 2013-10-21
- 实施
- 2014-10-01
This practice outlines irradiator installation qualification,operational qualification, performance qualification, and routine product processing dosimetric procedures to be followed in the irradiation of blood and blood components by the blood-banking community. If followed, these procedures will help to ensure that the products processed with ionizing radiation from gamma, X-radiation (bremsstrahlung), or electron sources receive absorbed doses within a predetermined range.
Practice for blood irradiation dosimetry
- ICS
- 11.020;17.240
- CCS
- C43
- 发布
- 2013-10-01
- 实施
Medical electron accelerators - Part 5: Constancy tests of functional performance characteristics
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2013-10
- 实施
Medical electrical equipment -- Part 2-28: Particular requirements for the basic safety and essential performance of X-ray tube assemblies for medical diagnosis
- ICS
- 11.040.55
- CCS
- C43
- 发布
- 2013-09-01
- 实施
Medical electrical equipment -- Part 2-45: Particular requirements for the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2013-09-01
- 实施
Photography - Intra-oral dental radiographic film and film packets - Manufacturer specifications (ISO 3665:2011); German version EN ISO 3665:2013
- ICS
- 37.040.25
- CCS
- C43
- 发布
- 2013-07
- 实施
This International Standard is applicable to ANTI-SCATTER GRIDS used in medical diagnostic Xray imaging equipment. ANTI-SCATTER GRIDS are used to reduce the incidence of SCATTERED RADIATION@ produced particularly in the body of the PATIENT@ upon the IMAGE RECEPTION AREA and thus to improve the contrast of the X-RAY PATTERN. This International Standard specifies the definitions@ determination and indication of characteristics of ANTI-SCATTER GRIDS. In this standard only LINEAR GRIDS are considered. Since at present only FOCUSED GRIDS are used in mammography@ this standard is restricted to FOCUSED GRIDS where MAMMOGRAPHIC ANTI-SCATTER GRIDS are concerned. This standard is not intended to be applied for ACCEPTANCE TESTS. This standard does not cover the homogeneity of performance over the area of a grid. This standard is intended to be applied for the determination of the characteristics of ANTISCATTER GRIDS under test conditions. These conditions are not usually available at the site of the RESPONSIBLE ORGANIZATION.
Diagnostic X-ray imaging equipment - Characteristics of general purpose and mammographic anti-scatter grids
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2013-07
- 实施
- 2013-07-12
Image quality assurance in diagnostic X-ray departments - Part 152: RöV acceptance test of X-ray installations for screen/film mammography
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2013-06
- 实施
Image quality assurance in diagnostic X-ray departments - Part 150: RöV acceptance test of medical radiographic and fluoroscopic X-ray equipment
- ICS
- 11.040.50;37.040.25
- CCS
- C43
- 发布
- 2013-06
- 实施
Medical X-ray equipment up to 300 kV - Rules of construction for structural radiation protection
- ICS
- 11.040.50;13.280
- CCS
- C43
- 发布
- 2013-06
- 实施
Medical X-ray equipment up to 300 kV - Rules for testing of radiation protection after installation, maintenance and essential modification
- ICS
- 11.040.50;13.280
- CCS
- C43
- 发布
- 2013-06
- 实施
Image quality assurance in diagnostic X-ray departments - Part 162: RöV acceptance test of X-ray installations for digital mammography
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2013-06
- 实施
Medical electrical equipment. Dosimeters with ionization chambers and/or semiconductor detectors as used in X-ray diagnostic imaging
- ICS
- 17.240
- CCS
- C43
- 发布
- 2013-04-30
- 实施
- 2013-04-30
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MR EQUIPMENT and MR SYSTEMS, hereafter referred to also as ME EQUIPMENT.This standard does not cover the application of MR EQUIPMENT beyond the INTENDED USE.If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.
Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
- ICS
- 11.040.55;35.240.80
- CCS
- C43
- 发布
- 2013-04
- 实施
Replace the existing first bullet with:"the general standard" designates IEC 606011-2005+A1:2012; Replace the existing second bullet with: "this collateral standard" designates IEC 60601-1-3-2008+A1:2013;
Amendment 1 to IEC 60601-1-3: Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment
- ICS
- 11.040.50;13.280
- CCS
- C43
- 发布
- 2013-04
- 实施
- 2013-05-03
