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
Medical electrical equipment - Part 2-45: Particular requirements for the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices (IEC 60601-2-45:2011 + A1:2015); German version EN 60601-2-45:2011 + A1:
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2017-01
- 实施
5.1 This practice establishes the basic parameters for the application and control of the CR examination method. This practice is written so it can be specified on the engineering drawing, specification, or contract. 5.2 Weld Examination—Additional information on weld examination may be found in Practice E1032, ISO 17636-2, or both. 5.3 Casting Examination—Additional information on casting examination may be found in Practice E1030. 5.4 Electronic Components—Radiographic examination of electronic components shall comply with Practice E1161. 5.5 Part-Specific Examination Technique—A detailed written procedure in the form of a part-specific examination technique (7.5) shall be documented for each part, or group of parts, and shall be approved by the Cognizant Radiographic Level 3. 5.6 Personnel Qualification—Personnel performing examinations to this practice shall be qualified in accordance with ISO 9712, NAS 410, EN 4179, ANSI/ASNT CP 189, or SNT-TC-1A and certified by the employer or certifying agency as applicable. Other equivalent qualification documents may be used when specified on the contract or purchase order. The applicable revision shall be the latest unless otherwise specified in the contractual agreement between parties. 5.7 System Qualification—All CR systems shall be qualified for their intended use. System qualification requirements are specified in subsection 7.1. 5.8 Process Control—All CR systems shall be monitored for long term stability (process control) as specified in subsection 7.1.4. 5.9 Preventative Maintenance—All CR systems and X-ray machines require periodic maintenance to ensure proper functionality. Preventative maintenance requirements are specified in subsection 6.2. 5.10 Environmental Conditions—CR systems should be operated within environmental conditions that are in compliance with manufacturer’s stated acceptable environmental conditions, e.g., temperature and humidity. When CR systems are operated outside the specified manufacturer’s environmental ranges, the system shall be qualified (7.1) for such conditions. 1.1 This practice establishes the minimum requirements for computed radiographic (CR) examina......
Standard Practice for Radiographic Examination Using Computed Radiography (Photostimulable Luminescence Method)
- ICS
- 87.060.10
- CCS
- C43
- 发布
- 2017
- 实施
Radiation protection rules for handling of unsealed radioactive material in medicine
- ICS
- 11.040.50;13.280
- CCS
- C43
- 发布
- 2016-11
- 实施
Diagnostic X-ray imaging equipment - Characteristics of general purpose and mammographic anti-scatter grids (IEC 60627:2013); German version EN 60627:2015
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-08
- 实施
Terms in the field of radiological technique - Part 8: Radiotherapy
- ICS
- 01.040.11;01.040.17;11.040.50;17.240
- CCS
- C43
- 发布
- 2016-08
- 实施
Radionuclide imaging devices - Characteristics and test conditions - Part 1: Positron emission tomographs (IEC 61675-1:2013); German version EN 61675-1:2014
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-08
- 实施
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 60601-2-1:2009 + A1:2014); German version EN 60601-2-1:2015
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-08
- 实施
Terms in the field of radiological technique - Part 3: Dosimetry
- ICS
- 01.040.11;11.040.50
- CCS
- C43
- 发布
- 2016-08
- 实施
Medical electrical equipment Dosimetric instruments for non-accessible measurement of X-ray tube voltage in diagnostic radiology
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-07-29
- 实施
- 2017-06-01
Technical conditions of 64-slice spiral X-ray computed tomography equipment
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-07-29
- 实施
- 2017-06-01
Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy (IEC 60601-2-54:2009 + Cor.:2010 + Cor.:2011 + A1:2015); German version EN 60601-2-54:2009 +
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-07
- 实施
Nuclear medicine instrumentation. Routine tests. Gamma radiation counting system
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-04-30
- 实施
- 2016-04-30
Medical electrical equipment - Part 2-11: Particular requirements for the basic safety and essential performance of gamma beam therapy equipment (IEC 60601-2-11:2013); German version EN 60601-2-11:2015
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-04
- 实施
本标准规定了自动控制式近距离治疗后装设备放射治疗计划系统（以下简称治疗计划系统）的性能和试验方法。本标准适用于使用Ir放射性后装治疗源的治疗计划系统。对于使用其他后装治疗源或者其他封装方式的源，参照使用本标准。
Radiotherapy treatment planning system for automatically-controlled brachytherapy afterloading equipment.Characteristics and test methods
- ICS
- 11.040.60
- CCS
- C43
- 发布
- 2016-03-23
- 实施
- 2017-01-01
本标准规定了放射治疗用多元限束装置（以下简称多元限束装置）的适用范围、术语、性能要求和试验方法。本标准适用于预期独立装配在外照射治疗机（以下简称治疗机）辐射头外部的多元限束装置，该装置与治疗机配合使用，对肿瘤病变区域进行放射治疗。本标准不适用于预期装配在治疗机辐射头内部以及仅有开或关两种状态的多元限束装置。
Multi-element beam limiting device used in radiotherapy.Characteristics and test methods
- ICS
- 11.040.60
- CCS
- C43
- 发布
- 2016-03-23
- 实施
- 2017-01-01
本标准规定了医用乳腺数字化X射线摄影用探测器（以下简称“探测器”）的术语和定义、组成、要求、试验方法、检验规则、标志、标签、使用说明书、包装、运输和贮存。本标准适用于具有单次曝光成像功能的用于乳腺数字化X射线设备的探测器，包括但不限于非晶硅探测器、非晶硒探测器、CCD探测器、CMOS探测器等。本标准不适用于：--普通摄影用探测器和牙科摄影用探测器；--计算机体层摄影用探测器；--动态或体层成像用探测器。
Medical digital X-ray image detector used in mammography
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-03-23
- 实施
- 2017-01-01
本标准规定了自动控制式近距离治疗后装设备的要求和试验方法。 本标准适用于自动控制式近距离治疗后装设备(以下简称“后装设备”)。
Automatically-controlled brachytherapy afterloading equipment
- ICS
- 11.040.60
- CCS
- C43
- 发布
- 2016-03-23
- 实施
- 2017-01-01
本标准适用于医用诊断X射线设备系统或部件的特性测定试验程序，该程序要求定义明确的辐射条件。除了乳腺摄影外，本标准不适用于为了改善辐射束的特性而特意选用具有不连续性辐射吸收元素的情况（例如用稀土滤过板）。有屏-片系统的感光度测量的辐射条件不包括在本标准中。本标准涉及用什么辐射条件产生辐射束的方法，这些辐射条件皆为测试实验室或制造商通常用来测定医用诊断X射线设备特性的测试条件。
Medical diagnostic X-ray equipment.Radiation conditions for use in the determination of characteristics
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-03-23
- 实施
- 2017-01-01
本标准规定了单光子发射及X射线计算机断层成像系统(以下简称“SPECT/CT”)的性能和试验方法。 本标准适用于SPECT/CT，不适用于独立的单光子发射断层成像装置(以下简称“SPECT”)和独立的X射线计算机体层摄影设备(以下简称“CT”)。
Performance characteristics and test methods of imaging system of single photon emission and X-ray computed tomograph
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-03-23
- 实施
- 2017-01-01
本标准规定了医用X射线设备（以下简称设备）的环境分组、要求、试验方法。本标准适用于医用X射线设备。
Environmental requirements and test methods for medical X-ray equipment
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2016-03-23
- 实施
- 2017-01-01
