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
Basic requirements for connectivity compliance of medical diagnostic X-ray imaging equipment Part 1: General requirements
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2020-06-30
- 实施
- 2021-06-01
Medical diagnostic X-ray radiation protective equipment Part 1: Determination of material attenuation properties
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2020-02-25
- 实施
- 2021-03-01
Medical diagnostic X-ray radiation protection equipment Part 2: Transparent protective panels
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2020-02-25
- 实施
- 2021-03-01
Performance and test methods of body surface optical positioning equipment for radiotherapy
- ICS
- 11.040.60
- CCS
- C43
- 发布
- 2020-02-21
- 实施
- 2021-06-01
本标准规定了钴-60远距离治疗机的型式和基本性能参数、技术要求、试验方法、检验规则等内容。 本标准适用于钻-60远距离治疗机，该机主要供医疗单位作放射治疗用。
Cobalt-60 telecobalt machine
- ICS
- 11.040.60
- CCS
- C43
- 发布
- 2019-05-31
- 实施
- 2020-12-01
X-ray image guided radiotherapy equipment performance and test methods
- ICS
- 11.040.60
- CCS
- C43
- 发布
- 2019-05-31
- 实施
- 2020-12-01
Radiation protection and detection requirements for X-ray imaging diagnosis in operating room
- ICS
- 13.280
- CCS
- C43
- 发布
- 2019-04-22
- 实施
- 2019-07-01
Special technical conditions for mobile X-ray computed tomography equipment
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2018-12-20
- 实施
- 2020-01-01
YY/T 0590的本部分规定了数字X射线成像装置量子探测效率(DQE)的测定方法。在制造商规定的医疗应用范围内的工作条件下量子探测效率(DQE)是照射量和空间频率的函数。 本部分适用于那些产生用于医疗诊断的数字格式影像的数字X射线成像装置。本部分的适用范围限于用于单次曝光成像的数字X射线摄影装置，例如CR系统、基于硒材料的成像系统，平板探测器，光学耦合CCD成像系统以及数字X射线影像增强器。 本部分不适用于： —乳腺摄影和牙科摄影用数字X射线成像装置； —计算机体层摄影设备； —对人体进行扫描成像的X线系统； —动态成像设备(在该系统中一系列影像被采集到，例如透视和心脏成像)。 上述设备不包括在本部分中是因为他们的许多参数(如辐射质量、几何关系、时间依赖性等)与常规的X射线摄影有很大区别，这些参数由已经完成的用于其他主题的各自的标准来规范，如同IEC和ISO中对感光速度和对比度的单独规定。
Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1: Determination of the detective quantum efficiency
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2018-11-07
- 实施
- 2019-11-01
本标准规定了医用诊断X射线管组件的分类、要求及试验方法。 本标准适用于医用诊断X射线管组件（以下简称X射线管组件）。该产品供医用诊断X射线设备配套使用。
General specifications of medical diagnostic X-ray tube assemblies
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2018-11-07
- 实施
- 2019-11-01
Special technical conditions for digital photography X-ray machines
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2018-09-28
- 实施
- 2019-10-01
Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy; Amendment 2
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2018-06-01
- 实施
- 2018-07-10
Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2018-06-01
- 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
- 2018-05-01
- 实施
本标准规定了放射治疗用体位固定装置热塑膜的性能要求和试验方法。本标准适用于放射治疗中用于体位固定的热塑膜。
Positioning devices for radiotherapy - Part 1: Thermoplastic films
- ICS
- CCS
- C43
- 发布
- 2018-04-01
- 实施
- 2018-04-01
Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
- ICS
- 11.040.40
- CCS
- C43
- 发布
- 2018-04-01
- 实施
本标准规定了乳腺X射线机(以下简称乳腺机)的术语、分类、要求和试验方法。 本标准适用于使用具有X射线胶片增感屏，采用接触式和放大式操作的乳腺摄影X射线机，该机专供医疗单位作乳腺X射线摄影之用。 本标准不适用于数字成像装置、活组织检查板和立体定位装置等专用附件。
Particular specifications for mammographic X-ray equipment
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2018-04-01
- 实施
- 2018-04-01
本标准规定了放射治疗激光定位系统的性能和试验方法。本标准适用于不同类型放射治疗及定位设备（例如钴-61远距离治疗机、医用电子加速器、放射治疗模拟机、放射治疗CT模拟机和放射治疗MRI模拟机等）中配套使用的外置激光定位系统，用于在患者皮肤上、患者固定装置及立体定向框架等配准装置上投射出位置参考标记，以便放射治疗时对患者进行定位。
Performance and test methods of laser positioning system for radiotherapy
- ICS
- CCS
- C43
- 发布
- 2018-04-01
- 实施
- 2018-04-01
Special technical conditions for mobile C-arm X-ray machines
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2018-01-19
- 实施
- 2019-01-01
This part of IEC 61948 describes test methods for POSITRON EMISSION TOMOGRAPHS (PET). As part of QUALITY CONTROL, this document is defining ROUTINE TESTS to be performed by the user of POSITRON EMISSION TOMOGRAPHS to maintain proper operation conditions. The results of these ROUTINE TESTS are compared to the REFERENCE DATA determined during or after ACCEPTANCE TEST. Methods used for ACCEPTANCE TESTS are described in IEC 61675-1:2013. In addition, today a POSITRON EMISSION TOMOGRAPH often includes X-RAY EQUIPMENT for COMPUTED TOMOGRAPHY (CT). For this document, PET/CT hybrid devices are considered to be state of the art, dedicated POSITRON EMISSION TOMOGRAPHS not including the X-ray component being special cases only. QUALITY CONTROL tests specific to only the CT component of the PET/CT are described in IEC 61223-2-6. The CT SCANNER also is subject to a TYPE TEST according to IEC 60601-1 and applicable collateral and particular standards.
Nuclear medicine instrumentation - Routine tests - Part 3: Positron emission tomographs
- ICS
- 11.040.50
- CCS
- C43
- 发布
- 2018-01-01
- 实施
