共找到 661 条与 治疗设备 相关的标准,共 45 页
Medical electrical equipment -- Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipment
Ultrasonics - Physiotherapy systems - Field specifications and methods of measurement in the frequency range 0,5 MHz to 5 MHz (IEC 87/769/CDV) (english version)
Medical electrical equipment – Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment
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
Medical electrical equipment - Part 2-21 : particular requirements for the basic safety and essential performance of infant radiant warmers
Medical electrical equipment - Part 2-50 : particular requirements for the basic safety and essential performance of infant phototherapy equipmen
IEC 60601-2-1:2009 applies to the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV, used for treatment of patients. This particular standard establishes requirements to be complied with by manufacturers in the design and construction of electron accelerators for use in radiotherapy; it does not attempt to define their optimum performance requirements. Its purpose is to identify those features of design that are regarded, at the present time, as essential for the safe operation of such medical electrical equipment. It places limits on the degradation of medical electrical equipment performance beyond which it can be presumed that a fault condition exists and where an interlock then operates to prevent continued operation of the me equipment. This third edition cancels and replaces the second edition published in 1998 and its Amendment 1 (2002). It constitutes a technical revision. This third edition addresses the following issues not covered in previous editions: - alignment with the new relevant collateral standards; - new technologies in radiotherapy, including stereotactic radiosurgery (SRS) and stereotactic radiotherapy (SRT), intensity modulated radiotherapy (IMRT), electronic imaging devices (e.g. EPID) and moving beam radiotherapy (dynamic therapy).
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
This International Standard applies to the Basic safety and essential Performance of external pacemakers powered by an internal electrical power source, hereafter referred to as ME Equipment.
Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source (IEC 60601-2-31:2020); German version EN IEC 60601-2-31:2020
Medical electrical equipment — Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment
Radiotherapy simulators — Functional performance characteristics
Radiotherapy simulators —Guidelines for functional performance characteristics
Radiotherapy simulators —Guidelines for functional performance characteristics
Medical electrical equipment — Part 2-3: Particular requirements for the basic safety and essential performance of short-wave therapy equipment
Radiotherapy simulators — Functional performance characteristics
Medical electrical equipment — Part 2-3: Particular requirements for the basic safety and essential performance of short-wave therapy equipment
Medical electrical equipment — Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment
1.1?This practice provides a structure for documenting test methods used to evaluate exoskeleton success criteria during a requested movement task and to ensure the movements can be completed to the criteria specified by the test requestor. The practice describes movement tasks,
Standard Practice for Movement Tests When Using an Exoskeleton
Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipment
本文件规定了掺铥光纤激光治疗机的型号规格标记、分类、组成、技术要求、试验方法、检验规则以及标签、说明书、包装、贮存等要求。
Thulium-doped fiber laser equipment
Copyright ©2007-2022 ANTPEDIA, All Rights Reserved
京ICP备07018254号 京公网安备1101085018 电信与信息服务业务经营许可证:京ICP证110310号