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现行 IEC 80601-2-49:2018
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Medical electrical equipment — Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment 医用电气设备 - 第2-49部分:基本安全和多功能病人监护设备基本性能的特殊要求
发布日期: 2018-03-09
IEC 80601-2-49:2018适用于多功能患者监护仪(以下简称医用电气设备或医疗电气系统)的基本安全和基本性能要求。本特殊标准适用于专业医疗机构、紧急医疗服务环境或家庭医疗环境中使用的多功能患者监护仪。 本文件的范围仅限于医用电气设备或医用电气系统,用于连接具有两个或多个生理监测装置的单个患者。 在本文件中,孕妇及其胎儿被视为单一患者。 本文件未规定ECG、有创血压和脉搏血氧饱和度等单独生理监测装置的要求。 与这些生理监测装置相关的特殊标准从独立医用电气设备的角度规定了要求。本特定标准阐述了与多功能患者监护仪相关的附加要求。多功能患者监护仪可以集成到其他医用电气设备或医疗电气系统中。在这种情况下,其他相关标准也适用。 本文件不适用于多功能患者监护仪的可植入部件。 第一版取消并取代了2011年发布的IEC 60601-2-49第二版。本版本构成技术修订版,与IEC 60601-1的现行版本和修订版、附属标准的新版本及其修订版保持一致。第208条作了重大修改,因为以前的许多要求现在由IEC 60601解决- 1-8.
IEC 80601-2-49:2018 applies to basic safety and essential performance requirements of multifunction patient monitors, hereafter referred to as ME equipment or medical electrical systems. This particular standard applies to multifunction patient monitors intended for use in professional healthcare facilities as well as in the emergency medical service environment or the home healthcare environment. The scope of this document is restricted to ME equipment or medical electrical systems intended for connection to a single patient that has two or more physiological monitoring units. For purposes of this document, a pregnant mother and her fetus(es) are considered a single patient. This document does not specify requirements for individual physiological monitoring units such as ECG, invasive pressure and pulse oximetry. The particular standards related to these physiological monitoring units specify requirements from the perspective of stand-alone ME equipment. This particular standard addresses the additional requirements related to multifunction patient monitors. Multifunction patient monitors can be integrated into other ME equipment or medical electrical systems. When this is the case, other relevant standards also apply. This document does not apply to implantable parts of multifunction patient monitors. This first edition cancels and replaces the second edition of IEC 60601-2-49, published in 2011. This edition constitutes a technical revision to align with the current edition and Amendment to IEC 60601-1, new versions of collateral standards and amendments thereto. Major changes are in Clause 208 because many of the former requirements are now addressed by IEC 60601-1-8.
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研制信息
归口单位: ISO/TC 121/SC 3
相似标准/计划/法规
现行
YY 0668-2008
医用电气设备 第2-49部分:多参数患者监护设备安全专用要求
Medical electrical equipment—Part 2-49:Particular requirements for the safety of multifunction patient monitoring equipment
2008-10-17
现行
UNE-EN 60601-2-49-2002
Medical electrical equipment -- Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment.
医用电气设备第2-49部分:多功能患者监护设备安全的特殊要求
2002-05-30
现行
GOST 30324.2.49-2012
Изделия медицинские электрические. Часть 2-49. Частные требования безопасности к многофункциональным мониторам пациента
医疗电气设备 第2-49部分 多功能病人监护设备安全的特殊要求
2012-05-24
现行
IEC 80601-2-49-2018+AMD1-2024 CSV
Medical electrical equipment - Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitors
医用电气设备.第2-49部分:多功能病人监护仪基本安全和基本性能的特殊要求
2024-09-11
现行
KS C IEC 80601-2-49
의료용 전기기기 — 제2-49부: 다기능 환자 감시장치의 기본 안전 및 필수 성능에 대한 개별 요구사항
多参数病人监护设备委员会电子医疗 病人监护 诊断设备医用电气设备第2-49部分:多功能病人监护机基本安全和基本性能的特殊要求
2020-12-30
现行
AAMI MP80601-2-49-2020
Medical electrical equipment - Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitors
医用电气设备第2-49部分:多功能病人监护仪基本安全和基本性能的特殊要求
2020-03-24
现行
IEC 80601-2-49-2018/Amd 1-2024
Medical electrical equipment — Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment — Amendment 1
医用电气设备第2-49部分:多功能患者监护设备基本安全和基本性能的特殊要求修改件1
2024-09-13
现行
DIN EN IEC 80601-2-49
Medical electrical equipment - Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment (IEC 80601-2-49:2018); German version EN IEC 80601-2-49:2019
医用电气设备.第2-49部分:多功能患者监护设备基本安全和基本性能的特殊要求(IEC 80601-2-49-2018);德国版本EN IEC 80601-2-49:2019
2020-10-01
现行
UNE-EN 60601-2-18-1997
MEDICAL ELECTRICAL EQUIPMENT. PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ENDOSCOPIC EQUIPMENT.
医用电气设备 第2部分:内窥镜设备安全的特殊要求
1997-11-26
现行
IEC 80601-2-49-2018/AMD1-2024
Amendment 1 - Medical electrical equipment - Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitors
修改件1-医用电气设备-第2-49部分:多功能患者监护仪基本安全和基本性能的特殊要求
2024-09-11
现行
GB 10793-2000
医用电气设备 第2部分:心电图机安全专用要求
Medical electrical equipment—Part 2:Particular requirements for the safety of electrocardiographs
2000-07-12
现行
UNE-EN 60601-2-25-1997
MEDICAL ELECTRICAL EQUIPMENT. PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ELECTROCARDIOGRAPHS.
医用电气设备 第2部分:心电图机安全的特殊要求
1997-03-04
现行
GOST 30324.25-1995
Изделия медицинские электрические. Часть 2. Частные требования безопасности к электрокардиографам
医疗电气设备 第2部分心电图安全的特殊要求
现行
GOST R 50267.25-1994
Изделия медицинские электрические. Часть 2. Частные требования безопасности к электрокардиографам
医疗电气设备 第2部分心电图安全的特殊要求
现行
JIS T 0601-2-208-2008
Medical electrical equipment -- Part 2-208: Particular requirements for the safety of electric potential equipment
医用电气设备第2-208部分:电势设备安全的特殊要求
2008-01-01
现行
CAN/CSA C22.2 No.60601-2-49-11(R2021)
Medical electrical equipment - Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment (Adopted IEC 60601-2-49:2011, second edition, 2011-02)
医用电气设备.第2-49部分:多功能患者监护设备基本安全和基本性能的特殊要求(采用IEC 60601-2-49:2011 第二版 2011-02)
2012-03-29
现行
GOST 30324.6-1995
Изделия медицинские электрические. Часть 2. Частные требования безопасности к аппаратам для микроволновой терапии
医疗电气设备 第二部分微波治疗设备安全的特殊要求
现行
GOST 30324.5-1995
Изделия медицинские электрические. Часть 2. Частные требования безопасности к аппаратам для ультразвуковой терапии
医疗电气设备 第二部分超声波治疗设备安全的特殊要求
现行
GOST R 50267.14-1993
Изделия медицинские электрические. Часть 2. Частные требования безопасности к аппаратам для электрошоковой терапии
医疗电气设备 第2部分电惊厥治疗设备安全的特殊要求
现行
GOST 30324.14-1995
Изделия медицинские электрические. Часть 2. Частные требования безопасности к аппаратам для электрошоковой терапии
医疗电气设备 第2部分电惊厥治疗设备安全的特殊要求