脉搏血氧测量设备检测

prEN 865-1992 医疗电气设备.脉搏血氧定量计.特殊要求

Medical electrical equipment; pulse oximeters; particular requirements

KS P ISO 9919-2007(2012 医用脉搏血氧仪要求

Pulse oximeters for medical use－Requirements

ASTM F1415-92 脉搏血氧计的标准规范

Standard Specification for Pulse Oximeters

EN ISO 11073-10404:2011 保健信息学.个人保健设备通信.第10404部分:设备规范.脉搏血氧计

Within the context of the ISO/IEEE 11073 family of standards for device communication,This standardestablishes a normative definition of communication

Health informatics - Personal health device communication - Part 10404: Device specialization - Pulse oximeter

KS X ISO/IEEE 11073-10404-2015(2020 健康信息学 - 个人健康设备通信第10404部分:设备专业化 - 脉搏血氧仪

Health informatics — Personal health device communication — Part 10404: Device specialization — Pulse oximeter

YY 0784-2010 医用电气设备 医用脉搏血氧仪设备基本安全和主要性能专用要求

引用GB 9706.1-2007的第1章,不包括以下内容。 修改(增加在1.1末尾处) 本标准详细描述了适用于人体使用的脉搏血氧仪设备的基本安全和主要性能的专用要求,该设备包括在正常使用中的任何必要的部件,如脉搏血氧监护仪、脉搏血氧探头、探头电缆延长线等。 这些要求也适用于经再加工的脉搏

Medical electrical equipment.Particular requirements for the basic safety and essential performance of pulse oximeter equipement for medical use

BS EN ISO 80601-2-61:2011 医用电气设备.对脉搏血氧计设备基本安全和基本性能的特殊要求

Subclause 1.1 of The general standard is replaced by: This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of PULSE

Medical electrical equipment. Particular requirements for basic safety and essential performance of pulse oximeter equipment

YY 9706.261-2023 医用电气设备 第2-61部分:脉搏血氧设备的基本安全和基本性能专用要求

本文件规定了脉搏血氧设备的基本安全和基本性能。本文件适用于人体使用的脉搏血氧设备和已再加工的脉搏血氧设备。脉搏血氧设备包括脉搏血氧监护仪，脉搏血氧探头和探头的电缆延长线。本文件适用但不限于预期在专业医疗机构，家庭护理环境和紧急医疗服务环境中估计患者的动脉血氧饱和度和脉率的脉搏血氧设备。本文件也适用于

ISO/IEEE 11073-10404:2022 健康信息学.设备互操作性.第10404部分:个人健康设备通信.设备专用化.脉搏血氧计

Health informatics — Device interoperability — Part 10404: Personal health device communication — Device specialization — Pulse oximeter

JIS T 80601-2-61:2014 医用电气设备. 第2-61部分: 脉搏血氧计设备基本安全和基本性能的特殊要求

Medical electrical equipment -- Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment

NF S95-158:2011 医用电气设备.第2-61部分:脉搏血氧仪设备的基本安全和基本性能的特殊要求

Medical electrical equipment - Part 2-61 : particular requirements for basic safety and essential performance of pulse oximeter equipment.

KS C ISO 80601-2-61:2020 医疗电气设备 - 第2-61部分:脉搏血氧仪设备的基本安全和基本性能的特殊要求

Medical electrical equipment — Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment

KS C ISO 80601-2-61:2014 医疗电气设备 第2-61部分：脉搏血氧仪设备的基本安全和基本性能的特殊要求

이 표준은 인체에 사용하도록 의도한 펄스옥시미터의 기본안전 및 필수성능(BASIC SAFETY and ESSENTIAL PERFORMANCE)에 관한 요구사항에 적용하며, 이하에서 ME기기(ME EQUIPMENT)라고 표기한다. 여기에는 펄스옥시미터모니터(PULSE

Medical electrical equipment — Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment

DIN EN ISO 11073-10404:2011 保健信息学.个人保健设备通信.第10404部分:设备规范.脉搏血氧计(ISO/IEEE 11073-10404-2010).英文版本EN ISO 11073-10404-2011

Within the context of the ISO/IEEE 11073 family of standards for device communication, this standard establishes a normative definition

Health informatics - Personal health device communication - Part 10404: Device specialization - Pulse oximeter (ISO/IEEE 11073-10404:2010); English version EN ISO 11073-10404:2011

ISO 18615:2020 中药 - 电子径向脉搏测量仪的一般要求

Traditional Chinese medicine — General requirements of electric radial pulse tonometric devices

ISO/IEEE 11073-10404:2010 保健信息学.个人保健设备通信.第10407部分:设备规范.脉冲血氧定量计

IMPORTANT NOTICE: This standard is not intended to ensure safety, security, health, or environmental protection in all circumstances. Implementers

Health informatics - Personal health device communication - Part 10404: Device specialization - Pulse oximeter

BS EN ISO 11073-10404:2011 健康信息学.个人健康设备通信.专门化设备.脉冲光电血氧计

Within the context of the ISO/IEEE 11073 family of standards for device communication, this standard establishes a normative definition

Health informatics. Personal health device communication. Device specialization. Pulse oximeter

T/ZMDS 10003-2016 可穿戴的健康类电气设备 第3部分:通过反射式光电容积脉搏波描记法测量脉率设备的性能和安全要求

主要内容包括：脉率测量范围和准确度、使用说明书、应用部分的温度、光辐射和生物相容性等方面的要求和试验方法

Body-worn electrical equipment for healthy purposes Part3: Performance and safety requirements for equipment intended for measuring pulse rate through reflecting photoplethysmography

T/ZMDS 10002-2016 可穿戴的健康类电气设备 第2部分:通过透射式光电容积脉搏波描记法测量脉率设备的性能和安全要求

主要内容包括：脉率测量范围和准确度、使用说明书、应用部分的温度、光辐射和生物相容性等方面的要求和试验方法

Body-worn electrical equipment for healthy purposes Part2: Performance and safety requirements for equipment intended for measuring pulse rate through transmission photoplethysmography

SNI 16-6360-2000 医用脉冲光电血氧剂

Pulse oximeters for medical use

ISO 18615:2020 中药 - 电子径向脉搏测量仪的一般要求

Traditional Chinese medicine — General requirements of electric radial pulse tonometric devices

YY 0126-1993 滚压式搏动血泵

本标准规定了滚压式搏动血泵的产品分类、技术要求、试验方法、检验规则及标志、包装、运输、贮存的要求。 本标准适用于人工心肺机中的滚压式搏动血泵，该产品供医疗单位用于心脏直视手术及抢救时，暂时代替心脏功能进行体外循环用

Rolling type pulsate blood pump

KS P ISO 18615:2019 中药 - 电动径向脉搏测量装置的一般要求

Traditional Chinese medicine — General requirements of electric radial pulse tonometric device

AS ISO 9919:2004 医用脉动式血氧计．要求

Specifies requirements for the safety of pulse oximeters, intended for use in the approximate measurement of the saturation of human arterial

Pulse oximeters for medical use - Requirements

ISO 9919:1992 医用脉动式血氧计 要求

Pulse oximeters for medical use; requirements

T/ZSA 5002.01-2017 可穿戴的健康类电气设备 第3部分:通过反射式光电容积脉搏波描记法测量脉率设备的性能和安全要求

本标准规定了预期通过反射式光电容积脉搏波描记法测量脉率的可穿戴的健康类电气设备的性能和安全要求。 本标准适用于通过反射式光电容积脉搏波描记法测量脉率的设备

SANS 1775-4:2009 静脉输液及输血设备(一次性使用菌包装).第4部分:中心静脉压(CVP)监测设备

Covers requirements for central venous pressure (CVP) monitoring sets intended for general medical use and sterile-packed for single use

Intravenous infusion and transfusion equipment (sterile-packed for single use) Part 4: Central venous pressure (CVP) monitoring sets

NF S94-203-1:2009 心血管植入物.血管内设备.第1部分:内脉管修复

Cardiovascular implants - Endovascular devices - Part 1 : endovascular prostheses.

DB51/T 1266-2011 心搏与血液循环模型

CSA Z9919-07-CAN/CSA-2007 医疗电子设备-为了保证基本安全和性能使用医用脉冲血氧计.特殊设备.第2版

Canadian Standards Association (CSA) standards are developed through a consensus standards development process approved by the Standards Council

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