现行

YY 0786-2010

医用呼吸道湿化器　呼吸湿化系统的专用要求
Respiratory tract humidifiers for medical use—Particular requirements for respiratory humidification systems

2010-12-27

现行

BS EN ISO 8185-2009

Respiratory tract humidifiers for medical use. Particular requirements for respiratory humidification systems
医用呼吸道加湿器 呼吸增湿系统的详细要求

2009-07-31

现行

UNE-EN ISO 8185-2009

Respiratory tract humidifiers for medical use - Particular requirements for respiratory humidification systems (ISO 8185:2007)
医用呼吸道加湿器.呼吸加湿系统的特殊要求（ISO 8185-2007）

2009-07-22

现行

GOST ISO 8185-2012

Увлажнители медицинские. Технические требования и методы испытаний
医疗用加湿器技术要求和试验方法

2012-05-24

现行

CAN/CSA Z8185-08(R2013)

Respiratory tract humidifiers for medical use - Particular requirements for respiratory humidification systems (adopted ISO Standard 8185, third edition, 2007-07-01)
医用呼吸道加湿器.呼吸加湿系统的特殊要求（采用ISO标准8185 第三版 2007-07-01）

2008-08-01

现行

GB/T 38800-2020

General technical requirements of modular isolation units for emergency medical use

2020-04-03

现行

BS EN ISO 15223-1-2021(CD-ROM)

Medical devices. Symbols to be used with information to be supplied by the manufacturer-General requirements
医疗设备 与制造商提供的信息一起使用的符号

2021-09-29

现行

GOST 31626-2012

Бинты гипсовые медицинские. Общие технические требования. Методы испытаний
巴黎石膏医疗用途 一般技术要求 测试方法

2012-05-24

现行

GOST 31508-2012

Изделия медицинские. Классификация в зависимости от потенциального риска применения. Общие требования
医疗产品 按照潜在的使用风险进行分类 一般要求

2012-05-24

现行

GB/T 44008-2024

应急医用模块化集成系统通用技术要求
General technical requirements of modular integrated system for emergency medical use

2024-04-25

现行

GOST R 57629-2017

Изделия медицинские. Общие требования безопасности и совместимости магистралей инфузионных однократного применения
医疗器械 一次性输液器的一般安全性和兼容性要求

现行

KS P ISO 15223-1

의료기기 — 의료기기의 라벨, 라벨링 및제공해야 할 정보에 사용하는 기호 — 제1부: 일반 요구사항
医疗器械 - 符合医疗器械标签 标签和信息要使用的符号 - 第1部分:一般要求

2019-11-25

现行

YY/T 0466.1-2016

医疗器械　用于医疗器械标签、标记和提供信息的符号　第1部分：通用要求
Medical devices—Symbols to be used with medical device labels,labelling and information to be supplied—Part 1:General requirements

2016-01-26

现行

BS EN 60601-1-12-2015+A1-2020

Medical electrical equipment-General requirements for basic safety and essential performance. Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment
医用电气设备

2020-09-04

现行

KS P ISO 15223-1

의료기기 — 제조자가 제공하는 정보에 사용하는 기호 — 제1부: 일반 요구사항
医疗器械.与制造商提供的信息一起使用的符号.第1部分:一般要求

2023-12-28

现行

ISO 15223-1-2021

Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements
医疗器械与制造商提供的信息一起使用的符号第1部分:一般要求

2021-07-06

现行

DIN 58959-7

Quality management in medical microbiology - Part 7: General requirements for the use of control strains
医学微生物学的质量管理.第7部分:控制菌株使用的一般要求

1997-06-01

现行

BS EN 60601-1-11-2015+A1-2021

Medical electrical equipment-General requirements for basic safety and essential performance. Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
医用电气设备

2021-08-20

现行

IEC 60601-1-12-2014

Medical Electrical Equipment — Part 1-12: General requirements for basic safety and essential performance — Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the emergency medical services environment
医用电气设备第1-12部分:基本安全和基本性能的一般要求附属标准:应急医疗服务环境中使用的医用电气设备和医用电气系统的要求

2015-11-18

现行

AS IEC 60601.1.12-2017

Medical electrical equipment, Part 1.12: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment
医用电气设备 第1.12部分:基本安全和基本性能的一般要求-附带标准:用于紧急医疗服务环境的医用电气设备和医用电气系统的要求

2017-06-23