
发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22
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Inhalational anaesthesia systems - Part 5 : anaesthetic ventilators.
This SAE Aerospace Recommended Practice (ARP) recommends performance requirements for test equipment used in dynamic testing of aviation oxygen
Dynamic Testing Systems for Oxygen Breathing Equipment
YY 0635本部分规定了由制造商提供或组装的,或由用户在制造商的指导下装配的麻醉呼吸系统的专用要求。本部分也包含对循环吸收组件、排气阀、吸入和呼出阀的要求,及在一些设计中组成吸人式麻醉系统的麻醉呼吸系统部件的要求,这些部件包括麻醉呼吸机的呼出气体通道。本部分不覆盖关于麻醉呼吸系统消除呼出二氧化碳的
Inhalational anaesthesia systems.Part 1:Anaesthetic breathing systems
This part of ABNT NBR ISO 8835 specifi es requirements for anaesthetic breathing systems that are supplied either assembled by the manufacturer
Testing methods for self-contained underwater breathing apparatus(SCUBA)
近年来,医学检验技术进展迅猛,临床检验逐渐过渡到检验医学.临床一线的医务工作者需紧跟发展趋势,全面,深入认识层出不穷的检验项目,并能够准确,有效解读常见检验项目的临床价值,这疑对提高临床诊断和治疗水平具有重要意义.临床检验项目繁多,影响检验结果解读的因素颇多,解读检验报告需充分了解检验方法和仪器的
Application analysis criteria for a number of indicators of intelligent health detection respiratory system
除下述内容外,GB 9706.1-2007第1章适用。 修改(在1.1末尾增加): 本标准规定了湿化系统(见3.6定义)的基本安全和基本性能的要求。也包括湿化系统中使用的特定的独立装置,如呼吸管路加热(呼吸管路加热丝)以及呼吸管路加热的控制装置(呼吸管路加热控制器)。呼吸管路其他方面的安全和
Respiratory tract humidifiers for medical use.Particular requirements for respiratory humidification systems
Inhalational anaesthesia systems - Part 2 : anaesthetic breathing systems.
Breathing system filters for anaesthetic and respiratory use - Non-filtration aspects
This Part of this European Standard specifies requirements for non-filtration aspects of breathing system filters (BSFs) intended for the filtration
Breathing system filters for anaesthetic and respiratory use - Non-filtration aspects
Breathing system filters for anaesthetic and respiratory use - Non-filtration aspects
Humidifiers for Medical Use - General Requirements for Humidification Systems
Respiratory tract humidifiers for medical use - Particular requirements for respiratory humidification systems
Breathing system filters for anaesthetic and respiratory use -- Non-filtration aspects
Inhalation anaesthesia systems. Part 2. Anaesthetic circle breathing systems
Inhalational anaesthesia systems - Part 2: Anaesthetic breathing systems
This part of ISO 8835 specifies requirements for anaesthetic breathing systems that are supplied either assembled by the manufacturer or for assembly
Inhalational anaesthesia systems - Part 2: Anaesthetic breathing systems (ISO 8835-2:2007); German version EN ISO 8835-2:2007
Inhalational anaesthesia systems - Part 2: Anaesthetic breathing systems
Inhalational anaesthesia systems-Part 2:Anaesthetic breathing systems for adults
この規格は,完成品として,又は製造業者の指示によって使用者が組み立てる部品の形で供給される吸入麻酔装置の循環式二酸化炭累(炭酸がス)吸収呼吸回路の要求事項を規定する
Inhalational anaesthesia systems -- Part 5: Anaesthetic circle breathing systems
Respiratory tract humidifiers for medical use —Particular requirements for respiratory humidification systems
YY 0635的本部分规定了由制造商提供或组装的,或由用户在制造商的指导下装配的,用于成人的吸入式麻醉呼吸系统的专用要求。本标准也包含对循环吸收组件、排气阀、吸气和呼气阀的要求,这些部件包括麻醉呼吸机的呼出气体通道和非操作者可拆卸的麻醉气体净化系统(AGSS)的任何部分。 本部分不覆盖关于呼吸系统
Inhalational anaesthesia systems.Part 1:Anaesthetic breathing system for adults
This part of ISO 8835 specifies requirements for inhalational anaesthetic breathing systems for adults which are supplied either assembled
Inhalational anaesthesia systems - Part 2: Anaesthetic breathing systems
Inhalational anaesthesia systems ?Part 2: Anaesthetic breathing systems Second Edition
Valve, Oxygen Mask, Combination Inhalation and Exhalation
Inhalational anaesthesia systems. Part 2. Anaesthetic circle breathing systems
YY/T 0735的本部分规定了用于麻醉呼吸用呼吸系统过滤器的非过滤方面,包括其连接端口、泄漏、阻流、包装、标识和提供的信息。试验方法预期用于临床呼吸系统中使用的BSF。 本部分不适用于其他类型的过滤器,如专门用于保护真空源或气体采样管路、对过滤器加压的气体或保护生理呼吸测量试验设备的过滤器
Breathing system filters for anaesthetic and respiratory use.Part 2:Non-filtration aspects








