BS ISO 18562-3:2017规定了气体中挥发性有机化合物（vocs）的排放试验 医疗设备、其零件或附件的路径，旨在提供呼吸 在所有环境中通过呼吸道向患者护理或供应物质。这方面的考验 该文件旨在量化由制造商添加到可吸入气流中的挥发性有机化合物的排放量 气体通道的材料。本文件确立了这些试验的验收标准。本文件阐述了气体通道产生的气流的潜在污染， 然后将其引导至患者。本文件适用于医疗器械在正常使用和使用中的预期使用寿命 考虑任何预期加工或再加工的影响。 本文件不涉及直接接触的气体通道表面的生物评估 与患者接触。直接接触表面的要求见ISO 10993 系列[1]。包含本文件所述气体通道的医疗设备、零件或附件 包括但不限于呼吸机、麻醉工作站（包括气体混合器）、呼吸 系统、氧气保存装置、氧气浓缩器、雾化器、低压软管组件、， 加湿器、热湿交换器、呼吸气体监测器、呼吸监测器、口罩、， 口罩、复苏器、呼吸管、呼吸系统过滤器、Y形管和任何呼吸系统 拟与此类装置一起使用的附件。孵化器的封闭室，包括 床垫和氧气罩的内表面被认为是气体通道，也是 本文件所述。本文件不涉及气源供应的气体中已经存在的污染 当医疗设备处于正常使用状态时。例如，来自医疗气体管道等气源的污染到达医疗设备 系统（包括管道出口中的止回阀）、连接的压力调节器出口或 ISO 18562系列并未涉及医疗气瓶或医疗器械内的室内空气。本文件旨在结合ISO 18562-1阅读。注:本文件旨在阐述相关的安全和环境基本原则 性能如附件B所示。 交叉引用:ISO 7396-1:2016ISO 14971:2007ISO 16000-6:2011ISO 18562-1:2017ASTM D5466-01ISO 10993ISO 16142-1:2016IEC 60601-1购买本文件时提供的所有现行修订均包含在购买本文件中。

BS ISO 18562-3:2017 specifies tests for the emissions of volatile organic compounds (vocs) from the gas pathways of a medical device, its parts or accessories, which are intended to provide respiratory care or supply substances via the respiratory tract to a patient in all environments. The tests of this document are intended to quantify emissions of vocs that are added to the respirable gas stream by the materials of the gas pathway. This document establishes acceptance criteria for these tests.This document addresses potential contamination of the gas stream arising from the gas pathways, which is then conducted to the patient.This document applies over the expected service life of the medical device in normal use and takes into account the effects of any intended processing or reprocessing.This document does not address biological evaluation of the surfaces of gas pathways that are in direct contact with the patient. The requirements for direct contact surfaces are found in the ISO 10993 series[1].Medical devices, parts or accessories containing gas pathways that are addressed by this document include, but are not limited to, ventilators, anaesthesia workstations (including gas mixers), breathing systems, oxygen conserving devices, oxygen concentrators, nebulizers, low-pressure hose assemblies, humidifiers, heat and moisture exchangers, respiratory gas monitors, respiration monitors, masks, mouth pieces, resuscitators, breathing tubes, breathing systems filters, Y-pieces and any breathing accessories intended to be used with such devices. The enclosed chamber of an incubator, including the mattress, and the inner surface of an oxygen hood are considered to be gas pathways and are also addressed by this document.This document does not address contamination already present in the gas supplied from the gas sources while medical devices are in normal use.EXAMPLE Contamination arriving at the medical device from gas sources such as medical gas pipeline systems (including the non-return valves in the pipeline outlets), outlets of pressure regulators connected or integral to a medical gas cylinder or room air taken into the medical device is not addressed by ISO 18562 series.This document is intended to be read in conjunction with ISO 18562-1.NOTE This document has been prepared to address the relevant essential principles of safety and performance as indicated in Annex B.Cross References:ISO 7396-1:2016ISO 14971:2007ISO 16000-6:2011ISO 18562-1:2017ASTM D5466-01ISO 10993ISO 16142-1:2016IEC 60601-1All current amendments available at time of purchase are included with the purchase of this document.