采用ISO 16571:2014，其中规定了医疗器械产生的羽流排放设备的设计、制造、安装、功能、性能、维护、维修、记录、测试和调试的要求和指南。

Adopts ISO 16571:2014 which specifies requirements and guidelines for the design, manufacture, installation, function, performance, maintenance, servicing, documentation, testing, and commissioning of equipment for evacuation of plume generated by medical devices.