接受检测人士只需呼气,便可得悉有否染疫。
美国食品及药物管理局(FDA)周四向一款能够透过呼气方式检测新冠病毒的设备发出紧急使用授权,是全美首次批准使用上述设备。
FDA称,名为“InspectIR COVID-19 Breathalyzer”的设备检测确诊及证实无染疫的准确率分别达到91.2%和99.3%,需在持有相关牌照的医疗保健提供者监督之下使用。它的体积与行李箱相若,可在医生诊症室、医院及流动检测场所使用,约3分钟左右便有结果。
FDA辖下医疗器械与放射健康中心负责人舒伦形容,上述设备又是一个快速创新的例子。
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