发布日期:2023年11月20日召回级别:Ⅱ级召回编号:RC-2023-RN-00941-1召回产品:ResMed磁吸式口罩产品批次:AirFit N10,AirFit N10 for Her,AirFit N20,AirFit N20 for Her,AirTouch N20,AirTouch N20 for Her,AirFit F20,AirFit F20 for ...发布日期:2023年11月20日召回级别:Ⅱ级召回编号:RC-2023-RN-00941-1召回产品:ResMed磁吸式口罩产品批次:AirFit N10,AirFit N10 for Her,AirFit N20,AirFit N20 for Her,AirTouch N20,AirTouch N20 for Her,AirFit F20,AirFit F20 for Her,AirTouch F20,AirTouch F20 for Her,AirFit F30,AirFit F30 for Her,注册登记号:300769和300768(Resmed Limited-CPAP/BiPAP口罩可重复使用).展开更多
文摘发布日期:2023年11月20日召回级别:Ⅱ级召回编号:RC-2023-RN-00941-1召回产品:ResMed磁吸式口罩产品批次:AirFit N10,AirFit N10 for Her,AirFit N20,AirFit N20 for Her,AirTouch N20,AirTouch N20 for Her,AirFit F20,AirFit F20 for Her,AirTouch F20,AirTouch F20 for Her,AirFit F30,AirFit F30 for Her,注册登记号:300769和300768(Resmed Limited-CPAP/BiPAP口罩可重复使用).