FDA宣布碧迪医疗于7月8日在美国扩大一级自愿召回范围,告知特定Alaris泵输液器最坏情况下的性能表现
FDA宣布碧迪医疗于7月8日在美国扩大一级自愿召回范围,告知特定Alaris泵输液器最坏情况下的性能表现
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