摘要:最近,美国FDA批准了美敦力公司推出的两种Visia AF植入式复律除颤器(ICD)用于诊断和治疗新房颤动患者。与目前美国市场上的植^式复律除颤器类似,这两种产品属于单室除颤器,按计划这两种产品将于今年夏天上市。美敦力此次获批的两种产品将能够帮助医生尽早确诊患者并及时治疗,从而最大限度降低患者发生更严重病情的风险。此次两种ICD产品爰用了最新算法,能够准确检测到患者心率不正常波动,从而及时发现患者出现心房颤动的征兆,该产品已经获得了CE认证。
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