Philips receives 510(k) clearance from the FDA for its professional defibrillator (Tempus LS- Manual), now offering its remote monitor and defibrillator solution (Tempus ALS) to EMS customers in the U.S.
Solution delivers real-time bidirectional data transfer for remote patient monitoring, giving EMS responders a new approach to pre-hospital care.
飛利浦的專業除顫器(Tempus LS-Manual)已獲得FDA的許可,提供美國EMS客戶結合遠端監測儀和除顫器之解決方案(Tempus ALS)。
該解決方案可提供雙向即時數據傳輸以進行遠端病人監測,從而提供完善的醫療照護。
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