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Patient Monitoring system
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Sotera Wireless Obtained an Approval From FDA for Its CNIBP Technology
Oct 12, 2013Sotera Wireless, a medical device company, has obtained an approval from the US Food and Drug Administration (FDA) for its continuous non-invasive blood pressure (cNIBP) technology, a new feature of the ViSi Mobile wireless patient ...
Tags: cNIBP Technology, Sotera Wireless
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Tensys Medical Obtained SFDA Approval for Its New Continuous
Aug 22, 2013Tensys Medical has obtained State Food & Drug Administration (SFDA) approval for its new continuous, non-invasive hemodynamic patient monitoring system in the People’s Republic of China. The TL-300 T-Line system comprises of a ...
Tags: SFDA Approval, Tensys Medical
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Covidien's Nellcor Pulse Oximeters Has Obtained 510(K) Clearance with Labeling From US FDA
May 29, 2013Patient monitoring and respiratory care devices provider Covidien's Nellcor Pulse Oximeters has obtained 510(k) clearance with labeling from US Food and Drug Administration (FDA). Nellcor Pulse Oximeters facilitates in noninvasive ...
Tags: Covidien's Nellcor, Medicine
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The Nellcor Pulse Oximetry Portfolio, Which Is Used to Measure Arterial Oxygen Saturation
May 23, 2013Covidien has announced that its Nellcor pulse oximetry portfolio received the US Food and Drug Administration (FDA) 510(k) clearance for motion claims. The Nellcor pulse oximetry portfolio, which is used to measure arterial oxygen ...
Tags: Covidien, Motion Claims
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Earlysense Patient Monitoring System in US Is Distributed by Welch Allyn
Feb 1, 2013US based global healthcare company Welch Allyn has entered into a collaboration agreement to distribute EarlySense's continuous, contact-free patient monitoring solution to hospitals across the US. The solution, EarlySense System, is ...
Tags: healthcare company, Welch Allyn, EarlySense patient monitoring solution
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Non-Invasive Hemodynamic Patient Monitoring System Has Obtained 510(K) Clearance
Jan 4, 2013Tensys Medical's new continuous, non-invasive hemodynamic patient monitoring system has obtained 510(k) clearance from the US Food and Drug Administration (FDA). The TL-300 system, a member of T-Line family, is designed for use in ...
Tags: Hemodynamic Patient Monitor, FDA Approval, TL-300 system
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Nellcor Bedside SpO2 Patient Monitoring System Is Introduced by Covidien
Dec 19, 2012Covidien will introduce its Nellcor Bedside SpO2 Patient Monitoring system at the European Society of Anesthesiology Congress held between 9-12 June 2012 in Paris, France. The Nellcor system utilizes OxiMax technology for monitoring ...
Tags: European Society of Anesthesiology Congress, Patient Monitoring system
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FDA Has Granted Clearance to Covidien's Nellcor Bedside SpO2 Patient Monitoring System
Dec 17, 2012The US Food and Drug Administration (FDA) has granted 510(k) clearance to Covidien's Nellcor bedside SpO2 patient monitoring system. The Nellcor bedside SpO2 monitor, which utilizes OxiMax technology, is designed for detecting heart rate ...
Tags: FDA, clearance, Nellcor, SpO2 patient monitoring system, SpO2 monitor
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Covidien Will Market Its Nellcor Bedside Respiratory Patient Monitoring System
Dec 5, 2012Covidien will market its Nellcor bedside respiratory patient monitoring system in the US and European Economic Area (EEA), following the Food and Drug Administration and CE mark approvals. The new system, which can connect to the ...
Tags: respiratory monitoring system, FDA, clinical technology
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