BreatheLink Mobile App for Overnight Oximetry Testing
The BreatheLink platform allows patients to transmit overnight oximetry data from their own smartphones, reducing the time required to set up home oxygen therapy.
The BreatheLink platform allows patients to transmit overnight oximetry data from their own smartphones, reducing the time required to set up home oxygen therapy.
The BreatheLink platform allows patients to transmit overnight oximetry data from their own smartphones, reducing the time required to set up home oxygen therapy.
Read MoreFrom assessing hypoxia and supplemental oxygen needs in respiratory patients to screening obstructive sleep apnea and evaluating dental sleep appliances, overnight pulse oximetry (OPO) offers noninvasive, cost-effective monitoring, as new technologies further streamline care.
Read MoreResearchers developed a soft, skin-like nasal patch to track sleep apnea breathing patterns without the need for bulky tubes or wires.
Read MoreThe new suite integrates workflows for COPD, lung nodules, and pulmonary embolism to improve patient follow-up and treatment times.
Read MoreThe CO Check Pro is designed for use in both smoking cessation programs and emergency healthcare settings for the detection of carbon monoxide poisoning.
Read MoreA Mayo Clinic study demonstrates that at-home monitoring provides actionable data and reduces the travel burden for post-transplant patients.
Read MoreA Mayo Clinic study indicates that home monitoring kits can identify early complications and reduce travel burdens for transplant recipients.
Read MoreResearchers developed a contactless method using radio frequency identification (RFID) technology to track respiratory function.
Read MoreSleep metrics from wrist monitors can identify which COPD patients may need more support during pulmonary rehab.
Read MoreMasimo Corp will be acquired by Danaher Corp for $9.9 billion, according to multiple media reports including Reuters.
Read MoreZoll Medical’s Zenix monitor/defibrillator is now approved under the European Union’s Medical Device Regulation 2017/745, commonly referred to as EU MDR.
Read MoreSalaera’s MaxO2 ME+p devices are designed to help hospitals meet monitoring guidelines and improve patient safety during respiratory therapies.
Read MoreSentec’s tCOM+ provides continuous carbon dioxide and oxygen data to improve workflow and support ventilator management across healthcare settings.
Read MoreThe Hans Rudolph SmartLab system with Insight software offers modular sensing and real-time analysis for research applications.
Read MoreNonin Medical’s WristOx2 Model 3150 offers oxygen saturation and pulse rate monitoring for patients in home and hospital settings.
Read MoreThe Vision system and weaning application use real-time data to identify emergent conditions and help clinicians reduce ventilator time.
Read MoreThe VitalFlow ECMO system is designed to simplify bedside monitoring and patient transport within healthcare facilities.
Read MoreHeartBeam’s 12-lead ECG synthesis software allows patients to obtain an ECG reading for their arrhythmia from the comfort of home, with results promptly reviewed by an on-demand, board-certified cardiologist.
Read MoreThe company’s Board of Directors has appointed industry veteran and respiratory therapist Todd Austin as Nonin Medical’s next CEO.
Read MoreA US-based jury ordered Apple to pay $634 million for infringing Masimo’s patent for blood oxygen monitoring technology in its Apple Watch.
Read MoreGE HealthCare’s Carevance patient monitor includes advanced patient monitoring and new perioperative hypotension management capability.
Read MoreThe INSPIRE Trial prospectively assesses pulse oximeter accuracy using a unique real-world study design and in the feasibility study showed no clinically significant bias between patients with light and dark skin tones and no occult hypoxemia.
Read MoreNihon Kohden has launched AlarmSense, an advanced, data-driven analytics solution designed to combat widespread alarm fatigue.
Read MoreZoll Medical’s Zenix monitor/defibrillator has received premarket approval (PMA) from the US FDA, according to the company.
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