Drive Medical Launches Unbound IQ Brand
The new portfolio includes smart monitoring and cueing devices designed to support proactive patient care and data-driven insights.
The new portfolio includes smart monitoring and cueing devices designed to support proactive patient care and data-driven insights.
The new portfolio includes smart monitoring and cueing devices designed to support proactive patient care and data-driven insights.
Read MoreBaxter has recommended removal of certain Duo-Vent solution sets used for administration of fluids to the patient’s vascular system.
Read MoreResmed has recommended corrections to certain Astral 100 and Astral 150 ventilators due to an issue that may result in interrupted therapy.
Read MoreNuvaira treated the first patient treated in a clinical trial evaluating a one-time lung denervation therapy for patients with specific COPD symptoms.
Read MoreHHS secretary Robert F Kennedy, Jr signed determinations to end COVID-19 emergency use authorizations for drugs, biological products, and medical devices because the emergency circumstances no longer exist.
Read MoreDynarex Corp launched a new Resp-O₂ Portable Oxygen Concentrator and a new line of infant- and pediatric-sized closed suction catheters.
Read MoreBaxter issued an Urgent Medical Device Correction notice for all Volara System patient circuits to be corrected prior to continued use, according to an FDA alert.
Read MoreHamilton Medical issued updated use instructions for certain coaxial breathing circuit sets used with Hamilton-C1, Hamilton T-1, and Hamilton-MR1 ventilators, according to an FDA alert.
Read MoreGE HealthCare has issued a letter to affected customers recommending Infant Resuscitation Systems and Warmers with a M1091607-R blender be corrected prior to continued use, according to an FDA alert.
Read MoreReact Health is removing certain VOCSN V+Pro units due to a potential oxygen leak condition prior to or during ventilation.
Read MoreFujifilm’s EB-710US Ultrasound Bronchoscope features a balloon-less design to streamline workflow and reduce infection risks during pulmonary care.
Read MoreA manufacturing error in the ventilator motor assembly may cause mechanical ventilation to fail before or during use, according to an FDA early alert.
Read MorePhase 1 results for the inhaled drug candidate ALX1 focus on safety and pharmacokinetics for the treatment of serious lung diseases.
Read MoreMechanical ventilation is one of the most common ICU interventions, and understanding and accurately interpreting ventilator graphics may reduce risks and improve patient outcomes.
Read MoreThe Draeger Evita V800 is designed to improve clinical workflows and support lung protection for patients of all ages.
Read MoreThe DeVilbiss by Drive 555 model is designed to improve provider efficiency and reduce operating costs for patients.
Read MorePhilips has issued a recall for Trilogy ventilators be corrected prior to continued use, according to an FDA alert. The alert includes Trilogy Evo, Trilogy EV300, Trilogy Evo O2, and Trilogy Evo Universal devices.
Read MoreRemote respiratory services enable Veterans to receive guided therapy and specialist consultations from home.
Read MorePerma Pure and Maxtec have unified under a new parent company, Salaera, to form a global technology platform for breath and gas systems.
Read MoreFor most chronic lung disease patients, their health depends on the consistent clearance of airway secretions. In this Q&A, RT will speak with industry leaders on advances in secretion clearance technology.
Read MoreKreg’s national agreement with Premier includes a breakthrough technology designation for a specialty bed that supports early mobility for bariatric patients.
Read MoreMaison, Porush & Theil — inventors of the pressure metered dose inhaler (pMDI) — will be posthumously inducted into the National Inventors Hall of Fame in May 2026.
Read MoreDry powder and soft mist inhalers—which have a lower carbon footprint than metered-dose inhalers (MDIs)—were associated with slightly better clinical outcomes for COPD patients.
Read MoreResmed’s new AirTouch F30i Comfort full face CPAP mask is now available in the United States, Canada, Australia, and New Zealand.
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