The defibrillation lead, approved for placement in the left bundle branch area, can deliver both life-saving shock therapy and physiologic pacing through the heart's natural electrical system.
A patient using a defibrillator died at a southern-based medical center after the device erupted in fire and burned his body.
The specialist biomed team at the Deaconess Midtown Hospital is using a Rigel UniPulse 400 defibrillator analyzer for the maintenance of its defibrillators.
The defibrillation lead, approved for placement in the left bundle branch area, can deliver both life-saving shock therapy and physiologic pacing through the heart's natural electrical system.
The government alleges that St. Jude failed to disclose serious adverse health events in connection with the premature depletion of the battery in certain models of its implantable defibrillators.
Read More
Placing an iPhone 12 or its magnet-containing MagSafe accessories near a pacemaker can interfere with the medical device’s ability to function.
Read More
FDA has changed the deadline for filing PMA applications for previously cleared AED accessories in response to the impact from COVID-19.
Read More
A formalized protocol to transfer AED data upon hospital arrival for cardiac arrest patients may help staff decision-making and lessen the strain on hospital resources.
Read More
Royal Philips has launched a wireless remote monitoring and defibrillator solution (Tempus ALS) for pre-hospital settings in the United States.
Read More
Philips has resumed the manufacturing and shipping of external defibrillators for the United States, following FDA notification that the injunction prohibiting those activities has been lifted.
Read More
The defibrillators market is forecast to reach $10.88 billion by 2022 from $9.32 billion in 2017 at a compound annual growth rate (CAGR) of 3.1%, according to market research firm ReportsnReports.
