FDA Guides Return to Pre-Pandemic Medical Device Enforcement, EUA Policies
The FDA finalized guidance that outlines recommendations regarding the transition of medical device enforcement policies to normal operations
The FDA finalized guidance that outlines recommendations regarding the transition of medical device enforcement policies to normal operations
Researchers reprocessed respirators using vaporized hydrogen peroxide and found that the devices maintained effectiveness with up to 25 cycles of re-use.
The COVID-19 pandemic caused an immeasurable number of delays to the healthcare supply chain, which included a large bulk order of ventilators in Iowa.
The FDA finalized guidance that outlines recommendations regarding the transition of medical device enforcement policies to normal operations
Both melt-blown filter and nanofiber filter N95 masks have similar performance at the time of first use, but after disinfecting and reusing, the nanofiber filter does not exhibit performance deterioration.
Read MoreThe VentMI pressure regulator is designed to allow the use of a single ventilator by multiple individuals.
Read MoreThe demand for infusion pumps has increased phenomenally due to the outbreak of COVID-19.
Read MoreIn response to the global need for ventilators amid the COVID-19 pandemic, Fitbit has quickly developed Fitbit Flow, an automatic resuscitator.
Read MoreIn a study of 12 healthy male volunteers, a wearable biosensor that is placed on the chest, called the VitalScout, provided an accurate assessment of physiological parameters—heart rate and respiration rate—that are used to calculate stress.
Read MoreThe Joint Commission will begin resuming some survey and review activities in June. But, the accrediting organization emphasizes, safety will be its first priority.
Read MoreThe guidance aims to mitigate equipment shortages by requiring manufacturers to communicate any interruptions in their supply chains that could affect hospitals’ ability to treat patients with COVID-19.