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VA Selects Philips to Create World’s Largest Tele-Critical Care System

Royal Philips has announced that the U.S. Department of Veterans Affairs (VA) has awarded a contract to Philips to expand VA’s tele-critical care program, creating the world’s largest system to provide veterans remote access to intensive care expertise, regardless of...

BD Launches First and Only Fully Sterile Povidone-Iodine and Isopropyl Alcohol Skin Preparation

BD (Becton, Dickinson and Company) has announced the availability of BD PurPrep patient preoperative skin preparation with sterile solution, the first and only fully sterile povidone-iodine plus isopropyl alcohol single-use antiseptic skin preparation (PVP-I; 0.83%...

PDI Receives Promising Testing Results of Super Sani-Cloth Wipes Against SARS-COV-2

PDI has generated data showing its Super Sani-Cloth wipes are effective against SARS-CoV-2, the virus that causes COVID-19. This is one of several of the company's hospital-grade disinfecting products being tested for efficacy against SARS-CoV-2 for submission to the...

New Dräger Solution Aims to Improve Long-Term Acute Care Outcomes

Dräger has leveraged its 100+ years of critical care expertise to develop a new solution designed specifically to address the needs of the long-term acute care (LTAC) environment. With Dräger’s solution, LTAC facilities can maintain quality throughout the continuum of...

FDA Issues Emergency Use Authorization for Ventilators

Yesterday, the U.S. Food and Drug Administration (FDA) took action to make more ventilators available to health care personnel in the United States. The FDA issued an emergency use authorization for ventilators, anesthesia gas machines modified for use as ventilators, and positive pressure breathing devices modified for use as ventilators (collectively referred to as “ventilators”), ventilator tubing connectors, and ventilator accessories.

Yesterday’s emergency use authorization allows ventilators, anesthesia gas machines modified for use as ventilators, and positive pressure breathing devices modified for use as ventilators, ventilator tubing connectors, and ventilator accessories to be used in health care settings during the coronavirus (COVID-19) pandemic.

Manufacturers and other stakeholders may submit a request to the FDA under the process outlined in the EUA to have their device(s) added to the EUA.

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