Siemens Healthineers Rapidpoint 500e Blood Gas Analyzer After Europe Launched in europe august 2019, siemens healthineers rapidpoint 500e blood gas analyzer – used for critically ill patients in acute care settings – receives u.s. fda clearance. the siemens healthineers blood gas portfolio is supporting covid 19 response efforts, where blood gas testing plays a critical role in managing infected patients. The rapidpoint® 500e system elevates siemens healthineers blood gas offering to a new level, allowing you to spend more time focused on patient care. implement a proven end to end blood gas solution that reduces the daily burden of device management and enables you to give your full care and attention where it matters most.
Siemens Rapidpoint 500 Blood Gas Analyzer Vrogue Co Empowered by technology. the rapidpoint® 500e system elevates siemens healthineers blood gas offering to a new level, allowing you to spend more time focused on patient care. implement a proven end to end blood gas solution that reduces the daily burden of device management and enables you to give your full care and attention where it matters. Siemens healthineers customer clinical education response to novel coronavirus (covid 19) available now! online pepconnect content for updating from atellica® solution v1.25 to v1.26 and above. click here! the website will be briefly unavailable at today from 10:00 11:00 pm est for unscheduled maintenance. Siemens healthineers ag (listed in frankfurt, germany: shl) is shaping the future of healthcare. as a leading medical technology company headquartered in erlangen, germany, siemens healthineers enables healthcare providers worldwide through its regional companies to increase value by empowering them on their journey towards expanding precision medicine, transforming care delivery, improving. News • blood gas testing aiding covid 19 efforts: fda clearance for blood gas analyzer siemens healthineers announced that its latest critical care testing solution, the rapidpoint 500e blood gas analyzer, has received clearance from the u.s. food and drug administration (fda), and is now available in the u.s., europe and countries requiring the ce mark.
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