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FDA investigates reports of urological endoscope infections

FDA investigates urological endoscopes

The Food and Drug Administration (FDA) announced it is investigating reports of infections associated with reprocessed urological endoscopes. The FDA received more than 450 medical device reports (MDRs) describing post-procedure patient infections or other contamination issues associated with reprocessing urological endoscopes. Andersen’s EOGas 4 presents an FDA-cleared terminal sterilization option for the urological endoscopes under investigation, as well as significantly longer and smaller diameter scopes.

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Andersenโ€™s EOGas 4 is ๐˜๐—ต๐—ฒ ๐—ณ๐—ถ๐—ฟ๐˜€๐˜, ๐—ฎ๐—ป๐—ฑ ๐—ผ๐—ป๐—น๐˜†, ๐˜€๐˜๐—ฒ๐—ฟ๐—ถ๐—น๐—ถ๐˜‡๐—ฎ๐˜๐—ถ๐—ผ๐—ป ๐˜€๐˜†๐˜€๐˜๐—ฒ๐—บ ๐—™๐——๐—” ๐Ÿฑ๐Ÿญ๐Ÿฌ(๐—ธ) ๐—ฐ๐—น๐—ฒ๐—ฎ๐—ฟ๐—ฒ๐—ฑ ๐—ณ๐—ผ๐—ฟ ๐˜๐—ฒ๐—ฟ๐—บ๐—ถ๐—ป๐—ฎ๐—น ๐˜€๐˜๐—ฒ๐—ฟ๐—ถ๐—น๐—ถ๐˜‡๐—ฎ๐˜๐—ถ๐—ผ๐—ป ๐—ผ๐—ณ ๐—ฑ๐˜‚๐—ผ๐—ฑ๐—ฒ๐—ป๐—ผ๐˜€๐—ฐ๐—ผ๐—ฝ๐—ฒ๐˜€ ๐—ฎ๐—ป๐—ฑ ๐—ฐ๐—ผ๐—น๐—ผ๐—ป๐—ผ๐˜€๐—ฐ๐—ผ๐—ฝ๐—ฒ๐˜€. A true game changer for healthcare facilities that sterilize these critical instruments. On a recent ๐—•๐—ฒ๐˜†๐—ผ๐—ป๐—ฑ ๐—–๐—น๐—ฒ๐—ฎ๐—ป podcast, Ted May, Andersen President and CEO, and Dr. Larry Muscarella of LFM Healthcare Solutions LLC, take you ๐—ถ๐—ป๐˜€๐—ถ๐—ฑ๐—ฒ ๐˜๐—ต๐—ฒ ๐˜€๐—ฐ๐—ถ๐—ฒ๐—ป๐—ฐ๐—ฒ behind this one-of-a-kind sterilization technology ๐—ฝ๐—ฟ๐—ผ๐˜ƒ๐—ฒ๐—ป ๐˜๐—ผ ๐˜€๐˜๐—ฒ๐—ฟ๐—ถ๐—น๐—ถ๐˜‡๐—ฒ the toughest endoscopes on the market. MORE…

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