2022/07/06 MiiS Disposable ENT Nasopharyngoscope Receives U.S. FDA 510(k) Clearance

MiiS announced United States Food and Drug Administration (FDA) 510(k) clearance for its first disposable nasopharyngoscope (EES 100), which has also obtained the Class II medical device license from Taiwan Food and Drug Administration (TFDA) in May.


EES 100 is comprised of a flexible insertion tube with fully integrated LEDs and micro camera module and is used in minimally invasive procedures. Its micro camera module provides high resolution image that details features for diagnosis. EES 100 offers the benefit of reducing the risk of a postoperative infection caused by cross-contamination thus improving patient outcomes. As a single-use endoscope, there is also no re-sterilization process involved nor extra cost incurred.


More information: https://www.miis.com.tw/products_detail.php?lang=us&id=83&last_page=2&last_id=

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