LUMENDI RECEIVES FDA 510(k) CLEARANCE FOR ... | 合法醫療器材資訊網
2018年5月29日—SecondGenerationEndoscopicAccessoryforEndolumenalProcedures...asterile,single-use,disposablemonopolarelectrosurgicaldeviceforcutting,...withthecommerciallyavailableDiLumenEIPwithnoseriousdevice ...
Lumendi is pleased to also report that, to date, clinicians in the U.S., several EU countries including Germany, France, Italy, Spain, and the U.K., as well as at the Chinese University of Hong Kong, have completed over 3,000 procedures with the commercially available DiLumen EZ Glide.
“These new products along with the strong market adoption of DiLumen EZ Glide will help accelerate Lumendi’s continued vision to migrate many invasive gastrointestinal surgeries that require hospital stays, higher risks of infection and longer recoveries to much less invasive endoluminal procedures with low complication rates, no hospital stays and very minimal recovery times.” said Dr. Johann. “In addition, based on our success impacting therapeutic procedures in the colon and using our current technology, we have recently started a development program in upper GI interventions tha...
April 17, 2018 Lumendi, LLC John J. Smith | 合法醫療器材資訊網
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LUMENDI RECEIVES 510(k) CLEARANCE FOR DILUMEN Ik ... | 合法醫療器材資訊網
LUMENDI RECEIVES FDA 510(k) CLEARANCE FOR ... | 合法醫療器材資訊網
October 30, 2018 Lumendi, LLC John J. Smith | 合法醫療器材資訊網
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【"羅曼迪" 內視鏡附件 (未滅菌)】許可證字號:衛部醫器輸壹字第021931號
器材品名:"羅曼迪"內視鏡附件(未滅菌)許可證字號:衛部醫器輸壹字第021931號註銷狀態:註銷日期:註銷理由:有效日期:2025/09/04...