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Home » FDA clears Ambu single-use duodenoscope

FDA clears Ambu single-use duodenoscope

July 17, 2020 By Chris Newmarker

Ambu aScope Duodeno single-use duodenoscope
Ambu’s aScope Duodeno single-use duodenoscope [Image courtesy of Ambu]
Ambu announced today that FDA has cleared its aScope Duodeno — a sterile, single-use duodenoscope meant to avoid the deadly superbug outbreaks that cropped up around reusable versions of the scopes.

Other companies — including Boston Scientific (NYSE:BSX),  Hoya’s (TYO:7741) Pentax subsidiary, and Olympus (TYO:7733) — have been releasing either fully disposable duodenoscopes or duodenoscopes with disporable endcaps or disposable elevators.

Duodenoscopes provide a less invasive way than traditional surgery to drain fluids from pancreatic and biliary ducts blocked by cancerous tumors, gallstones or other gastrointestinal conditions — with an estimated 600,000 procedures conducted annually in the United States.

FDA has been pushing duodenoscope makers to change designs, and CMS has been working to speed up Medicare beneficiaries’ access to single-use endoscopes.

“At Ambu, we are determined to advance patient safety through innovative design of single-use devices, and we are excited to improve safety for the 2 million patients each year who require an ERCP (endoscopic retrograde cholangio-pancreatography) procedure,” said Juan Jose Gonzalez, CEO of Ambu A/S (Copenhagen, Denmark).

“It’s no longer necessary to balance the necessity of the procedure against the risk of infection from a reusable endoscope. Now, both doctor and patient can focus on diagnosis and treatment by using a sterile, single-use duodenoscope,” Gonzalez said in a news release.

Ambu will initiate a 500-patient post-market study at multiple U.S. centers and will release a sub-set of the study during Q1 of its 2020/21 financial year.

Ambu plans to introduce 15 new devices across all major areas of endoscopy over the next three years. The company in May announced the launch of its Ambu aView 2 Advance display unit for use with endoscopes in Europe and the U.S.

Filed Under: 510(k), Endoscopic, Featured, Food & Drug Administration (FDA), News Well, Regulatory/Compliance Tagged With: Ambu, duodenoscope

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About Chris Newmarker

Chris Newmarker is the executive editor of WTWH Media life science's news websites and publications including MassDevice, Medical Design & Outsourcing and more. A professional journalist of 18 years, he is a veteran of UBM (now Informa) and The Associated Press whose career has taken him from Ohio to Virginia, New Jersey and, most recently, Minnesota. He’s covered a wide variety of subjects, but his focus over the past decade has been business and technology. He holds bachelor’s degrees in journalism and political science from Ohio State University. Connect with him on LinkedIn or email at [email protected].

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