Ambu has obtained 510(k) regulatory clearance from the US Food and Drug Administration (FDA) for its new-generation duodenoscopy solution, the aScope Duodeno 2 and aBox 2, which is designed for ...
From October 2011 to September 2012, 16 patients underwent loop duodeno-enterostomies for bariatric surgery. Explicit written informed consent for operation and data recording was obtained from ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback