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Ambu to launch US FDA approved sterile, single-use duodenoscope, aScope Duodeno
The Ambu, a company develop, produce and market diagnostic and life-supporting devices for hospitals and rescue services, announced that it has received 510(k) clearance from the US Food and Drug Administration (FDA) for aScope Duodeno on 17 July 2020 and is now ready for commercial launch as planned
US FDA Approved Sterile, Single-use Duodenoscope, | 20/07/2020 | By Darshana | 524
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