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  • Penumbra Announces FDA Approval of RED 62 Perfusion Catheter »Cardiology2.0

    Penumbra, Inc. (NYSE: PEN) is a global healthcare company focused on innovative therapies. Its RED™ 62 reperfusion catheter has been approved by the U.S. Food and Drug Administration (FDA) 510(k)

  • This amphibious electric tricycle (and camper) costs $14,600

    A Latvian startup has developed an amphibious electric tricycle that will take you from the road to the water to the campsite — if you’re willing to pay a premium for your next recreati

  • Darryl Rozelle Discusses Medical Molding That Is FDA Approved

    As a professional engineer, Darryl Rozelle from Chaska, Minnesota, solves complex problems. With over 30 years of experience, Darryl Rozelle specializes in manufacturing process development. Medica

  • Biliary obstruction and pancreatitis after duodenal stent placement in the descending duodenum: a retrospective study | BMC Gastroenterology | Full Text

    BMC Gastroenterology volume  22, Article number: 257 (2022 ) Cite this article

    Metal

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  • Catheter Coatings Market Opportunity Analysis, Trends, and Business Strategies | Forecast- 2023 – mainlander.nz

    According to a new report published by Allied Market Research, titled, “Catheter Coatings Market by Material and Type:  Opportunity Analysis and Industry Forecast, 2019–2026,”the global

  • Arrow International Inc recalls Arrow-Trerotola Over-The-Wire PTD Kit percutaneous thrombolysis device: 7Fr due to separation risk | Food and Drug Administration

    .gov means it is official. Federal government websites usually end in .gov or .mil. Before sharing sensitive information, make sure you are visiting a federal government website.

    The website

  • Catheter Stabilization Devices Market – Challenges to Implement Digital Transformation, Key Players – Koninklijke Philips N.V PARI Pharma Allied Healthcare. – Industrial IT

    Your Go To News Portal

    New York, United States: Our group of research wizards has designed and outlined an exceptional report on the Catheter Stabilization Devices market that includes a 3

  • Intra-aortic balloon pumps recalled due to fluid leak issue

    The FDA announced it designated a recall of intra-aortic balloon pumps due to problems related to fluid leak as class 1, the most serious type.

    The recall by Getinge/Datascope/Maquet of th

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