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Chris Newmarker on Muck Rack

Chris Newmarker

Verified
Minneapolis
As seen in: Drug Discovery & Development, Mass Device, Medical Design & Outsourcing, Medical Tubing + Extrusion, Pharmaceutical Processing World, Entrepreneur, Inc., NewsBreak, The Robot Report, R&D World, Robotics Business Review, Medical Device and Diagnostic Industry (MDDI), Finance & Commerce, Our Community Now, Qmed and
A journalist for over 20 years, I am executive editor of Life Sciences at WTWH Media. Media outlets include MassDevice, Medical Design & Outsourcing and more.
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Articles

Philips has a new single-transducer offering for its women’s health ultrasound

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By Chris Newmarker Verified
| Mass Device Verified
The eV14-2v is meant to minimize the need to switch between transducers during ultrasound exams in gynecology and obstetrics. [Image courtesy of Philips] Philips (NYSE: PHG)  is expanding its obstetrics and gynecology ultrasound portfolio with the introduction of the eV14-2v transvaginal transducer. FDA 510(k) cleared and CE-marked, the eV14-2v combines image quality and broad clinical capabilities in a single lightweight transducer, according to Philips.
Open in Who Shared View Duplicates (8) Issue with article?

Globus Medical wins CE mark for Excelsius3D imaging system

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By Chris Newmarker Verified
| Mass Device Verified
The Excelsius3D intelligent 3-in-1 imaging system [Image courtesy of Globus Medical] Globus Medical (NYSE: GMED) has secured a CE mark for its Excelsius3D intelligent 3-in-1 imaging system for spine and cranial procedures. The regulatory approval in the EU, announced yesterday, comes five years after the system’s FDA clearance in the U.S. With a CE mark, Audubon, Pennsylvania–based Globus kicks off commercialization of Excelsius3D in the European Union and United Kingdom.
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Medtronic says Endurant stent graft’s new CE mark could boost use for ruptured AAA

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By Chris Newmarker Verified
| Medical Tubing + Extrusion Verified
The Endurant stent graft system. [Image courtesy of Medtronic] Medtronic (NYSE: MDT) has secured a CE mark for its Endurant stent graft, removing a treatment warning related to its use in ruptured abdominal aortic aneurysms (AAA). The Minnesota-run medtech giant received a similar FDA labeling change in late 2025. A ruptured AAA occurs when the main artery in the abdomen bursts, causing severe internal bleeding and the need for immediate emergency surgical intervention.
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