Successful large bore closure with a device that is simple to use and does not require pre-closure, saving valuable time during the most delicate interventional procedures.
Low complication rates for fast reliable biomechanical closure with rapid hemostasis, potentially reducing costs.1a,b
Reproducible results, inspiring confidence in achieving successful closure.1c
“FDA premarket approval is another important milestone for the MANTA™ Vascular Closure Device,” said Stewart Strong, President and General Manager of the Interventional business unit of Teleflex. “Our commercial efforts in 2019 will include a measured launch of the MANTA™ Device to ensure strong initial outcomes with key thought leading physicians as we further invest in building the commercial infrastructure to support the long-term growth of MANTA™ Device revenues.”
About Teleflex Incorporated
Teleflex is a global provider of medical technologies designed to improve the health and quality of people’s lives. We apply purpose driven innovation – a relentless pursuit of identifying unmet clinical needs – to benefit patients and healthcare providers. Our portfolio is diverse, with solutions in the fields of vascular access, interventional cardiology and radiology, anesthesia, emergency medicine, surgical, urology and respiratory care. Teleflex employees worldwide are united in the understanding that what we do every day makes a difference. For more information, please visit teleflex.com.
Teleflex is the home of Arrow®, Deknatel®, Hudson RCI®, LMA®, Pilling®, Rusch®, UroLift®, and Weck® – trusted brands united by a common sense of purpose.
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