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Tuesday, October 4, 2022



SunMed Receives the European Union (EU) Medical Device Regulation (MDR) Certification

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Grand Rapids, MI, September 16, 2022 –(PR.com)– SunMed, a global leader in consumable medical devices for anesthesia and respiratory care, has received Medical Device Regulation (MDR) certification from the European Union (EU) on nine categories of its medical devices.

SunMed, a significant provider of medical products, celebrates its EU MDR certification for Salter Labs product families, including Pressure Infusers (InfuseIT™), Humidifiers, Aerosol Masks, Nebulizers, Monitor Masks, Oxygen Masks, Oxygen Tubing, Oxygen Cannulas and Capnography Cannulas. The EU MDR certification means these products meet the essential requirements of the latest regulatory standards required for medical devices in Europe. Hank Struik, Chief Executive Officer, said, “SunMed is excited to meet this milestone EU MDR achievement enabling us to provide products to the EU which are critical to our customers and the patients they serve. This also…

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