The Cuviva RPM Platform is now certified according to MDR Class IIa. This makes Cuviva RPM Platform one of the first complete platforms certified according to MDR Class IIa for Remote Patient Monitoring and Hospital at Home. The certification demonstrates increased patient safety and efficiency of healthcare, and opens up for further extensive development.
Philips and Masimo have announced an expansion of their partnership to augment patient monitoring capabilities in home telehealth applications with the Masimo W1 advanced health tracking watch.
PENTAX Medical, a division of HOYA Group, has obtained CE marks for two of its latest innovations; PENTAX Medical INSPIRA, the new premium video processor, and the i20c video endoscope series. Developed with a focus on healthcare providers’ needs, the new video processor maintains compatibility with PENTAX Medical’s recent endoscope models, and sets new standards […]
Five years ago, JVCKENWOOD redesigned its monitors from the ground up and launched the i3 Series – kicking off a success story. At first glance, the new housing design stood out; the displays were significantly narrower than in the previous generation.
RQM+ has launched its clinical trial services division to complete its full complement of MedTech contract research organization (CRO) services.
Bayer’s iodine-based contrast agent Ultravist-300, -370 is now approved for contrast-enhanced mammography (CEM) in the EU. The product can be used to evaluate and detect lesions of the breast as an adjunct to mammography (with or without ultrasound) or as an alternative when a magnetic resonance imaging (MRI) is contraindicated or unavailable.
Genesis Medical Plastics has developed production-scale calendering to convert medical grade and implantable PEEK into thin sheet and film. The technology adds to the medical polymer conversion services it provides in injection moulding, extrusion of machinable shapes, and CNC machining.
Varian, a Siemens Healthineers company, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA), as well as CE mark, for Halcyon and Ethos radiotherapy systems featuring Varian’s HyperSight imaging solution. On February 1, a cancer patient at Penn Medicine became the first person in the world to be treated on a Halcyon […]
ASPIVIX SA, an innovator and developer of medical technologies to advance gynaecological care, announced that Carevix, its novel cervical stabilizer, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA). This next generation device for routine procedures in gynaecology will allow millions of women across the USA access to significantly less painful treatments […]
Medical device provider Mindray has become one of the first manufacturers in the world to receive certification for its defibrillators, under the European Union’s newest Medical Device Regulation (MDR).
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