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Author Archive for: panglobal
Entries by panglobal
Cuviva receives MDR certification – paves the way for international growth
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 expand partnership to improve telehealth for patients and clinicians with Masimo W1 Watch
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 launches new premium video processor and endoscope series
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 […]
JVCKENWOOD monitors get tech upgrade
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+ launches clinical trial services
RQM+ has launched its clinical trial services division to complete its full complement of MedTech contract research organization (CRO) services.
Bayer’s Ultravist approved for contrast-enhanced mammography in EU
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 introduces implantable PEEK film
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 receives FDA clearance, CE Mark for Halcyon and Ethos radiotherapy systems
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’s Carevix soft-suction cervical device receives FDA clearance
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 […]