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Archive for category: Product News

Products News

Cuviva receives MDR certification – paves the way for international growth

, 23 February 2023/in Product News /by panglobal

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.

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https://interhospi.com/wp-content/uploads/sites/3/2023/02/Schermafbeelding-2023-02-23-om-12.58.57-e1677153789118.png 1324 2146 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2023-02-23 12:01:562023-02-23 12:04:08Cuviva receives MDR certification – paves the way for international growth

Philips and Masimo expand partnership to improve telehealth for patients and clinicians with Masimo W1 Watch

, 23 February 2023/in Product News /by panglobal

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.

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https://interhospi.com/wp-content/uploads/sites/3/2023/02/masimo-w1-photo.download-scaled.jpg 1248 2560 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2023-02-23 11:54:202023-02-23 11:54:20Philips and Masimo expand partnership to improve telehealth for patients and clinicians with Masimo W1 Watch

PENTAX Medical launches new premium video processor and endoscope series

, 23 February 2023/in Product News /by panglobal

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 […]

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https://interhospi.com/wp-content/uploads/sites/3/2023/02/Pentax_INSPIRA.jpg 1672 2507 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2023-02-23 11:49:352023-02-23 11:49:35PENTAX Medical launches new premium video processor and endoscope series

JVCKENWOOD monitors get tech upgrade

, 23 February 2023/in Product News /by panglobal

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.

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https://interhospi.com/wp-content/uploads/sites/3/2023/02/JVCKENWOOD_monitor.png 1130 1416 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2023-02-23 11:45:352023-02-23 11:45:35JVCKENWOOD monitors get tech upgrade

RQM+ launches clinical trial services

, 23 February 2023/in Product News /by panglobal

RQM+ has launched its clinical trial services division to complete its full complement of MedTech contract research organization (CRO) services.

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Bayer’s Ultravist approved for contrast-enhanced mammography in EU

, 23 February 2023/in Product News /by panglobal

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.

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https://interhospi.com/wp-content/uploads/sites/3/2023/02/bayer_ultravist.jpg 1280 1124 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2023-02-23 11:36:012023-02-23 11:36:01Bayer’s Ultravist approved for contrast-enhanced mammography in EU

Genesis Medical Plastics introduces implantable PEEK film

, 23 February 2023/in Product News /by panglobal

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.

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https://interhospi.com/wp-content/uploads/sites/3/2023/02/Genesis-PEEK-film.png 678 906 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2023-02-23 11:31:282023-02-23 11:31:28Genesis Medical Plastics introduces implantable PEEK film

Varian receives FDA clearance, CE Mark for Halcyon and Ethos radiotherapy systems

, 23 February 2023/in Product News /by panglobal

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 […]

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https://interhospi.com/wp-content/uploads/sites/3/2023/02/Varian-Halcyon.png 1076 1678 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2023-02-23 11:26:532023-02-23 11:26:53Varian receives FDA clearance, CE Mark for Halcyon and Ethos radiotherapy systems

ASPIVIX’s Carevix soft-suction cervical device receives FDA clearance

, 23 February 2023/in Product News /by panglobal

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 […]

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https://interhospi.com/wp-content/uploads/sites/3/2023/02/ASPIVIX-Carevix.png 1140 1834 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2023-02-23 11:22:172023-02-23 11:22:17ASPIVIX’s Carevix soft-suction cervical device receives FDA clearance

Mindray defibrillators amongst the world’s first to receive EU Medical Device Regulation certification

, 23 February 2023/in Product News /by panglobal

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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https://interhospi.com/wp-content/uploads/sites/3/2023/02/Mindrays-BeneHeart-Defibrillator-1-scaled.jpg 1634 2560 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2023-02-23 11:16:462023-02-23 11:16:46Mindray defibrillators amongst the world’s first to receive EU Medical Device Regulation certification
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