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Archive for category: Product News

Products News

Paragon 28 introduces intramedullary nail system for fibular fracture repair

Paragon 28 introduces intramedullary nail system for fibular fracture repair

, 28 October 2024/in Product News /by panglobal

Paragon 28, Inc. has launched the Phantom® Fibula Nail System, offering a less invasive approach to fibular fracture treatment in ankle injuries. The system, designed to provide an alternative to traditional plate and screw fixation, purportedly addresses some of the complications associated with external fixation methods.

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https://interhospi.com/wp-content/uploads/sites/3/2024/10/Paragon_28.jpg 962 1347 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2024-10-28 01:00:492024-10-28 07:55:56Paragon 28 introduces intramedullary nail system for fibular fracture repair
GE Healthcare Venue PoC ultrasound

GE HealthCare expands point-of-care ultrasound portfolio with new Venue Sprint and enhanced Venue systems

, 25 October 2024/in Product News /by panglobal

GE HealthCare has introduced the Venue Sprint, a new tablet-based ultrasound device, alongside enhancements to its existing Venue family of point-of-care ultrasound (POCUS) systems. The launch aims to address the growing demand for portable, high-quality imaging solutions in various clinical settings.

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https://interhospi.com/wp-content/uploads/sites/3/2024/10/GE-Venue-PoC-ultrasound.jpg 968 776 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2024-10-25 08:00:202024-10-17 13:15:44GE HealthCare expands point-of-care ultrasound portfolio with new Venue Sprint and enhanced Venue systems
GE Healthcare Versana Premier ultrasound

GE HealthCare unveils Versana Premier ultrasound system for multi-purpose practices

, 24 October 2024/in Product News /by panglobal

GE HealthCare has introduced the Versana Premier, a new multi-purpose ultrasound system designed to meet the diverse needs of healthcare professionals across various clinical specialties. The system, which forms part of the Versana ultrasound family, incorporates artificial intelligence (AI) and automated productivity tools to streamline workflow and improve clinical efficiency.

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https://interhospi.com/wp-content/uploads/sites/3/2024/10/Versana-Premier-ultrasound.jpg 829 795 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2024-10-24 08:00:572024-10-17 13:10:09GE HealthCare unveils Versana Premier ultrasound system for multi-purpose practices
Catalyst OrthoScience

Catalyst OrthoScience receives FDA clearance for novel shoulder fracture system

, 23 October 2024/in Product News /by panglobal

Catalyst OrthoScience, a medical technology company specialising in shoulder arthroplasty, has announced FDA 510(k) clearance for its Catalyst Fracture Shoulder System. The system, designed for reverse shoulder arthroplasty in cases of proximal humeral fractures (PHFs), aims to tackle the complexities associated with tuberosity fixation and healing.

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https://interhospi.com/wp-content/uploads/sites/3/2024/10/Catalyst-OrthoScience.jpg 1077 1915 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2024-10-23 08:00:222024-10-17 12:56:09Catalyst OrthoScience receives FDA clearance for novel shoulder fracture system
New flow cytometry guidelines support bioAffinity’s lung cancer test

New flow cytometry guidelines support bioAffinity’s lung cancer test

, 22 October 2024/in Product News /by panglobal

bioAffinity Technologies’ Vice President of Diagnostics, Dr Jennifer Rebeles, has contributed to a new set of guidelines for flow cytometry testing on rare matrix samples. The peer-reviewed paper, published in Cytometry Part B: Clinical Cytometry, addresses the challenges and considerations in validating assays with unique sample types.

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https://interhospi.com/wp-content/uploads/sites/3/2024/10/lungs.jpg 936 1230 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2024-10-22 08:00:572024-10-17 12:58:02New flow cytometry guidelines support bioAffinity’s lung cancer test
Atricure EnCompass Clamp

AtriCure’s EnCompass Clamp receives CE mark approval

, 21 October 2024/in Product News /by panglobal

AtriCure has announced regulatory approval for the sale of its EnCompass® Clamp in CE-marked countries within the European Union. This development follows the device’s FDA 510(K) clearance and subsequent launch in the United States in 2022.

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https://interhospi.com/wp-content/uploads/sites/3/2024/10/Atricure-EnCompass-Clamp.jpg 700 1314 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2024-10-21 08:30:272024-10-17 12:59:08AtriCure’s EnCompass Clamp receives CE mark approval
ARIETTA 750 FF ENDO

FUJIFILM Healthcare Europe expands compatibility of ARIETTA 750 FF ENDO ultrasound system

FUJIFILM, ultrasound, 23 September 2024/in Imaging, Product News, Ultrasound /by panglobal

FUJIFILM Healthcare Europe has announced that its high-end ultrasound system, the ARIETTA 750 FF ENDO, is now compatible with FUJIFILM’s ultrasound endoscopes and endobronchial ultrasound scope. This advancement allows clinicians to fully leverage FUJIFILM’s endoscopic technology during diagnostic and therapeutic procedures.

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https://interhospi.com/wp-content/uploads/sites/3/2024/09/arietta-750-ff-endo-and-scopes.png 537 816 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2024-09-23 10:29:252024-09-23 10:29:25FUJIFILM Healthcare Europe expands compatibility of ARIETTA 750 FF ENDO ultrasound system
Vitestro autonomous blood drawing device

Autonomous blood drawing device receives CE marking

blood, CE Mark, phlebotomy, 28 August 2024/in Product News /by panglobal

Vitestro, a Dutch medical robotics firm, has announced that its autonomous blood drawing device has received CE marking, making it the first such device to be approved for commercial use in the European Union. This milestone, achieved in July 2024, signifies the device’s compliance with the European Medical Device Regulation (MDR) standards for safety and […]

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https://interhospi.com/wp-content/uploads/sites/3/2024/08/VITESTRO.jpg 1333 2000 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2024-08-28 10:00:282024-08-27 13:35:00Autonomous blood drawing device receives CE marking
Synchron BCI

Synchron integrates generative AI into brain-computer interface platform

BCI, Neurotechnology, OpenAI, paralysis, Synchron, 15 July 2024/in Neurology, Product News /by panglobal

Neurotechnology firm Synchron has announced the incorporation of OpenAI’s generative artificial intelligence (AI) into its brain-computer interface (BCI) platform, introducing a novel chat feature. This integration aims to enhance the capabilities of Synchron’s BCI technology, enabling individuals with severe paralysis and loss of upper limb mobility to interact with digital interfaces through thought alone.

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https://interhospi.com/wp-content/uploads/sites/3/2024/07/Synchron_II.jpg 1440 2560 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2024-07-15 09:32:422024-07-15 09:32:42Synchron integrates generative AI into brain-computer interface platform
Oticon Medical Sentio System

Oticon Medical’s transcutaneous bone conduction hearing system receives FDA clearance

FDA, hearing loss, Oticon Medical, Sentio System, transcutaneous, 15 July 2024/in Product News /by panglobal

Oticon Medical has announced that its Sentio System, the company’s first active transcutaneous bone conduction hearing system, has received clearance from the U.S. Food and Drug Administration (FDA). This innovative system aims to provide the established benefits of the company’s Ponto System whilst offering a transcutaneous option.

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https://interhospi.com/wp-content/uploads/sites/3/2024/07/Oticon_Sentio.jpg 662 716 panglobal https://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png panglobal2024-07-15 09:13:322024-07-15 09:13:32Oticon Medical’s transcutaneous bone conduction hearing system receives FDA clearance
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