Medical Device Developments’ Post

𝗗𝗮𝗶𝗹𝘆 𝗡𝗲𝘂𝗿𝗼-𝗯𝗶𝘁𝗲𝘀 🧠: 🩸Rapid Medical 𝗖𝗼𝗺𝗽𝗹𝗲𝘁𝗲𝘀 𝗜𝗻𝗶𝘁𝗶𝗮𝗹 𝗡𝗲𝘂𝗿𝗼𝘃𝗮𝘀𝗰𝘂𝗹𝗮𝗿 𝗖𝗮𝘀𝗲𝘀 𝗶𝗻 𝘁𝗵𝗲 𝗨𝗦𝗔 𝗙𝗼𝗹𝗹𝗼𝘄𝗶𝗻𝗴 𝗙𝗗𝗔 𝗖𝗹𝗲𝗮𝗿𝗮𝗻𝗰𝗲 𝗼𝗳 𝗜𝘁𝘀 𝗔𝗰𝘁𝗶𝘃𝗲 𝗔𝗰𝗰𝗲𝘀𝘀 𝗦𝗼𝗹𝘂𝘁𝗶𝗼𝗻 Rapid announced this year at SNIS 2024, the first procedures in the USA of their DRIVEWIRE 24 breakthrough device. DRIVEWIRE 24 redefines interventional access by providing an active 𝙙𝙚𝙛𝙡𝙚𝙘𝙩𝙖𝙗𝙡𝙚 𝙩𝙞𝙥 that controls and steers a range of catheters directly to the target vessels. 🤔𝗪𝗵𝘆 𝗱𝗼𝗲𝘀 𝘁𝗵𝗶𝘀 𝗺𝗮𝗸𝗲 𝘁𝗵𝗲𝗺 𝗱𝗶𝗳𝗳𝗲𝗿𝗲𝗻𝘁? Conventional access devices are reactive and rely on external forces to reach their target. DRIVEWIRE's active technology selects turns on-demand and handles the complexity of navigating the vascular highway with ease. ⭐This provides 𝙝𝙞𝙜𝙝-𝙥𝙚𝙧𝙛𝙤𝙧𝙢𝙖𝙣𝙘𝙚 𝙞𝙣𝙩𝙧𝙖𝙫𝙖𝙨𝙘𝙪𝙡𝙖𝙧 𝙨𝙩𝙚𝙚𝙧𝙞𝙣𝙜.  ⭐The device also features variable support to articulate a wide range of micro and intermediate catheters without advanced forerun or additional support devices. 🥼In the 2 cases completed by Shahram Majidi, DRIVEWIRE 24 navigated the aspiration catheter directly to the M2 arterial occlusion for first-pass excellent reperfusion. In the second case, DRIVEWIRE navigated complex turns to place 2 flow diverters in a large, multilobed aneurysm. 𝘾𝙤𝙣𝙜𝙧𝙖𝙩𝙪𝙡𝙖𝙩𝙞𝙤𝙣𝙨 to Rapid Medical!!! Ronen Eckhouse, Walid Haddad Shimon Eckhouse Giora Kornblau https://lnkd.in/e22gXu8M

This is the Mid-bore vascular closure we’ve all been waiting for!! *Provides fastest to Hemostasis on the market. *PEG Sealant shown to dissolve 3x faster than collagen in recent randomized, multi-center study. * Easy to use ergonomic handle with very few steps, tension indicator and balloon inflation indicator. * Improve patient satisfaction with little to no pain during deployment. * Increase productivity with patients going home same day as procedure. #CordisGoBeyond

ONLY the InterStim™ systems provide a visual display of therapy settings so your patient can easily see their current amplitude.¹,² See what sets the InterStim™ system apart: https://bit.ly/3OQrs20 Risks may include surgical, device, and stimulation-related complications. See important safety info: https://bit.ly/4fchaUL 1. Medtronic Patient User Guide Model A510/A51200 (M974740A30 rev. C) and Model A51300 (M017457C001 rev. A) 2. Axonics Remote Control User Manual, US, 110-0125-001rN, 05-2023.

🎤 From Concept to Care: Benjamin Rieck at MedTech Malta 2024 🌍 Benjamin Joas Rieck delivered an insightful presentation at this year’s MedTech World in Malta, titled: "From Concept to Care: Navigating the Journey of Cardiovascular Medical Devices from Design to Patient." 💡 While we’re not entirely sure what happened to our slides during the presentation, Benjamin still managed to deliver key insights on how to navigate the complex journey of MedTech innovations. 🙌 Couldn’t make it to the session? Watch the full presentation here: https://lnkd.in/g-UucyA5 🎥 Let us know your thoughts, and feel free to reach out if you’d like to discuss how we can help navigate your MedTech journey! #AngioConsult #MedTechMalta #InnovationInHealth #MedicalDevices #CardiovascularCare #FromConceptToCare

BCBN Feed: Improving strategies for managing patients with pacemakers https://lnkd.in/gE-GWChG A large new study aims to reduce the time, cost, and complexity involved with managing patients who have pacemakers and implantable cardioverter-defibrillators. ... [...]

The Lode Corival has been at the forefront of ergometry since its first release in 1980. 🚴♂️ Building on decades of expertise, the Corival CPET combines precision and comfort with modern technology. From its 7-watt starting load to seamless ECG and pulmonary device integration, it’s designed to deliver accurate and reliable results for every patient. Discover how this trusted legacy continues to advance medical diagnostics. 🔗Learn more about the Corival CPET: https://lnkd.in/eXZ9963n #ergometer #cardiopulmonary #exercise

🏥 FDA clears Gentuity, LLC HF-OCT Imaging System for PCI imaging The imaging system, combined with the Vis-Rx Micro-Imaging Catheter, is now approved for use before and after percutaneous coronary intervention (PCI). This approval makes the Gentuity HF-OCT Imaging System the only intravascular imaging platform specifically indicated for assessing coronary vessels pre-and post-intervention. This allows physicians to access real-time, actionable insights in as little as one second, enhancing decision-making and improving procedural efficiency while minimising contrast use. Read more online: https://lnkd.in/er9h-8QB 📰 Follow Medical Device Developments to receive the latest medical device news daily and to subscribe to our weekly newsletter #MedicalDeviceDevelopments #medicaldevices #medicalmanufacturing

💞Stereotaxis secures China’s NMPA approval for Magbot Catheter Magbot is a single-use magnetic saline-irrigated radiofrequency ablation catheter designed and developed by Shanghai MicroPort EP Medtech, Stereotaxis’ collaborator in China. MicroPort EP is a China-based leading medical device company that has a portfolio of cardiovascular medical devices for the diagnosis and treatment of arrythmias. Stereotaxis and MicroPort EP previously announced their collaboration in August 2021. Magbot is indicated for the ablation of drug-resistant persistent atrial fibrillation, atrioventricular nodal re-entrant tachycardia, and atrioventricular re-entrant tachycardia. Read more online: https://lnkd.in/e6jctDHs 📰 Follow Medical Device Developments to receive the latest medical device news daily and to subscribe to our weekly newsletter #MedicalDeviceDevelopments #medicaldevices #medicalmanufacturing

Jason Hannon, CEO of Mainstay, breaks down the impact of ReActiv8’s recent full-body MRI conditional labeling approvals in the UK, EU, and Australia. ReActiv8 patients in these regions can now receive MRI scans with their implanted device, removing one more barrier for those who could benefit from this groundbreaking therapy. To learn more, read the full press release → https://lnkd.in/e3sFBmPJ. The MRI approvals were achieved in connection with Mainstay receiving certificates issued by its Notified Body confirming conformity with the Medical Device Regulations (MDR) of both the European Union and the United Kingdom. Specific scan conditions and safety information are provided in the ReActiv8 MRI Guidelines manuals for each territory. #mainstaymedical #reactiv8 #multifidusdysfunction #chroniclowbackpain #restorativetherapy #thinkrestorative #restorativerevolution #lowbackpain #clbp #helpingpatients #patientfocus #puttingpatientsfirst

AAMI has new UV disinfection guidance in the works! This forthcoming document will impact medical device manufacturers and end users who work with ultraviolet light disinfection. Alpa Patel from Nelson Labs joined us in the studio during AAMI’s Fall Sterilization Standards Week to discuss how UV was widely adopted during the COVID-19 pandemic and why new guidance is needed. #Sterilization #Sterileprocessing https://lnkd.in/ekeiEJii