Forty-eight patients were randomized to receive a single-chamber ICD and 52 for implantation of a dual-chamber ICD. Patient characteristics are shown in Table 1. No statistically significant ...

BIOTRONIK SE & Co. KG, a leading manufacturer of implantable cardiac devices and pioneer of wireless remote monitoring technologies, today announced the first implantations of the Lumax DX System, a ...

These studies are required by FDA for product evaluation, and are designed to assess the safety and efficacy of BIOTRONIK’s existing single- and dual-chamber Entovis pacemaker systems and Setrox 53 ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Back to Healio A novel implantable cardioverter ...

Please provide your email address to receive an email when new articles are posted on . Abbott announced that the FDA has approved its Aveir VR single-chamber leadless pacemaker for the treatment of ...

Single-chamber Devices Receive CE Mark for Full Body MRI Scans Without Positioning Restrictions MINNEAPOLIS - Medtronic, Inc., today announced CE (Conformité Européenne) Mark and commercial launch of ...

Routine placement of atrial leads is common during implantable cardioverter-defibrillator (ICD) implantation for primary prevention despite guidelines that discourage it—now there are new ...

Dublin, Oct. 09, 2019 (GLOBE NEWSWIRE) -- The "Interventional Cardiology: Implantable Pacemaker Products" report has been added to ResearchAndMarkets.com's offering. The global market for implantable ...

The product is Abbott’s Aveir system, which is the world’s first approved dual-chamber pacemaker. Other leadless pacemakers are single chamber, meaning they connect to one chamber in the patient’s ...

The introduction of dual-chamber pacing in current ICD has facilitated and improved the treatment of ICD recipients with concomitant standard dual-chamber pacemaker indication. Whether dual-chamber ...