The ENERGEN ICD, with the 4 SITE DF4 connector system, is designed to streamline the implant procedure and make the thinnest, long lasting high energy devices in the world even smaller. Safety Topic / Subject Article Text 167: . boston scientific energen icd mri safety. FINELINETM II: 4456, 4457, 4458, 4459 (Not valid with VITALIO MRI. This site is Exclusively Sponsored by BRACCO, Cardiac Pacemakers, Implantable Cardioverter Defibrillators (ICDs), and Cardiac Monitors. Details About Your Boston Scientific ENERGENImplantable Cardioverter Defibrillator (ICD) What is an ICD? S-ICD System - Important Safety Information. INGEVITYTM+:7840, 7841, 7842 The date by which the label of a device states the device must or should be used. Your physician should discuss all potential benefits and risks with you and describe the appropriate medical care. This date is required to be part of the UDI when included on the label in order to provide the means to track the device back to its manufacturing source or otherwise allow the history of the device manufacturing, packaging, labeleing, distribution and use to be determined. Learn a few simple modifications that can help increase your overall well-being. ENDOTAK RELIANCETM 4-SITETM (DF4): 0262, 0263, 0265, 0266, 0272, 0273, 0275, 0276, 0282, 0283, 0285, 0286, 0292, 0293, 0295, 0296 In patients with an implanted ICD (Figure 4, Supplementary material online, Movie 1), the conventional LGE tech- nique led to 69.2% (53.8-92.3%) artefact-free segments with a wide range of. The information outlines answers to commonly asked questions about ICDs and S-ICDs and a summary about your deviceincluding a photograph and dimensions. Use of these devices may cause serious injuries or death. If you have any device implanted in your chest or body, its safefor you to have a CT scan. Status Post Boston Scientific Emblem Mri S Icd Model Number A219, supplied by Boston Scientific Corporation, used in various techniques. The Boston Scientific S-ICD is an implantable cardioverter defibrillator that is intended to provide electrical shock to stop dangerously fast heart rhythms and pacing for a short time. An official website of the United States government, : Additional relevant information about the device that is not already captured as a distinct GUDID data attribute. Implantable pulse generator, pacemaker (non-CRT), Coronary atherosclerosis of native coronary artery. This document contains Boston Scientific CRM devices that are approved by the FDA as MR-Conditional as of August 2019. Catalog Number: Company Name: BOSTON SCIENTIFIC CORPORATION. This medical procedure uses high-frequency, high-intensity electromagnetic waves for physical therapy. PDF Urgent Field Safety Notice MRI Compatibility - BOSTON SCIENTIFIC
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