CARTO VISITAG™ Module settings are user defined based on the user’s clinical experience and medical judgment. By using this site, you agree to our Legal Notice and Privacy Policy. The data does not indicate the effectiveness of RF energy application. CARTO 3 advanced 3D mapping system, integration, scalability and insights for electrophysiology diagnosis and treatment.
* In the U.S., THERMOCOOL® Navigation Catheters are approved for drug refractory recurrent symptomatic paroxysmal atrial fibrillation, when used with CARTO® Systems (excluding NAVISTAR® RMT THERMOCOOL® Catheter). IRVINE, CA – August 27, 2020 – Johnson & Johnson Medical Devices Companies* today announced the launch of Biosense Webster, Inc.’s CARTO ® 3 System Version 7 and the CARTO PRIME ™ Mapping Module. CARTO System, CARTO Smarttouch, Biosense Webster, Inc.
© Biosense Webster, Inc. 2015-2017. The third-party trademarks used herein are trademarks of their respective owners. This site last updated on February 15, 2018. with Therapeutic cardiovascular navigational catheters, Learn more about how Johnson & Johnson is mobilizing to address the COVID-19 pandemic at. CARTO PRIME ® Mapping Module offers a suite of tools that may help to shorten ablation time 1. This site is published by Biosense Webster, Inc. which is solely responsible for its contents. Bertaglia E, Bella PD, Tondo C, Proclemer A, Bottoni N, De Ponti R, et al. The clinical significance of utilizing the CARTO® CFAE Module to help identify areas with complex fractionated atrial electrograms for catheter ablation of atrial arrhythmias, such as atrial fibrillation, has not been established by clinical investigations. Journal of Cardiovascular Electrophysiology 2004;15,3:310-315. ... As part of the Biosense Webster policy of continuous product development we reserve the right to change product specifications without prior notification.
046549-180503, 046550-180522. Click here for our California Health Care Compliance Information and AdvaMed Code. In the US, 4mm Catheters (NAVISTAR®, CELSIUS®, EZ STEER® (NAV and Non-Nav)) have a “General Indication” for creation of endocardial lesions in patients 4 years of age and older. Capitalized product names are trademarks of Biosense Webster, Inc. Biosense Webster THERMOCOOL® Catheters are indicated for Type I Atrial Flutter in patients 18 years of age or older. Biosense Webster, Inc. does not recommend any settings for the CARTO VISITAG™ Module. This high-performance mapping is fully integrated into the CARTO ® System. The NAVISTAR® THERMOCOOL® and EZ STEER® THERMOCOOL® NAV Catheters are FDA approved for the treatment of drug refractory recurrent symptomatic paroxysmal atrial fibrillation, when used with compatible three-dimensional electroanatomic mapping systems. Always verify catheter tip location using fluoroscopy or IC signals and consult the CARTO® System User Guide regarding recommendations for fluoroscopy use. This “General Indication” includes treatment of Ventricular Tachycardia. © Biosense Webster, Inc. 2014-2015. THERMOCOOL® Navigation Catheters are approved for recurrent drug/device refractory sustained monomorphic ventricular tachycardia (VT) due to prior myocardial infarction (MI) in adults (excluding THERMOCOOL® SF Catheters). Europace 2009;11:1004-1010. Important Information: Prior to use, refer to the “instructions for use” supplied with these devices for indications, contraindications, side effects, suggested procedure, warnings and precautions. Third party trademarks used herein are trademarks of their respective owners. Always verify catheter tip location using fluoroscopy or IC signals and consult the CARTO® System User Guide regarding recommendations for fluoroscopy use.
Sporton S, Earley M, Nathan A, and Schilling R, Electroanatomic versus fluoroscopic mapping for catheter ablation procedures: A prospective randomized study.
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