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Johnson & Johnson Biosense Webster: Biosense Webster Announces CE Mark approval in Europe for VARIPULSE Pulsed Field Ablation (PFA) Platform

Johnson & Johnson Biosense Webster: Biosense Webster Announces CE Mark approval in Europe for VARIPULSE Pulsed Field Ablation (PFA) Platform
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Biosense Webster Announces CE Mark approval in Europe for VARIPULSE™ Pulsed Field Ablation (PFA) Platform

Börse Express - Biosense Webster Announces CE Mark approval in Europe for VARIPULSE™ Pulsed Field Ablation (PFA) Platform

Biosense Webster, Inc., a global leader in cardiac arrhythmia treatment and part of Johnson & Johnson MedTech, today announced European CE mark approval of the VARIPULSEā„¢ Platform for the treatment of symptomatic drug refractory recurrent paroxysmal atrial fibrillation (AF) using pulsed field ablation (PFA). The VARIPULSEā„¢ Platform is comprised.

J&J: CE Mark approval for Varipulse platform -February 29, 2024 at 10:40 am EST

J&J announces that Biosense Webster today announced the European CE Mark approval of the Varipulse platform for the treatment of symptomatic drug-refractory paroxysmal atrial fibrillation by pulsed.

J&J s Biosense Webster s Varipulse PFA system wins CE mark

J&J MedTech's Biosense Webster unit announced today that it won CE mark approval for its Varipulse pulsed field ablation platform.

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