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CONNEQT Pulse

CardieX gets FDA approval for the CONNEQT Pulse, a unique vascular biometric monitor

CardieX Limited announced its new arterial health monitor, the CONNEQT Pulse (Pulse), has received 510(k) clearance from the U.S. Food and Drug Administration (FDA). Pulse is the only vital signs monitor targeted at home, clinician, and clinical trial use that provides measurements of both brachial blood pressure (the pressure at your arm) and central blood pressure (the pressure at your aorta/heart) in addition to multiple other vascular health biomarkers.

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PlaClin-M

PlaClin-M, for Safe Environments in the Pandemic Era

CodeSteri, a leading provider of disinfection solutions, is proud to announce the launch of PlaClin-M, a revolutionary device designed to help ensure a clean and safe environment in offices, commercial establishments, and public spaces. CodeSteri started from the Korean government project to combat new infectious diseases by the incumbent professor and MD of Hanyang University Emergency Medicine, Seoul.

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Cardiac Structure and Function

Ancora Heart’s AccuCinch System Demonstrates Significant Improvement in Quality of Life

Ancora Heart, Inc., a company developing a completely transcatheter device-based therapy to address heart failure (HF), announced that patients treated with the investigational AccuCinch® Ventricular Restoration System demonstrated improvement in HF patient outcomes and beneficial changes in the structure of the heart. The 12-month data were presented as part of a late-breaking clinical science session at the Technology and Heart Failure Therapeutics conference (THT 2023) and simultaneously published in the Journal of Cardiac Failure.

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SIFT-MS, Syft Tracer TM

Syft Technologies Announces Next Generation SIFT-MS, Syft Tracer™

Syft Technologies today announced the release of its next generation Selected Ion Flow Tube Mass Spectrometry (SIFT-MS) technology, Syft Tracer™, at Pittcon 2023. This innovation of real-time, direct injection mass spectrometry (MS) offers platform advancements such as greater sensitivity, unparalleled performance stability, and high reproducibility and repeatability that make the system an industry-scalable solution. Analytical workflows that require fast time to data, high throughput, and continuous operation will benefit significantly from Syft Tracer capabilities.

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SURGVISION'S EXPLORER AIR

The U.S. Food and Drug Administration has granted 510(k) clearance to SurgVision's Explorer Air® II

SurgVision, a high-tech company developing pioneering solutions for fluorescence-guided surgical and interventional oncology, part of the Bracco Group, announces that it has received 510(k) clearance from the U.S. Food and Drug Administration for the EXPLORER AIR® II for use with Pafolacianine (CYTALUX, On Target Laboratories Inc.) during intraoperative fluorescence imaging.

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