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Cardiovascular Devices News

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136-150 of 2702 results
St. Jude Medical wins CE mark approval for SyncAV CRT software
By MDBR Staff Writer
Medical device firm St. Jude Medical has received CE mark approval for its SyncAV CRT software and Quadra Assura MP CRT-Defibrillator (CRT-D) with full-body magnetic resonance (MR) labeling.
Specialty Devices > Cardiovascular Devices > News
Biotronik introduces new Solia S ProMRI conditional pacing lead in US
By MDBR Staff Writer
Germany-based medical technology firm Biotronik has introduced a new Solia S ProMRI conditional pacing lead in the US.
Specialty Devices > Cardiovascular Devices > News
Fujifilm presents next generation of Synapse Cardiovascular at ASE
By MDBR Staff Writer
FUJIFILM Medical Systems U.S.A. will showcase the latest generation of Synapse Cardiovascular, a premier cardiology image management and reporting solution with new module enhancements for echocardiography, at the American Society of Echocardiography (ASE) 27th Annual Scientific Sessions, from June 10-14 at the Washington State Convention Center in Seattle, Washington.
Specialty Devices > Cardiovascular Devices > News
STENTYS receives CE mark approval for its longest Xposition stent
By MDBR Staff Writer
STENTYS, a medical technology company commercializing the world's first and only Self-Apposing coronary stent, announces that it has received CE Marking for the longest version of its Xposition S Sirolimus-eluting self-apposing stent.
Specialty Devices > Cardiovascular Devices > News
Nokia launches Withings Body Cardio device
By MDBR Staff Writer
Nokia Technologies introduced Withings Body Cardio device, which has been developed for use in cardiovascular health assessment.
Specialty Devices > Cardiovascular Devices > News
Micro Interventional Devices wins CE mark approval for Permaseal transapical access and closure device
By MDBR Staff Writer
Micro Interventional Devices (MID) has secured CE mark approval for its Permaseal transapical access and closure device.
Specialty Devices > Cardiovascular Devices > News
BioVentrix gets FDA IDE approval to start Revivent TC system trial
By MDBR Staff Writer
BioVentrix has obtained investigational device exemption (IDE) approval from the US Food and Drug Administration (FDA) to start its clinical trial to evaluate the safety and effectiveness of the Revivent TC transCatheter ventricular enhancement system.
Specialty Devices > Cardiovascular Devices > News
Biotronik introduces new CardioMessenger Smart portable monitoring device in US
By MDBR Staff Writer
Cardiovascular medical technology firm Biotronik has introduced a new CardioMessenger Smart portable monitoring device in the US.
Specialty Devices > Cardiovascular Devices > News
Direct Flow Medical announces DISCOVER trial three-year results
By MDBR Staff Writer
Direct Flow Medical, a medical device company developing and commercializing transcatheter heart valve therapy products to treat structural heart disease, presented three-year results from its prospective, multicenter DISCOVER Trial at the EuroPCR meeting in Paris.
Specialty Devices > Cardiovascular Devices > News
St. Jude Medical announces US launch of Trifecta surgical valve with Glide technology
By MDBR Staff Writer
St. Jude Medical, a global medical device company, today announced the U.S. launch of the company’s most advanced tissue valve — the Trifecta valve with Glide Technology (GT) — for the treatment of patients diagnosed with unhealthy, damaged or malfunctioning aortic heart valves.
Specialty Devices > Cardiovascular Devices > News
Mitralign to highlight Trialign system at EuroPCR 2016
By MDBR Staff Writer
Mitralign, an innovative developer of direct transcatheter mitral and tricuspid valve repair solutions will present its Trialign system for transcatheter tricuspid repair at the EuroPCR conference, one of the world’s leading conferences on cardiology.
Specialty Devices > Cardiovascular Devices > News
NeoChord gets FDA IDE approval to start clinical study of DS1000 chordae delivery system
By MDBR Staff Writer
Medical device firm NeoChord has secured investigational device exemption (IDE) approval from the US Food and Drug Administration (FDA) to start a clinical study for its DS1000 artificial chordae delivery system.
Specialty Devices > Cardiovascular Devices > News
Corvia Medical gets CE mark approval for InterAtrial shunt device
By MDBR Staff Writer
Corvia Medical has received CE mark approval for its InterAtrial shunt device (IASD) to treat heart failure with preserved ejection fraction (HFpEF) or diastolic heart failure.
Specialty Devices > Cardiovascular Devices > News
St. Jude Medical announces MultiPoint pacing IDE study results
By MDBR Staff Writer
St. Jude Medical, a global medical device company, announced presentation of the MultiPoint Pacing (MPP) Investigational device exemption (IDE) Clinical Study results during a late-breaking clinical trial session at the Heart Rhythm Society's (HRS) 37th annual scientific sessions.
Specialty Devices > Cardiovascular Devices > News
Ligand acquires portfolio of synthetic royalty and milestone rights from CorMatrix Cardiovascular for $17.5m
By MDBR Staff Writer
Ligand Pharmaceuticals announces the acquisition of economic rights to multiple programs owned by CorMatrix.
Specialty Devices > Cardiovascular Devices > News
136-150 of 2702 results