The US Food and Drug Administration (FDA) has granted 510(k) approval to Surefire Medical's High-Flow Microcatheter. The Surefire Microcatheter, comprising of expandable tip, is designed to deliver therapy with higher infusion ...
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Surefire Medical's new line of Angiographic catheters. Angiographic Catheter line features a large inner lumen of 0.054 inches which enables interventional ...
ETView Medical has obtained European pre-market clearance for Viva-EB line of endobronchial blockers. The Viva-EB product family are designed to provide endobronchial blockade of the right or left lung for thoracic surgical procedures ...
Tags: Viva-EB line of endobronchial blockers, clinical application, CE Mark
Nipro has entered into a five-year agreement to distribute Infraredx's TVC intravascular imaging system for true vessel characterization of coronary artery disease in Japan. The TVC imaging system incorporates near infrared ...
One StockDuq Holdings has filed a patent infringement case against Becton, Dickinson and Company in the US District Court for the Western District of Tennessee for continuing to infringe One StockDuq's Patent. The patent No. 5,704,914 ...
The European Union has granted CE mark approval to BiO2 Medical's inferior vena cava(IVC)filter for use in critically ill patients who are at increased risk of pulmonary embolism and temporarily contraindicated for anticoagulation therapy. ...
Tags: European Union, CE mark approval, BiO2 Medical, IVC filter
Intertronics, a developer of software and hardware solutions for automated measurement and analysis systems, has released new medical device adhesive guides focusing on needle bonding and catheter assembly. The new selector guides, from ...
Tags: Intertronics, medical device, adhesive guides, needle bonding
Medtronic has obtained regulatory clearance from the US Food and Drug Administration (FDA) for the expanded indication of use of its tubular stent graft for the endovascular repair of isolated lesions (excluding dissections) of the ...
Maquet Cardiovascular has gained US and European marketing rights for its new SENSATION PLUS 7.5Fr. 40Cc intra-aortic balloon (IAB) catheter, following the US Food and Drug Administration (FDA) and CE mark approvals respectively. The ...
Tags: marketing rights, catheter, FDA
The US Food and Drug Administration (FDA) has approved St Jude Medical's Amplatzer Vascular Plug 4. Amplatzer Plug is delivered using a standard diagnostic catheter and is designed for use in transcatheter embolization procedures ...
Tags: FDA, Amplatzer Vascular Plug 4, embolization
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Semprus BioSciences' vascular access catheter, designed to provide peripheral access to the central venous system. Using Semprus Sustain technology, the ...
The European Union has granted CE mark to W.L.Gore&Associates'endovascular stent-graft with a new 35 mm trunk-ipsilateral leg and 36 mm aortic extender. Inserted through a catheter-based delivery technique,the GORE EXCLUDER AAA ...
Tags: GORE, European Union, CE mark, aortic business
Developer of innovative vascular access products Catheter Connections announced that it teamed up with Merit Medical Systems, a manufacturer and marketer of proprietary disposable devices used primarily in cardiology and radiology. As per ...
Tags: Dualcap Distribution, vascular access products, Merit Medical Systems
St Jude Medical has implanted the first patient with its Portico Transcatheter aortic heart valve designed to treat patients with severe aortic stenosis who are at high risk of needing open-heart surgery, using the Transapical delivery ...
Tags: portico transcatheter aortic heart valve, St Jude Medical
Clinical stage biopharmaceutical company, Tocagen, has entered into a partnership agreement with MRI Interventions and Brainlab. Under the collaboration, Tocagen will use MRI Interventions' ClearPoint neuro intervention system at selected ...