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Cappella Medical Devices Ltd Company Profile

00:22 EDT 19th May 2013 | BioPortfolio

Cappella, Inc. is a medical device company that develops novel solutions for the treatment of complex coronary artery disease (CAD) focused on protecting the coronary sidebranch arteries. Cappella’s Sideguard® coronary sidebranch technology offers interventional cardiologists a straightforward, effective, and easy to use solution that preserves the sidebranch of diseased coronary arteries by protecting the ostium while minimizing plaque shift. The Sideguard delivery system features a proprietary split-sheath, balloon released, technology that ensures precise placement on the ostial borderline. The Sideguard self-expanding, nitinol, stent promotes continuous wall apposition and positive remodelling and its unique trumpet-shaped design conforms to varying characteristics of the sidebranch ostium. The Cappella Sideguard system is currently CE mark approved and is being distributed throughout Europe and South America. Cappella Medical Devices Ltd., Galway, Ireland is the R&D and manufacturing subsidiary of Cappella, Inc. For more information, please visit the Cappella Medical Systems website at www.cappella-med.com.


News Articles [ 645 Associated News Articles listed on BioPortfolio]

Cappella Medical Announces Excellent Long Term Follow-Up Results for Its Sideguard® Technology at TCT 2012

Cappella Medical Devices Ltd (Cappella), a medical device company developing dynamic solutions for the treatment of coronary bifurcation disease, today announced the multic...

Pepperdine University Hosts Grammy Nominated Artists and Unique Festival Devoted to Christian A Cappella Music from Around the World

MALIBU, Calif., May 9, 2013 (GLOBE NEWSWIRE) -- More than 600 singers and advocates of a cappella music will converge on Malibu, California this week for a distinctive and eclectic festival dedicated...

U.S. Medical Devices Markets Reimbursement Trends Analysis in New Research Report at ReportsnReports.com

Dallas, Texas (PRWEB) May 04, 2013 Changing Regulatory and Reimbursement Scenario for Medical Devices in the US Market looks at the regulatory landscape and reimbursement scenario in the US for fou...

How can we get high quality routine data to monitor the safety of devices and procedures?

Difficulties with medical devices and discussions at the European Commission about new regulations have focused attention on how to introduce devices and procedures safely.1 2 Both medical devices......

Frost & Sullivan: Appropriate Channel Partners Vital in the Highly Fragmented Medical Devices Distribution Market in VITSK

SINGAPORE, Dec. 10, 2012 /- The medical devices distribution market in Vietnam, Indonesia, Thailand, and South Korea (VITSK) is highly fragmented, with 1428 distributors in Vietnam alone. This is due...

Making Medical Devices Safer at Home

Today, medical devices are often used at home,enabling people with medical conditions to lead full, active lives. However, consumers using them face many challenges. FDA is working to make these devic...

Medical Device Commercial Leaders Forum, 7-9 October 2013, Brussels, Belgium

3 EVENTS IN ONE: Day 1: Innovative Customer-Centric Commercial Models For Devices Day 2-3: STREAM 1 - Sales Force Effectiveness for Medical Devices Day 2-3: STREAM 2 - Multi-Channel & Digital Marketin...

Argon Medical Devices releases OptionELITE Retrievable Vena Cava Filter

Continuing our commitment to provide best-in-class medical devices for the prevention of recurrent pulmonary embolism, Argon Medical Devices, Inc. takes another step forward with the launch of the Opt...

PubMed Articles [ 484 Associated PubMed Articles listed on BioPortfolio]

Use of the Sideguard (Cappella) stent in bifurcation lesions: a real-world experience.

Aims: The Sideguard® stent (Cappella Medical Devices Ltd, Galway, Ireland), is a novel nitinol self-expanding dedicated bifurcation stent that flares proximally at the ostium of the side branch (SB)...

How medical devices are regulated in the UK.

Excluding medicines, most other healthcare products are medical devices.1 It is estimated that around 38 million people in the UK "have contact with" a medical device every day,2 and there are more th...

Authorization procedure of clinical trials with medical devices : First practical analysis of the BfArM.

The 4th amendment of the Medical Device Law introduced the authorization procedure for clinical trials with medical devices. The Federal Institute for Drugs and Medical Devices ("Bundesinstitut für A...

Reusable invasive medical devices: clean and prepare.

In England, there are approximately 170 NHS hospitals managed by acute trusts, where over 4.2million surgical procedures are performed annually (NHS, 2012; Royal College of Surgeons, 2012). The majori...

Biomaterials in medical devices: An Interview with Jörg Vienken of Fresenius Medical Care, Germany.

Biomaterial and biopolymer research have significant impact on the development as well as application of biotechnology. Biotechnology Journal recently attended the "Nanomaterials for Biomedical Techno...

Clinical Trials [ 1012 Associated Clinical Trials listed on BioPortfolio]

Assessment of Myocardial Disease in Man Using Novel Non-invasive Diagnostic Tools

This study will be testing two devices which are designed to detect cardiovascular disease in patients as early as possible. As there are now many therapies to prevent and treat this cond...

Satisfaction With Placement of Implantable Venous Access Devices in Patients With Solid Tumors

RATIONALE: Gathering information about patients with solid tumors who have implantable venous access devices may help doctors learn more about patient satisfaction. PURPOSE: This phase I...

Safety of Catheter Lock With or Without Heparin in Implanted Central Venous Catheters

Long-term central venous access devices are considered as safe for the administration of medication as chemotherapy, but are also used for blood sampling. For years these catheters have be...

Oral Fluid Screening Devices

This research includes the evaluation of a checklist and on-site screening devices to pre-select drivers suspected of being drug-impaired. The reliability of a limited number of promising...

ATHERO: Advanced Technology Halting Early Re-Stenosis and Occlusion

The rise of minimal access surgery has heralded the approval of a number of endovascular devices with similar indications. This is particularly true for the treatment of lower extremity is...

Companies [ 1848 Associated Companies listed on BioPortfolio]

Cappella Medical Devices Ltd

Cappella, Inc. is a medical device company that develops novel solutions for the treatment of complex coronary artery disease (CAD) focused on protecting the coronary sidebranch a...

Cappella Medical Devices Limited

Cappella, Inc. develops novel solutions for the treatment of complex coronary artery disease (CAD) - specifically bifurcation disease. Cappella’s Sideguard® coronary sideb...

Cappella Medical Devices, Ltd.

Cappella, Inc. is a medical device company, developing novel solutions for the treatment of complex Coronary Artery Disease (CAD) and specifically bifurcation vascular disease. Ca...

Cappella, Inc.

Cappella, Inc. is a medical device company, developing novel solutions for the treatment of complex Coronary Artery Disease (CAD), specifically bifurcation disease. Cappella’...

Cappella Inc.

Cappella, Inc. is a medical device company, developing novel solutions for the treatment of complex Coronary Artery Disease (CAD) and specifically bifurcation vascular disease. Cappella's initial prod...

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