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Defibrillation leads
PHRI analysis shows reliability benefits of Optim-insulated defibrillation leads
Defibrillation leads : 13 May, 2013
The Population Health Research Institute (PHRI), an academic health science research institute, has conducted a further independent analysis of data received from ongoing prospective registries that monitor the performance of St Jude Medical's Durata and Riata ST Optim implantable cardioverter defibrillator (ICD) leads.
 
St Jude Medical reveals initial findings from Riata lead evaluation study
Defibrillation leads : 17 July, 2012
St Jude Medical is reporting initial findings from the Riata Lead Evaluation Study.
 
St Jude Medical launches Riata Lead Communication website
Defibrillation leads : 27 December, 2011
St Jude Medical is launching a Riata Lead Communication website which is dedicated to providing physicians a compilation of important communications and updated information regarding the recent Riata and Riata ST Silicone Defibrillation Leads Class I recall.
 
Resuscitation equipment manufacturer hits Fortune 100
Defibrillation leads : 21 September, 2009
At a time when many companies are concentrating on survival, Zoll is growing fast enough to reach number 85 in Fortune’s 100 listing on the back of strong demand for data management and the company’s wearable defibrillator
 
Frst human implants of Endotak Reliance 4-Site defibrillation leads are completed
Defibrillation leads : 13 May, 2009
The first human implants of the Boston Scientific's Endotak Reliance 4-Site defibrillation lead system have been completed.
 
Sorin's Isoline defibrillation leads receive approval fro Japanese authorities
Defibrillation leads : 12 December, 2008
Sorin Group has received Japanese approval for its Isoline defibrillation leads which are now released to the Japanese market.
 
Medtronic Sprint Quattro Secure S single coil defibrillation lead receives US FDA approval
Defibrillation leads : 04 December, 2008
Medtronic has received US Food and Drug Administration (FDA) approval of the Medtronic Sprint Quattro Secure S single coil defibrillation lead (Model 6935) for use with implantable defibrillators in patients at risk for dangerous tachyarrhythmias (fast heartbeats) and sudden cardiac arrest.
 
Study indicates Medtronic’s Lead Integrity Alert improves early identification of ICD lead fractures
Defibrillation leads : 19 November, 2008
A study published in journal Circulation (November 18, 2008) reports that Medtronic’s Lead Integrity Alert (LIA) significantly improves early identification of potential implantable cardioverter-defibrillator (ICD) lead fractures.
 
Mechanical dilator sheath technology simplifies pacemaker lead extraction
Defibrillation leads : 28 August, 2008
As many as 200 medical centres in the USA have adopted Cook Medical’s Evolution Mechanical Dilator Sheath technology that utilises venous entry during pacemaker lead extraction procedures.
 
St Jude Medical receives Japanese regulatory approval for high-voltage defibrillation lead
Defibrillation leads : 06 August, 2008
St Jude Medical has received regulatory approval, in addition to reimbursement approval, from the Japanese Ministry of Health, Labour and Welfare (MHLW), for the Durata defibrillation lead, the company's next-generation high-voltage lead.
 
Medtronic’s Attain StarFix OTW (over-the-wire) lead receives FDA approval
Defibrillation leads : 18 June, 2008
Medtronic has received US Food and Drug Administration approval for the Medtronic Attain StarFix OTW (over-the-wire) lead (Model 4195) which is the first-ever active fixation left-heart lead for cardiac resynchronization therapy (CRT).
 
New heart failure lead receives US FDA approval
Defibrillation leads : 19 May, 2008
Boston Scientific has received US FDA approval of its Acuity Spiral left ventricular lead for use with cardiac resynchronization therapy defibrillators (CRT-D) and cardiac resynchronization therapy pacemakers (CRT-P), both of which treat heart failure.
 
High-voltage lead performance study shows positive results
Defibrillation leads : 16 May, 2008
St Jude Medical has announced the results from the largest actively monitored, multi-site lead performance evaluation ever conducted for an ICD lead family.
 
St Jude pacing lead receives FDA and CE MArk approval
Defibrillation leads : 14 May, 2008
St Jude Medical has received US FDA and European CE Mark approvals of the IsoFlex Optim pacing lead.
 
Isoline range of defibrillation leads receive US FDA approval
Defibrillation leads : 14 March, 2008
ELA Medical, a Sorin Group company, has received the US Food and Drug Administration's approval to market the Isoline range of defibrillation leads.
 
Boston Scientific’s left ventricular lead receives CE Mark approval
Defibrillation leads : 03 March, 2008
Boston Scientific has received CE Mark approval of the company’s Acuity Spiral left ventricular lead for use with cardiac resynchronization therapy defibrillators and cardiac resynchronization therapy pacemakers, both of which treat heart failure.
 
St Jude Medical’s QuickFlex family of left-heart leads receive key approvals
Defibrillation leads : 23 January, 2008
St Jude Medical’s QuickFlex family of left-heart leads to treat heart failure patients has received the US Food and Drug Administration (FDA) and European CE Mark approval.
 
St Jude’s Durata defibrillation lead receives FDA and CE Mark approvals
Defibrillation leads : 17 January, 2008
St Jude Medical has announced US Food and Drug Administration (FDA) and European CE Mark approvals of the company’s Durata defibrillation lead.
 
Medtronic’s Sprint Quattro defibrillation lead receive Japanese regulatory approval
Defibrillation leads : 17 December, 2007
Medtronic has received Japanese regulatory approval for the Sprint Quattro (Model 6944 and 6947) steroid-eluting right ventricular lead used with implantable cardioverter-defibrillators (ICDs) that detect and treat rapid and potentially lethal heart rhythms.
 
Distribution of Sprint Fidelis defibrillation leads is suspended by Medtronic
Defibrillation leads : 15 October, 2007
Medtronic has voluntarily suspended worldwide distribution of the Sprint Fidelis family of defibrillation leads because of the potential for the leads to fracture.
 
 
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