Tender For supply of srph154080-mri conditional pacing system with accessories for delivery of cardiac resynchronization therapy. system should include a current generation mri conditional crt pulse generator, bipolar steroid-eluting atrial and ventricular lead s and a quadripolar left ventricular ( coronary sinus ) lead and accessories ( lead in troducers, sheaths or guiding catheters etc.,). should provide independently progr ammable right and left ventricular pulse outputs and interventricular delay ( with t he choices of right ventricular alone, left ventricular alone or biventricular pacin g as well as the choice of which ventricle is to be paced first with optimization of del ay for pacing of other ventricle ). should have features like negative av hysteresis a nd triggered modes for continuous delivery of crt. should have advanced features for detection and management and prevention of atrial tachycardias and atrial fibri llation as well as detailed data storage of all arrhythmias and therapy as well as tr ends over time. should have features for management of atrial fibrillation including mode switch, ventricular rate management etc., pulse generator should be suitable for use with either an endocardial lv lead or an epimyocardial lead for lv stimulatio n. lv leads should have optimal features for introduction, positioning and fixation an d documented low displacement rates. unit: no.
Tender For supply of srph154052-single chamber rate responsive pacemaker (system should be mri conditional) with appropriate bipolar mri conditional lead. should have the lat est technological features to provide proportionate, smooth and appropriate re sponse of pacing rate to increased metabolic demand. should be suitable for use in adult and children. should have sufficient programming flexibility for using in atri um (where sensitivity should be adjustable to 0.25mv or lower) and / or ventricle an d should be supplied with low profile atrial / ventricular mri compatible lead. (to b e specified when taking delivery). the lead should be low profile (7f or smaller intr oducer) and should be steroid eluting. should be capable of high energy output pa cing with pulse amplitude of up to at least 6.0v and pulse width up to atleast 1.0ms. t he pacing system should have maximum flexibility of programming, data storage an d display for ease of clinical follow up and diagnosis of malfunction. should be co vered by life warranty. (providing pacing therapy for the duration of patients life time). should provide free of charge the latest programmer with appropriate soft ware which should have facilities for simultaneous display of multiple surface ec g leads, intracardiac electrograms, event markers, electronic calipers and for r ecording the same both on paper and in electronic storage media e.g. compact disc s etc., the safety and efficacy of the pacing system should be documented in scient ific publications. unit:no