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Supply of Srph154036-Mri Conditional Dual Chamber Pacemaker Rate Responsive Ddd R With Appropriate Atrial And Ventricular Bipolar Steroid Eluting Lead Mri Conditi Onal With Life Warranty Provision Of Pacing Therapy For The Use Of The Patients Lif E-Time Including Any No. Of Pulse Generator Replacements As Clinically Required. S Hould Have The Latest Technological Features To Provide Proportionate, Smooth A Nd Appropriate Response Of Pacing Rate To Increased Metabolic Demand, Should Pr Ovide For Atrial And Ventricular Pacing And Sensing With Choice Of At Least 16 Mode S Of Operation, Appropriate Safety Features To Avoid Cross Talk, Optimum Flexibilit Y Of Programming Including Minimal Av Delay Of 30Msec Or Less And Atrial Sensitivit Y Of 0.2Mv Or Less, Detailed Data Storage With Easy Retrieval And Display Of Advanc Ed Diagnostics For Ease Of Clinical Follow Up & Maximal Longevity. Should Be Capabl E Of Programming For Prolonging Longevity And Maximal Cost Effectiveness. Shoul D Be Capable Of Providing Reliable Ventricular Capture With Lowest Battery Drain S O As To Provide Maximum Longevity Of The Pacing System. Preferably As An Automati C Feature Where The Pulse Generator Can Perform A Periodic Threshold Test And R Eliably Verify Ventricular Capture And Adjust Ventricular Pulse Output Parameter S To Minimize Battery Drain Without Compromising Patient Safety. Should Have Feat Ures For Automatic Management Of Arrhythmias Including Pacemaker Mediated Arr Hythmias As Well As Automatic Mode Switching Mode Switch Should Be To And From Ddd To Ddi/Vvir, Provision Of Rate Responsive Pacing After Mode Switch And Automat Ic Reversion To Ddd After Termination Of Mode Switch Triggering Arrhythmias. Sho Uld Have Algorithms To Promote Intrinsic Conduction. Both Atrial And Ventricular Channels Should Have Provision For High Energy Output I.E. Up To At Least 6.0 Volts Pulse Amplitude And Pulse Width Up To Atleast 1.0 Ms, Follow Up Diagnosis And Repro Gramming Should Be Rendered As Effective As Possible Through Provision Of Adequ Ate Information Management Systems On The Programmer. Mri Compatible Leads Sho Uld Be Bipolar, Steroid Eluting And Low Profile Either Tined Or Active Fixation Type 7F Or Smaller Introducer Individually. Leads Should Be From The Same Manufacture R I.E. Manufactured By The Same Company As The Pulse Generator, Not Outsourced A Nd Marketed By Another Company. Pulse Generator And Leads Should Be Suitable Fo R Adult And Paediatric Patients. The Manufacturer / Supplier Should Submit Proof O F Supply To A Major Government Institute. Publications Supporting The Safety And E Fficacy Of The Pacemaker Device And The Leads In Clinical Use Should Be Available In Peer Reviewed Journals. The Latest Programmer With Up Dated Software Should Be Available At All Times Permanently In The Hospital. The Programmer Should Have Fac Ilities For Simultaneous Display Of Multiple Surface Ecg Leads, Intracardiac Electr Ograms, Event Markers, Electronic Calipers And For Recording The Same Both On P Aper And In Electronic Storage Media E.G. Compact Disc Etc., Unit:No
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