Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. / Mri Conditional Dual Chamber Pacemaker Rate Responsive (Dddr).Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. / Mri Conditional Dual Chamber Pacemaker Rate Responsive (Dddr).,Srphc82278095-Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization T Herapy. System Should Include A Current Generation Mri Conditional Crt

Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. / Mri Conditional Dual Chamber Pacemaker Rate Responsive (Dddr).Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. / Mri Conditional Dual Chamber Pacemaker Rate Responsive (Dddr).,Srphc82278095-Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization T Herapy. System Should Include A Current Generation Mri Conditional Crt Pulse Generator, Bipolar Steroid-Eluting Atria L And Ventricular Leads And A Left Ventricular ( Coronary Sinus ) Lead And Accessories ( Lead Introducers, Sheaths Or G Uiding Catheters Etc.,). Should Provide Independently Programmable Right And Left Ventricular Pulse Outputs And Inter Ventricular Delay ( With The Choices Of Right Ventricular Alone, Left Ventricular Alone Or Biventricular Pacing As Well As The Choice Of Which Ventricle Is To Be Paced First With Optimization Of Delay For Pacing Of Other Ventricle ). Should Have Features Like Negative Av Hysteresis And Triggered Modes For Continuous Delivery Of Crt. Should Have Advanced F Eatures For Detection And Management And Prevention Of Atrial Tachycardias And Atrial Fibrillation As Well As Detaile D Data Storage Of All Arrhythmias And Therapy As Well As Trends Over Time. Should Have Features For Management Of A Trial 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 Stimulation. Lv Leads Should Have Optimal Features F Or Introduction, Positioning And Fixation And Documented Low Displacement Rates. ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 3.00 , Srphc82278090-Mri Conditional Dual Chamber Pacemaker Rate Responsive (Dddr) With Appropriate Atrial And Ventricular Bipolar Steroid Eluting Lead (Mri Conditional) With Life Warranty Provision Of Pacing Therapy For The Use O F The Patients Life-Time Including Any No. Of Pulse Generator Replacements As Clinically Required. Should Have The Lates T Technological Features To Provide Proportionate, Smooth And Appropriate Response Of Pacing Rate To Increased Meta Bolic Demand, Should Provide For Atrial And Ventricular Pacing And Sensing With Choice Of At Least 16 Modes Of Operation, Appropriate Safety Features To Avoid Cross Talk, Optimum Flexibility Of Programming (Including Minimal Av De Lay Of 30Msec Or Less And Atrial Sensitivity Of 0.2Mv Or Less), Detailed Data Storage With Easy Retrieval And Display Of A Dvanced Diagnostics For Ease Of Clinical Follow Up & Maximal Longevity. Should Be Capable Of Programming For Prolon Ging Longevity And Maximal Cost Effectiveness. Should Be Capable Of Providing Reliable Ventricular Capture With Lowes T Battery Drain So As To Provide Maximum Longevity Of The Pacing System.( Preferably As An Automatic Feature Where Th E Pulse Generator Can Perform A Periodic Threshold Test And Reliably Verify Ventricular Capture And Adjust Ventricula R Pulse Output Parameters To Minimize Battery Drain Without Compromising Patient Safety). Should Have Features For Au Tomatic Management Of Arrhythmias (Including Pacemaker Mediated Arrhythmias) 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 Automa Tic Reversion To Ddd After Termination Of Mode Switch Triggering Arrhythmias). Should Have Algorithms To Promote Int Rinsic Conduction. Both Atrial And Ventricular Channels Should Have Provision For High Energy Output I.E. Up To At Leas T 6.0 Volts Pulse Amplitude And Pulse Width Up To Atleast 1.0 Ms, Follow Up Diagnosis And Reprogramming Should Be Ren Dered As Effective As Possible Through Provision Of Adequate Information Management Systems On The Programmer. Mri Compatible Leads Should Be Bipolar, Steroid Eluting And Low Profile Either Tined Or Active Fixation Type (7F Or Smaller I Ntroducer Individually). Leads Should Be From The Same Manufacturer I.E. Manufactured By The Same Company As The Pul Se Generator, Not Outsourced And Marketed By Another Company. Pulse Generator And Leads Should Be Suitable For Ad Ult And Paediatric Patients. The Manufacturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. Publications Supporting The Safety And Efficacy Of The Pacemaker Device And The Leads In Clinical Use Should Be Availab Le In Peer Reviewed Journals. The Latest Programmer With Up Dated Software Should Be Available At All Times Permanent Ly In The Hospital. The Programmer Should Have Facilities For Simultaneous Display Of Multiple Surface Ecg Leads, Intrac Ardiac Electrograms, Event Markers, Electronic Calipers And For Recording The Same Both On Paper And In Electronic S Torage Media E.G. Compact Disc Etc., ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 30.00