Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. System Should Include A Current Generation Mri Conditional Crt Pulse Generator,............... Mri Conditional Single Chamber Implantable Cardioverter Defibrillator System With Df - 4 Lead With Other Accessories For Detection And Management Of Tachycardia (Vt/Vf), Therapy And For Bradycardia Therapy With Ventricular Pacing And Anti- Tachycardia Pacing..............Mri Conditional Pacing System With

Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. System Should Include A Current Generation Mri Conditional Crt Pulse Generator,............... Mri Conditional Single Chamber Implantable Cardioverter Defibrillator System With Df - 4 Lead With Other Accessories For Detection And Management Of Tachycardia (Vt/Vf), Therapy And For Bradycardia Therapy With Ventricular Pacing And Anti- Tachycardia Pacing..............Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. System Should Include A Current Generation Mri Conditional Crt Pulse Generator,............... Mri Conditional Single Chamber Implantable Cardioverter Defibrillator System With Df - 4 Lead With Other Accessories For Detection And Management Of Tachycardia (Vt/Vf), Therapy And For Bradycardia Therapy With Ventricular Pacing And Anti- Tachycardia Pacing..............,Srphc82278100-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 Quadripolar Left Ventricular ( Coronary Sinus ) Lead And Accessories ( Lead Introducers, Sheaths Or Guiding Catheters Etc.,). Should Provide Independently Programmable Right And Left Ventricular Pulse Outp Uts And Interventricular Delay ( With The Choices Of Right Ventricular Alone, Left Ventricular Alone Or Biventricular P Acing 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. Shou Ld Have Advanced Features For Detection And Management And Prevention Of Atrial Tachycardias And Atrial Fibrillation As Well As Detailed Data Storage Of All Arrhythmias And Therapy As Well As Trends Over Time. Should Have Features For Management Of Atrial Fibrillation Including Mode Switch, Ventricular Rate Management Etc., Pulse Genera Tor Should Be Suitable For Use With Either An Endocardial Lv Lead Or An Epimyocardial Lead For Lv Stimulation. Lv Leads Should Have Optimal Features For Introduction, Positioning And Fixation And Documented Low Displacement Rates. ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 4.00 , Srphc82278110-Mri Conditional Single Chamber Implantable Cardioverter Defibrillator System With Df - 4 Lea D With Other Accessories For Detection And Management Of Tachycardia (Vt/Vf), Therapy And For Bradycardia Therapy W Ith Ventricular Pacing And Anti-Tachycardia Pacing. It Should Be Capable Of Delivering Maximum Energy Of 35 J Or More W Ith Acceptable Limits Throughout The Lifetime Of The Device. It Should Automatically Alert The Patient In The Event Of Ba Ttery Or Lead Fault. Data Storage, Retrieval And Display Should Be Efficient And User Friendly. Data Storage Should Inc Lude Episode Details, Therapy Delivered And Results And Electrogram Storage And Should Be Comprehensive. Bradycard Ia Pacing (Including Independently Programmable Parameters For High Output For Post Shock Pacing) Should Be Available. Warranty Terms Should Be Specified Clearly Along With The Quotation. Firms Should Submit Detailed Literature Of The Item In A Bulletin/Tutorial Format Which Should Contain All The Details About The Product. Compliance Statement Of Each Specification To Be Submitted. The Safety And Efficacy Of The Icd System In Clinical Use Sho Uld Be Documented In Scientific Publications. The Firm Quoting The Tender Should Submit A Letter Of Authorisation From The Principal Firm/Original Equipment Manufacturer. The Manufacturer/Supplier Should Submit Proof Of Supply Of The Ite M To Major Government Institutes. The System Should Be Approved By Dcgi And A Copy Of Dcgi Approval Should Be Enclos Ed. All The Above Mentioned Specifications Are Essential And Mandatory And Should Be Submitted At The Time Of Initial T Ender Submission. ] Page 1 Of 6 Run Date/Time: 21/09/2026 17:07:11Stores/Southern Rly Tender Document