Mri Conditional Dual Chamber / Mri Conditional Crt D System / Mri Conditional Dual Chamber.Mri Conditional Dual Chamber / Mri Conditional Crt D System / Mri Conditional Dual Chamber.,Srphc82278075-Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System With Appropria Te Atrial And Ventricular Pace / Sense Leads And Option Of Dual Shocking Coil Leads And Accessories. System Should Hav E Advanced Features For The Reliable Detection And Management Of Ventricular Tachycardia And V

Mri Conditional Dual Chamber / Mri Conditional Crt D System / Mri Conditional Dual Chamber.Mri Conditional Dual Chamber / Mri Conditional Crt D System / Mri Conditional Dual Chamber.,Srphc82278075-Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System With Appropria Te Atrial And Ventricular Pace / Sense Leads And Option Of Dual Shocking Coil Leads And Accessories. System Should Hav E Advanced Features For The Reliable Detection And Management Of Ventricular Tachycardia And Ventricular Fibrillatio N, Including Features To Differentiate Supra-Ventricular Tachycardia From Ventricular Tachycardia And Features To Av Oid Inappropriate Shocks, Tiered Therapy Delivery, Choice Of Atp Protocols And Shock Energies, And Should Be Capable O F Delivering Maximum Energy Of 35J Or More And Should Have Features For Management Of High Defibrillation Energy Req Uirement. Charge Times Should Be Within Clinically Acceptable Limits Throughout The Lifetime Of The Device. Leads Shoul D Be Low Profile And Choice Of Both Active Or Passive Fixation Leads Should Be Available. Should Have Features For Aut Omatically Alerting The Patient In The Event Of A Battery Or Lead Fault. Data Storage, Retrieval And Display Should Be E Fficient And User Friendly. Data Storage Should Include Episode Details, Therapy Delivered And Results And Electrogra M Storage And Should Be Comprehensive. Bradycardia Pacing (Including Independently Programmable Parameters For Hi Gh Output For Post-Shock Pacing) Should Be Available. Warranty Terms Should Be Specified Clearly Along With The Quot Ation. Firms Should Submit Detailed Literature Of The Item In A Bulletin/Tutorial Format Which Should Contain All The De Tails About The Product. Compliance Statement Of Each Specification To Be Submitted. The Firm Quoting The Tender Shou Ld Submit A Letter Of Authorisation From The Principal Firm/Original Equipment Manufacturer. The Manufacturer / Suppli Er Should Submit Proof Of Supply To A Major Government Institute. The Safety And Efficacy Of The Icd Device And The Lea D In Clinical Use Should Be Documented In Scientific Publications. All The Above Mentioned Specifications Are Essential A Nd Mandatory And Should Be Submitted At The Time Of Initial Tender Submission. ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 2.00 , Srphc82278070-Mri Conditional Crt D System With Quadripolar Lv Lead Along With Other Accessories For Delivery Of Cardiac Resynchronization Therapy And Automatic Cardioversion Or Defibrillation. System Should Include A Current Generation Mri Conditional Crt-D Pulse Generator, Bipolar Steroid Eluting Atrial And Right Ventricular Defibri Llation Lead And A Quadripolar Left Ventricular Lead With Lead Introducers, Sheaths Or Guiding Catheters Etc.Device F Ollowup And Management Should Be Efficient And User Friendly And Telemetry Data Trasnmission And Display Should Be Extremely Quick And Simple.Detailed Logs Of Episode Data,Egms And Therapy And Response Should Be Available. ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 2.00 , Srphc82278080-Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System With Appropria Te Atrial And Ventricular Pace / Sense Leads With Df - 4 Connector And Option Of Dual Shocking Coil Leads And Accessori Es. System Should Have Advanced Features For The Reliable Detection And Management Of Ventricular Tachycardia And Ventricular Fibrillation, Including Features To Differentiate Supra-Ventricular Tachycardia From Ventricular Tachycar Dia And Features To Avoid Inappropriate Shocks, Tiered Therapy Delivery, Choice Of Atp Protocols And Shock Energies, A Nd Should Be Capable Of Delivering Maximum Energy Of 35J Or More And Should Have Features For Management Of High D Efibrillation Energy Requirement. Charge Times Should Be Within Clinically Acceptable Limits Throughout The Lifetime Of The Device.Leads Should Be Low Profile And Choice Of Both Active Or Passive Fixation Leads Should Be Available. Should Have Features For Automatically Alerting The Patient In The Event Of A Battery Or Lead Fault. Data Storage, Retrieval A Nd Display Should Be Efficient And User Friendly. Data Storage Should Include Episode Details, Therapy Delivered And Re Sults And Electrogram Storage And Should Be Comprehensive. Bradycardia Pacing (Including Independently Programma Ble 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 Whi Ch Should Contain All The Details About The Product. Compliance Statement Of Each Specification To Be Submitted. The Fi Rm Quoting The Tender Should Submit A Letter Of Authorisation From The Principal Firm/Original Equipment Manufacture R. The Manufacturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. The Safety And Efficacy O F The Icd Device And The Lead In Clinical Use Should Be Documented In Scientific Publications. All The Above Mentioned Sp Ecifications Are Essential And Mandatory And Should Be Submitted At The Time Of Initial Tender Submission. ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 5.00