Tender For Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System With Df - 4 Connector And Option Of Dual Shocking Coil., chennai-Tamil Nadu

Supply Of Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System With Df - 4 Connector And Option Of Dual Shocking Coil.Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System With Df - 4 Connector And Option Of Dual Shocking Coil.,Sr Ph 154066-Mri Conditional Dual Chamber Implantable Cardioverter Defibril Lator System With Appropriate Atrial And Ventricular Pace / Sense Leads With Df - 4 Co Nnector And Option Of Dual Shocking Coil Leads And Accessories. System Should Have Advanced Features For The Reliable Detection And Management Of Ventricular Tachyc Ardia And Ventricular Fibrillation, Including Features To Differentiate Supra-Ventric Ular Tachycardia From Ventricular Tachycardia And Features To Avoid Inappropriate Shocks, Tiered Therapy Delivery, Choice Of Atp Protocols And Shock Energies, And Sh Ould Be Capable Of Delivering Maximum Energy Of 35J Or More And Should Have Featur Es For Management Of High Defibrillation Energy Requirement. Charge Times Should B E Within Clinically Acceptable Limits Throughout The Lifetime Of The Device.Leads Shou Ld Be Low Profile And Choice Of Both Active Or Passive Fixation Leads Should Be Availa Ble. Should Have Features For Automatically Alerting The Patient In The Event Of A Bat Tery Or Lead Fault. Data Storage, Retrieval And Display Should Be Efficient And User F Riendly. Data Storage Should Include Episode Details, Therapy Delivered And Results And Electrogram Storage And Should Be Comprehensive. Bradycardia Pacing (Includin G Independently Programmable Parameters For High Output For Post-Shock Pacing) S Hould Be Available. Warranty Terms Should Be Specified Clearly Along With The Quota Tion. 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 Eac H Specification To Be Submitted. The Firm Quoting The Tender Should Submit A Letter Of Authorisation From The Principal Firm/Original Equipment Manufacturer. The Manufac Turer / Supplier Should Submit Proof Of Supply To A Major Government Institute. The Safety And Efficacy Of The Icd Device And The Lead In Clinical Use Should Be Documente D In Scientific Publications. All The Above Mentioned Specifications Are Essential And M Andatory And Should Be Submitted At The Time Of Initial Tender Submission. Unit:No [Quantity Tolerance (+/-): 5 %Age , Item Category : Normal , Total Po Value Variation Permitted: Max 8 Lacs ] ]

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INR 56300.0 /-

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