Tender For Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System, chennai-Tamil Nadu

Supply Of Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator Systemmri Conditional Dual Chamber Implantable Cardioverter Defibrillator System,Srph154064-Mri Conditional Dual Chamber Implantable Cardioverter Defibrill Ator System With Appropriate Atrial And Ventricular Pace / Sense Leads And Option Of Dual Shocking Coil Leads And Accessories. System Should Have Advanced Features Fo R The Reliable Detection And Management Of Ventricular Tachycardia And Ventricular Fibrillation, Including Features To Differentiate Supra-Ventricular Tachycardia From Ventricular Tachycardia And Features To Avoid Inappropriate Shocks, Tiered Therapy Delivery, Choice Of Atp Protocols And Shock Energies, And Should Be Capable Of Deliv Ering Maximum Energy Of 35J Or More And Should Have Features For Management Of Hi Gh Defibrillation Energy Requirement. Charge Times Should Be Within Clinically Accep Table Limits Throughout The Lifetime Of The Device. Leads Should Be Low Profile And Ch Oice Of Both Active Or Passive Fixation Leads Should Be Available. Should Have Feature S For Automatically Alerting The Patient In The Event Of A Battery Or Lead Fault. Data Storage, Retrieval And Display Should Be Efficient And User Friendly. Data Storage Sh Ould Include Episode Details, Therapy Delivered And Results And Electrogram Storag E And Should Be Comprehensive. Bradycardia Pacing (Including Independently Progra Mmable Parameters For High Output For Post-Shock Pacing) Should Be Available. Warr Anty 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 Sub Mitted. 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 To A Major Government Institute. The Safety And Efficacy Of T He Icd Device And The Lead In Clinical Use Should Be Documented In Scientific Publicatio Ns. All The Above Mentioned Specifications Are Essential And Mandatory 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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