Tender For 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-, chennai-Tamil Nadu

Supply Of 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. It Should Be Capable Of Delivering Maximum Energy Of 35 J Or More With Acceptable Limits Throughout The Lifetime Of The Device. It Should Automatically Alert The Patient In The Event Of Battery Or Lead Fault. Data Storage, Retrieval And Display Should Be Efficient And User Friendly. Data Storage Should Include Episode Details, Therapy Delivered And Results And Electrogram Storage And Should Be Comprehensive. Bradycardia 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 Should 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 Item To Major Government Institutes. The System Should Be Approved By Dcgi And A Copy Of Dcgi Approval Should Be Enclosed. All The Above Mentioned Specifications Are Essential And Mandatory And Should Be Submitted At The Time Of Initial Tender Submission. Unit:Nomri 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. It Should Be Capable Of Delivering Maximum Energy Of 35 J Or More With Acceptable Limits Throughout The Lifetime Of The Device. It Should Automatically Alert The Patient In The Event Of Battery Or Lead Fault. Data Storage, Retrieval And Display Should Be Efficient And User Friendly. Data Storage Should Include Episode Details, Therapy Delivered And Results And Electrogram Storage And Should Be Comprehensive. Bradycardia 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 Should 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 Item To Major Government Institutes. The System Should Be Approved By Dcgi And A Copy Of Dcgi Approval Should Be Enclosed. All The Above Mentioned Specifications Are Essential And Mandatory And Should Be Submitted At The Time Of Initial Tender Submission. Unit:No,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. It Should Be Capable Of Delivering Maximum Energy Of 35 J Or More With Acceptable Limits Throughout The Lifetime Of The Device. It Should Automatically Alert The Patient In The Event Of Battery Or Lead Fault. Data Storage, Retrieval And Display Should Be Efficient And User Friendly. Data Storage Should Include Episode Details, Therapy Delivered And Results And Electrogram Storage And Should Be Comprehensive. Bradycardia 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 Should 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 Item To Major Government Institutes. The System Should Be Approved By Dcgi And A Copy Of Dcgi Approval Should Be Enclosed. All The Above Mentioned Specifications Are Essential And Mandatory And Should Be Submitted At The Time Of Initial Tender Submission. Unit:No

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