Supply Of Mri Conditional Dual Chamber Pacemaker Rate Responsive (Dddr), Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System, perambalur-Tamil Nadu

Supply Of Mri Conditional Dual Chamber Pacemaker Rate Responsive (Dddr), Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator Systemmri Conditional Dual Chamber Pacemaker Rate Responsive (Dddr), Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System,Srphc154036-Mri Conditional Dual Chamber Pacemaker Rate Responsive (Dddr) With Appropriate Atrial And Ve Ntricular Bipolar Steroid Eluting Lead (Mri Conditional) With Life Warranty Provision Of Pacing Therapy For The Use Of T He Patients Life-Time Including Any No. Of Pulse Generator Replacements As Clinically Required. Should Have The Latest T Echnological Features To Provide Proportionate, Smooth And Appropriate Response Of Pacing Rate To Increased Metabo Lic Demand, Should Provide For Atrial And Ventricular Pacing And Sensing With Choice Of At Least 16 Modes Of Operatio N, Appropriate Safety Features To Avoid Cross Talk, Optimum Flexibility Of Programming (Including Minimal Av Delay Of 30 Msec Or Less And Atrial Sensitivity Of 0.2Mv Or Less), Detailed Data Storage With Easy Retrieval And Display Of Advanced Diagnostics For Ease Of Clinical Follow Up & Maximal Longevity. Should Be Capable Of Programming For Prolonging Lon Gevity And Maximal Cost Effectiveness. Should Be Capable Of Providing Reliable Ventricular Capture With Lowest Batter Y Drain So As To Provide Maximum Longevity Of The Pacing System.( Preferably As An Automatic Feature Where The Pulse G Enerator Can Perform A Periodic Threshold Test And Reliably Verify Ventricular Capture And Adjust Ventricular Pulse O Utput Parameters To Minimize Battery Drain Without Compromising Patient Safety). Should Have Features For Automatic Management Of Arrhythmias (Including Pacemaker Mediated Arrhythmias) As Well As Automatic Mode Switching (Mode S Witch Should Be To And From Ddd To Ddi/Vvir, Provision Of Rate Responsive Pacing After Mode Switch And Automatic Reve Rsion To Ddd After Termination Of Mode Switch Triggering Arrhythmias). Should Have Algorithms To Promote Intrinsic C Onduction. Both Atrial And Ventricular Channels Should Have Provision For High Energy Output I.E. Up To At Least 6.0 Vo Lts Pulse Amplitude And Pulse Width Up To Atleast 1.0 Ms, Follow Up Diagnosis And Reprogramming Should Be Rendered A S Effective As Possible Through Provision Of Adequate Information Management Systems On The Programmer. Mri Compat Ible Leads Should Be Bipolar, Steroid Eluting And Low Profile Either Tined Or Active Fixation Type (7F Or Smaller Introdu Cer Individually). Leads Should Be From The Same Manufacturer I.E. Manufactured By The Same Company As The Pulse Generator, Not Outsourced And Marketed By Another Company. Pulse Generator And Leads Should Be Suitable For Adul T And Paediatric Patients. The Manufacturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. P Ublications Supporting The Safety And Efficacy Of The Pacemaker Device And The Leads In Clinical Use Should Be Availabl E In Peer Reviewed Journals. The Latest Programmer With Up Dated Software Should Be Available At All Times Permanentl Y In The Hospital. The Programmer Should Have Facilities For Simultaneous Display Of Multiple Surface Ecg Leads, Intracardiac Electrograms, Event Markers, Electronic Calipers And For Recording The Same Both On Paper And In Electr Onic Storage Media E.G. Compact Disc Etc., Unit:No ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 30.00 , Srphc154064-Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System With Appropriate Atrial And Ventricular Pace / Sense Leads And Option Of Dual Shocking Coil Leads And Accessories. System Should Have A Dvanced Features For The Reliable Detection And Management Of Ventricular Tachycardia And Ventricular Fibrillation I Ncluding 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 Deli Vering Maximum Energy Of 35J Or More And Should Have Features For Management Of High Defibrillation Energy Requirem Ent. Charge Times Should Be Within Clinically Acceptable Limits Throughout The Lifetime Of The Device. Leads Should Be L Ow Profile And Choice Of Both Active Or Passive Fixation Leads Should Be Available. Should Have Features For Automatic Ally 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 Should Include Episode Details Therapy Delivered And Results And Electrogram Storag E And Should Be Comprehensive. Bradycardia Pacing (Including Independently Programmable Parameters For High Outpu T For Post-Shock Pacing) Should Be Available. Warranty Terms Should Be Specified Clearly Along With The Quotation. Fir Ms Should Submit Detailed Literature Of The Item In A Bulletin/Tutorial Format Which Should Contain All The Details Abo Ut The Product. Compliance Statement Of Each Specification To Be Submitted. 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 The Icd Device And The Lead In Clinica L Use Should Be Documented In Scientific Publications. All The Above Mentioned Specifications Are Essential And Mandat Ory And Should Be Submitted At The Time Of Initial Tender Submission. Unit:No ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 2.00

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