tender for mri conditional pacing system with accessories for delivery of cardiac resynchronization therapy. / mri conditional dual chamber pacemaker rate responsive (dddr)., srphc82278090-mri conditional dual chamber pacemaker rate responsive (dddr) with appropriate atrial and ventricular bipolar steroid eluting lead (mri conditional) with life warranty provision of pacing therapy for the use o f the patients life-time including any no. of pulse generator replacements as clinically required. should have the lates t technological features to provide proportionate, smooth and appropriate response of pacing rate to increased meta bolic demand, should provide for atrial and ventricular pacing and sensing with choice of at least 16 modes of operation, appropriate safety features to avoid cross talk, optimum flexibility of programming (including minimal av de lay of 30msec or less and atrial sensitivity of 0.2mv or less), detailed data storage with easy retrieval and display of a dvanced diagnostics for ease of clinical follow up & maximal longevity. should be capable of programming for prolon ging longevity and maximal cost effectiveness. should be capable of providing reliable ventricular capture with lowes t battery drain so as to provide maximum longevity of the pacing system.( preferably as an automatic feature where th e pulse generator can perform a periodic threshold test and reliably verify ventricular capture and adjust ventricula r pulse output parameters to minimize battery drain without compromising patient safety). should have features for au tomatic management of arrhythmias (including pacemaker mediated arrhythmias) as well as automatic mode switching ( mode switch should be to and from ddd to ddi/vvir, provision of rate responsive pacing after mode switch and automa tic reversion to ddd after termination of mode switch triggering arrhythmias). should have algorithms to promote int rinsic conduction. both atrial and ventricular channels should have provision for high energy output i.e. up to at leas t 6.0 volts pulse amplitude and pulse width up to atleast 1.0 ms, follow up diagnosis and reprogramming should be ren dered as effective as possible through provision of adequate information management systems on the programmer. mri compatible leads should be bipolar, steroid eluting and low profile either tined or active fixation type (7f or smaller i ntroducer individually). leads should be from the same manufacturer i.e. manufactured by the same company as the pul se generator, not outsourced and marketed by another company. pulse generator and leads should be suitable for ad ult and paediatric patients. the manufacturer / supplier should submit proof of supply to a major government institute. publications supporting the safety and efficacy of the pacemaker device and the leads in clinical use should be availab le in peer reviewed journals. the latest programmer with up dated software should be available at all times permanent ly in the hospital. the programmer should have facilities for simultaneous display of multiple surface ecg leads, intrac ardiac electrograms, event markers, electronic calipers and for recording the same both on paper and in electronic s torage media e.g. compact disc etc.,

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Tender18 provides end-to-end professional bidding support and documentation advisory for Tender For Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. / Mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr)., Srphc82278090-mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr) With Appropriate Atrial And Ventricular Bipolar Steroid Eluting Lead (mri Conditional) With Life Warranty Provision Of Pacing Therapy For The Use O F The Patients Life-time Including Any No. Of Pulse Generator Replacements As Clinically Required. Should Have The Lates T Technological Features To Provide Proportionate, Smooth And Appropriate Response Of Pacing Rate To Increased Meta Bolic Demand, Should Provide For Atrial And Ventricular Pacing And Sensing With Choice Of At Least 16 Modes Of Operation, Appropriate Safety Features To Avoid Cross Talk, Optimum Flexibility Of Programming (including Minimal Av De Lay Of 30msec Or Less And Atrial Sensitivity Of 0.2mv Or Less), Detailed Data Storage With Easy Retrieval And Display Of A Dvanced Diagnostics For Ease Of Clinical Follow Up & Maximal Longevity. Should Be Capable Of Programming For Prolon Ging Longevity And Maximal Cost Effectiveness. Should Be Capable Of Providing Reliable Ventricular Capture With Lowes T Battery Drain So As To Provide Maximum Longevity Of The Pacing System.( Preferably As An Automatic Feature Where Th E Pulse Generator Can Perform A Periodic Threshold Test And Reliably Verify Ventricular Capture And Adjust Ventricula R Pulse Output Parameters To Minimize Battery Drain Without Compromising Patient Safety). Should Have Features For Au Tomatic Management Of Arrhythmias (including Pacemaker Mediated Arrhythmias) As Well As Automatic Mode Switching ( Mode Switch Should Be To And From Ddd To Ddi/vvir, Provision Of Rate Responsive Pacing After Mode Switch And Automa Tic Reversion To Ddd After Termination Of Mode Switch Triggering Arrhythmias). Should Have Algorithms To Promote Int Rinsic Conduction. Both Atrial And Ventricular Channels Should Have Provision For High Energy Output I.e. Up To At Leas T 6.0 Volts Pulse Amplitude And Pulse Width Up To Atleast 1.0 Ms, Follow Up Diagnosis And Reprogramming Should Be Ren Dered As Effective As Possible Through Provision Of Adequate Information Management Systems On The Programmer. Mri Compatible Leads Should Be Bipolar, Steroid Eluting And Low Profile Either Tined Or Active Fixation Type (7f Or Smaller I Ntroducer Individually). Leads Should Be From The Same Manufacturer I.e. Manufactured By The Same Company As The Pul Se Generator, Not Outsourced And Marketed By Another Company. Pulse Generator And Leads Should Be Suitable For Ad Ult And Paediatric Patients. The Manufacturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. Publications Supporting The Safety And Efficacy Of The Pacemaker Device And The Leads In Clinical Use Should Be Availab Le In Peer Reviewed Journals. The Latest Programmer With Up Dated Software Should Be Available At All Times Permanent Ly In The Hospital. The Programmer Should Have Facilities For Simultaneous Display Of Multiple Surface Ecg Leads, Intrac Ardiac Electrograms, Event Markers, Electronic Calipers And For Recording The Same Both On Paper And In Electronic S Torage Media E.g. Compact Disc Etc., . Our senior analysts help you decode the complete project guidelines, manage accurate costing sheets, and complete error-free submissions on the official platform used by Southern Railway SR.

Most online bids face rejection during the initial evaluation round due to avoidable errors like uploading blurred document scans, submitting expired DSCs, or missing critical experience papers required for Tender For Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. / Mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr)., Srphc82278090-mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr) With Appropriate Atrial And Ventricular Bipolar Steroid Eluting Lead (mri Conditional) With Life Warranty Provision Of Pacing Therapy For The Use O F The Patients Life-time Including Any No. Of Pulse Generator Replacements As Clinically Required. Should Have The Lates T Technological Features To Provide Proportionate, Smooth And Appropriate Response Of Pacing Rate To Increased Meta Bolic Demand, Should Provide For Atrial And Ventricular Pacing And Sensing With Choice Of At Least 16 Modes Of Operation, Appropriate Safety Features To Avoid Cross Talk, Optimum Flexibility Of Programming (including Minimal Av De Lay Of 30msec Or Less And Atrial Sensitivity Of 0.2mv Or Less), Detailed Data Storage With Easy Retrieval And Display Of A Dvanced Diagnostics For Ease Of Clinical Follow Up & Maximal Longevity. Should Be Capable Of Programming For Prolon Ging Longevity And Maximal Cost Effectiveness. Should Be Capable Of Providing Reliable Ventricular Capture With Lowes T Battery Drain So As To Provide Maximum Longevity Of The Pacing System.( Preferably As An Automatic Feature Where Th E Pulse Generator Can Perform A Periodic Threshold Test And Reliably Verify Ventricular Capture And Adjust Ventricula R Pulse Output Parameters To Minimize Battery Drain Without Compromising Patient Safety). Should Have Features For Au Tomatic Management Of Arrhythmias (including Pacemaker Mediated Arrhythmias) As Well As Automatic Mode Switching ( Mode Switch Should Be To And From Ddd To Ddi/vvir, Provision Of Rate Responsive Pacing After Mode Switch And Automa Tic Reversion To Ddd After Termination Of Mode Switch Triggering Arrhythmias). Should Have Algorithms To Promote Int Rinsic Conduction. Both Atrial And Ventricular Channels Should Have Provision For High Energy Output I.e. Up To At Leas T 6.0 Volts Pulse Amplitude And Pulse Width Up To Atleast 1.0 Ms, Follow Up Diagnosis And Reprogramming Should Be Ren Dered As Effective As Possible Through Provision Of Adequate Information Management Systems On The Programmer. Mri Compatible Leads Should Be Bipolar, Steroid Eluting And Low Profile Either Tined Or Active Fixation Type (7f Or Smaller I Ntroducer Individually). Leads Should Be From The Same Manufacturer I.e. Manufactured By The Same Company As The Pul Se Generator, Not Outsourced And Marketed By Another Company. Pulse Generator And Leads Should Be Suitable For Ad Ult And Paediatric Patients. The Manufacturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. Publications Supporting The Safety And Efficacy Of The Pacemaker Device And The Leads In Clinical Use Should Be Availab Le In Peer Reviewed Journals. The Latest Programmer With Up Dated Software Should Be Available At All Times Permanent Ly In The Hospital. The Programmer Should Have Facilities For Simultaneous Display Of Multiple Surface Ecg Leads, Intrac Ardiac Electrograms, Event Markers, Electronic Calipers And For Recording The Same Both On Paper And In Electronic S Torage Media E.g. Compact Disc Etc., in Tamil Nadu.

Eligibility for outstation bidders depends entirely on the terms set inside the document for Tender For Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. / Mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr)., Srphc82278090-mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr) With Appropriate Atrial And Ventricular Bipolar Steroid Eluting Lead (mri Conditional) With Life Warranty Provision Of Pacing Therapy For The Use O F The Patients Life-time Including Any No. Of Pulse Generator Replacements As Clinically Required. Should Have The Lates T Technological Features To Provide Proportionate, Smooth And Appropriate Response Of Pacing Rate To Increased Meta Bolic Demand, Should Provide For Atrial And Ventricular Pacing And Sensing With Choice Of At Least 16 Modes Of Operation, Appropriate Safety Features To Avoid Cross Talk, Optimum Flexibility Of Programming (including Minimal Av De Lay Of 30msec Or Less And Atrial Sensitivity Of 0.2mv Or Less), Detailed Data Storage With Easy Retrieval And Display Of A Dvanced Diagnostics For Ease Of Clinical Follow Up & Maximal Longevity. Should Be Capable Of Programming For Prolon Ging Longevity And Maximal Cost Effectiveness. Should Be Capable Of Providing Reliable Ventricular Capture With Lowes T Battery Drain So As To Provide Maximum Longevity Of The Pacing System.( Preferably As An Automatic Feature Where Th E Pulse Generator Can Perform A Periodic Threshold Test And Reliably Verify Ventricular Capture And Adjust Ventricula R Pulse Output Parameters To Minimize Battery Drain Without Compromising Patient Safety). Should Have Features For Au Tomatic Management Of Arrhythmias (including Pacemaker Mediated Arrhythmias) As Well As Automatic Mode Switching ( Mode Switch Should Be To And From Ddd To Ddi/vvir, Provision Of Rate Responsive Pacing After Mode Switch And Automa Tic Reversion To Ddd After Termination Of Mode Switch Triggering Arrhythmias). Should Have Algorithms To Promote Int Rinsic Conduction. Both Atrial And Ventricular Channels Should Have Provision For High Energy Output I.e. Up To At Leas T 6.0 Volts Pulse Amplitude And Pulse Width Up To Atleast 1.0 Ms, Follow Up Diagnosis And Reprogramming Should Be Ren Dered As Effective As Possible Through Provision Of Adequate Information Management Systems On The Programmer. Mri Compatible Leads Should Be Bipolar, Steroid Eluting And Low Profile Either Tined Or Active Fixation Type (7f Or Smaller I Ntroducer Individually). Leads Should Be From The Same Manufacturer I.e. Manufactured By The Same Company As The Pul Se Generator, Not Outsourced And Marketed By Another Company. Pulse Generator And Leads Should Be Suitable For Ad Ult And Paediatric Patients. The Manufacturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. Publications Supporting The Safety And Efficacy Of The Pacemaker Device And The Leads In Clinical Use Should Be Availab Le In Peer Reviewed Journals. The Latest Programmer With Up Dated Software Should Be Available At All Times Permanent Ly In The Hospital. The Programmer Should Have Facilities For Simultaneous Display Of Multiple Surface Ecg Leads, Intrac Ardiac Electrograms, Event Markers, Electronic Calipers And For Recording The Same Both On Paper And In Electronic S Torage Media E.g. Compact Disc Etc.,. While many public sector projects allow national competitive bidding, certain localized works require local offices or specific registration metrics in Perambalur.

If this procurement is routed through the central marketplace, an active GeM Seller ID is mandatory to supply items. Tender18 offers complete assistance for brand cataloging, profile creation, and vendor assessment required officially by Southern Railway SR

To register an eligible bid for these contracts, companies must prepare their core compliance documents. Vendors operating across Tamil Nadu must ensure they possess a valid GST registration, permanent account number (PAN), and active Class-3 Digital Signature Certificates.

This public procurement cycle is specifically looking for qualified vendors and suppliers who can provide high-quality solutions. The operational execution, delivery, and deployment of these materials must be managed locally within the Perambalur region.

The estimated project cost and budget thresholds can be reviewed directly inside the tender document. Bidders can analyze these qualification files to check if their firm meets the financial capability criteria specified for Tender For Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. / Mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr)., Srphc82278090-mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr) With Appropriate Atrial And Ventricular Bipolar Steroid Eluting Lead (mri Conditional) With Life Warranty Provision Of Pacing Therapy For The Use O F The Patients Life-time Including Any No. Of Pulse Generator Replacements As Clinically Required. Should Have The Lates T Technological Features To Provide Proportionate, Smooth And Appropriate Response Of Pacing Rate To Increased Meta Bolic Demand, Should Provide For Atrial And Ventricular Pacing And Sensing With Choice Of At Least 16 Modes Of Operation, Appropriate Safety Features To Avoid Cross Talk, Optimum Flexibility Of Programming (including Minimal Av De Lay Of 30msec Or Less And Atrial Sensitivity Of 0.2mv Or Less), Detailed Data Storage With Easy Retrieval And Display Of A Dvanced Diagnostics For Ease Of Clinical Follow Up & Maximal Longevity. Should Be Capable Of Programming For Prolon Ging Longevity And Maximal Cost Effectiveness. Should Be Capable Of Providing Reliable Ventricular Capture With Lowes T Battery Drain So As To Provide Maximum Longevity Of The Pacing System.( Preferably As An Automatic Feature Where Th E Pulse Generator Can Perform A Periodic Threshold Test And Reliably Verify Ventricular Capture And Adjust Ventricula R Pulse Output Parameters To Minimize Battery Drain Without Compromising Patient Safety). Should Have Features For Au Tomatic Management Of Arrhythmias (including Pacemaker Mediated Arrhythmias) As Well As Automatic Mode Switching ( Mode Switch Should Be To And From Ddd To Ddi/vvir, Provision Of Rate Responsive Pacing After Mode Switch And Automa Tic Reversion To Ddd After Termination Of Mode Switch Triggering Arrhythmias). Should Have Algorithms To Promote Int Rinsic Conduction. Both Atrial And Ventricular Channels Should Have Provision For High Energy Output I.e. Up To At Leas T 6.0 Volts Pulse Amplitude And Pulse Width Up To Atleast 1.0 Ms, Follow Up Diagnosis And Reprogramming Should Be Ren Dered As Effective As Possible Through Provision Of Adequate Information Management Systems On The Programmer. Mri Compatible Leads Should Be Bipolar, Steroid Eluting And Low Profile Either Tined Or Active Fixation Type (7f Or Smaller I Ntroducer Individually). Leads Should Be From The Same Manufacturer I.e. Manufactured By The Same Company As The Pul Se Generator, Not Outsourced And Marketed By Another Company. Pulse Generator And Leads Should Be Suitable For Ad Ult And Paediatric Patients. The Manufacturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. Publications Supporting The Safety And Efficacy Of The Pacemaker Device And The Leads In Clinical Use Should Be Availab Le In Peer Reviewed Journals. The Latest Programmer With Up Dated Software Should Be Available At All Times Permanent Ly In The Hospital. The Programmer Should Have Facilities For Simultaneous Display Of Multiple Surface Ecg Leads, Intrac Ardiac Electrograms, Event Markers, Electronic Calipers And For Recording The Same Both On Paper And In Electronic S Torage Media E.g. Compact Disc Etc., by Southern Railway SR

You can download the commercial Bill of Quantities (BOQ) spreadsheet directly using the secure link provided on this page. The BOQ file contains the item descriptions and rate filling forms officially validated for Tender For Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. / Mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr)., Srphc82278090-mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr) With Appropriate Atrial And Ventricular Bipolar Steroid Eluting Lead (mri Conditional) With Life Warranty Provision Of Pacing Therapy For The Use O F The Patients Life-time Including Any No. Of Pulse Generator Replacements As Clinically Required. Should Have The Lates T Technological Features To Provide Proportionate, Smooth And Appropriate Response Of Pacing Rate To Increased Meta Bolic Demand, Should Provide For Atrial And Ventricular Pacing And Sensing With Choice Of At Least 16 Modes Of Operation, Appropriate Safety Features To Avoid Cross Talk, Optimum Flexibility Of Programming (including Minimal Av De Lay Of 30msec Or Less And Atrial Sensitivity Of 0.2mv Or Less), Detailed Data Storage With Easy Retrieval And Display Of A Dvanced Diagnostics For Ease Of Clinical Follow Up & Maximal Longevity. Should Be Capable Of Programming For Prolon Ging Longevity And Maximal Cost Effectiveness. Should Be Capable Of Providing Reliable Ventricular Capture With Lowes T Battery Drain So As To Provide Maximum Longevity Of The Pacing System.( Preferably As An Automatic Feature Where Th E Pulse Generator Can Perform A Periodic Threshold Test And Reliably Verify Ventricular Capture And Adjust Ventricula R Pulse Output Parameters To Minimize Battery Drain Without Compromising Patient Safety). Should Have Features For Au Tomatic Management Of Arrhythmias (including Pacemaker Mediated Arrhythmias) As Well As Automatic Mode Switching ( Mode Switch Should Be To And From Ddd To Ddi/vvir, Provision Of Rate Responsive Pacing After Mode Switch And Automa Tic Reversion To Ddd After Termination Of Mode Switch Triggering Arrhythmias). Should Have Algorithms To Promote Int Rinsic Conduction. Both Atrial And Ventricular Channels Should Have Provision For High Energy Output I.e. Up To At Leas T 6.0 Volts Pulse Amplitude And Pulse Width Up To Atleast 1.0 Ms, Follow Up Diagnosis And Reprogramming Should Be Ren Dered As Effective As Possible Through Provision Of Adequate Information Management Systems On The Programmer. Mri Compatible Leads Should Be Bipolar, Steroid Eluting And Low Profile Either Tined Or Active Fixation Type (7f Or Smaller I Ntroducer Individually). Leads Should Be From The Same Manufacturer I.e. Manufactured By The Same Company As The Pul Se Generator, Not Outsourced And Marketed By Another Company. Pulse Generator And Leads Should Be Suitable For Ad Ult And Paediatric Patients. The Manufacturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. Publications Supporting The Safety And Efficacy Of The Pacemaker Device And The Leads In Clinical Use Should Be Availab Le In Peer Reviewed Journals. The Latest Programmer With Up Dated Software Should Be Available At All Times Permanent Ly In The Hospital. The Programmer Should Have Facilities For Simultaneous Display Of Multiple Surface Ecg Leads, Intrac Ardiac Electrograms, Event Markers, Electronic Calipers And For Recording The Same Both On Paper And In Electronic S Torage Media E.g. Compact Disc Etc., within the Tamil Nadu jurisdiction

The official timeline and deadline details for Tender For Mri Conditional Pacing System With Accessories For Delivery Of Cardiac Resynchronization Therapy. / Mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr)., Srphc82278090-mri Conditional Dual Chamber Pacemaker Rate Responsive (dddr) With Appropriate Atrial And Ventricular Bipolar Steroid Eluting Lead (mri Conditional) With Life Warranty Provision Of Pacing Therapy For The Use O F The Patients Life-time Including Any No. Of Pulse Generator Replacements As Clinically Required. Should Have The Lates T Technological Features To Provide Proportionate, Smooth And Appropriate Response Of Pacing Rate To Increased Meta Bolic Demand, Should Provide For Atrial And Ventricular Pacing And Sensing With Choice Of At Least 16 Modes Of Operation, Appropriate Safety Features To Avoid Cross Talk, Optimum Flexibility Of Programming (including Minimal Av De Lay Of 30msec Or Less And Atrial Sensitivity Of 0.2mv Or Less), Detailed Data Storage With Easy Retrieval And Display Of A Dvanced Diagnostics For Ease Of Clinical Follow Up & Maximal Longevity. Should Be Capable Of Programming For Prolon Ging Longevity And Maximal Cost Effectiveness. Should Be Capable Of Providing Reliable Ventricular Capture With Lowes T Battery Drain So As To Provide Maximum Longevity Of The Pacing System.( Preferably As An Automatic Feature Where Th E Pulse Generator Can Perform A Periodic Threshold Test And Reliably Verify Ventricular Capture And Adjust Ventricula R Pulse Output Parameters To Minimize Battery Drain Without Compromising Patient Safety). Should Have Features For Au Tomatic Management Of Arrhythmias (including Pacemaker Mediated Arrhythmias) As Well As Automatic Mode Switching ( Mode Switch Should Be To And From Ddd To Ddi/vvir, Provision Of Rate Responsive Pacing After Mode Switch And Automa Tic Reversion To Ddd After Termination Of Mode Switch Triggering Arrhythmias). Should Have Algorithms To Promote Int Rinsic Conduction. Both Atrial And Ventricular Channels Should Have Provision For High Energy Output I.e. Up To At Leas T 6.0 Volts Pulse Amplitude And Pulse Width Up To Atleast 1.0 Ms, Follow Up Diagnosis And Reprogramming Should Be Ren Dered As Effective As Possible Through Provision Of Adequate Information Management Systems On The Programmer. Mri Compatible Leads Should Be Bipolar, Steroid Eluting And Low Profile Either Tined Or Active Fixation Type (7f Or Smaller I Ntroducer Individually). Leads Should Be From The Same Manufacturer I.e. Manufactured By The Same Company As The Pul Se Generator, Not Outsourced And Marketed By Another Company. Pulse Generator And Leads Should Be Suitable For Ad Ult And Paediatric Patients. The Manufacturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. Publications Supporting The Safety And Efficacy Of The Pacemaker Device And The Leads In Clinical Use Should Be Availab Le In Peer Reviewed Journals. The Latest Programmer With Up Dated Software Should Be Available At All Times Permanent Ly In The Hospital. The Programmer Should Have Facilities For Simultaneous Display Of Multiple Surface Ecg Leads, Intrac Ardiac Electrograms, Event Markers, Electronic Calipers And For Recording The Same Both On Paper And In Electronic S Torage Media E.g. Compact Disc Etc., are available inside the detailed notification files. Bidders planning to target this contract in Perambalur should check the official portal schedule early to complete their online technical and financial submission well before the closing hours.