Railways Government Departments Closing in 0 days TDR #52187199

Supply Of Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System

Issued by Government Departments · perambalur, Tamil Nadu
Tender Value
Ref. Documents
Estimated cost
Bid Submission
28 Nov 2025
0 days left
EMD
76880
Bank guarantee accepted
Document Fee
Ref. Documents
Non-refundable
Tender Type
Online

Tender Overview

Competition Type
NCB
Bidding Type
Tender
Location / State
perambalur → Tamil Nadu
EMD Exemption
Not Available
Quantity
Not Available

Project Description

Supply Of Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator Systemmri Conditional Dual Chamber Implantable Cardioverter Defibrillator System,Srphc154066-Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System With Appropriate Atrial And Ventricular Pace / Sense Leads With Df - 4 Connector And Option Of Dual Shocking Coil Leads And Accessories. System Should Have Advanced Features For The Reliable Detection And Management Of Ventricular Tachycardia And Ven Tricular 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 Sh Ould Be Capable Of Delivering Maximum Energy Of 35J Or More And Should Have Features For Management Of High Defibril Lation Energy Requirement. Charge Times Should Be Within Clinically Acceptable Limits Throughout The Lifetime Of The D Evice.Leads Should Be Low Profile And Choice Of Both Active Or Passive Fixation Leads Should Be Available. Should Have Features For Automatically Alerting The Patient In The Event Of A Battery Or Lead Fault. Data Storage Retrieval And Dis Play 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 Pa Rameters For High Output For Post-Shock Pacing) Should Be Available. Warranty Terms Should Be Specified Clearly Alon G With The Quotation. Firms Should Submit Detailed Literature Of The Item In A Bulletin/Tutorial Format Which Should Co Ntain All The Details About The Product. Compliance Statement Of Each Specification To Be Submitted. The Firm Quoting T He Tender Should Submit A Letter Of Authorisation From The Principal Firm/Original Equipment Manufacturer. The Manuf Acturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. The Safety And Efficacy Of The Icd Dev Ice And The Lead In Clinical Use Should Be Documented In Scientific Publications. 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 ] ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 5.00 , Srphc154061-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 Wit H Ventricular Pacing And Anti-Tachycardia Pacing. It Should Be Capable Of Delivering Maximum Energy Of 35 J Or More Wit H Acceptable Limits Throughout The Lifetime Of The Device. It Should Automatically Alert The Patient In The Event Of Batt Ery Or Lead Fault. Data Storage, Retrieval And Display Should Be Efficient And User Friendly. Data Storage Should Inclu De 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 It Em 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 Scientifi C Publications. The Firm Quoting The Tender Should Submit A Letter Of Authorisation From The Principal Firm/Original Eq Uipment 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 Mentio Ned Specifications Are Essential And Mandatory And Should Be Submitted At The Time Of Initial Tender Submission. Unit:N O ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 8.00

BOQ

Sl. No. Item Description
1Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System
2SRPHC154066-MRI CONDITIONAL DUAL CHAMBER IMPLANTABLE CARDIOVERTER DEFIBRILLATOR SYSTEM WITH APPROPRIATE ATRIAL AND VENTRICULAR PACE / SENSE LEADS WITH DF - 4 CONNECTOR AND OPTION OF DUAL SHOCKING COIL LEADS AND ACCESSORIES.SYSTEM SHOULD HAVE ADVANCED FEATURES FOR 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 DELIVERING MAXIMUM ENERGY OF 35J OR MORE AND SHOULD HAVE FEATURES FOR MANAGEMENT OF HIGH DEFIBRILLATION ENERGY REQUIREMENT. CHARGE TIMES SHOULD BE WITHIN CLINICALLY ACCEPTABLE LIMITS THROUGHOUT THE LIFETIME OF THE DEVICE.LEADS SHOULD BE LOW PROFILE AND CHOICE OF BOTH ACTIVE OR PASSIVE FIXATION LEADS SHOULD BE AVAILABLE. SHOULD HAVE FEATURES 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 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 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 CLINICAL USE SHOULD BE DOCUMENTED IN SCIENTIFIC PUBLICATIONS. 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 ] ]ACHD/Surg.Store/RH/PER, SR chennai Tamil Nadu 5.00
3 SRPHC154061-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 EACHSPECIFICATION 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 GOVERNMENTINSTITUTES. 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 ]ACHD/Surg.Store/RH/PER, SR chennai Tamil Nadu 8.00

AI Tender Summary

OUR REF NO 52187199
AUTHORITY Government Departments
TENDER VALUE Ref. Documents
LAST DATE 28-11-2025
Authority
Authority Name Southern Railway
Work Description Supply Of Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator Systemmri Conditional Dual Chamber Implantable Cardioverter Defibrillator System,Srphc154066-Mri Conditional Dual Chamber Implantable Cardioverter Defibrillator System With Appropriate Atrial And Ventricular Pace / Sense Leads With Df - 4 Connector And Option Of Dual Shocking Coil Leads And Accessories. System Should Have Advanced Features For The Reliable Detection And Management Of Ventricular Tachycardia And Ven Tricular 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 Sh Ould Be Capable Of Delivering Maximum Energy Of 35J Or More And Should Have Features For Management Of High Defibril Lation Energy Requirement. Charge Times Should Be Within Clinically Acceptable Limits Throughout The Lifetime Of The D Evice.Leads Should Be Low Profile And Choice Of Both Active Or Passive Fixation Leads Should Be Available. Should Have Features For Automatically Alerting The Patient In The Event Of A Battery Or Lead Fault. Data Storage Retrieval And Dis Play 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 Pa Rameters For High Output For Post-Shock Pacing) Should Be Available. Warranty Terms Should Be Specified Clearly Alon G With The Quotation. Firms Should Submit Detailed Literature Of The Item In A Bulletin/Tutorial Format Which Should Co Ntain All The Details About The Product. Compliance Statement Of Each Specification To Be Submitted. The Firm Quoting T He Tender Should Submit A Letter Of Authorisation From The Principal Firm/Original Equipment Manufacturer. The Manuf Acturer / Supplier Should Submit Proof Of Supply To A Major Government Institute. The Safety And Efficacy Of The Icd Dev Ice And The Lead In Clinical Use Should Be Documented In Scientific Publications. 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 ] ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 5.00 , Srphc154061-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 Wit H Ventricular Pacing And Anti-Tachycardia Pacing. It Should Be Capable Of Delivering Maximum Energy Of 35 J Or More Wit H Acceptable Limits Throughout The Lifetime Of The Device. It Should Automatically Alert The Patient In The Event Of Batt Ery Or Lead Fault. Data Storage, Retrieval And Display Should Be Efficient And User Friendly. Data Storage Should Inclu De 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 It Em 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 Scientifi C Publications. The Firm Quoting The Tender Should Submit A Letter Of Authorisation From The Principal Firm/Original Eq Uipment 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 Mentio Ned Specifications Are Essential And Mandatory And Should Be Submitted At The Time Of Initial Tender Submission. Unit:N O ] Achd/Surg.Store/Rh/Per, Sr Chennai Tamil Nadu 8.00
Basic Detail
Tender No 02256625
Bidding Type Tender
Location
City perambalur
State Tamil Nadu
Key Dates
Publish Date 06 Nov 2025
Submission Date 28 Nov 2025
Open Date 01 Jan 0001
Finance
Tender Value Ref. Documents
Tender Fee Ref. Documents
EMD 76880
Exemption Not Available
Document List
59afad7a-515a-4611-a062-987aa0a23c7e.pdf

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Tender Timeline

Nov 06, 2025
11:30 IST

Tender Published

Tender notice published.

Completed
Nov 28, 2025
17:00 IST

Bid Submission Deadline

Online submission via eProcurement portal.

Completed

Tender Documents

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pdf

59afad7a-515a-4611-a062-987aa0a23c7e.pdf

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