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Tender Notice for Temporary bipolar pacing catheter,Totally Subcutaneously automated implantable cardiovertor defibri

Bid Publish Date

23-Oct-2024, 1:26 pm

Bid End Date

13-Nov-2024, 2:00 pm

Progress

Issue23-Oct-2024, 1:26 pm
AwardPending
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Quantity

10

Categories 13

A tender has been published for The issuing authority Temporary bipolar pacing catheter, Totally Subcutaneously automated implantable cardiovertor defibri. Quantity: 10 by. Submission Deadline: 13-11-2024 14: 00: 00. Check eligibility and apply.

Documents 4

GeM-Bidding-7015933.pdf

Main Document

BOQ Document

BOQ

BOQ Document

BOQ

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

Bill of Quantities (BOQ) 7 Items

Item # Title Description Quantity Unit Consignee Delivery (Days)
1 Temporary bipolar pacing catheter Temporary bipolar pacing catheter 1 no oicprocurementcell 21
2 Totally Subcutaneously automated implantable cardiovertor defibrillator SICD which is MRI safe allong with all accessories and subcutaneous leads. Totally Subcutaneously automated implantable cardiovertor defibrillator SICD which is MRI safe allong with all accessories and subcutaneous leads. 1 no oicprocurementcell 21
3 Smartphone app based remote monitoring enabled whole body MRI safe single chamber implantable cardiovertor defibrillator Smartphone app based remote monitoring enabled whole body MRI safe single chamber implantable cardiovertor defibrillator SC AICD which delivers 40 joules energy with programmable tilt and pulse with programming. 1 no oicprocurementcell 21
4 smartphone app based remote monitoring enabled 3T whole body MRI safe dual chamber implantable cardiovertor defibrillator smartphone app based remote monitoring enabled 3 T whole body MRI safe dual chamber implantable cardiovertor defibrillator DC AICD with 40 J with programmable tilt and pulse width programming 2 no oicprocurementcell 21
5 Smartphone app based 3T MRI whole body MRI safe implantable cardiac resynchranisation therapy with 40J defibrillator Smartphone app based 3T MRI whole body MRI safe implantable cardiac resynchranisation therapy with 40J defibrillator CRT D with programmable defib pulse width programming and device based atrioventricular optimization 2 no oicprocurementcell 21
6 3 T whole body safe mri dual chamber pacemaker with deflectable His Bundle pacing catheter HIS bundle pacemaker with mapping capabilities 3T whole body safe mri dual chamber pacemaker with deflectable His Bundle pacing catheter HIS bundle pacemaker with mapping capabilities 1 no oicprocurementcell 21
7 3T full body MRI safe Dual Chamber pacemaker DDDR with transvenous leads and introducer sheaths. 3T full body MRI safe Dual Chamber pacemaker DDDR with transvenous leads and introducer sheaths. 2 no oicprocurementcell 21

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Frequently Asked Questions

## FAQs
What are the eligibility requirements for this tender?

The eligibility requirements include being a registered entity with a minimum average annual turnover of 20 Lakhs over the last three years. A minimum experience of 3 years in supplying similar medical devices is also necessary. Additionally, MSEs may enjoy exemptions related to experience and turnover.

What certificates are required during the bidding process?

Bidders must provide a variety of certificates, including proof of turnover, compliance documentation for BoQ specifications, and, depending on the offer, an OEM authorization certificate. Proper documentation is critical to demonstrate eligibility.

How can bidders register for this tender?

To register for the tender, bidders must create an account on the GeM portal. Once registered, they can participate in the bidding process by submitting their offers electronically along with required documentation.

What document formats are accepted for submission?

The accepted document formats typically include PDF and scanned copies of certificates and compliance documents. All submissions should be digitally uploaded through the GeM portal to maintain standards and security.

What are the technical specifications for medical devices?

Technical specifications generally outline safety, functionality, and compatibility with hospital equipment. Each item, such as the temporary bipolar pacing catheter and automated implantable cardioverter defibrillator, must comply with requisite regulations and should be backed by supporting documentation.

What quality standards must be met for the supplied products?

Implementation of recognized quality standards as per medical device regulations is required. Bidders must ensure that their products meet local and national certification standards and are validated through appropriate testing.

Are there any compliance requirements for product offerings?

Yes, all product offerings must comply with national health regulations and standards for medical devices. Bidders should provide evidence of compliance with necessary regulatory frameworks.

What are the criteria for testing the medical devices?

The testing criteria may include validation of device functionality, safety assessments, and conformity with technical specifications outlined in the submission documents. Bidders may be asked to provide samples for testing during the evaluation process.

What are the details for the Earnest Money Deposit (EMD)?

The tender may require bidders to submit an Earnest Money Deposit (EMD). The EMD safeguards against bid withdrawal and generally forms part of the overall financial requirements detailed in the tender documentation.

What are the performance security requirements?

Upon acceptance of the tender, successful bidders may be required to submit performance security to guarantee compliance with the terms of the contract. This is typically expressed as a percentage of the contract value and must be maintained for the contract duration.

What are the payment terms for successful bidders?

Payment terms will be outlined in the contract negotiated post-award of the bid. Generally, payments are structured around delivery milestones, with possible provisions for advance payments as specified.

How will bids be evaluated and selected?

Bids will be evaluated based on their adherence to eligibility criteria, technical compliance, and bidder past performance. The selection process is structured to identify offers best suited to meet quality and budgetary requirements.

How will bidders be notified of the tender results?

Bidder notifications regarding the results will typically occur through the GeM portal. Bidders should ensure their accounts are updated to receive notifications directly related to their submissions.

What are the benefits for MSEs in this tender?

MSEs enjoy special conditions such as exemptions from certain experience requirements, designed to foster competitive opportunities and incorporate smaller bidders into the supply chain.

Are there provisions for startups?

Startups are not provided with exemptions related to experience and turnover in this tender, ensuring that all bidders demonstrate a consistent operational history before being considered.

How does this tender comply with 'Make in India' policies?

This tender promotes local manufacturing by prioritizing vendors who align with the 'Make in India' initiative, encouraging domestic production and innovation within the medical supplies arena.

What are the local content and procurement rules applicable here?

Local content and procurement rules dictate that bids prioritize local suppliers, ensuring that domestic entities are supported through public procurement processes and enhancing local business opportunities.

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