PAC 07 - Department of Military Affairs - Indian Army

UEG 100 uL Kloehn Syringe,UEG 500 uL Kloehn Syringe,UEG 2500 uL Kloehn Syringe,Generic PM Kit Dimen

Goods
Qty:48

Tender Timeline

Tender Issue
June 14, 2025 at 1:13 PM

Tender Description

Tender Title: PAC 07

Tender Reference Number: 142ea10a6

Issuing Authority/Department:
Department of Military Affairs, Ministry of Defence

Scope of Work and Objectives

The PAC 07 tender aims to procure essential medical equipment and supplies which include various types of Kloehn Syringes (100 uL, 500 uL, and 2500 uL), along with a Generic PM Kit for medical operations and related components such as ET CO2 Sampling lines and Water traps specifically for GE Healthcare applications. The objective is to enhance healthcare efficiency and operational readiness concerning military and medical applications.

Tender BOQ Items

7 Items
1.

UEG 100 uL Kloehn Syringe

Qty:6
Unit:pack
30
2.

UEG 500 uL Kloehn Syringe

Qty:6
Unit:pack
30
3.

UEG 2500 uL Kloehn Syringe

Qty:6
Unit:pack
30
4.

Generic PM Kit Dimension EXL

Generic PM Kit Dimension EXL 200

Qty:3
Unit:pack
30
5.

ET CO2 Sampling line for GE

ET CO2 Sampling line for GE Healthcare anaesthesia apparutus

Qty:25
Unit:pkt
30
6.

Water trap for GE Healthcare

Water trap for GE Healthcare Anaesthesia apparatus

Qty:1
Unit:no
30
7.

O2 sensor for GE Healthcare

O2 sensor for GE Healthcare anaeasthesia apparatus

Qty:1
Unit:no
30

General Information

Item Category
UEG 100 uL Kloehn Syringe , UEG 500 uL Kloehn Syringe , UEG 2500 uL Kloehn Syringe , Generic PM Kit Dimension EXL , ET CO2 Sampling line for GE , Water trap for GE Healthcare , O2 sensor for GE Healthcare
Ministry Name
Organisation Name

Financial Information

OEM Average Turnover
₹18.00 Lakh (s)
Minimum Turnover
₹3.00 Lakh (s)
Bid Offer Validity
180 (Days)
Past Performance
50 %
Arbitration Clause
No
Mediation Clause
No

Evaluation and Technical Information

Evaluation Method
Item wise evaluation/
RA Qualification Rule
50% Lowest Priced Technically Qualified Bidders
Inspection Required
Yes
Technical Clarifications Time
2 Days

Tender Documents

4 Documents
GeM-Bidding-7951059.pdfMain Document
BOQ DocumentBOQ BOQ
BOQ DocumentBOQ BOQ
GEM General Terms and Conditions DocumentGEM_GENERAL_TERMS_AND_CONDITIONS

Documents Required from Seller

  • Experience Criteria
  • Past Performance
  • Bidder Turnover
  • Certificate (Requested in ATC)
  • OEM Authorization Certificate
  • OEM Annual Turnover
  • Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria
  • the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer

Frequently Asked Questions

The eligibility requirements include being a registered entity capable of delivering medical devices, possessing the necessary licenses and certifications as per medical standards. Bidders need to demonstrate quality assurance metrics and compliance with local procurement regulations.

Submitting a bid requires certifications that comply with medical device regulations. This includes product quality certifications, ISO standards, and any specific certifications related to medical-grade supplies. It is crucial for bidders to present these required certificates clearly and accurately to ensure compliance.

The registration process involves creating an account on the designated procurement portal. Potential bidders need to submit their business details, including tax identification and certification documents. Completing this process grants access to tender documentation and submission features.

Documents must be submitted in formats specified within the tender guidelines, generally accepted formats include PDF and DOCX. All submissions must be clear, legible, and formatted according to the requirements outlined in the tender document.

Yes, the tender includes provisions specifically aimed at MSEs, enhancing their accessibility to government projects. These benefits can include reduced submission requirements, assistance in the documentation process, and added consideration during the evaluation phase to promote local entrepreneurship and support the ‘Make in India’ initiative.

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