ENDO CONSUMABLES - Department of Military Affairs - Indian Army

Libre Freestyle Glucose Monitoring Sensor,Free style optium Neo H Glucose Test Strips,Freestyle Opt

Goods
Qty:677
EMD: ₹6,300

Tender Timeline

Tender Issue
June 10, 2025 at 10:21 AM

Tender Description

Tender Title: ENDO CONSUMABLES
Reference Number: 16ebf3642
Issuing Authority/Department: Department of Military Affairs, Ministry of Defence

The ENDO CONSUMABLES tender aims to procure essential medical supplies, specifically targeting the Libre Freestyle Glucose Monitoring Sensor and associated products, including Free style optium Neo H Glucose Test Strips and Freestyle Optium Neo H Beta Ketones Test Strips. This solicitation seeks to secure a total quantity of 677 units across various, clearly defined items which will ensure the availability of crucial components for glucose and ketone monitoring.

Tender BOQ Items

6 Items
1.

Libre Freestyle Glucose Monitoring Sensor

As per uploaded file

Qty:60
Unit:no
28
2.

Free style optium Neo H Glucose Test Strips

As per uploaded file

Qty:500
Unit:no
28
3.

Freestyle Optium Neo H Beta Ketones Test strip

As per uploaded file

Qty:60
Unit:no
28
4.

Disposable for insulin pump Quickset and Reservoir 10 disp per pkt

As per uploaded file

Qty:12
Unit:pkt
28
5.

FREE STYLE LIBRE READER

As per uploaded file

Qty:30
Unit:no
28
6.

REAL TIME CONTINUOUS GLUCOSE MONITORING SYSTEM CGMS

As per uploaded file

Qty:15
Unit:box
28

General Information

Item Category
Libre Freestyle Glucose Monitoring Sensor , Free style optium Neo H Glucose Test Strips , Freestyle Optium Neo H Beta Ketones Test strip , Disposable for insulin pump Quickset and Reservoir 10 disp per pkt , FREE STYLE LIBRE READER , REAL TIME CONTINUOUS GLUCOSE MONITORING SYSTEM CGMS
Ministry Name
Organisation Name
State

Financial Information

EMD Amount
₹6,300.00
OEM Average Turnover
₹3.00 Lakh (s)
Minimum Turnover
₹3.00 Lakh (s)
Bid Offer Validity
180 (Days)
Past Performance
50 %
Arbitration Clause
Yes (Arbitration clause document) as per DoE OM No.F.1/2/2024-PPD dated 03.06.2024 Arbitration should not be routinely included in contracts
Mediation Clause
Yes (Mediation clause document) as per DoE OM No.F.1/2/2024-PPD dated 03.06.2024 mediation clause should not be routinely included in contracts and pre- litigation mediation can be taken up without any such clause also

Evaluation and Technical Information

Evaluation Method
Item wise evaluation/
RA Qualification Rule
H1-Highest Priced Bid Elimination
Inspection Required
Yes
Technical Clarifications Time
2 Days

Tender Documents

7 Documents
GeM-Bidding-7894601.pdfMain Document
Other DocumentsOTHER
Other DocumentsOTHER
BOQ DocumentBOQ BOQ
BOQ DocumentBOQ BOQ
Buyer uploaded ATC documentATC ATC
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 with relevant experience in supplying medical devices. Bidders should present their legal documents, compliance certificates, and a history of similar supply contracts to demonstrate their capabilities and qualifications.

Bidders need to provide various certificates such as ISO certifications, product-specific compliance documents, and any additional quality assurance certificates that ensure the medical supplies meet the industry’s safety and quality standards.

The registration process involves registering on the designated procurement platform, submitting the relevant documentation, including company details and product specifications, and ensuring that all requirements are met according to the guidelines laid out in the tender documents.

Submissions must be made in standard formats, including PDF and Word documents. It is essential that all files are clear, legibly formatted, and easily accessible to facilitate the evaluation process by the tender committee.

Yes, the tender specifies that all products must comply with defined quality standards established for medical devices. Testing criteria include ensuring that all items meet safety regulations, undergo quality assurance checks, and possess necessary certifications to validate their performance and reliability in medical applications.

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