Indian Army Blood Collection Tube Procurement Tender 2025 India ISO 9001 BIS Type Test
Indian Army
JALANDHAR, PUNJAB
Bid Publish Date
24-Feb-2026, 9:51 am
Bid End Date
06-Mar-2026, 10:00 am
Location
Progress
Quantity
49000
Category
Blood Collection Tube
Bid Type
Single Packet Bid
Public procurement opportunity for Indian Navy Blood Collection Tube (Q2) in MUMBAI, MAHARASHTRA. Quantity: 49000 issued by. Submission Deadline: 06-03-2026 10: 00: 00. View full details and respond.
Main Document
CATALOG Specification
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS
Indian Army
JALANDHAR, PUNJAB
N/a
SOUTH ANDAMAN, ANDAMAN & NICOBAR
Employees State Insurance Corporation
N/a
SHIMOGA, KARNATAKA
N/a
JAMNAGAR, GUJARAT
Tender Results
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| Category | Specification | Requirement |
|---|---|---|
| GENERAL | Product Description | Blood Collection Tube |
| GENERAL | Usage | Single-Use (Disposable) |
| GENERAL | Sterility | Sterile |
| TECHNICAL INFORMATION | Type of Tube | Vacuum Blood Collection Tube (Evacuated Tube) |
| TECHNICAL INFORMATION | Material of Tube | Polyethylene Terephthalate (PET) |
| TECHNICAL INFORMATION | Non toxic, leakproof and crack resistance material | Yes |
| TECHNICAL INFORMATION | Transparency | Transparent |
| TECHNICAL INFORMATION | Negative air pressure present inside the tube | Yes |
| TECHNICAL INFORMATION | Additive | 3.2% Sodium Citrate |
| TECHNICAL INFORMATION | Draw volume of blood sample | 3 mL |
| TECHNICAL INFORMATION | Cap Color | Light Blue |
| TECHNICAL INFORMATION | Patient Utility | Adult |
| TECHNICAL INFORMATION | Graduation marking | Yes |
| TECHNICAL INFORMATION | Label on tube for Identification | Yes |
| CERTIFICATIONS | Compliance to Medical Device Rules (MDR) 2017 as amended till date | Yes |
| CERTIFICATIONS | Availability of valid medical device license for the product issued from the competent authority defined under Drugs and Cosmetic Act 1940 and Rules made there under as amended till date | Yes |
| CERTIFICATIONS | Manufacturer Certification | ISO:13485 (Latest) |
| CERTIFICATIONS | Availability of Test Report for each supplied batch/product as per Medical Device Rules (MDR) 2017 as amended till date | Yes |
| CERTIFICATIONS | Submission of all necessary certifications, licenses and test reports to the buyer at the time of bid submission and/or along with supplies as per buyer requirement | Yes |
| SHELF LIFE | Minimum shelf life of the product at the time of delivery to the consignee | 3/4 th of Total Shelf Life |
| ADVANCE SAMPLE | Agree to provide advance sample of the product for buyer's approval after award of contract and before commencement of supply in case of bidding only | Yes |
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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
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Main Document
CATALOG Specification
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS