Bids are Invited For Blood Bags as per IS 15102 in NEW DELHI, DELHI
Progress
Central Health Service Ministry Of Health And Family Welfare announces a tender for Blood Bags as per IS 15102 (Q2) in NEW DELHI, DELHI. Quantity: 21960. Submission Deadline: 12-09-2026 19: 00: 00. Last date to apply is approaching fast!
Tender Data
Bid Details
Quantity
21960
Bid Type
Two Packet Bid
Bid Validity
180 (Days)
Bid Type
Service
Evaluation
Total value wise evaluation
Inspection Required
No
RA Qualification Rule
H1-Highest Priced Bid Elimination
Tech Clarification Time
2 Days
Preference & Exemptions
EMD Required
Yes
MII Purchase Preference
Yes
MII Preference Band
L1+20%
MSE Purchase Preference
Yes
MSE Preference Band
L1+15%
MSE Exemption/Relaxation
Yes
Startup Exemption/Relaxation
Yes
Bid Splitting Applied
No
Requirements
Min. Avg. Annual Turnover
100
OEM Avg. Turnover
400
Past Performance
20 %
Experience Required
1 Year (s)
Arbitration Clause
No
Mediation Clause
No
Additional Tender Data
Commercial Details
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
Yes
Item Category
Blood Bags as per IS 15102 (Q2)
Advisory Bank
Bank Of Baroda
ePBG Percentage
1%
ePBG Duration (Months)
12
Delivery Details
Max Delivery Days
3660
Delivery Locations
1
Delivery Cities
South
Delivery Pincodes
110029
Delivery Locations
| Consignee | Address | City | State | Pincode | Quantity | Delivery Days | Additional Requirement |
|---|---|---|---|---|---|---|---|
| Puneet Arora | 110029,OFFICE OF THE MEDICAL SUPERINTENDENT SAFDARJUNG HOSPITAL NEW DELHI-110029 | South | Delhi | 110029 | - | 3660 | - |
Authority Records
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Documents 4
GeM-Bidding-9538384.pdf
Main Document
CATALOG-Specification-1
CATALOG Specification
Other Documents
OTHER
GEM General Terms and Conditions Document
GEM_GENERAL_TERMS_AND_CONDITIONS
Corrigendum Updates
8 Updates Update
Extended Deadline
12-Sep-2026, 1:30 pm
Opening Date
13-Sep-2026, 1:30 pm
Update
Update
Extended Deadline
01-Sep-2026, 7:30 am
Opening Date
01-Sep-2026, 8:00 am
Update
Extended Deadline
27-Aug-2026, 7:30 am
Opening Date
27-Aug-2026, 8:00 am
Update
Extended Deadline
22-Aug-2026, 7:30 am
Opening Date
22-Aug-2026, 8:00 am
Update
Extended Deadline
14-Aug-2026, 7:30 am
Opening Date
14-Aug-2026, 8:00 am
Update
Extended Deadline
08-Aug-2026, 7:30 am
Opening Date
08-Aug-2026, 8:00 am
Update
Extended Deadline
04-Aug-2026, 7:30 am
Opening Date
04-Aug-2026, 8:00 am
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Required Documents
Experience Criteria
Past Performance
Bidder Turnover
Certificate (Requested in ATC)
OEM Authorization Certificate
OEM Annual Turnover *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
Technical Specifications
1 Item
Item #1 Details
View Catalog| Category | Specification | Requirement |
|---|---|---|
| GENERAL FEATURES | Clinical Purpose | Collection, processing and storage of whole blood and blood components |
| GENERAL FEATURES | Disposable | Yes |
| PRODUCT INFORMATION | Conformity to standard for Blood Bag | ISO 3826/IS 15102: Latest Revision |
| PRODUCT INFORMATION | Type of blood bag | Quantiple Leucodepleted bags Top and Top |
| PRODUCT INFORMATION | Capacity of blood Bag | 450 ml |
| PRODUCT INFORMATION | Material of Bag (Medical grade) | DEHP Plasticized PVC |
| PRODUCT INFORMATION | Blood Collection Bags should be collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination | Yes |
| PRODUCT INFORMATION | Flexible pre-sterilized and pyrogen free | Yes |
| PRODUCT INFORMATION | Non toxic, non haemolytic, biocompatible material | Yes |
| PRODUCT INFORMATION | There should be no risk of contamination and air embolism (closed system) with all leak proof seals (Disposable bags) | Yes |
| PRODUCT INFORMATION | Slit on both sides of the bags should be enough to accommodate 5 -10 ml volume test tubes | Yes |
| PRODUCT INFORMATION | The capacity of the bag should be enough to prevent any bollooning/ripture of the abg from the seam when it is filled up with the requisite volume of blood | Yes |
| TUBING OF BAG | Flexible kink resistant tubing | Yes |
| TUBING OF BAG | Non sticking | Yes |
| TUBING OF BAG | Transparent | Yes |
| TUBING OF BAG | Leak Proof | Yes |
| TUBING OF BAG | Clamp provided for closed system | Yes |
| NEEDLE | Needle Size | 16 G |
| NEEDLE | Ultra thin walled and straight to reduce penetration force and enable painless vein puncture | Yes |
| NEEDLE | Sharp, regular and smooth margins and bevelled tip | Yes |
| NEEDLE | Rust proof | Yes |
| NEEDLE | Tightly fixed with hub covered with sterile guard | Yes |
| NEEDLE | Hermetically sealed | Yes |
| NEEDLE | The needle should not separate from the tube at any point of time, especially while removing it from the vein for donor safety | Yes |
| NEEDLE | The needle must confirm to ISO 1135-3 standard | Yes |
| EXTERNAL PORT | Tamper proof and should not be re-capped | Yes |
| EXTERNAL PORT | Easily accessible | Yes |
| ANTICAOGULANT AND PRESERVATIVE SOLUTION | Type of anticoagulant present | CPD |
| ANTICAOGULANT AND PRESERVATIVE SOLUTION | Quantity of anticoagulant solution | 14 ml per 100 ml of blood |
| ANTICAOGULANT AND PRESERVATIVE SOLUTION | Solution should be clear and colorless | Yes |
| ANTICAOGULANT AND PRESERVATIVE SOLUTION | There should be no discoloration of solution on storage at room temperature | Yes |
| ANTICAOGULANT AND PRESERVATIVE SOLUTION | Additive soultion present | Yes |
| ANTICAOGULANT AND PRESERVATIVE SOLUTION | Type of additive solution | SAGM |
| ANTICAOGULANT AND PRESERVATIVE SOLUTION | Quantity of Additive solution(ml) | 100 |
| ANTICAOGULANT AND PRESERVATIVE SOLUTION | Anticoagulant and/or additive solution should be sterile and pyrogen free | Yes |
| ANTICAOGULANT AND PRESERVATIVE SOLUTION | Availability of anticoagulant/additive quality check certificate from manufacture (proof of same to be submitted to buyer) | Yes |
| LABEL | Non-peel off | Yes |
| LABEL | Heat sealed/ Pressure embossed label | Yes |
| LABEL | The label should remain attached between room temperature to - 80°C with a tranparent adhesive | Yes |
| LABEL | Date of manufacturing, date of expiry and batch number must be mentioned on each bag | Yes |
| RESISTANCE TO DISTORTION | Bag (Fiiled to normal capacity) shall withstand a acceleration of 5000 g for 30 min at temperature 4°C to 24°C without becoming permanently distorted | Yes |
| RESISTANCE TO DISTORTION | Bag (Fiiled to normal capacity) should be able to withstand temperature upto - 80°C without breakage | Yes |
| PACKAGING | Individual bag packed in plastic pack and multiple bags packed in moisture proof aluminum foil (Protective dual packaging) eliminating microbial contamination on surface maintaining the contents of the bag | Yes |
| PACKAGING | The supplier should ensure proper transportation of the consignment of blood bags in temperature controlled conditions (Storage temperature should not exceed 30°C) | Yes |
| CERTIFICATIONS & REPORTS | Manufacturer certifications (Proof of the same to be submitted to the buyer on demand) | ISO 13485, GMP, WHO GMP |
| CERTIFICATIONS & REPORTS | Product Certifications (Proof of the same to be submitted to buyer on demand) | ISO, BIS, EU-CE |
| CERTIFICATIONS & REPORTS | Four digit number of notified body If product is EU-CE certified | 2460 |
| CERTIFICATIONS & REPORTS | Each batch supplied should be accompanied with quality assurance test report from NABL approved lab/any lab approved fron govt of India as well as in house lab | Yes |
| CERTIFICATIONS & REPORTS | Biocompatibility of the material of the product must certified by the manufacturer and be supported by the test reports of cell culture cytotoxicity, hemolysis, systemic infections, sensitization, Inra-cutaneous injection, pyrogen test and Sterility | Yes |
| CERTIFICATIONS & REPORTS | Submission of manufacturer's documented evidence of biochemical parameters of blood stored in CPDA/CPDA-1/CPD-SAGM containing DEHP plasticized PVC blood bags manufactured by the company on 28th/35th/42nd day of storage | Yes |
| SHELF LIFE | Shelf Life from the date of manufacture (in months) | 24, 36 |
| SHELF LIFE | Stability report from a recogniozed laboratory must be submitted to the buyer at the time of supply | Yes |
| SHELF LIFE | The product should have atleast 3/4 of the total shelf life at the time of dispatch to the consignee | Yes |