GEM

Open Tender for Blood Bags as per IS 15102,Blood Bags as per IS 15102,Blood Bags as per IS 15102,Blood Bags as per in VADODARA, GUJARAT

Bid Publish Date

29-Jun-2026, 3:49 pm

Bid End Date

14-Jul-2026, 4:00 pm

EMD

₹86,900

Value

₹1,22,19,800

Location

VALSAD , GUJARAT

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Progress

Issue29-Jun-2026, 3:49 pm

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Quantity

51408

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

Bid To RA Enabled

Yes

Item Category

Blood Bags as per IS 15102 (Q2)

Authority Records

HEALTH AND FAMILY WELFARE DEPARTMENT

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Documents 9

GeM-Bidding-9319961.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

CATALOG-Specification-2

CATALOG Specification

CATALOG-Specification-3

CATALOG Specification

CATALOG-Specification-4

CATALOG Specification

CATALOG-Specification-5

CATALOG Specification

CATALOG-Specification-6

CATALOG Specification

Buyer uploaded ATC document

ATC

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Posted: 11 November 2024

Closed: 2 December 2024

GEM

Technical Specifications 6 Items

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	Quadruple (top and bottom)
PRODUCT INFORMATION	Capacity of blood Bag	350 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	Length of tubing from primary bag to needle	≥ 80 Cm
TUBING OF BAG	The tubing should have same ID/segment number as that on the bag	Yes
TUBING OF BAG	The tubes should have multiple printed ID/segment numbers	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)	80
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	Availability of valid drug license issued from competent authority defined under Drugs and Cosmetics Act, 1940 (Proof of the same to be submitted to buyer on demand)	For Manufacture, For Sale
CERTIFICATIONS & REPORTS	Manufacturer certifications (Proof of the same to be submitted to the buyer on demand)	ISO 13485
CERTIFICATIONS & REPORTS	Product Certifications (Proof of the same to be submitted to buyer on demand)	ISO
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

Item #2 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	Quadruple (top and bottom)
PRODUCT INFORMATION	Capacity of blood Bag	350 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	Length of tubing from primary bag to needle	≥ 80 Cm
TUBING OF BAG	The tubing should have same ID/segment number as that on the bag	Yes
TUBING OF BAG	The tubes should have multiple printed ID/segment numbers	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)	80
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	Availability of valid drug license issued from competent authority defined under Drugs and Cosmetics Act, 1940 (Proof of the same to be submitted to buyer on demand)	For Manufacture, For Sale
CERTIFICATIONS & REPORTS	Manufacturer certifications (Proof of the same to be submitted to the buyer on demand)	ISO 13485, GMP
CERTIFICATIONS & REPORTS	Product Certifications (Proof of the same to be submitted to buyer on demand)	ISO, EU-CE
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

Item #3 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	Quadruple (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	Length of tubing from primary bag to needle	≥ 80 Cm
TUBING OF BAG	The tubing should have same ID/segment number as that on the bag	Yes
TUBING OF BAG	The tubes should have multiple printed ID/segment numbers	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	Availability of valid drug license issued from competent authority defined under Drugs and Cosmetics Act, 1940 (Proof of the same to be submitted to buyer on demand)	For Manufacture, For Sale
CERTIFICATIONS & REPORTS	Manufacturer certifications (Proof of the same to be submitted to the buyer on demand)	ISO 13485
CERTIFICATIONS & REPORTS	Product Certifications (Proof of the same to be submitted to buyer on demand)	ISO, BIS, EU-CE
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

Item #4 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	Quadruple (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	Length of tubing from primary bag to needle	≥ 80 Cm
TUBING OF BAG	The tubing should have same ID/segment number as that on the bag	Yes
TUBING OF BAG	The tubes should have multiple printed ID/segment numbers	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	Availability of valid drug license issued from competent authority defined under Drugs and Cosmetics Act, 1940 (Proof of the same to be submitted to buyer on demand)	For Manufacture, For Sale
CERTIFICATIONS & REPORTS	Manufacturer certifications (Proof of the same to be submitted to the buyer on demand)	ISO 13485, GMP
CERTIFICATIONS & REPORTS	Product Certifications (Proof of the same to be submitted to buyer on demand)	ISO, BIS, EU-CE
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

Item #5 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	Quadruple (top and bottom)
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	Length of tubing from primary bag to needle	≥ 80 Cm
TUBING OF BAG	The tubing should have same ID/segment number as that on the bag	Yes
TUBING OF BAG	The tubes should have multiple printed ID/segment numbers	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	Availability of valid drug license issued from competent authority defined under Drugs and Cosmetics Act, 1940 (Proof of the same to be submitted to buyer on demand)	For Manufacture, For Sale
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	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

Item #6 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	Quadruple (top and bottom)
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	Length of tubing from primary bag to needle	≥ 80 Cm
TUBING OF BAG	The tubing should have same ID/segment number as that on the bag	Yes
TUBING OF BAG	The tubes should have multiple printed ID/segment numbers	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	Availability of valid drug license issued from competent authority defined under Drugs and Cosmetics Act, 1940 (Proof of the same to be submitted to buyer on demand)	For Manufacture, For Sale
CERTIFICATIONS & REPORTS	Manufacturer certifications (Proof of the same to be submitted to the buyer on demand)	ISO 13485, GMP
CERTIFICATIONS & REPORTS	Product Certifications (Proof of the same to be submitted to buyer on demand)	ISO, EU-CE
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
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

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CATALOG Specification

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GeM-Bidding-9319961.pdf

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Blood Bags as per IS 15102,Blood Bags as per IS 15102,Blood Bags as per IS 15102,Blood Bags as per

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Documents 9

GeM-Bidding-9319961.pdf

CATALOG-Specification-1

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CATALOG-Specification-5

CATALOG-Specification-6

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CATALOG-Specification-4

CATALOG-Specification-5

CATALOG-Specification-6

Buyer uploaded ATC document

GEM General Terms and Conditions Document