BLOOD COLLECTING UNIT
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Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.
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The contract specifies the procurement of 2 packages of 200 blood collecting units each, totaling 400 units, with each unit being a winged blood collecting device at 23 gauge by 12 inches. The item is identified by NSN 6632-01-378-0273 and has been classified by the FDA as a Class II medical device, requiring compliance with registration, listing, labeling, and good manufacturing practices despite the absence of a 510(k) requirement. All packaging must meet commercial standards as outlined in the procurement document and adhere to Medical Marking Standard No. 1, which supersedes MIL-STD-129; packaging must protect against damage and ensure safe delivery via common carrier at the lowest cost to Fort Campbell, Kentucky. Documentation referencing the DLA Master List of Technical and Quality Requirements applies, with the revision in effect on the solicitation issue date controlling compliance. The bidder must clearly state the commercial item and part number being supplied, and the contracting official must submit a referral in EBS to verify regulatory compliance, including manufacturer details and item description. Delivery is required within 20 days of award, with the solicitation closing on August 5, 2026.
General Info
Agency
NAICS
Place of Performance
BLDG 5505A WICKHAM AVE, FORT CAMPBELL, KY, 42223-5000, USSet-Aside
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Organization & Contact Information
Full Description
BLOOD COLLECTING UNIT, WINGED, 23GA BY 12", 200S
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RA001: THIS DOCUMENT INCORPORATES TECHNICAL AND/OR QUALITY REQUIREMENTS
(IDENTIFIED BY AN 'R' OR AN 'I' NUMBER) SET FORTH IN FULL TEXT IN THE
DLA MASTER LIST OF TECHNICAL AND QUALITY REQUIREMENTS FOUND ON THE WEB
AT:
http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx
FOR SIMPLIFIED ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE SOLICITATION ISSUE DATE OR THE AWARD DATE CONTROLS. FOR LARGE ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE RFP ISSUE DATE APPLIES UNLESS A SOLICITATION AMENDMENT INCORPORATES A FOLLOW-ON REVISION, IN WHICH CASE THE AMENDMENT DATE CONTROLS.
RQ011: REMOVAL OF GOVERNMENT IDENTIFICATION FROM NON-ACCEPTED SUPPLIES
APPLICABLE TO ALL MEDICAL ACQUISITIONS:
PACKAGING AND PACKING SHALL BE COMMERCIAL AS
SPECIFIED IN THE PROCUREMENT DOCUMENT.
EACH COMPLETE UNIT SHALL BE PROPERLY PACKAGED
IN A SUITABLE SEALED UNIT CONTAINER CAPABLE
OF PROTECTING THE CONTENTS FROM DAMAGE AND/OR
BREAKAGE.
UNITS SHALL BE PACKED IN SUITABLE COMMERCIAL
EXTERIOR (SHIPPING) CONTAINERS (EXPORT WHEN
NECESSARY) WHICH SHALL INSURE ACCEPTANCE AND
SAFE DELIVERY BY COMMON OR OTHER CARRIER, AT
THE LOWEST RATE, TO POINT OF DELIVERY CALLED
FOR IN THE CONTRACT OR ORDER.
MATERIAL MUST BE MARKED IAW MEDICAL MARKING
STANDARD NO. 1. THIS SUPERCEDES ALL REFERENCES
TO MIL-STD-129.
COPIES OF MEDICAL MARKING STANDARD NO. 1
(MMS NO. 1) MAY BE OBTAINED BY CONTACTING DLA
TROOP SUPPORT VIA EMAIL TO fssb@dla.mil. MMS NO. 1 IS ALSO AVAILABLE ONLINE AT: https://www.dla.mil/Logistics-Operations/Packaging/
U/I PG OF 200S BIDDER SHALL SPECIFY CO & P/N BEING SUPPLIED THIS ITEM HAS BEEN DESIGNATED A MEDICAL DEVICE BY FDA. . This device or drug is regulated by the FDA. Note to Buyers: The contracting official shall send a referral in EBS to the product specialist for confirmation. Please include bidder name and bidder contact information, manufacturer name, manufacturer part number, and item description. REGULATION 862.1675 CLASS II EVEN THOUGH A 510(K) IS NOT REQUIRED, IT IS NECESSARY TO MEET OTHER REQUIREMENTS FOR MARKETING. THESE INCLUDE: REGISTRATION AND LISTING, LABELING OR GMP'S.
SPE2DH-26-T-5609
SECTION B
1 PG = 200 EA
ADEQUATE DATA FOR THE NSN/Part Number: 6632-01-378-0273 Quantity: 2 PG Purchase Request: 7017653344QTY: 2 Delivery: 20 days ADO
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