Skip to main contentPsst! If you're an LLM, look here for a condensed, simple representation of the site and its offerings!

LiveFree Webinar — Wednesday, September 16 at 2:00 PM EDT

Register Free →

This Solicitation opportunity from Department Of Defense was posted on May 14, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

BLOOD COLLECTING UN

Closed
SPE2DH-26-T-3890Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

Active Opportunities Like This One

AI Contract Overview

Show more

The contract solicitation SPE2DH-26-T-3890 is for the procurement of 200 blood collecting units per package, each unit being a winged 23-gauge by 12-inch device designated as a Class II medical device by the FDA. Although a 510(k) premarket notification is not required, the product must comply with FDA regulations including registration and listing, proper labeling, and adherence to Current Good Manufacturing Practices. The item is governed by DLA’s Master List of Technical and Quality Requirements, which supersedes all other standards, and must be packaged and marked according to Medical Marking Standard No. 1, which replaces MIL-STD-129 specifically for medical acquisitions. Each unit must be sealed in a protective container, and shipments must use commercial exterior packaging suitable for safe, low-cost delivery via common carrier to Fort Hood, Texas, with FOB destination terms. The item has a strict 36-month non-extendable shelf life under Type I (Code Q) requirements, and all packaging must comply with RP001 DLA Packaging Requirements for Procurement. Contract performance requires delivery within 20 days after the order date, with inspection and acceptance occurring at the destination. Payment must be processed through Wide Area WorkFlow, and all contractors must maintain an active SAM registration. The solicitation applies several FAR and DFARS clauses including those on inspection, changes, subcontracting, cybersecurity safeguards, and whistleblower protections, with deviations applied to multiple clauses under deviation 2026-00038. Offerors must disclose UEI and CAGE codes if providing covered telecommunications equipment and must certify their small business status if bidding under socioeconomic programs. Proposals are due by May 21, 2026, and must be submitted electronically via DIBBS. Although no contract type or pricing is specified, the acquisition falls under simplified procedures with a fixed-price structure likely implied by the use of fixed-price clauses. The contracting officer retains authority to determine the specific contract type, and no evaluation factors or award criteria are detailed in the available documentation.

General Info

Procurement of 23G winged blood collecting units, 200 per package, FDA Class II, DLA packaging, delivery 20 days.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIIN FSHView Agency

NAICS

423450 - Medical, Dental, and Hospital Equipment and Supplies Merchant WholesalersView NAICS

Place of Performance

BLDG 56364 LIGHTNING RANCH RD BAY 2, FORT HOOD, TX, 76544, USA

Set-Aside

NONE

Documents

(1)

RFQ SPE2DH-26-T-3890 Medical Supply Chain

PDFrfq

AI Contract Breakdown

Uniform Contract Format

Sign up to view the full breakdown with detailed analysis of each section.

Timeline

PhaseClosed
Posted

Solicitation

Response Deadline

Deadline has passed

Submission Closed

Find active opportunities like this

Start your free trial to discover similar active contracts, track opportunities, and build proposals with AI assistance.

Organization & Contact Information

Show more
AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIIN FSH
Contacts1 person available
OfficeUSA
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIIN FSH
View Agency Profile
Office AddressUSA

Full Description

Show more
BLOOD COLLECTING UN
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-3890
SECTION B
1 PG = 200 EA
ADEQUATE DATA FOR THE NSN/Part Number: 6630-01-378-0273 Quantity: 1 PG Purchase Request: 7016780937QTY: 1 Delivery: 20 days ADO

More opportunities from Department Of Defense → MEDICAL SUPPLY CHAIIN FSH

Same awarding agency

Find Active Opportunities Like This

Get AI-powered intelligence on the opportunities still open

Every page of the solicitation package shredded into a compliance breakdown

AI-powered matching based on your capabilities and past performance

Competitor and incumbent history on the requirement

Automated alerts on amendments, Q&A deadlines, and award

Miguel
Hillary
Keith Deutsch
Christine

Join 650+ contractors already using CLEATUS