This Solicitation opportunity from Department Of Defense was posted on May 10, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.
TEST KIT, HUMAN IMMU
Contract Overview
Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.
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AI Contract Overview
The contract specifies the procurement of a human immunodeficiency virus (HIV) detection test kit designed to identify HIV-1/2 antigen/antibody combo. Each package includes five test cards with five tests per card, housed in an aluminum ziplock pouch, accompanied by a desiccant package, chase buffer prepared for whole blood samples, a quick reference guide, package insert, 25 subject information notices, a customer letter, 25 disposable capillary tubes, and 25 disposable workstations. The unit of issue is one package containing 25 complete test kits. The delivered product must meet strict technical and quality standards as outlined by the Defense Logistics Agency (DLA), including adherence to packaging, labeling, and marking requirements consistent with Medical Marking Standard No. 1 to ensure safe transport and identification. The test kits carry an 18-month non-extendable shelf life, with no more than two months elapsed from manufacture to delivery, and all labeling must include manufacture and expiration dates, contract and lot numbers. Packaging must be commercial-grade, sealed to protect contents from damage, and suitable for shipment to the designated delivery point at the lowest transportation rate. The contract references applicable DLA packaging and quality mandates and includes requirements for removal of government identification on non-accepted supplies. The solicitation is issued by the Department of Defense’s Medical Supply Chain and delivery is expected within 83 days. Contact for the solicitation is Mary-Kathryn Donahue, with the procurement identified under solicitation SPE2DS-26-T-062L.
General Info
Agency
NAICS
Place of Performance
ATTN CL VIII MED REQ PROCES ACT, APO, AE, 09227-0000, USSet-Aside
Timeline
Submission Closed
Organization & Contact Information
Full Description
TEST KIT, HUMAN IMMUNODEFICIENCY VIRUS DETECTION
FEATURES DETERMINE HIV-1/2 AG/AB COMBO TEST;
CONTAINS: FIVE TEST CARDS (5 TESTS/CARD) CONTAINED IN ALUMINUM ZIPLOCK
POUCH; ONE DESICCANT PACKAGE; ONE 2.5 ML CHASE BUFFER PREPARED IN
PHOSPHATE BUFFER (FOR TESTING WHOLE BLOOD SAMPLES); ONE QUICK REFERENCE
GUIDE; ONE PACKAGE INSERT; 25 SUBJECT INFORMATION NOTICE; ONE CUSTOMER
LETTER; 25 DISPOSABLE CAPILLARY
TUBES; 25 DISPOSABLE WORKSTATION.
UNIT OF ISSUE: PG (25 EACH PER PACKAGE)
..
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.
..
RD003, COVERED DEFENSE INFORMATION POTENTIALLY APPLIES
..
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
..
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:
SPE2DS-26-T-062L
SECTION B
https://www.dla.mil/Logistics-Operations/Packaging/
.. RS013: Shelf-life requirement RS001 for a TYPE I (CODE K) item with a shelf life of 18 months (non-extendable) applies to this item.
SHALL HAVE A SHELF LIFE OF 18 MONTHS. NOT MORE THAN 2 MONTHS SHALL HAVE ELAPSED FROM DATE OF MANUFACTURE TO DATE OF DELIVERY TO THE GOVERNMENT. . SHELF LIFE MARKINGS SHALL BE IN ACCORDANCE WITH THE LATEST REVISION OF MMS1C.
. ALL LABELS SHALL INCLUDE:
DATE OF MANUFACTURE, EXPIRATION, OR RETEST DATE CONTRACT NUMBER/LOT NUMBER. .. ADEQUATE DATA FOR THE NSN/Part Number: 6550-01-692-1809 Quantity: 1 PG Purchase Request: 7016657888QTY: 1 Delivery: 83 days ADO
