This Solicitation opportunity from Department Of Defense was posted on April 12, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.
TEST KIT, HUMAN IMMU
Contract Overview
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AI Contract Overview
The contract is for a human immunodeficiency virus (HIV) detection test kit designed for in vitro use, providing qualitative, visually read results through an immunoassay. The kit delivers faster detection compared to conventional antibody-only tests and can be used with various human specimen types, including serum, plasma, capillary whole blood, and venous whole blood. Uniquely, it may differentiate acute HIV-1 infection by detecting HIV-1 P24 antigen when antibody tests are negative. Each package contains 25 tests organized as five test cards with five tests each, accompanying consumables such as disposable capillary tubes, a chase buffer, workstation, desiccant, and instructional materials. Storage conditions require maintenance between 2 to 30 degrees Celsius, and the item has a non-extendable shelf life of 18 months. Packaging and shipping must adhere to commercial standards specified in the procurement document, including proper sealing and protection to prevent damage during transport. The material requires marking according to Medical Marking Standard No. 1, superseding MIL-STD-129, with instructions available from DLA Troop Support. The contract emphasizes regulatory compliance with FDA requirements and mandates that bidders specify the source and part number of the supplied kits. Delivery is stipulated at destination within five days of order placement, with an exact delivery date expected by mid-April 2026. The acquisition is facilitated through the Department of Defense’s Medical Supply Chain, supporting military medical operations, and includes detailed logistical instructions ensuring safe and compliant supply distribution.
General Info
Agency
Contract Value
$463NAICS
Place of Performance
USASet-Aside
Awardee
Award Issued Date
Documents
(1)AI Contract Breakdown
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Timeline
Submission Closed
Organization & Contact Information
Full Description
TEST KIT, HUMAN IMMUNODEFICIENCY
VIRUS DETECTION
IN VITRO, VISUALLY READ, QUALITATIVE
IMMUNOASSAY GIVES FASTER RESULTS THAN
CONVENTIONAL TESTS THAT RELY SOLELY ON
PRESENCE OF HIV-1/2 ANTIBODIES; CAN BE
USED WITH HUMAN SERUM, PLASMA, CAPILLARY
(FINGERSTICK) WHOLE BLOOD OR VENIPUNCTURE
(VENOUS) WHOLE BLOOD; MAY DISTINGUISH
ACUTE HIV-1 INFECTION FROM ESTABLISHED
HIV-1 INFECTION WHEN SPECIMEN IS POSITIVE
FOR HIV-1 P24 ANTIGEN AND NEGATIVE FOR
ANTI-HIV-1 AND ANTI-HIV-2 ANTIBODIES;
25 PER PACKAGE; 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
.
STORE AT 2-30 DEGREES C (36-86 DEGREES F)
.
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.
. UNIT OF ISSUE PACKAGE, PG, OF 25S . 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.
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RQ011: REMOVAL OF GOVERNMENT IDENTIFICATION FROM NON-ACCEPTED SUPPLIES
.
BIDDER SHALL SPECIFY SOURCE AND
PART NUMBER BEING SUPPLIED.
.
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. .
APPLICABLE TO ALL MEDICAL ACQUISITIONS:
SPE2DS-26-T-9169
SECTION B
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/
RD003, COVERED DEFENSE INFORMATION POTENTIALLY APPLIES
DOVE MEDICAL SUPPLY LLC 6YAE8 P/N ALR-7D2648
ABBOTT LABORATORIES INC. 33110 P/N 7D2648
DLA issues this document using the DoD authorized unit of issue, please refer to the following URL to determine the corresponding ANSI X12 unit of issue.
https://view.officeapps.live.com/op/view.aspx?src=https%3A%2F%2Fwww.dla.mil%2FPortals%2F104%2FDocuments% 2FDLMS%2FeApplications%2FLogDataAdmin%2FUnitofIssueandPurchaseUnit.xlsx&wdOrigin=BROWSELINK
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0001 7016289024 0001 PG 1.000
NSN/MATERIAL:6550016921809
DELIVERY (IN DAYS):0005
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA MIL-STD-2073-1E
QUP:001 PRES MTHD:ZZ CLNG/DRY:Z PRESV MAT:ZZ
WRAP MAT:ZZ CUSH/DUNN MAT:ZZ CUSH/DUNN THKNESS:Z
UNIT CONT:ZZ OPI:A
INTRMDTE CONT:ZZ INTRMDTE CONT QTY:ZZZ
PACK CODE:U
MARKING SHALL BE IN ACCORDANCE WITH MIL-STD-129.
SPE2DS-26-T-9169
SECTION B
PR: 7016289024 PRLI: 0001 CONT’D
SPECIAL MARKING CODE:ZZ -ZZ Special Requirements
PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
STORE AT 2-30 DEGREES C (36-86 DEGREES F) 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/
BULK BREAK POINT:
W81X9C
0002 CS BN CO A DISTRIBUTI
ROSE BARRACKS BLDG 728 AWCF SSF
SUDLAGER STRASSE
VILSECK 92249
DE
FOR TRANSPORTATION SEE DLAD DLAD PROC NOTE C19. FOR FIRST DESTINATION TRANSPORTATION SEE DLAD PROC NOTE
C20 AND CONTRACT
FREIGHT SHIPPING ADDRESS:
W81X9C
0002 CS BN CO A DISTRIBUTI
ROSE BARRACKS BLDG 728 AWCF SSF
SUDLAGER STRASSE
VILSECK 92249
DE
MARKFOR
W81X9C
0002 CS BN CO A DISTRIBUTI
ROSE BARRACKS BLDG 728 AWCF SSF
SUDLAGER STRASSE
VILSECK 92249
SPE2DS-26-T-9169
SECTION B
PR: 7016289024 PRLI: 0001 CONT’D
DE
M/F: (TCN) W81X9C60990598
RDD: 113
PROJ: 9GU TP 1
SUPP ADD: W9046W SIG: C
FOR GOVERNMENT USE ONLY: (IPD) 02
DIC: A01 DIST: V ADV: 2A FC: Z9
Need Ship Date:00/00/0000 Original Required Delivery Date:04/14/2026
SPE2DS-26-T-9169 NSN/Part Number: 6550-01-692-1809 Quantity: 1 PG Purchase Request: 7016289024QTY: 1 Delivery: 5 days ADO
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