This Solicitation opportunity from Department Of Defense was posted on May 11, 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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The contract is for the procurement of Human Immunodeficiency Virus (HIV-1/2) Antigen/Antibody Combo Test Kits, with a total quantity of three packaging groups (PG), each containing 25 test kits. Each test kit includes five test cards, a desiccant package, a 2.5 mL chase buffer prepared in phosphate buffer for whole blood testing, a quick reference guide, a package insert, 25 subject information notices, one customer letter, 25 disposable capillary tubes, and 25 disposable workstations. The item is identified by NSN 6550-01-692-1809 and is governed by the DLA Master List of Technical and Quality Requirements through RA001, which applies to all technical and quality specifications referenced in the solicitation. The product must have a non-extendable shelf life of 18 months, with no more than two months elapsed between the date of manufacture and delivery to the government, and all packaging must comply with Medical Marking Standard No. 1 (MMS No. 1), superseding MIL-STD-129, with labels clearly showing the date of manufacture, expiration date, and contract/lot number. Packaging and shipping must meet RP001 DLA Packaging Requirements and MIL-STD-2073-1E, ensuring protection against damage and safe transport via commercial carriers at the lowest cost to the designated delivery point, with primary delivery to APO AE 09227-0000 and a secondary location in Kaiserslautern, Germany. The contract is a simplified acquisition under FAR 52.213-4, amended by Class Deviations 2025-00003 and 2025-00004, and employs a deviation-based contract type clause (52.216-1 Alt I) allowing offerors to propose alternative contract structures. It incorporates mandatory clauses for equal opportunity, combating trafficking in persons, employment eligibility verification, sustainable products, cybersecurity, and system for award management maintenance, all applied under Deviation 2026-00038. Inspection and acceptance occur at the destination, with shared responsibility between the contractor and government, and delivery is due 83 days after award under FOB destination terms. The award will be based on a trade-off evaluation considering both price and non-price factors including cybersecurity
General Info
Agency
Contract Value
$1,425NAICS
Place of Performance
ATTN CL VIII MED REQ PROCES ACT, APO, AE, 09227-0000, USASet-Aside
Awardee
Award Issued Date
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-064N
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: 3 PG Purchase Request: 7016742260QTY: 3 Delivery: 83 days ADO
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