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
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The contract is for a Human Immunodeficiency Virus (HIV-1/2) Ag/Ab Combo Test Kit, identified by NSN 6550-01-692-1809, with a unit of issue of PG (25 kits per package). Each kit includes five test cards with one test per card, stored in an aluminum ziplock pouch, along with one desiccant package, one 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 product must have a shelf life of 18 months with no more than two months elapsed from the date of manufacture to the date of delivery to the government. All labeling must comply with Medical Marking Standard No. 1C, including the date of manufacture, expiration date, and contract or lot number. Packaging must be commercial, sealed, and designed to protect against damage or breakage, with exterior shipping containers suitable for safe delivery via common carrier at the lowest rate. Marking and labeling adhere to MMS No. 1, superseding MIL-STD-129, and storage conditions must remain within 2–30°C (36–86°F). Delivery is required within 83 days after order placement to the destination facility in Kaiserslautern, Germany, under FOB Destination terms, meaning title and risk transfer upon arrival. The contract references technical and quality requirements from the DLA Master List and incorporates multiple FAR and DFARS clauses related to cybersecurity, hazardous materials, employment practices, sustainability, whistleblower protections, and information safeguarding. Cybersecurity compliance requires adherence to NIST SP 800-171, implementation of DFARS 252.204-7012 for safeguarding covered defense information, and reporting of cyber incidents. Invoicing must be completed electronically through Wide Area WorkFlow, and the product is subject to strict compliance with DLA packaging and marking standards. The solicitation was issued on May 10, 2026, with responses due by May 18, 2026, through the DIBBS portal, under NAICS code 339113 for medical and dental instrument manufacturing.
General Info
Agency
Contract Value
$481NAICS
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-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
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