This Solicitation opportunity from Department Of Defense was posted on July 16, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.
TEST KIT, HUMAN CHORION
Contract Overview
Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.
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AI Contract Overview
This procurement is for TEST KIT, HUMAN CHORIONIC GONADOTROPIN DETERMINATION, a qualitative diagnostic tool used for the early detection of pregnancy by identifying human chorionic gonadotropin (hCG) in serum or urine with a sensitivity of 25 MIU/mL. Each unit consists of 50 tests, including test cassettes, pipettes, package inserts, and procedure cards, packaged in commercial-grade sealed containers designed to protect against damage and breakage. The total quantity required is two packages, equivalent to 100 tests, to be delivered within 20 days after receipt of order to Fort Stewart, Georgia, under FOB Destination terms. The item must be stored at room temperature between 15°C to 30°C (59°F to 86°F) and has a mandatory 18-month shelf life, non-extendable, with no more than three months elapsed from date of manufacture to government delivery. All labels must include the date of manufacture, expiration or retest date, and contract or lot number, adhering strictly to the latest revision of Medical Marking Standard No. 1 (MMS1C), which supersedes MIL-STD-129. Compliance with FDA Regulation 862.1155 Class II is required, including proper labeling, registration, and adherence to Good Manufacturing Practices. The contract incorporates quality and technical requirements from the DLA Master List of Technical and Quality Requirements, with packaging and shipping following RP001 and IP025 standards where applicable. The item is classified as a Type I (Code K) shelf-life item, and delivery must meet strict aging constraints. All hazardous materials must be labeled according to the Hazard Communication Standard unless governed by other federal statutes such as the Federal Food, Drug and Cosmetics Act. Offerors must submit a Safety Data Sheet prior to award, and failure to do so renders them nonresponsible. The solicitation is a small business set-aside under NAICS code 621410, issued as a Request for Quotations with an automated award possibility if no first article testing is required. Bidders must specify their source and part number, and if submitting alternate products, must provide complete data packages for both approved and alternate items. Electronic invoicing via WAWF is mandatory, and contractors must maintain an active SAM registration. The contract includes multiple Federal Acquisition Regulation clauses covering cybersecurity, whistleblower protections, export controls, trafficking
General Info
Agency
NAICS
Place of Performance
BLDG 1509 WEST 6TH STREET, FORT STEWART, GA, 31314-5185, USASet-Aside
Timeline
Submission Closed
Organization & Contact Information
Full Description
TEST KIT, HUMAN CHORIONIC GONADOTROPIN DETERMINATION
FOR THE QUALITATIVE DETECTION OF HUMAN
CHORIONIC GONADOTROPIN (HCG) IN SERUM
OR URINE FOR THE EARLY DETECTION OF
PREGNANCY, 25 MIU/ML SENSITIVITY, INCLUDES
TEST CASSETTES, PIPETTES, PACKAGE INSERT<(>,<)>
AND PROCEDURE CARD, 50 TESTS
UNIT OF ISSUE: PG (50 EACH PER PACKAGE)
1 PG = 50 EA
..
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-244H
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 3 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.
..
STORE AT ROOM TEMPERATURE (15 C to 30 C/59 F to 86 F) .. BIDDER: PLEASE SPECIFY SOURCE AND PART NUMBER BEING SUPPLIED.
ADEQUATE DATA FOR THE NSN/Part Number: 6550-01-607-9206 Quantity: 2 PG Purchase Request: 7017515662QTY: 2 Delivery: 20 days ADO
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