This Solicitation opportunity from Department Of Defense was posted on July 27, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.
TEST KIT, E COLI DETECT
Contract Overview
Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.
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The contract is for a single unit of an E. coli detection test kit designed to identify and differentiate the O157 and H7 antigens, containing essential components including two 4 mL reagent vials for O157 and H7 latex testing, one 4 mL control latex, two 3 mL positive and negative controls, disposable slides, and stir sticks, all packaged for 50 individual tests. The product requires refrigeration at 2 to 8 degrees Celsius (36 to 46 degrees Fahrenheit) and must not be frozen. It has a strictly non-extendable shelf life of five months, with no more than three weeks allowed to have passed from the date of manufacture to the date of government delivery. Labeling must conform to Medical Marking Standard No. 1, specifying the date of manufacture, expiration date, contract number, and lot number, superseding MIL-STD-129 for all medical items. Packaging must be commercial-grade, with each unit sealed in a protective container and shipped in suitable exterior packaging for safe transit via common carrier to the delivery point, an APO address with ZIP code 09898, under FOB Destination terms. The item must also comply with hazard communication standards and other regulatory requirements for medical diagnostics. Delivery is due within 20 days after award, and the contract value is not specified due to blank pricing fields. The procurement falls under a simplified acquisition process with a fixed-price contract type, governed by numerous FAR and DFARS clauses addressing ethical conduct, equal opportunity, trafficking in persons, cybersecurity, safeguarding controlled information, and prohibition of hazardous substances such as hexavalent chromium. The contractor must adhere to stringent information security protocols including NIST SP 800-171, safeguarding covered defense information, and cyber incident reporting, as well as ensure compliance with federal regulations on labeling, traceability, and medical device standards. All proposals must be submitted electronically through the DLA Internet Bid Board System by the specified deadline, with no attachments or supplemental documents provided beyond the base solicitation.
General Info
Agency
NAICS
Place of Performance
USE TAC 2 FOR SHIPPING, APO, AE, 09898, USASet-Aside
Timeline
Submission Closed
Organization & Contact Information
Full Description
TEST KIT,E COLI DETECTION
DETECTS AND DIFFERENTIATES 0157 AND H7 ANTIGENS. CONTAINS POSITIVE AND
NEGATIVE CONTROLS, STIRRING STICKS AND DISPOSABLE SLIDES; 50 TESTS PER
KIT; CONTAINS 1 X 4 ML O157 TEST LATEX; 1 X 4 ML H7 TEST LATEX; 1 X 4 ML
CONTROL LATEX; 1 X 3 ML O157:H7 POSITIVE CONTROL; 1 X3 ML NEGATIVE
CONTROL; DISPOSABLE SLIDES; STIR STICKS
REQUIRES REFRIGERATION STORAGE BETWEEN 2 TO 8 DEGREES CELSIUS
(36 TO 46 DEGREES FAHRENHEIT) DO NOT FREEZE
UNIT OF ISSUE: EA (EACH)
..
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.
SPE2DS-26-T-259C
SECTION B
MMS NO. 1 IS ALSO AVAILABLE ONLINE AT:
https://www.dla.mil/Logistics-Operations/Packaging/
.. RS007: Shelf-life requirement RS001 for a TYPE I (CODE E) item with a shelf life of 5 months (non-extendable) applies to this item. SHALL HAVE A SHELF LIFE OF 5 MONTHS. NOT MORE THAN 3 WEEKS 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: 6550-01-444-7825 Quantity: 1 EA Purchase Request: 7017568896QTY: 1 Delivery: 20 days ADO
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