This Solicitation opportunity from Department Of Defense was posted on July 28, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.
TEST KIT, FECAL RAPID
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The test kit is a rapid fecal diagnostic tool designed for the qualitative detection of Entamoeba histolytica pathogens in human stool specimens, specifically for patients exhibiting symptoms of diarrhea or dysentery. It utilizes a membrane enzyme immunoassay in a single-use cassette format to identify the organism’s adherin, delivering results within 30 minutes without the need for specialized instrumentation. The kit has an analytical sensitivity of 0.2 ng/mL and is intended for use in clinical settings requiring swift diagnosis. Each package contains 25 tests and must be stored under refrigeration between 2 to 8 degrees Celsius; freezing is prohibited. The product has a non-extendable shelf life of 12 months from manufacture, and no more than one month may have elapsed from the date of manufacture to the date of delivery to the government. Labeling must include the date of manufacture, expiration or retest date, contract number, and lot number, all in compliance with Medical Marking Standard No. 1. Packaging must meet commercial standards ensuring protection from damage and safe transport via common carrier, with exterior containers suitable for shipping and export if required. The item is governed by DLA technical and quality requirements, packaging standards, and defense information protocols. The NSN is 6550-01-671-9115, with a purchase request quantity of one package, slated for delivery within 20 days to Fort Bliss, Texas, under solicitation SPE2DS-26-T-278B, issued by the Department of Defense’s Medical Supply Chain.
General Info
Agency
NAICS
Place of Performance
21287 LIGHT INFANTRY AVENUE, FORT BLISS, TX, 79918-2527, USASet-Aside
Timeline
Submission Closed
Organization & Contact Information
Full Description
TEST KIT,FECAL RAPID
FEATURES FECAL PARASITE TEST KIT, RAPID, ENT. HISTOLYTICA; ELISA TEST
FOR THE DETECTION OF ENTAMOEBA HISTOLYTICA PATHOGENS IN FECAL SPECIMENS.
RAPID MEMBRANE ENZYME IMMUNOASSAY FOR THE QUALITATIVE DETECTION OF
ADHESIN FROM ENTAMOEBA HISTOLYTICA IN A SINGLE USE CASSETTE. IT IS
INTENDED FOR USE WITH HUMAN FECAL SPECIMENS FROM PATIENTS WITH DIARRHEA
OR DYSENTERY AS AN AID IN THE DIAGNOSIS OF E. HISTOLYTICA
GASTROINTESTINAL INFECTION. RESULTS IN 30 MINUTES WITHOUT
INSTRUMENTATION. ANALYTICAL SENSITIVITY 0.2 NG/ML. STORE AT 2 TO 8
DEGREES C; 25 TESTS.
REQUIRES REFRIGERATION STORAGE BETWEEN 2 TO 8 DEGREES CELSIUS
(36 TO 46 DEGREES FAHRENHEIT) DO NOT FREEZE
UNIT OF ISSUE PG (25 TESTS 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
SPE2DS-26-T-278B
SECTION B
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/
.. RS011: Shelf-life requirement RS001 for a TYPE I (CODE H) item with a shelf life of 12 months (non-extendable) applies to this item.
SHALL HAVE A SHELF LIFE OF 12 MONTHS. NOT MORE THAN 1 MONTH 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: 6550-01-671-9115 Quantity: 1 PG Purchase Request: 7017631792QTY: 1 Delivery: 20 days ADO
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