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TEST KIT, E COLI DETECT

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SPE2DS-26-T-219UFederal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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The test kit is designed for the detection and differentiation of E. coli O157 and H7 antigens, containing all necessary components for 50 tests including O157 and H7 latex reagents, control latex, positive and negative controls, disposable slides, and stirring sticks. It requires refrigerated storage between 2 to 8 degrees Celsius and must not be frozen. The unit of issue is each, and the item is classified as a Type I (Code E) medical product with a non-extendable shelf life of five months from manufacture, with no more than three weeks elapsed between manufacture and government delivery. Labeling must include the date of manufacture, expiration or retest date, contract number, and lot number, following the latest revision of Medical Marking Standard No. 1, which supersedes MIL-STD-129. Packaging must meet commercial standards to ensure protection from damage and safe delivery via common carriers, with all exterior containers suitable for transport to the specified delivery point in APO, 09898. Technical and quality requirements referenced under RA001, packaging standards under RP001, and handling of government identification under RQ011 are incorporated. The item carries the NSN 6550-01-444-7825 and is subject to the solicitation SPE2DS-26-T-219U with a delivery deadline of 20 days ADO.

General Info

E. coli test kit solicitation NSN 6550-01-444-7825 due July 15, 2026, via DIBBS, DLA managed.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSFView Agency

NAICS

621410 - Family Planning CentersView NAICS

Place of Performance

USE TAC 2 FOR SHIPPING, APO, AE, 09898, US

Set-Aside

NONE

Documents

(1)

SPE2DS-26-T-219U.pdf

PDF

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Timeline

1 update
PhaseSolicitation
Posted

Solicitation

Amendment 1

Contract was updated

Response Deadline

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
Contacts1 person available
OfficeUS
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
View Agency Profile
Office AddressUS

Full Description

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TEST KIT,E COLI DETECTION
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-219U
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: 7017431124QTY: 1 Delivery: 20 days ADO

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