TEST KIT, SYPHILIS D
Contract Overview
Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.
AI Contract Overview
The contract pertains to the procurement of Test Kit, Syphilis D, a rapid plasma reagin card test used for the qualitative and semi-quantitative detection of antilipid antibodies in serum, commonly associated with syphilis and other acute or chronic conditions. The test kit delivers results in eight minutes and is classified as moderate complexity under CLIA, requiring refrigerated storage between 2 to 8 degrees Celsius and must not be frozen. Each pack contains 100 units, and the unit of issue is a PG. The item has a strict 12-month shelf life with no extensions permitted, and delivery to the government must occur within one month of manufacture to ensure product integrity. Labeling must include the date of manufacture, expiration or retest date, and contract or lot number, all in accordance with Medical Marking Standard No. 1, which supersedes MIL-STD-129 for medical supplies. Packaging must be commercial-grade, sealed to prevent damage, and shipped in exterior containers suitable for safe delivery via common carrier at the lowest cost to the designated FPO destination, with export packaging required when applicable. The solicitation, issued under DLA Master Solicitation Revision 105 and identified as SPE2DS-26-T-237L, requires electronic submission via DIBBS by July 21, 2026, with delivery mandated within 20 days of award. The contract includes a total estimated value of approximately $10,376.86 across multiple line items with unit prices ranging from $80.00 to $119.00 per pack. The item is subject to stringent regulatory compliance including DFARS clauses for hazardous material labeling under 252.223-7001, which mandates OSHA-compliant labels and pre-award submission of label samples, and ocean transportation requirements under 252.247-7023, mandating the use of U.S.-flag vessels unless a waiver is approved. All deliveries must be accepted at destination under FAR 52.246-2, and invoicing is exclusively through Wide Area WorkFlow with no paper submissions permitted. The contract includes affirmative representations for small business status, diversity certifications, compliance with cybersecurity standards including NIST SP 800-171, and prohibitions on the acquisition of prohibited telecommunications equipment or services. The contractor must also comply with trafficking in persons, employment verification
General Info
Agency
NAICS
Place of Performance
USNS COMFORT T AH 20, FPO, AE, 09566-4008, USSet-Aside
Timeline
Response Deadline
Organization & Contact Information
Full Description
TEST KIT, SYPHILIS DETECTION
RAPID PLASMA REAGIN CARD TEST MACROSCOPIC NONTREPONEMAL PROCEDURE; A
VARIATION OF THE STANDARD VDRL AND MAY BE USED TO OBTAIN QUALITATIVE AND
SEMI-QUANTATIVE RESULTS; CARDIOLIPIN CHARCOAL MICROPARTICLE TEST;
ANTIGEN DETECTS AN ANTILIPID ANTIBODY REAGIN PRESENT IN SERUM OF
SYPHILITIC PATIENTS AND IN SERUM OF PATIENTS OF OTHER ACUTE OR CHRONIC
DISEASES; RESULTS IN 8 MINUTES; CLIA COMPLEXITY: MODERATE
REQUIRES REFRIGERATION STORAGE BETWEEN 2 TO 8 DEGREES CELSIUS
(36 TO 46 DEGREES FAHRENHEIT) DO NOT FREEZE
UNIT OF ISSUE: PG (100 EA PER PG)
..
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
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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
SPE2DS-26-T-237L
SECTION B
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 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.
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ADEQUATE DATA FOR THE NSN/Part Number: 6550-01-508-1788 Quantity: 1 PG Purchase Request: 7017325271QTY: 1 Delivery: 20 days ADO
