This Solicitation opportunity from Department Of Defense was posted on May 31, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

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CONTROL, RESPIRATORY

Closed

SPE2DS-26-T-111VFederal

Submission Closed06/08/2026, 05:00:00 PM UTC

Contract Overview

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

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POSTED

6 days ago

DEADLINE

in 5 days

AI Contract Overview

The contract requires the supply of the BioFire RP2.1/RP2.1Plus Control Panel, a diagnostic quality control product consisting of 12 synthetic nucleic acid vials suspended in a non-infectious buffer solution, intended for in vitro use with the FilmArray instrument to monitor detection and identification of respiratory pathogens. Each kit contains six positive and six negative controls sufficient for six quality control runs and is identified by NSN 6550-01-690-4435. The item must be furnished with a shelf life of exactly 18 months, non-extendable, with no more than two months elapsed between manufacture and delivery to the government. Storage requirements mandate frozen conditions between -25°C and -15°C (-13°F to 5°F), and labeling must include the date of manufacture, expiration or retest date, and contract/lot number in compliance with Medical Marking Standard No. 1, superseding MIL-STD-129. Packaging must be commercial, using sealed unit containers and suitable exterior shipping containers capable of ensuring safe delivery to the point of delivery in APO 09227-0000 via FOB Destination terms, with palletization following DLA packaging standards and all marking adhering to MMS1C. The procurement is issued under solicitation SPE2DS-26-T-111V by the Department of Defense through DLA Troop Support with a delivery deadline of 83 days after award, and compliance with the Berry Amendment and Buy American Act is required. Contractors must submit quotes via DIBBS and maintain active SAM registration, with all representations in SAM current. The contract incorporates numerous Federal Acquisition Regulation clauses including those on equal opportunity, combating trafficking, employment verification, sustainable products, hazardous materials identification, changes, default, and inspection at destination per FAR 52.246-2. Additionally, the contract mandates adherence to NIST SP 800-171 cybersecurity requirements, electronic payment submission through Wide Area Workflow with specific documentation for fixed-price line items, and submission of hazardous material safety data sheets with labels. Offers must specify the source and part number being supplied, and payment requests must follow WAWF procedures with appropriate receiving reports and certifications, including vessel representation for ocean transport if applicable. All contract terms are subject to deviation updates as specified in the solicitation, and the product is subject to potential DX or DO priority rating under DPAS regulations.

General Info

Supply of Biofire RP2.1 Control Panel for respiratory pathogen testing, frozen storage, 18-month shelf life.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing

Place of Performance

ATTN CL VIII MED REQ PROCES ACT, APO, AE, 09227-0000, USA

Set-Aside

NONE

Documents

RFQ SPE2DS-26-T-111V Medical Supply Chain

rfq

High

AI Contract Breakdown

Uniform Contract Format

Timeline

PhaseClosed

PostedMay 31

Solicitation

Response DeadlineJun 8

Deadline has passed

Submission Closed

06/08/2026, 05:00:00 PM UTC

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Organization & Contact Information

AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

Contacts1 person available

OfficeUSA

Organization / AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

Office AddressUSA

Contacts

Marc Canalichio

contact@example.gov

+1 (555) 000-0000

Full Description

CONTROL,RESPIRATORY
CONTROL, RESPIRATORY PANEL
THE BIOFIRE RP2.1/RP2.1PLUS CONTROL PANEL
CONSISTS OF 12 VIALS SYNTHETIC NUCLEIC ACID
SUSPENDED IN A NON-INFECTIOUS SOLUTION OF
BUFFERS, PRESERVATIVES AND STABILIZERS; IT
IS INTENDED FOR IN VITRO USE AS A QUALITY
CONTROL TO MONITOR THE DETECTION AND
IDENTIFICATION OF RESPIRATORY PATHOGENS AS
PERFORMED BY THE FILMARRAY RP2.1 PANEL ASSAY
ON THE FILMARRAY INSTRUMENT; EACH KIT CONTAINS
ENOUGH REAGENT FOR 6 QUALITY CONTROL RUNS
UNIT ISSUE: KT (KIT CONTAINS 12 TUBES X 300UL, 6 POSITIVE CONTROLS AND 6
NEGATIVE CONTROLS)
..
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.
SPE2DS-26-T-111V
SECTION B
COPIES OF MEDICAL MARKING STANDARD NO. 1
(MMS NO. 1) MAY BE OBTAINED BY CONTACTING DLA
TROOP SUPPORT VIA EMAIL TO contact@example.gov. MMS NO. 1 IS ALSO AVAILABLE ONLINE AT: 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 2 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.
.
REQUIRES FROZEN STORAGE AT -25° CELSIUS TO -15° CELSIUS (-13° FAHRENHEIT
TO 5° FAHRENHEIT).
..
BIDDER: PLEASE SPECIFY SOURCE AND PART
NUMBER BEING SUPPLIED.
ADEQUATE DATA FOR THE NSN/Part Number: 6550-01-690-4435 Quantity: 1 KT Purchase Request: 7016978984QTY: 1 Delivery: 83 days ADO