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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NAICS: 325413

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AI Contract Overview

This contract covers the supply of the Biofire RP2.1/RP2.1 Plus Control Panel, a diagnostic quality control kit designed for in vitro use to monitor the detection and identification of respiratory pathogens using the FilmArray RP2.1 Panel Assay on the FilmArray instrument. The kit contains 12 vials of synthetic nucleic acid in a non-infectious solution, split evenly between six positive and six negative control samples, providing enough reagent for six quality control runs. The product requires frozen storage at temperatures between -25° to -15° Celsius and has a non-extendable shelf life of 18 months, with delivery conditioned to ensure no more than two months have elapsed from manufacturing to government receipt. Packaging and labeling must comply with specific medical packaging standards to ensure protection and safe transport, including marking in accordance with Medical Marking Standard No. 1, which supersedes previous military standards. The contract stipulates adherence to a series of technical and quality requirements, and the product must be commercially packed in sealed unit containers suitable for shipping. The solicitation requires bidders to specify the source and part number of the product supplied, and the contract is intended for delivery within an 83-day period to an APO location. The Department of Defense's Medical Supply Chain manages this acquisition under strict regulatory compliance to maintain the quality and integrity of the control panel for respiratory testing.

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 View NAICS

Place of Performance

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

Set-Aside

NONE

Documents

(1)

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

PDF•rfq

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

OfficeUS

Organization / Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF

Office AddressUS

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 fssb@dla.mil. 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