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TEST KIT, INFLUENZA +B

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SPE2DS-26-T-251AFederal

Contract Overview

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

AI Contract Overview

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The contract specifies the procurement of a rapid diagnostic test kit for the qualitative detection of influenza A and B antigens directly from nasal swabs, nasal washes, or nasal aspirates. Each kit contains 25 individual tests, with results available within 10 minutes, and the kits are designed for room temperature storage between 59°F and 86°F. The product is intended as an aid in the rapid differential diagnosis of acute influenza infections and is identified by NSN 6550-01-531-2897 with a unit of issue of one kit per order. Strict shelf-life requirements mandate a minimum of 24 months from manufacture to expiration, with no more than three months having passed from the date of manufacture to the date of delivery to the government. Labeling must include the date of manufacture, expiration or retest date, and contract or lot number, in compliance with Medical Marking Standard No. 1, which supersedes MIL-STD-129. Packaging must be commercial-grade, sealed, and protective, with exterior shipping containers ensuring safe, low-cost delivery to the designated delivery point in Groton, Connecticut. The contract enforces compliance with federal regulations regarding hazardous communication, requiring suppliers to provide Safety Data Sheets aligned with OSHA’s Hazard Communication Standard as amended under the Globally Harmonized System, along with compliant labeling as per 29 C.F.R. 1910.1200. Suppliers must also certify employee training on these updated SDS and labeling requirements. Additionally, all documentation must adhere to DLA’s technical and quality requirements referenced in the DLA Master List, and government identification must be removed from non-accepted supplies. The solicitation, issued under contract number SPE2DS-26-T-251A, has a response deadline of July 27, 2026, and requires delivery within five days of award. The product falls under NAICS code 621410 and is managed by the Department of Defense’s Medical Supply Chain Medical Surgical Functional Service Facility, with Seth Tootell designated as the primary point of contact.

General Info

Procurement of 25-test influenza A/B rapid diagnostic kits, room temperature stable, 24-month shelf life, delivery to Groton, CT, within five days of award.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSFView Agency

NAICS

621410 - Family Planning CentersView NAICS

Place of Performance

ATTN: SSN 801, GROTON, CT, 06340-4905, US

Set-Aside

NONE

Documents

(1)

Request for Quotations SPE2DS-26-T-251A

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Timeline

PhaseSolicitation
Posted

Solicitation

Response Deadline

Submission deadline

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
Contacts
Seth Tootell
contact@example.gov
+1 (555) 000-0000

Full Description

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TEST KIT,INFLUENZA +B TEST
TEST KIT,INFLUENZA A+B TEST
FEATURES QUALITATIVE DETECTION OF INFLUENZA TYPE A AND TYPE B
ANTIGENS DIRECTLY FROM NASAL SWAB, NASAL WASH AND/OR NASAL ASPIRATE
SPECIMENS. TEST IS INTENDED AS AN AID IN THE RAPID DIFFERENTIAL
DIAGNOSIS OF ACUTE INFLUENZA TYPE A AND TYPE B VIRUS INFECTION; 25 TESTS
PER KIT; RESULTS IN 10 MINUTES; STORAGE AT ROOM TEMPERATURE 59°F TO 86°F
(15°C TO 30°C)
UNIT OF ISSUE: KT (25 TESTS PER KIT)
..
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. MMS NO. 1 IS ALSO AVAILABLE ONLINE AT: https://www.dla.mil/Logistics-Operations/Packaging/
SPE2DS-26-T-251A
SECTION B
..
RS016: Shelf-life requirement RS001 for a TYPE I (CODE M) item with a shelf life of 24 months (non-extendable) applies to this item.
SHALL HAVE A SHELF LIFE OF 24 MONTHS.
NOT MORE THAN 3 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.
..
RQ034: HAZARDOUS COMMUNICATION STANDARD NOTICE
Hazard Communication Standard Notice:
Effective June 1, 2015, Federal Standard No. 313-E, Material Safety Data, Transportation Data and Disposal Data for Hazardous Materials Furnished to Government Activities, establishes the requirement for preparation and submission of Safety Data Sheets (SDS) in lieu of Material Safety Data Sheets (MSDS) by suppliers who provide hazardous materials to government activities.
The Occupational Safety and Health Administration (OSHA) has modified its Hazard Communication Standard (HCS) to conform to the United Nations Globally Harmonized System of Classification and Labeling of Chemicals. As a result of this change, GSA revised Federal Standard No. 313-E requiring Safety Data Sheets for classifying chemicals and communicating the applicable information on labels.
In accordance with the revised standard after June 1, 2015:
1. Suppliers will be required to submit, to the contracting officer for review and approval prior to award, safety data sheets consistent with the requirements found at 29 C.F.R. 1910.1200 for hazardous materials delivered to the Government.
2. Suppliers will also be required to submit, to the contracting officer for review and approval prior to award, Hazardous Communication Standard (HCS) labels in accordance with 29 C.F.R. 1910.1200 requirements or current Consumer Product Safety Act (CPSA), Federal Hazardous Substance Act (FHSA) labels when subject to labeling requirements under those statutes. This product labeling is required for hazardous materials delivered to the Government.
3. Finally, suppliers must train their employees on the new safety data sheets, hazardous communication labels, and requirements of 29 C.F.R. 1910.1200.
For more information on SDS, refer to OSHAs website, available at:
https://www.osha.gov/law-regs.html
For information on 29 C.F.R. 1910.1200, refer to the below link:
https://www.osha.gov/dsg/hazcom/index.html .. ADEQUATE DATA FOR THE NSN/Part Number: 6550-01-531-2897 Quantity: 1 KT Purchase Request: 7017542881QTY: 1 Delivery: 5 days ADO

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CATHETERIZATION KIT, URThe contract specifies the procurement of a urethral catheterization kit, identified by NSN 6515-01-615-2124, containing a 16 Fr Foley catheter with a 2000 mL anti-reflux valve bag, designed for infection control and including a complete set of sterile accessories: drape, underpad, specimen container, five prep balls, povidone-iodine solution, gloves, dual prefilled syringes (10 cc sterile water and 10 cc lubricant), and forceps. Each unit is packaged as a sealed tray of ten kits, with the unit of issue defined as a packaged group of ten. The product must have a mandatory 36-month shelf life, with no more than five months elapsed from manufacture to government delivery. Labeling must include NSN, manufacturer and CAGE code, date of manufacture or expiration, contract number, and lot number, in compliance with Medical Marking Standard No. 1, which replaces MIL-STD-129. Packaging must meet commercial standards under DLA’s RP001 requirements, protect against damage, and be shipped in suitable exterior containers to ensure safe, low-cost delivery to the destination. All packaging and labeling must adhere to DLA’s Master List of Technical and Quality Requirements, which override any conflicting standards like ASTM D3951. The product is FDA-regulated and subject to referral verification in EBS. Delivery is FOB destination, with zero tolerance for quantity variance. Two shipments totaling one package each are required, with delivery deadlines of July 22 and July 23, 2026, to Fort Bragg, North Carolina, and USS Charleston, respectively. All shipments must use traceable transportation methods, prohibiting parcel post, and palletization must comply with DLA packaging guidelines.
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NAICS: 339113
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DRESSING, OCCLUSIVE, ADHThis contract specifies the procurement of TEGADERM Transparent Occlusive Adhesive Dressings, each measuring 2.375 inches wide by 2.750 inches in length, intended for use as a sterile dressing for peripheral and central intravenous catheters or as a wound covering. The product is to be supplied in individually packaged units, with a unit of issue consisting of 100 packages per lot. The dressings must have a shelf life of 36 months from the date of manufacture, and no more than five months may have elapsed between the manufacturer’s date and delivery to the government. All markings must comply with Medical Marking Standard No. 1, which replaces MIL-STD-129, and must include the date of manufacture, expiration or retest date, contract number, and lot number. Packaging must adhere to commercial standards, ensuring protection from damage during transit, with interior units sealed in suitable containers and exterior shipping containers designed for safe, low-cost delivery via common carrier to the specified point of delivery, including FPO destinations. The item is identified by NSN 6510-01-234-8943, with a required quantity of three packages, and delivery must occur within 20 days of award. The solicitation number is SPE2DS-26-T-255V, with a response deadline in July 2026, and all technical and quality requirements referenced under R-numbers are governed by the DLA Master List of Technical and Quality Requirements in effect at the time of solicitation. The supplier must clearly state the source and part number being offered, and government identification must be removed from any non-accepted supplies in accordance with RQ011.
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CURETTE, EARThe contract pertains to the procurement of a pediatric ear curette with a flexible loop, measuring seven inches in length, featuring a blunt blade edge made of plastic, supplied in cases of fifty units each. The item is identified by the NSN 6515-01-290-8955 under solicitation SPE2DS-26-T-255L, with a response deadline of July 27, 2026, and a requirement for delivery within 20 days after award. Suppliers must specify the source and part number being offered, and all medical acquisitions must adhere to commercial packaging standards ensuring each unit is sealed in a protective container and packed in commercial shipping containers suitable for safe transport at the lowest cost to the designated delivery point in Fort Campbell, 42223-0000. Marking must comply with Medical Marking Standard No. 1, replacing all references to MIL-STD-129, and copies of this standard are available through DLA Troop Support or online. The solicitation incorporates technical and quality requirements from the DLA Master List, with the applicable revision determined by the solicitation or award date. Packaging must also meet DLA-specific requirements, and non-accepted supplies must have government identification removed. This procurement falls under NAICS code 339112 and is administered by the Department of Defense’s Medical Supply Chain MD Surg FSF.
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TEST STRIPS, GLUCOSEThe contract specifies the procurement of Prodigy AutoCode blood glucose test strips, a no-coding product compatible with all Prodigy pocket meters, utilizing oxidase technology for safer and more accurate results without GDH-PQQ technology. These strips feature capillary action for automatic blood sample intake and are approved for alternate site testing. Each box contains 50 strips, with the unit of issue being BX, and the order quantity is two boxes. The items must comply with stringent packaging and labeling requirements, including commercial packaging standards per Medical Marking Standard No. 1, which supersedes MIL-STD-129, and must be marked with the date of manufacture, expiration or retest date, contract number, and lot number. A non-extendable shelf life of 24 months is mandated, with no more than three months allowed to have passed from the date of manufacture to delivery to the government. The strips are subject to DLA packaging and quality requirements as defined in the DLA Master List of Technical and Quality Requirements, and the NSN 6550-01-680-9339 must be supplied with verified source and part number. The solicitation, issued under SPE2DS-26-T-256F, requires delivery within 20 days and is managed by the Department of Defense’s Medical Supply Chain.
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CUFF, SPHYGMOMANOMETERThe contract specifies the procurement of pediatric-sized non-invasive blood pressure cuffs, with bladder dimensions of 3.5 inches in width and 7.1 inches in length, designed for limb circumferences between 18 and 26 centimeters. This item serves as a replacement component for NSNs 6515-01-582-4060 and 6515-01-582-4072, and is identified by NSN 6515-01-593-8773 and Philips part number 40401B. Three units are required, each to be delivered as a single unit of issue, with a firm delivery deadline of 20 days after award, FOB destination, and no variance permitted in quantity. All packaging and labeling must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and must also meet ASTM D3951 standards, with DLA Master List of Technical and Quality Requirements taking precedence. Packaging must ensure protection from damage and be suitable for commercial shipping, using sealed unit containers and secure exterior shipping containers capable of safe transport at the lowest rate. The shipment must be traceable and cannot be sent via parcel post. Delivery is to the U.S. Air Force Medical Command at Fort Sam Houston, San Antonio, Texas, with the required delivery date set for July 23, 2026. The supplier, Philips North America LLC, must adhere to all DLA packaging and marking requirements under RP001 and ensure full compliance with government procurement specifications for medical equipment.
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DRAPE, WOUND CAREThe contract is for sterile disposable paper wound care drapes measuring 18 inches by 26 inches, supplied in packages of 300 units each. These drapes are designed to provide a sterile field during medical procedures and include an inner repellent layer to prevent moisture penetration. The product is identified by NSN 6515-01-568-3821, with a single package requested under purchase request 7017567293. Delivery is required within 20 days of award. The solicitation is issued under contract number SPE2DS-26-T-254M with a response deadline of July 27, 2026, and was posted on July 21, 2026. Performance is to be delivered to Dover AFB, ZIP 19902-7307. Bidders must specify the source and part number being offered. The contract incorporates technical and quality requirements from the DLA Master List, subject to specific revision controls based on acquisition type and amendment dates. It also includes DLA packaging standards, provisions for removal of government identification from non-accepted supplies, and potential applicability of covered defense information requirements. The contracting office is under the Department of Defense’s Medical Supply Chain MD Surg FSF, with Patrick Esposito listed as the primary point of contact.
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NEEDLE, ACUPUNCTUREThe contract is for the procurement of Seirin J-type acupuncture needles, specification .30mm diameter by 30mm length, supplied in boxes of 100 needles each, with a total quantity of four boxes. The needles must meet specific packaging requirements mandated by the Medical Marking Standard No. 1, which supersedes MIL-STD-129, and must be sealed in unit containers that protect against damage or breakage, while exterior shipping containers must ensure safe delivery at the lowest carrier rate to the designated delivery point. The item is classified as a Type I (Code Q) shelf-life item with a strict 36-month non-extendable shelf life, and all technical and quality requirements are governed by the DLA Master List of Technical and Quality Requirements referenced in the solicitation. The needles are identified by NSN 6515-01-680-9021 and must be sourced as specified, with full vendor details including part number and source clearly provided in the bid. Packaging, marking, and compliance with DLA standards are mandatory, including the removal of government identification from non-accepted supplies. The solicitation number is SPE2DS-26-T-255M, with a response deadline of July 27, 2026, and a required delivery within five days of award. The contract is managed by the Department of Defense’s Medical Supply Chain under the office of Patrick Esposito, with all documentation and standards accessible through official DLA portals.
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