This Solicitation opportunity from Department Of Defense was posted on July 9, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.
INTRAOSSEOUS INFUSI
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The intraosseous infusion system, designated as the T.A.L.O.N. IO needle, is a manual, FDA-cleared device designed for tactical advanced lifesaving applications, providing immediate vascular access through seven anatomical sites: the sternum, bilateral proximal humerus, bilateral proximal tibia, and bilateral distal tibia. Each set includes a 15-gauge needle measuring 1.8 mm by 38.5 mm in length and a 16-gauge sternal locator measuring 1.65 mm by 23.6 mm, both constructed from 304 stainless steel, and are sterile, latex-free, and non-pyrogenic. Units are packaged in sets of six, with each package containing one IO needle, one sternal locator, one EZ-Connect adapter, one quick reference card, and one wristband. The product must have a minimum shelf life of 48 months, with no more than seven months elapsed from manufacture to government delivery. The NSN is 6515-01-642-7919, and the unit of issue is a package of six. Technical and quality requirements are governed by the DLA Master List of Technical and Quality Requirements, with compliance dictated by the revision effective on the solicitation or award date. Packaging must adhere to DLA standards, and government identification must be removed from non-accepted supplies. Bidders are required to specify the source and part number. The solicitation, numbered SPE2DS-26-T-219K, was posted on July 9, 2026, with responses due by July 15, 2026, and delivery is required within 20 days of award to San Antonio, Texas, under a federal procurement with NAICS code 336310.
General Info
Place of Performance
1920 HARRY WURZBACH HWY, SAN ANTONIO, TX, 78209-6097, USASet-Aside
Documents
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Timeline
Submission Closed
Organization & Contact Information
Full Description
INTRAOSSEOUS INFUSION SYSTEM
USED TACTICALLY FOR ADVACNCED LIFESAVING
IO NEEDLE (T.A.L.O.N.), PROVIDES FDA
CLEARED MANUAL IO DEVICE WITH 7 STE
ACCESS (STERNUM, BILATERAL, PROXIMAL HUMERUS<(>,<)>
BILATERAL PROXIMAL TIBIA, AND BILATERAL DISTAL
TIBIA), STERILE, LATEX FREE, NON-PRYOGENIC<(>,<)>
NEEDLE SIZE IS 15 GA 1.8MM X 38.5 MM LONG, STERNAL
LOCATOR SIZE IS 16 GA 1.65MM X 23.6 MM LONG<(>,<)>
NEEDLE AND STERNAL LOCATOR MATERIAL<(>,<)>
304 STAINLESS STEEL, 6 INDIVIDUALLY PACKAGED
SETS PER PACKAGE; NEEDLE SET EZ-IO T.A.L.O.N. PACKAGE INCLUDES THE
FOLLOWING:
(1) MANUAL IO NEEDLE
(1) STERNAL LOCATOR
(1) 1 EZ CONNECT
(1) 1 QUICK REFERENCE CARD
(1) WRISTBAND
UNIT OF ISSUE PG (PACKAGE OF 6 EACH)
1 PG = 6 EA
SHALL HAVE A SHELF LIFE OF 48 MONTHS. NOT MORE THAN 7 MONTHS SHALL HAVE
ELAPSED FROM DATE OF MANUFACTURE TO DATE OF DELIVERY TO THE GOVERNMENT.
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.
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RQ011: REMOVAL OF GOVERNMENT IDENTIFICATION FROM NON-ACCEPTED SUPPLIES
BIDDER: PLEASE SPECIFY SOURCE AND PART NUMBER BEING SUPPLIED.
ADEQUATE DATA FOR THE NSN/Part Number: 6515-01-642-7919 Quantity: 1 PG Purchase Request: 7017429363QTY: 1 Delivery: 20 days ADO
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