INTRAOSSEOUS INFUSION
Contract Overview
Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.
AI Contract Overview
Solicitation SPE2DS-27-T-0080 is a request for quotation issued by the Department of Defense, specifically the DLA Troop Support Medical Supply Chain, for the procurement of an FDA cleared Intraosseous Infusion System (NSN 6515-01-642-7919) used for advanced tactical lifesaving. The required equipment is a manual IO device providing access to seven sites, including the sternum, bilateral proximal humerus, bilateral proximal tibia, and bilateral distal tibia. Each package consists of six individually packaged sets, with each set containing a 15 GA manual IO needle, a 16 GA sternal locator made of 304 stainless steel, one EZ Connect, one quick reference card, and one wristband. The supplies must be sterile, latex-free, non-pyrogenic, and maintain a shelf life of 48 months, with no more than seven months elapsed from the date of manufacture to the date of government delivery. The contract requires delivery of one package to Minot, North Dakota, within 20 days after order. Shipping, inspection, and acceptance are all designated as FOB Destination. Packaging must comply with ASTM D3951 and RP001, while marking and labeling must adhere to MIL-STD-129 and the Hazard Communication Standard for any hazardous materials. The award process is governed by the DLA Master Solicitation for Automated Simplified Acquisitions Revision 105, with a price evaluation preference for HUBZone concerns. Administrative requirements include the use of the Wide Area WorkFlow system for invoicing and compliance with various FAR and DFARS clauses regarding cybersecurity, domestic sourcing, and the safeguarding of covered defense information.
General Info
Place of Performance
3420 2ND ST NE, MINOT, ND, 58703-0527, USASet-Aside
Timeline
Response Deadline
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: 7018581661QTY: 1 Delivery: 20 days ADO
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