6515--Phantom Cervical Medical Instrument
Closed Pre-Solicitation Posted
Not the latest version. See the latest solicitation from .
- Solicitation number
- 36C24726Q0533
- Agency
-
Veterans Integrated Service Network 7
Veterans Health Administration, Department of Veterans Affairs
- Responses due
- Set-aside
- Service-Disabled Veteran-Owned Small Business
Opportunity facts
- NAICS code
- 339112 Surgical and Medical Instrument Manufacturing
- Place of performance
- VA Medical Center 1670 Clairmont Rd
- Points of contact
Notice details come from SAM.gov. Updated .
About this opportunity
The Department of Veterans Affairs Veterans Health Administration Veterans Integrated Service Network 7 intends to solicit Phantom Cervical Medical Instruments under a Service-Disabled Veteran-Owned Small Business set-aside, with offers due May 15, 2026 at 12:00 PM Eastern Time. Only VIP-verified SDVOSB firms are eligible for award.
Place of performance is the VA Medical Center at 1670 Clairmont Road, Decatur, Georgia, with the contracting office in Montgomery, Alabama. The requirement is subject to quick turnaround for replacing outdated and obsolete instruments. All instruments must comply with VHA Directive 1116, which establishes national policy and procedures for reprocessing, sterilization, and oversight of critical and semi-critical reusable medical devices in VA medical facilities, and VHA Directive 1220, which establishes infrastructure and complexity requirements for VA medical facilities performing invasive procedures to ensure patient safety and compliance with federal standards.
Vendors must submit offers that meet or exceed all requirements detailed in the Statement of Work included in the forthcoming RFQ. Offers that differ from stated requirements must include a detailed description demonstrating how the proposed solution meets or exceeds the specifications to be considered for award. All offers are submitted to Quincy.Alexander@VA.GOV.
Notice text
ON OR BEFORE MAY 12, 2026 I WILL POST A SOLICITATION FOR SURGICAL INSTRUMENTS THAT WILL BE A SDVOSB SET ASIDE. ONLY VIP VERIFIED SDVOSB s WILL BE CONSIDERED FOR AWARD THAT OFFERS MEET OR EXCEED THE REQUIREMENT LISTED IN THE SOW OF THE SOLICITATION. VENDOR MUST REVIEW THE SOW INSERTED IN THE RFQ IN DETAIL TO COMPLY WITH WHAT S BEING REQUIRED. THIS REQUIREMENT IS SUBJECT TO A QUICK TURN-AROUND TO REPLACE OUTDATED AND/OR OBSOLETE INSTRUMENTS. IF YOUR OFFER IS DIFFERENT THAN WHAT S BEING REQUIRED YOU MUST GIVE A COMPLETE DESCRIPTION OF YOUR OFFER IN DETAILS OF HOW IT MEETS OR EXCEED THE REQUIREMENT TO BE CONSIDERED. ALL OFFERS ARE TO BE SUBMITTED TO QUINCY.ALEXANDER@VA.GOV ON OR BEFORE MAY 15, 2026 12PM EST.
PLEASE NOTE:
VHA Directive 1116 establishes national policy and procedures for the proper reprocessing, sterilization, and oversight of critical and semi-critical reusable medical devices in VA medical facilities.
Purpose and Scope
VHA Directive 1116(2), issued on March 23, 2016, provides detailed procedures for decontamination, high-level disinfection (HLD), and sterilization of critical and semi-critical reusable medical instruments and equipment in VA facilities, ensuring patient safety and compliance with federal standards (VHA Directive 1116(2). The directive applies anywhere sterile processing or HLD occurs within VA medical facilities and establishes national standards for environmental controls, equipment standardization, and quality assurance
VHA Directive 1220 establishes the infrastructure and complexity requirements for VA medical facilities performing invasive procedures to ensure patient safety and appropriate facility capabilities.
Purpose and Scope
VHA Directive 1220, titled Facility Procedure Complexity Designation Requirements to Perform Invasive Procedures in Any Clinical Setting, sets policy and guidance for matching VA medical facility infrastructure to the complexity of invasive procedures performed. It defines the Invasive Procedure Complexity Model, which combines the Procedure Infrastructure Matrix (PIM) and the Invasive Procedure Complexity Matrix (IPCM) to assign complexity designations to procedures and ensure facilities have the necessary resources, personnel, and support services for safe care (VHA Directive 1220)
Files
| File | Type | Posted |
|---|---|---|
| 36C24726Q0533_1.docx | DOCX document |
Notice history
| Notice | Type | Posted |
|---|---|---|
| 6515--Phantom Cervical Medical Instrument | Solicitation | |
| This notice | Pre-Solicitation |
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