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6515--Phantom Cervical Medical Instrument

Sector: Commercial • Location: VA Medical Center 1670 Clairmont Rd Decatur, Ga 30033

Source: SAM.gov

Tender
Presolicitation

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 RE

Status
Prospective
Sector
Commercial, Residential, Manufacturing (Industrial), Hospital
Location
United States of America
Updated
3 Nov 2026
Source
SAM.gov

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The tender “6515--Phantom Cervical Medical Instrument” is a tender record in Taiyo, linked to the Commercial sector. It is issued for works, goods, or services related to VA Medical Center 1670 Clairmont Rd Decatur, Ga 30033.

Participants

Not available for this record.

Status

Original status

presolicitation

Taiyo status

Prospective

Taiyo last update

2026-11-03

Contact

Not available for this record.

Description

Description

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 THIS REQUIREMENT IS SUBJECT TO A QUICK TURN-AROUND TO REPLACE OUTDATED AND/OR OBSOLETE INSTRUMENTS.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)

Original sector

Not Identified

Location

Country

United States of America (USA)

Source

Source

SAM.gov

URL

More Details

Record type

Tender

Sector

Commercial, Residential, Manufacturing (Industrial), Hospital

Article published date

2026-05-13

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