This Government Contract opportunity from Department Of Veterans Affairs was posted on June 1, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

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6525--Intravascular Imaging and Physiology Guidance System

Closed

36C26326Q0552_2Federal

Submission Closed06/12/2026, 09:00:00 PM UTC

Contract Overview

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

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NAICS: 334510

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FA2396 USAF Afmc Afrl Pzl Afrl Pzle

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ACTIVE DEVICES DIVISION

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STARTER KIT, DIGITAL DE

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ANALYZER, BLOOD CHOLEST

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MEDICAL SUPPLY CHAIIN FSH

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1 day ago

DEADLINE

in 5 days

AI Contract Overview

The Department of Veterans Affairs, through Network Contract Office 23, is conducting a sources sought notice for the procurement of an Intravascular Imaging and Physiology Guidance System to enhance Percutaneous Coronary Interventions at the Minneapolis VA Healthcare System. The requirement specifies the acquisition of two AVVIGO+ Integrated Guidance Systems and one AVVIGO+ Mobile Guidance System, both branded as equal to the Avvigo+ IVUS, with integrated High-Definition Intravascular Ultrasound, Fractional Flow Reserve, and distal pressure wire capabilities. Technical specifications demand a 60MHz or higher transducer, automatic lumen assessment, automated pullback, angiogram co-registration, side branch detection, stent assessment, and a 3.1F catheter profile. The systems must include a medical-grade touch screen tablet, battery, power supply, installation guide, and a one-year standard manufacturer warranty, with the integrated system also containing up to five FFR LINKS and the mobile system including one FFR LINK. Delivery must be made to the VA Medical Center’s Bldg. 70 Warehouse in Minneapolis, Minnesota, under FOB Destination terms, with installation and training to be completed no later than 60 days after award and shipping occurring within 30 days of award. Delivery is restricted to business hours Monday through Friday, excluding federal holidays, and coordination with on-site Biomedical Staffing is mandatory. Respondents must comply with federal acquisition regulations including FAR 52.225-2(b), requiring a Buy American Certificate that clearly identifies the item and its country of origin, and must affirm whether the product is a U.S.-made end product. The acquisition is subject to the Nonmanufacturer Rule under FAR 52.219-33, meaning entities not manufacturing the product must demonstrate the manufacturer’s identity and socioeconomic status. All respondents must provide their organization’s name, UEI number, address, and socioeconomic classification under NAICS code 334510 for Electromedical and Electrorherapeutic Apparatus Manufacturing, with a 1,250-employee size standard. Small businesses must estimate the percentage of work they will perform versus subcontract, and all must submit authorization agreements with the manufacturer, a capability statement detailing compliance with the technical requirements, and confirmation of SAM registration under the correct NAICS code. Proposals must be submitted via email to the designated Contract Specialist by the deadline of June 12, 2026, at 4: