Supply of Class III Implantable Pulse Generator (IPG)

The contract involves the procurement and delivery of a single FDA-approved Implantable Pulse Generator classified as a Class III medical device for use in neuromodulation therapy. This device is subject to stringent regulatory standards due to its invasive nature and critical role in patient care, requiring full compliance with FDA quality and safety protocols. The item will be supplied under a subcontract arrangement through the Department of Veterans Affairs, specifically managed by the 250-NETWORK Contract Office 10, with the North American Industry Classification System code 334510 indicating its alignment with medical equipment manufacturing. The contract was posted on July 1, 2026, and the place of performance is not specified, suggesting flexibility in delivery location to meet clinical needs. While no set-aside designation or point of contact is provided, the procurement is intended to fulfill a specific therapeutic requirement for a veteran patient, emphasizing precision, reliability, and adherence to medical guidelines. The transaction is conducted through the federal contracting system via the SAM.gov platform, ensuring transparency and compliance with federal acquisition regulations governing high-risk medical devices.