Attachment 6 - MANDATORY ITEM-BY-ITEM COUNTRY-OF-ORIGIN AND PLACE-OF-MANUFACTURE DISCLOSURE.xlsx

This is a mandatory country-of-origin and place-of-manufacture disclosure template for the Axion BioSystems Maestro Pro Microelectrode Array (MEA) System solicitation. The template requires vendors to provide detailed information for ten contract line item numbers (CLINs) covering the core equipment and consumables required under solicitation CBER-2026-135659 issued by the FDA's Center for Biologics Evaluation and Research.

The disclosure requirements apply to the following items: the Maestro Pro 768-Channel MEA/Impedance System, Neural Module, MEA Viability Module, installation and training services, miscellaneous equipment and supplies, shipping (if applicable), CytoView MEA 48-Well Plates, CytoView MEA 96-Well Plates, MEA Creator Kit, and 3DMap MEA Plates. For each CLIN, vendors must identify the manufacturer, brand/model, part number, place of manufacture (by city and state/country), country of origin, and whether the end product qualifies as U.S.-Made, Designated-Country, or Other. The template also includes rows for computer equipment, monitors, and other accessories or supply items as needed. This disclosure document is intended to ensure compliance with Buy American Act requirements and trade agreement provisions applicable to this commercial products procurement conducted under simplified acquisition procedures.