Opportunity
SAM #FDA-HFP-2026-134777-AMENDMENT1
FDA Procurement of Biotage TurboVap LV Solvent Evaporation Systems and Accessories
Buyer
FDA Office of the Associate General Counsel for Administrative Law
Posted
August 04, 2026
Respond By
August 10, 2026
Identifier
FDA-HFP-2026-134777-AMENDMENT1
NAICS
334516
The FDA Human Foods Program is seeking to procure two Biotage TurboVap LV solvent evaporation systems and associated accessories for the Denver Human and Animal Food Laboratory. - Government Buyer: - U.S. Food and Drug Administration (FDA) - Human Foods Program (HFP), Office of Regulatory Testing and Surveillance - Office of Operations (OO)/ Office of Finance, Budget, and Acquisitions (OFBA)/ Office of Acquisitions and Grants Services (OAGS)/ Division of Acquisition Operations (DAO)/ Service Contracts Branch (SCB) - OEM Highlight: - Biotage is the specified Original Equipment Manufacturer (OEM) - Products Requested: - 2 x Biotage TurboVap LV Systems (Part Number: 415000) - Solvent evaporation system supporting 48-position racks for 10-20mm tubes - Features: vortex gas shearing, heated water bath, touchscreen interface, compatibility with compressed air or nitrogen, and use with specified solvents - 2 x TurboVap LV Multi Rack (48 Positions, 10-20mm Tubes) (Part Number: 414964) - 2 x Mains Cord (US/CA) (Part Number: C65902SP) - Unique/Notable Requirements: - Systems must be brand name or equal to Biotage TurboVap LV - Delivery required within 60 days of award - Minimum one-year manufacturer warranty from government acceptance - Equipment must support high-throughput, reproducible, and efficient solvent evaporation for laboratory sample preparation
Description
The purpose of this procurement is to acquire two (2) solvent evaporation systems capable of high-throughput, reproducible, and efficient solvent evaporation during sample preparation. The systems shall be used to remove organic solvents from extracted samples, leaving concentrated residues for further analytical processing. The equipment shall improve laboratory efficiency, reduce analyst handling time, and ensure consistent analyte concentration prior to instrumental analysis.