Opportunity

SAM #FDA-HFP-2026-134777

FDA Solicits Biotage TurboVap LV Solvent Evaporation Systems and Accessories for Food Safety Lab

Buyer

FDA Office of the Associate General Counsel for Administrative Law

Posted

July 31, 2026

Respond By

August 10, 2026

Identifier

FDA-HFP-2026-134777

NAICS

334516

The U.S. Food and Drug Administration (FDA) Human Foods Program is seeking to acquire advanced laboratory equipment to enhance food safety testing capabilities. - Government Buyer: - U.S. Food and Drug Administration (FDA) - Human Foods Program (HFP), Office of Regulatory Testing and Surveillance (ORTS) - Office of Acquisitions and Grants Services (OAGS), Division of Acquisition Operations (DAO), Service Contracts Branch (SCB) - OEM Highlight: - Biotage is specified as the OEM for the TurboVap LV solvent evaporation systems and accessories - Products Requested: - Two (2) Biotage TurboVap LV solvent evaporation systems (Part Number: 415000) - Two (2) TurboVap LV Multi Racks, 48 positions for 10-20mm tubes (Part Number: 414964) - Two (2) Mains Cords for US/CA (Part Number: C65902SP) - Quantities: - Each product line item is requested in a quantity of two - Notable Requirements: - Systems must be brand name or equal to Biotage TurboVap LV - Equipment will be used to improve sample preparation efficiency and reproducibility in food safety testing - Delivery required within 60 days of award - Minimum one-year warranty from date of government acceptance - Purpose: - To remove organic solvents from extracted samples, leaving concentrated residues for further analytical processing - To increase laboratory throughput and reduce analyst handling time

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.

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