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  4. ›BioRad QX200 Droplet Digital PCR System

U.S. Department Of Health And Human Services·Maryland

BioRad QX200 Droplet Digital PCR System

Closes 6/8/2026$100k – $200kRequest for Quotation
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Description

The Food and Drug Administration (FDA) is seeking a quote for the Bio-Rad QX200 Droplet Digital PCR System. The system must include all required components, software, installation, training, warranty coverage, and other requirements identified in the Statement of Work. The quoted system shall include a minimum one (1) year manufacturer warranty, and offerors shall provide separate pricing for an option one (1) year extended warranty/service plan. Key requirements include: • Compatibility with ongoing validated research workflows and existing assay development activities • The system must be the Bio-Rad QX200 Droplet Digital PCR System • The warranty shall include all labor, travel, replacement parts, technical support, and corrective maintenance necessary to maintain the instrument in accordance with Original Equipment Manufacturer (OEM) specifications • Any maintenance, repairs, or replacement of components performed under the warranty shall be conducted by OEM-trained or OEM-authorized personnel using OEM-approved parts

Attached files

Contact

Jennifer Mun(Contracting Officer)

[email protected]

Key dates

Opened
6/1/2026
Closes
6/8/2026
Duration
30 days

Last updated

Details

Type
Request for Quotation
Industry
Healthcare and Medical Services
NAICS
334516
Solicitation №
75F40126Q00195

Budget estimate

$100,000 – $200,000

The budget for this opportunity is not explicitly stated, but based on the context of purchasing a Bio-Rad QX200 Droplet Digital PCR System, the cost could range from $100,000 to $200,000. This estimate is based on the assumption that the system's price includes all required components, software, installation, training, and warranty coverage. Factors influencing the likely payment range include the complexity of the system, the level of training and support required, and the cost of any additional components or services needed to meet the FDA's requirements.

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