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Supply of Cytation 9 Multimode Reader or Equivalent Instrument

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Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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This contract involves the procurement, delivery, and installation of a Cytation 9 Multimode Reader or an equivalent turnkey laboratory instrument. The contractor is responsible for providing the complete package, which includes hardware, software, on-site training for users, and warranty support to ensure the instrument's optimal operation. The equipment must comply with FDA standards and meet the requirements of Section 508, which pertains to accessibility. The contract is being managed by the FDA Office of Acquisition and Grant Services within the Department of Health and Human Services. The place of performance is located in Silver Spring, with the solicitation posted on June 12, 2026, and responses due by June 18, 2026. It falls under the NAICS code 334516, indicating it relates to manufacturing of instruments and related equipment. This subcontract aims to equip the FDA with advanced laboratory tools while ensuring regulatory compliance and support services are provided.

General Info

Procurement and installation of FDA-compliant Cytation 9 Reader with training, warranty, and accessibility.

Agency

Department Of Health And Human Services → FDA Office Of Acq Grant Svcs

NAICS

334516 - Analytical Laboratory Instrument Manufacturing View NAICS

Place of Performance

Silver Spring, MD, 20993, USA

Set-Aside

NONE

Documents

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No documents available

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Timeline

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Organization & Contact Information

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AgencyDepartment Of Health And Human Services → FDA Office Of Acq Grant Svcs
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Health And Human Services → FDA Office Of Acq Grant Svcs
Office AddressN/A
ContactsNo contact information available

Full Description

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Procurement, delivery, and installation of one Cytation 9 Multimode Reader or equivalent turn-key laboratory instrument, including hardware, software, on-site training, and warranty support. Contractor must ensure FDA acceptance and compliance with Section 508.

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