BPA for Ortho/Quidel Blood Bank Reagents and Consumables
Contract Overview
Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.
AI Contract Overview
The Indian Health Service’s Lawton Service Unit is seeking to establish a Blanket Purchase Agreement for the procurement of name-brand Ortho/Quidel reagents, consumables, and quality control materials essential for maintaining laboratory operations. These supplies must be specifically compatible with the Ortho MTS and Ortho Vision Swift instruments and fully comply with federal clinical laboratory standards outlined in 42 CFR Part 493. The solicitation, identified as IHS1526434, is open to Indian Small Business Economic Enterprises and falls under NAICS code 334516, targeting vendors capable of supplying certified, branded laboratory products to support blood bank testing within federal health regulations. Responses are due by August 14, 2026, and all materials must be delivered to the designated performance location in Oklahoma with a ZIP code of 73507. The procurement is managed by the Indian Health Service under the Department of Health and Human Services, with primary contact information provided through Audrey Yackeyonny at the Oklahoma City office. This BPA aims to ensure consistent, reliable access to critical diagnostic supplies while supporting economic opportunities for certified Indian small businesses.
General Info
Agency
NAICS
Place of Performance
OK, 73507, USASet-Aside
Timeline
Response Deadline
Organization & Contact Information
Full Description
The Lawton Service Unit (LSU), Indian Health Service (IHS), has a requirement to establish a Blanket Purchase Agreement (BPA) for the procurement of Ortho/Quidel reagents, consumables, and quality control materials necessary to support ongoing laboratory operations. Procurement must be name-brand Ortho/Quidel laboratory reagents and supplies that must be compatible with the Ortho MTS and Orth Vision Swift machines and comply with federal clinical laboratory testing regulations under 42 CFR Part 493
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