Redacted J&A or a Cost-Per-Test (CPT) Agreement to include reagents, instrument/equipment, consumables, controls, and any necessary services to conduct Flow Cytometry Requirement 23-P-0054
Summary
AI-generated · Jan 22, 2026FDA-approved flow cytometry instrumentation is being sought, along with all necessary reagents, consumables, controls, and related services to perform flow cytometry analyses. The system must support fully automated discrete random-access operation.
Additional requirements include storing reagents at FDA-approved storage levels, barcode identification, printing one patient-result per page, and the ability to interface with the Military Health System Genesis, comply with RMF, and be HIPAA-compliant. This requirement is described as a redacted Justification and Approval (J&A) or a Cost-Per-Test (CPT) arrangement.
This requirement was for a FDA Approved Flow Cytometry Instrumentation must be able to have fully automated discrete random-access capabilities; be able to store reagents at the Food and Drug Administration (FDA) storage levels; be capable of barcode identification; be able to print patient results as one per page; have the ability to interface with the Military Health System (MHS) Genesis and the Risk Management Framework (RMF) and Health Insurance Portability and Accountability Act (HIPAA) compliant.
From Justification posted on Jan 21, 2026Notice history
1Details
Award Information
Contacts
Phone
2102213446
Phone
2102213446
Agency
Place of Performance
USA