D.1 VA DIRECTIVE 6550 APPENIDX A.docx

VA Directive DOCX document 13 KB Posted

Attached to
6640--COPAN WASP LAB SYSTEM (VA-25-00029956)
Solicitation number
36C25525Q0122_1
Issued by

About this file

The document is a detailed technical specification for a VA Saint Louis Health Care System solicitation (Solicitation Number: 36C25525Q0122_1) to procure a COPAN Walkaway Specimen Processor (WASP) for the John Cochran facility. The system must weigh less than 1,600 lbs, include peripherals like a touch screen monitor and barcode reader, and have advanced microbiological processing capabilities such as custom streaking patterns, multiple media type acceptance, sample traceability, and slide preparation for gram staining.

Key requirements include network connectivity to VISTA, Cerner compatibility, white-glove installation within 30 days of delivery, on-site training for clinical and biomedical staff, and a comprehensive one-year warranty covering parts, labor, and software updates. The vendor must provide two copies of operator and service manuals, respond to technical calls within 8 hours, ship replacement parts within 48 hours, and deliver the equipment within 90 business days of contract completion. Additional considerations include potential trade-in options, extended warranty possibilities, and service training opportunities. The solicitation emphasizes the need for a fully functional, technologically advanced laboratory specimen processing system that meets VA security and operational standards.

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Other versions and copies of VA Directive 6550

File Revision Posted Attached to
VA Directive 6550 20_Feb_2025 Med Devices.pdf Feb 20, 2025 R699--On-Site Document Shredding Services UNRESTRICTED
VA Directive 6550 - New Appendix A - published Jun. 2023.pdf Jun 2023 JUN 2026 Equipment Only Consolidation
VA Directive 6550 - New Appendix A - published Jun. 2023.pdf Jun 2023 6525--JUN 2026 Equipment Only Consolidation
VA Directive 6550 - New Appendix A - published Jun. 2023.pdf Jun 2023 6525--JUN 2026 Equipment Only Consolidation
VA Directive 6550 - New Appendix A - published Jun. 2023.pdf Jun 2023 6525--CFM SPECIAL EQ Consolidation
VA Directive 6550 - New Appendix A - published Jun. 2023.docx Jun 2023 6525--MAY 2026 Consolidation - HTME with Extended Installation Services (includes Turnkey Services)
VA Directive 6550 - New Appendix A - published Jun. 2023.pdf Jun 2023 6525--MAR 2026 Equipment Only Consolidation
VA Directive 6550 - New Appendix A - published Jun. 2023.pdf Jun 2023 6525--PACT Act Leases Special FEB FY26 EQ Consolidation
VA Directive 6550 - New Appendix A - published Jun. 2023.docx Jun 2023 6525--JAN 2026 Consolidation - HTME with Extended Installation Services (includes Turnkey Services)
VA Directive 6550 - New Appendix A - published Jun. 2023.pdf Jun 2023 6525--DEC FY2025 Equipment Only Consolidation
VA Directive 6550 - New Appendix A - published Jun. 2023 02.pdf Jun 2023 6525--DEC FY2025 Equipment Only Consolidation
VA Directive 6550 - New Appendix A - published Jun. 2023.docx Jun 2023 6525--SEP 2025 Consolidation - HTME with Extended Installation Services (Includes Turnkey Services)
VA Directive 6550 - New Appendix A - published Jun. 2023.pdf Jun 2023 6525--SEP 2025 Equipment Only Consolidation
Attachment 0001 - VA Directive 6550 Appendix A.pdf Revision not stated 6640--Electrophoresis Testing for the Albany, Buffalo, and Syracuse VA Medical Centers
Attachment 1 VA Directive 6550 Appendix A.pdf Revision not stated 6515--Anesthesia Units
Attachment 1 VA Directive 6550 Appendix A.pdf Revision not stated 6515--Anesthesia Units
Attachment 1 VA Directive 6550 Appendix A.pdf Revision not stated 6515--Anesthesia Units
VA Directive 6550 2.pdf Revision not stated 6640--554 (LAB) | NEW | RTPCR GI and Respiratory Testing
VA Directive 6550 App A Fillable.pdf Revision not stated 6640--New Blanket Purchase Agreement for Molecular Testing- Strep ID, Respiratory Panel, and Blood Culture ID.
VA Directive 6550.pdf Revision not stated 6640--554 (LAB) | NEW | RTPCR GI and Respiratory Testing
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Who attaches VA Directive 6550

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D.2 MDS2 - MANUFACURER DISCLOSURE STATEMENT FOR MEDICAL DEVICE SECURITY

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