VA Directive 6550 - New Appendix A.pdf

VA Directive PDF 165 KB Posted

Attached to
6525--SEP 2024 Equipment Only Consolidation - Amendment 0004
Solicitation number
36A79725Q0002
Issued by

About this file

This document is VA Directive 6550 Appendix A, which is required to be completed for all procurements of network-connected medical devices and non-network-connected medical devices that store sensitive information. It covers details such as the equipment category, manufacturer, model, application, device type, operating system, wireless connectivity, enterprise risk analysis, patching, auditing, antivirus, endpoint management, authentication, encryption, data storage, and cloud connectivity. The document provides technical requirements and considerations for these medical devices to be deployed within the VA network.

The related federal contract opportunity is for a SEP 2024 Equipment Only Consolidation, solicitation number 36A79725Q0002, issued by the Department of Veterans Affairs National Acquisition Center. This appears to be a solicitation for the procurement of various types of equipment, though the specific products or services required are not detailed in the provided information.

View the file

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
Show all 20

Who attaches VA Directive 6550

Other files

File Type Posted
SF30 - Amendment 0004.pdf PDF
SEP 2024 Equipment Only Consolidation Schedule - Revised2.pdf PDF
CORRECT 695B48007_XR US VAMC MILWAUKEE WI_COMPLIANCE MATRIX_UPDATED2.xlsx XLSX spreadsheet
Amendment 0004 - Continuation Page.pdf PDF
SF30 - Amendment 0003.pdf PDF
358B49001 - 695B48011.zip ZIP file
SEP 2024 EQ Consolidation - Schedule of Line Items w QA - ROUND 2.xlsx XLSX spreadsheet
SEP 2024 Equipment Only Consolidation Schedule - Revised.pdf PDF
Amendment 0003 - Continuation Page.pdf PDF
SF30 Amendment 0002.pdf PDF
644B48042 - XR US VAMC PHOENIX AZ_Compliance matrix updated.xlsx XLSX spreadsheet
Amendment 0002 - Continuation Page.pdf PDF
644B48043 - XR US VAMC PHOENIX AZ_Compliance matrix updated.xlsx XLSX spreadsheet
SEP 2024 EQ Consolidation - Schedule of Line Items w QA.xlsx XLSX spreadsheet
Amendment 0001 - Continuation Page.pdf PDF
SEP 2024 EQ Consolidation - Schedule of Line Items w QA - Updated.xlsx XLSX spreadsheet
573B45026 - 644B48042.zip ZIP file
SF30 Amendment 0001.docx DOCX document
644B48043 - 757B50001.zip ZIP file
358B49001 - 573B45024.zip ZIP file
Vendor Folders.zip ZIP file
691B40053 - 757B50001.zip ZIP file
516B40042 - 548B40010.zip ZIP file
499B49018 - 516B40041.zip ZIP file
548B40020 - 558B49028.zip ZIP file
654B30016 - 673B40053.zip ZIP file
673B40056 - 691B40052.zip ZIP file
SEP 2024 EQ Consolidation - RFO.pdf PDF
Memorandum for Training.pdf PDF
629B40355 - 654B30014.zip ZIP file
558B49030 - 596B40037.zip ZIP file
SEP 2024 Equipment Only Consolidation Schedule.pdf PDF
36A79725Q0002_1.docx DOCX document
SEP 2024 EQ Consolidation - Schedule of Line Items.xlsx XLSX spreadsheet
Vendor Workup Spreadsheet - 36A79725Q0002.xlsx XLSX spreadsheet
101EH2069 - 499B49015.zip ZIP file
596B40038 - 621B40006.zip ZIP file
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Text version

VA Directive 6550 Appendix A

VA DIRECTIVE 6550 Appendix A – To be completed for all procurements of network-connected medical devices and non-network-connected medical devices that store sensitive information. For client/server systems, a separate 6550 Appendix A is required for each the client and the medical server.

1.1 Equipment Category (VA-MDNS)

1.2 Manufacturer

1.3 Model

1.4 NSI Number (if known)

1.5 Application Name and Software Version #

1.6 Requesting Service

1.7 VISN

1.8 Facility Name

1.9 Facility Number

1.10 Manufacturer Point of Contact

Phone Number E-mail address

1.11 Biomedical Engineering Point of Contact

Phone Number E-mail address

1.12 Responsible Service if Biomedical Engineering is NOT the Primary System Manager for system maintenance, support and lifecycle management

1.13 Medical Device Type Discrete device

Software Client Application server

1.14 Device Description (i.e. equipment function and systems it communicates with)

1.15 MDIA VLAN Number for installation (if known)

1.16 Device Operating System (OS)

Please include OS build level.

Review support status for Windows OS versions here.

Procurement of devices with unsupported operating systems is prohibited. Unsupported operating systems are OSs that are not supported by the manufacturer and have reached the end of the OS lifecycle as published by the OS manufacturer (i.e. no further security patches will be released for the OS by the manufacturer after the OS end-of-life nor will be available by other methods such as extended warranty purchases from the OS manufacturer).

1.17 Does the device support wireless network connection? Yes No If yes, what is the FIPS 140-2 or 140-3 certification number?

If no, does the vendor support the installation of FIPS 140-2 or 140-3 wireless cards? Yes No

Procurement of devices using 802.11 wireless networking that are not FIPS 140-2 or 140-3 compliant is prohibited.

1.18 Does the device have an existing, active Enterprise Risk

Analysis (ERA)? Yes No

If yes, what is the ERA number?

If the device has a direct connection to Cerner or EHRM interface, does the device have an existing MedMod ERA? Yes No

If yes, what is the MedMod ERA number?

**Note that the ERA must be for the same make, model, and application software version to apply to the requested device. A new ERA is required for major software or operating system updates (e.g. version 2.0 to 3.0) but is not required for minor updates (e.g. version 2.0 to version 2.1).

If an ERA exists for the requested device, completion of the 6550 Appendix A is not required beyond this point. Please sign to certify that an existing ERA is available for the requested device and forward the document to either the Area Manager or

ISSO for signature, as appropriate. Please note that if the device is an EHRM device, a MedMod ERA is required.

2.1 Can the OS be automatically patched? Yes No

**Note that devices that do not support automated patching via the VHA MD Update Server (MDUS) or via vendor channels impose a significantly higher risk to the VA network.

If patching is not automated, what is the patching process and/or limitations?

2.2 For applications and sub-applications (e.g., Java, Apache) on the device, is automatic patching or updating supported? Yes No

**Note that devices that do not support automated patching impose a significantly higher risk to the VA network.

If patching is not automated, what is the patching process and/or limitations?

2.3 Is a device hardening guide available? Yes No

2.4 Does the device have logging or other auditing mechanisms in place? Yes No

If yes, can these logs be exported to a syslog or similar server?

2.5 Does the device include a database? Yes No

If yes, what is the database version and type (e.g., SQL, Oracle)?

**Note that procuring and deploying devices with unsupported database versions imposes a significantly higher risk to the VA network.

Does the vendor support database conversion from SSN to electronic data interchange personal identifier (EDIPI)? Yes No No PHI

Does the vendor database support multiple identifiers? Yes No No PHI

2.6 Can the device run Defender, ESET, or McAfee antivirus? Yes No

**Note that devices that do not support VA-approved antivirus scanning or an antivirus scanning solution managed by the vendor impose a significantly higher risk to the VA network.

If antivirus is not supported, what are the AV processes and/or the limitations?

2.7 Can a commercial-off-the-shelf (COTS) endpoint management system be installed (e.g., IBM Big Fix, Goverlan, SCCM)? Yes No

If so, which one(s)?

2.8 For Windows-based devices, can the existing Microsoft service be enabled to communicate with the VHA SMAK-AM server?

Yes No Non-Windows-based system

If no, has the vendor agreed to provide a complete software and application inventory for all system components as per FISMA requirements?

Yes No

**Note that devices that do not support communication with the SMAK-AM server or for which the vendor does not agree to provide a complete software inventory impose a significantly higher risk to the VA network.

2.9 Does the device support the use of two-factor authentication? Yes No **Note that devices that do not support two-factor authentication impose a significantly higher risk to the VA network. Please review the VA’s requirements for two-factor authentication here.

Does the device require interactive login service accounts?

**Note that devices that require interactive login service accounts impose a significantly higher risk to the VA network.

2.10 Will the device be joined to the VA domain? Yes No

**Note that devices that are not joined to the domain impose a significantly higher risk to the VA network.

2.11 Does the device allow for encryption of the data drive or OS drives? Yes No

What level of encryption is allowed?

2.12 Are post-quantum cryptography (PQC) ciphers being used for this implementation? Yes No

2.13 What method of encryption is used for data in transit? SSL

HTTPS

TLS (version: )

SFTP

None Other:

**Note that use of SSL is prohibited and that TLS versions 1.0/1.1 impose a significantly higher risk to the VA network.

2.14 Is sensitive data stored at rest on the device? Yes No

If yes, how many records can be stored on the device? <500 >500 If yes, does the device support on demand purging of data from the local hard drive? Yes No

2.15 Will sensitive data be stored outside of the VA network (e.g.

cloud-based service provider – excludes Electronic Medical Record connection)?

Yes No

2.16 Does the device send/receive VA data to/from an external, vendor-managed cloud? Yes No

If yes, has the cloud platform been approved by the VA Digital Transformation Center (DTC)?

To determine approval status, please visit the Digital VA Product Marketplace.

Yes No

If yes, what is the cloud type, determined by the VA DTC? Software as a Service (SaaS) Managed Service

If SaaS, what is the FedRAMP package ID?

If SaaS, is it FedRAMP authorized? Yes No Is there an approved VA ATO for the cloud platform? Yes No

2.17 Is connectivity external to the VA required for device

operation? Yes No

2.18 Is connectivity external to the VA required for device support? No Yes - VA S2S VPN Yes - VA Citrix Yes – VA Azure Virtual Desktop Yes – Other

If other, describe the remote access method.

What is the MOU/ISA number?

2.19 How many IP addresses are required?

2.20 What kind of IPs does the device use? Static IP DHCP

**Devices should be deployed with static IPs unless DHCP is required.

2.21 Is IPv6 supported? Yes No

If yes, please list any limitations.

2.22 If server-based, select one from each column: Vendor-provided

VHA-provided Other - describe

Physical server Virtual host Cloud virtual host

2.23 If server-based, list server specifications (cores, RAM, power, storage) and rack space.

Attach additional documentation, as needed.

2.24 Does the device use Java? Yes No

2.25 Does the device utilize machine learning/artificial intelligence? Yes No

2.26 What type of vulnerability scanning is allowed on the device? Active Passive Both

If active, is credentialed scanning allowed? Yes No

2.27 If the device uses digital signatures, is it compliant with FIPS 186-4? Yes No N/A

2.28 Does this system include a pre-production (test) environment? Yes No

2.29 Does the device support backups? Yes No

Does this procurement include a backup solution? Yes No N/A

2.30 Does this device include an HL7 interface? Yes No

If yes, what will the HL7 interface be used for? Orders Results Billing (DFT)

ADT

Other:

If the requested device does not have an EHRM approved connection or interface to Cerner, completion of the 6550 Appendix A is not required beyond this point. Please sign this document and route it for signature, as appropriate.

2.31 Does the device have an EHRM approved Cerner interface?

For more information, please reference the approved EHRM interface list and the EHRM IO HTM SharePoint site

Yes No

If no, has an NSR been submitted for interface approval? Yes No NSR Number:

If no, to which security authorization boundary will this device/system be added?

For more information on MedMod zones and MD-LITE, please reference the EHRM IO HTM SharePoint site or contact the EHRM IO HTM team at EHRMIOHTM@va.gov.

MedMod Zone 6A MedMod Zone 6B

MD-LITE

Other

If no, what is the proposed EHR connection(s)/integration(s) type(s)?

For additional guidance, please contact the EHRM IO HTM team at EHRMIOHTM@va.gov.

Openlink (HL7) Compass Router (DICOM) EHR Gateway (Non-DICOM Image Routing) Cerner Connectivity Engine (CCE) CCE Terminal Server (CCE-TS) Separate HL7 Interface/Middleware Server None Other:

Submittal/Approval

Biomedical Engineering Date

Area Manager* Date

*Area manager signature only required for client/server medical systems. Please sign within 10 business days of receipt.

Information Systems Security Officer** Date

** Please sign within 5 business days of receipt and return the document to Biomedical Engineering and the Area Manager. If an ERA is required, please submit this form with the ERA package to the Specialized Device Cybersecurity Department (SDSD) to initiate the ERA process.

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