6515--PORTABLE RO SYSTEM FOR INPATIENT DIALYSIS "BRAND NAME ONLY" OEM LETTER FROM THE MANUFACTURER IS REQUIRED. IF NO OEM LETTER VENDOR WILL BE CONSIDERED NON-RESPONSIVE.

SOL #: 36C24526Q0446Sources Sought

Overview

Buyer

Veterans Affairs
Veterans Affairs, Department Of
245-NETWORK CONTRACT OFFICE 5 (36C245)
LINTHICUM, MD, 21090, United States

Place of Performance

Place of performance not available

NAICS

Surgical and Medical Instrument Manufacturing (339112)

PSC

Medical And Surgical Instruments, Equipment, And Supplies (6515)

Set Aside

No set aside specified

Timeline

1
Posted
Apr 13, 2026
2
Response Deadline
Apr 17, 2026, 7:00 PM

Qualification Details

Fit reasons
  • NAICS alignment with historical contract wins in similar service areas.
  • Scope strongly matches core technical capabilities and delivery model.
Risks
  • Past performance thresholds may require one additional teaming partner.
  • Potential clarification needed on staffing minimums before bid/no-bid.
Next steps

Validate eligibility requirements, assign capture owner, and schedule partner outreach to confirm teaming strategy before submission planning.

Quick Summary

The U.S. Department of Veterans Affairs (VA) is conducting market research through a Request for Information (RFI) to identify qualified sources for Portable RO (Reverse Osmosis) Machines for the Washington DC VA Medical Center. This is a "BRAND NAME ONLY" requirement, and an OEM Distributor/Authorization Letter is mandatory for all responses. Responses are due by April 17, 2026, at 3:00 PM EST.

Scope of Work

The VA requires the supply and installation of specific portable RO machines and related components. This includes four units each of: AquaC 15 Amp, Portable Softener (with salt tablet kit), AquaCaddy V2 Backflow Prevention/RPZ, AquaCaddy V2 Bolt on HD Conn.Kit, AquaCaddy V2 Booster Pump, Aqua Caddy - Dual Carbon Block, and AAMI Water Profile Kit. Additionally, four units of installation services and two units of system technician training are required. All items are specified as "BRAND NAME ONLY" with corresponding Manufacturer Part Numbers (MPNs).

Key Requirements for Response

  • Mandatory OEM Letter: An OEM Distributor/Authorization Letter from the manufacturer is required. Failure to provide this will result in disqualification.
  • Certifications: Completion of the Buy American-Free Trade Agreements-Israeli Trade Act Certificate (FAR 52.225-4) is mandatory.
  • Questions: Vendors must answer 14 specific questions covering business size, manufacturer/distributor status, OEM authorization, contract numbers (FSS/GSA, NAC/SAC, SEWP V), general pricing, company information (Legal Name, UEI), warranty, point of contact, and estimated delivery timeframes.
  • Registration: Prospective awardees must be registered with SAM.gov and complete representations and certifications. SDVOSB and VOSB socio-economic categories must be verified on the SBA website.
  • Delivery: Required within 60 days from contract award to the Washington DC VA Medical Center warehouse.

Contract & Timeline

  • Type: Sources Sought / Request for Information (RFI) for market research purposes.
  • Intended Contract Type: Firm-Fixed Price (FFP).
  • Set-Aside: None specified; market research will determine the acquisition strategy, including potential for a total Small Business Set-Aside. Vendors should indicate their business size status.
  • Response Due: April 17, 2026, 3:00 PM EST.
  • Published: April 13, 2026.

Additional Notes

This RFI is for information and planning purposes only and does not constitute a solicitation or guarantee a contract award. Responses will be used to identify responsible sources and inform future acquisition decisions. Proprietary information should be clearly marked. Submissions are voluntary and at no cost to the Government. The Principal NAICS Code is 339112 - Surgical and Medical Instrument Manufacturing.

People

Points of Contact

Mohsin AbbasContract SpecialistPRIMARY

Files

Files

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Versions

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Sources Sought
Posted: Apr 13, 2026
6515--PORTABLE RO SYSTEM FOR INPATIENT DIALYSIS "BRAND NAME ONLY" OEM LETTER FROM THE MANUFACTURER IS REQUIRED. IF NO OEM LETTER VENDOR WILL BE CONSIDERED NON-RESPONSIVE. | GovScope