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Request for Prototype Proposals (RPP) — Anesthesia Workstation System (AWS) Prototype

DEPT OF DEFENSE › DEPT OF THE ARMY › W6QK ACC-APG

Response deadlineOct 8, 2026 4:00 PM EDT · 2 days left
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Key decision factors

Response deadline
Oct 8, 2026 4:00 PM EDT · 2 days left
Posted
Sep 8, 2026 12:00 AM EDT
Notice type
Solicitation
Set-aside
Not provided or not applicable
PSC
6515 — Medical and Surgical Instruments, Equipment, and Supplies
Place of performance
Frederick, Maryland
Current status
Closing soon

Notice details

Official status
Closing soon
Normalized group
Bid opportunity
Notice ID
25afc09116754c249c0ed97cbd5fe418
Solicitation number
W91CRB-26-AWSP

Description

Displayed as sanitized plain text from SAM.gov. Retrieved Sep 9, 2026 10:23 PM EDT.

1.0 Overview The U.S. Army Contracting Command (ACC), on behalf of Portfolio Acquisition Executive (PAE) Maneuver Ground, Project Manager Maneuver Medical Systems (PM M2S), is issuing this Request for Prototype Proposals (RPP) to solicit prototype project proposals for a modernized Anesthesia Workstation System (AWS). This RPP is issued pursuant to the Other Transaction Authority (OTA) under 10 U.S.C. § 4022. This is a DIRECT OTA and is NOT a solicitation for a procurement contract under the Federal Acquisition Regulation (FAR). Consortium membership is not required to respond to this RPP. 2.0 Mission Need & Scope The U.S. Army requires a Commercial-Off-The-Shelf (COTS) or Non-Developmental Item (NDI) anesthesia workstation system capable of supporting life-saving medical operations in austere environments at Role of Care (ROC) 3 with little to no modification. The system must overcome the capability gaps of legacy systems, specifically regarding interoperability with Army Oxygen Generation Systems, heavy logistical footprint (weight), and proprietary maintenance constraints. The Government intends to award one (1) OT Agreement for the delivery of two (2) prototype units. These units will undergo rigorous operational testing by the Medical Test and Evaluation Activity (MTEAC) and environmental testing conducted in accordance with MIL-STD-810H. Proposed solutions must be FDA-cleared for human use and Trade Agreements Act (TAA) compliant. A high priority for this effort is organic supportability. The Government strongly prefers systems designed to be maintainable by military Biomedical Equipment Technicians (BMETs) at the Field and Depot levels without reliance on proprietary vendor service contracts. 3.0 Follow-On Production Authority In accordance with 10 U.S.C. § 4022(f), this OT Agreement is issued with a provision for follow-on production. Upon successful prototype completion and validation, the Government may award a follow-on production contract or OT Agreement for approximately one hundred and eighty (180) AWS units without further competitive procedures. 4.0 Proposal Submission Instructions All proposal instructions, technical specifications (CODS and APAs), and evaluation criteria are detailed in the attached Request for Prototype Proposals (RPP) document. Questions: All questions must be submitted in writing via email to the Agreements Officer and Agreements Specialist no later than 15:00 ET on 17 September 2026. Proposals: Proposals must be submitted via DoD SAFE file transfer or secure email no later than 16:00 ET on 01 October 2026. Communications: Unauthorized contact with program office personnel or technical end-users regarding this RPP may result in disqualification. All communications must be directed to the points of contact listed below. Attachments The Final RPP Document (which includes Appendix E) The Standalone ADRL Document Attachment A (The blank TAA Certificate) Attachment C / OTA Articles Points of Contact Primary Point of Contact: Timothy Compton Agreements Officer Email: timothy.j.compton7.civ@army.mil Secondary Point of Contact: Roxanne A. Dalrymple Agreements Specialist Email: roxanne.a.dalrymple.civ@army.mil

Attachments

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Contacts

Roxanne Dalrymple
Secondary
roxanne.a.dalrymple.civ@army.mil

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Detected in

  • Solicitation document“n be performed using standard, non-proprietary tools and diagnostic equipment. Any requirement for proprietary diagnostic software, specialized vendor-only calibration tools, or proprietary training certifications to per”
  • Solicitation document“k-resistant flow meters for manual ventilation. Physical mechanical backup required if electronic flow control is used. Minimum Required 5 Connection compatibility The system shall be compatible with universal ventilator”

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