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This Sources Sought opportunity from Department Of Defense was posted on March 22, 2016. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Aircrew Bladder Relief Capability

Closed
N00421-16-RFI-1004Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

Active Opportunities Like This One

NAICS: 334510
New
Federal
Automated Ultrasound-Based, Super Intelligence (SI)-Enabled Fracture Detection
Solicitation # BARDA-FY27-10192026
The Center for Biomedical Advanced Research and Development Authority (BARDA) has issued Sources Sought Notice BARDA-FY27-10192026 to identify innovative medical countermeasure technologies for the rapid triage of musculoskeletal injuries, such as fractures and soft tissue injuries of extremities. This request for information is intended for planning and market research purposes to assess commercially available or nearing-commercial technologies that utilize Super Intelligence (SI) and machine learning for automated ultrasound-based fracture detection. The goal is to find standalone, point-of-care devices that can operate in emergency departments, urgent care centers, and austere field settings without relying on traditional imaging infrastructure like X-ray or CT scans. The desired technology must feature automated volumetric capture, 3D-rotatable modeling, and SI-enabled image processing that outperforms human imaging experts and has undergone FDA 510k clearance processes. BARDA is interested in ruggedized, portable units with sufficient battery life for disaster response, interoperability with electronic health record systems, and minimal training requirements for non-specialist operators. Potential acquisition strategies being explored include direct purchases, leases, or vendor-managed inventory arrangements. Interested small businesses and other than small business concerns under NAICS code 334510 must submit their capabilities statements by 1:00 p.m. Eastern Time on November 18, 2026. Submissions must include separate Technical and Business Representation sections, each limited to 10 pages in 12-point Times New Roman font, and be emailed to Justin Moore and Richard Hall. Responses should detail the company's manufacturing capabilities within the United States, regulatory maturity, supply chain resilience, and cybersecurity standards for handling sensitive patient health information.
Barda - Aspr / Daappo / Barda Dcma

POSTED

about 2 hours ago

DEADLINE

in 29 days
NAICS: 334510
New
Federal
Electro-Therapeutic Modalities for Pain Management (ETMPM) - Transcutaneous Electrical Nerve Stimulation (TENS) Procurement Program
Solicitation # 36C79126R0011
The Department of Veterans Affairs is soliciting proposals under Solicitation Number 36C79126R0011 to establish multiple Firm-Fixed-Price, Indefinite Delivery/Indefinite Quantity (IDIQ) base contracts for the Electro-Therapeutic Modalities for Pain Management (ETMPM) and Transcutaneous Electrical Nerve Stimulation (TENS) Procurement Program. This national program provides FDA-cleared electro-therapeutic devices and accessories to support non-opioid pain management across 168 VA Medical Centers and over 1,000 Community Based Outpatient Clinics. The scope includes portable TENS units, portable Interferential Current (IFC) devices, thermal and non-thermal Short-Wave Diathermy devices, and portable Neuromodulation systems for headache disorders, along with associated accessories such as electrodes and lead wires. All products must be OEM-new, feature a one-year warranty, and meet universal Minimum Technical Requirements, including FDA 510(k) clearance for home use. The procurement utilizes a VA Tiered Set-Aside Evaluation Approach, prioritizing Service-Disabled Veteran-Owned Small Businesses (Tier 1), followed by Veteran-Owned Small Businesses (Tier 2), other small business concerns (Tier 3), and finally other-than-small business concerns (Tier 4). Evaluation is based on a per CLIN/SLIN basis; CLINs X001 through X004 are awarded using the Lowest Price Technically Acceptable (LPTA) methodology, while CLIN X005 is evaluated via a Best Value Tradeoff process weighted at 60% Technical, 25% Price, and 15% Past Performance. Responsive proposals must be submitted electronically by October 30, 2026, at 3:00 PM CDT, and must include a signed SF 1449, a Technical Capability Statement, FDA clearance letters, and required certifications including the Buy American or Trade Agreements certificates depending on the offeror's business size. Additionally, product samples must be shipped to the Denver Logistics Service facility in Golden, Colorado, by the same deadline.
Commodities & Services Acquisition Service (36C791)

POSTED

4 days ago

DEADLINE

in 10 days

General Info

NAICS

334510 - Electromedical and Electrotherapeutic Apparatus Manufacturing

Place of Performance

PATUXENT RIVER, MD, 20670, USA

Set-Aside

NONE

Documents

0

No documents available

Documents will appear here when they are available.

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Uniform Contract Format

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Timeline

2 updates
PhaseClosed
Posted

Sources Sought

Notice updated

Response deadline added: Apr 12, 2016. The notice title changed. NAICS code added: 334510. The notice description changed. The point of contact changed.

Notice updated

The notice description changed.

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → Naval Air Warfare Center Air Division
Contacts2 people available
OfficePATUXENT RIVER, MD, 20670-1545, USA
Office AddressPATUXENT RIVER, MD, 20670-1545, USA
Contacts
Lauren S. Morgan
Sabana N MooreContract Specialist

Full Description

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To promote early exchanges of information with industry in accordance with FAR Subpart 15.2 Naval Air Systems Command, Aircrew Systems (NAVAIR-4.6.7.2) at Patuxent River, Maryland is conducting market research by issuing this Request for Information (RFI). NAVAIR is requesting information to identify qualified sources to provide commercially available, non-developmental for a bladder relief device. Interested parties are invited to describe their capabilities and provide a sample of their product to include proposed solutions, current state of technology maturity, and ability to meet the capabilities listed below. A description of the product, its capabilities, and supporting documentation (including specification sheets, test results) is requested. RFI responses are limited to 25 pages. The product sample as well as product information will be submitted at NO expense to the Government. The sample product and corresponding product information will NOT be returned. The samples maybe tested based on its demonstrated ability to meet performance requirements. It is also requested that pricing be included with the submitted product and information. Proprietary data MUST be marked on a page-by-page basis and will be kept confidential and protected in accordance with the Uniform Trades Secret Act. Interested parties should state whether their product is available commercially, and if there is a textile in the product the information shall indicate whether it is made domestically of domestic textiles (must be Berry Amendment compliant - manufacturers must list the origin and place of manufacturing operations of all components). The bladder relief device submitted in response to this RFI will aid the Government in seeking information on products that best meet as many of the following characteristics as possible and determine if further development of a product meeting the requirements listed below is required. - 1. Provide the capability for all aircrew members to obtain bladder relief on typical missions up to 3 hours in duration and multiple uses on long-duration missions up to 12 hours without physiological adverse side effects such as skin irritation, prolonged exposure to urine, hot spots, pinching, rubbing, etc. - 2. Provide bladder relief for male and female aircrew. A unisex design is not required. - 3. Should not restrict movement of aircrew before, during, or after flight. - 4. Operate in an aircraft environment which will include: exposure to Electro-magnetic Interference (EMI), high humidity, high and low temperatures (-20'C/-4'F to +70'C/158'F), dust, rain, static electricity, etc. - 5. Operate on commercially available batteries (if applicable). If the device has an electronic operating component, it should not weigh in excess of 16 ounces, including batteries and preference is given to smaller size devices that can fit into a pocket. - 6. Provide hands-free urine collection. - 7. Should not interfere with operation of the aircraft. - 8. Be flame resistant and not ignite in highly explosive atmospheres. - 9. Device should not interfere with performance of duty or result in aircrew unstrapping from seat nor with emergency egress procedures. - 10. Device should allow the user to don the device or applicable components while donning flight gear without assistance, or don without undressing just prior to going to the flight line. The device should be compatible with Life Support Systems flight gear and be discrete in appearance when worn. - 11. Device should require minimal maintenance which can be performed by the user. - 12. Device shall have no special disposal requirements (disposal shall be in regular trash service). The North American Industry Classification System (NAICS) codes for this acquisition are 315999 - General, 334510 Electromedical and Electrotherapeutic Apparatus Manufacturing, 339920 - Sporting Goods, 339999 - Other misc, Interested companies should address all technical questions to Tara Capecci, Code 4.6.7.2, and (610) 746-3599. Please submit all RFI responses and samples to Naval Air Warfare Center, Code 2.5.1.6., Sabana Moore Barnes, 22473 Millstone Road BLDG 505 Patuxent River, MD 20670-2055. Interested companies should send only contractual questions to the Contract Specialist at the following email address: Lauren.S.Morgan@Navy.mil. All submissions should reference the synopsis number N00421-16-RFI-1004 on the mailing container and all enclosed documents. The deadline for responses is 12 April 2016, which is 21 days after RFI release. All Companies should indicate whether they are a small, small disadvantaged, 8(a), or large business. Respondents must clarify if their firm can provide commercial or non-developmental items that could be modified, or the technology and expertise for development, to meet the Government's needs. This announcement is NOT A REQUEST FOR PROPOSAL nor does the Government intend to pay for any information submitted in response to this synopsis. This synopsis does not commit the Government to award a contract. This synopsis is for market research only and any procurement resulting from this announcement will be synopsized separately.

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