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This Combined Synopsis/Solicitation opportunity from Department Of Veterans Affairs was posted on July 22, 2019. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

65--Commercial Item - Supply Restock of Artificial Larynges and Associated Items (VA-19-00032947)

Awarded
36C79119Q0014Federal

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The Department of Veterans Affairs is seeking proposals for the restocking of Artificial Larynges at the Denver Logistic Center in Golden, Colorado. Eligible vendors must be FDA Class 1 Device Registered and provide equipment that meets FDA 21 CFR 874.3375 standards. The requirement is divided into four categories: digital extra-oral, analog extra-oral, analog intra-oral, and digital intra-oral devices. All requested devices must be hand-held, battery-operated, and feature manual volume and pitch controls, as well as a manually depressed button to produce sound vibrations. Extra-oral models must support both neck/cheek placement and intra-oral tube use, while intra-oral models are dedicated solely to tube placement. Each device must include a commercial warranty of at least one year, and applicable models must include necessary batteries, chargers, and oral adaptors.

General Info

Contract Value

$0

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

555 Corporate Circle;Golden CO 80401 USA, CO, USA

Set-Aside

NONE

Award Issued Date

Documents

0

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Timeline

1 update
PhaseAwarded
Posted

Combined Synopsis

Notice updated

Response deadline changed from Aug 2, 2019 to Jul 22, 2019. The notice description changed.

Awarded

Contract was awarded

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Veterans Affairs → Commodities & Services Acquisition Service (36C791)
ContactsNo contacts available
OfficeDENVER, CO, 80225, USA
Office AddressDENVER, CO, 80225, USA
ContactsNo contact information available

Full Description

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The VA Denver Logistic Center (DLC) intends to issue a Request for Proposals (RFP) for the restocking of Artificial Larynges at the Denver Logistic Center, located in Golden, CO. The contractor shall minimally provide and deliver an FDA Device Registered (FDA 21 CFR 874.3375) Artificial Larynx that meets or exceeds the technical specifications described below in this section. Digital Extra-Oral Artificial Larynx Device (B.5.1 CLIN 01) The artificial larynx shall meet the following minimum technical requirements and minimum functions: The device is used to produce speech in the absence of a functioning larynx. The device functions extra-orally by manual placement against neck or cheek surface; and intra-orally by intra-oral tube placement in the oral cavity with use of an oral adaptor and intra-oral tube. When pressed against the skin on the neck or outer cheek sound vibrations are conducted through the neck or cheek tissue into the pharynx and oral/nasal cavities and shaped by the articulators (tongue, lips) to produce speech. When the oral adaptor is used, the intra-oral tube transmits sound directly into the oral cavity. The digital device must be hand-held; battery-operated, capable of working with rechargeable battery/batteries, include a battery charger, and include at least two rechargeable batteries. The device must produce sound and include a manual volume control with a high/low range of volume. The device must also have a range of pitch/tone settings with an internal and/or external pitch/tone setting adjustment(s). The device must include an oral adaptor and intra-oral tubes. The device must have a manually depressed button that produces sound vibrations. The device must include a commercial warranty that meets or exceeds one year. Analog Extra-Oral Artificial Larynx Device (B.5.2 CLIN 02) The artificial larynx shall meet the following minimum technical requirements and minimum functions: The device is used to produce speech in the absence of a functioning larynx. The device functions extra-orally by manual placement against neck or cheek surface; and intra-orally by intra-oral tube placement in the oral cavity with use of an oral adaptor and intra-oral tube. When pressed against the skin on the neck or outer cheek sound vibrations are conducted through the neck or cheek tissue into the pharynx and oral/nasal cavities and shaped by the articulators (tongue, lips) to produce speech. When the oral adaptor is used, the intra-oral tube transmits sound directly into the oral cavity. The analog device must be hand-held; battery-operated, capable of working with rechargeable battery/batteries, include a battery charger, and include at least two rechargeable batteries. The device must produce sound and include a manual volume control with a high/low range of volume. The device must also have a range of pitch/tone settings with an internal and/or external pitch/tone setting adjustment(s). The device must include an oral adaptor and intra-oral tubes. The device must have a manually depressed button that produces sound vibrations. The device must include a commercial warranty that meets or exceeds one year. Analog Intra-Oral Artificial Larynx Device (B.5.3 CLIN 03) The artificial larynx shall meet the following minimum technical requirements and minimum functions: The device is used intra-orally to produce speech in the absence of a functioning larynx. The device functions by intra-oral tube placement in the oral cavity. Sound vibration is conducted through a thin tube placed directly into the oral cavity where it can be shaped by the articulators (tongue, lips) to produce speech. The analog device is a dedicated intra-oral device and cannot be used by manual placement against the neck or cheek surface. The analog device must be battery powered, hand-held, and have a manually depressed button that activates sound which is conducted from the device through the intra-oral tube directly into the oral cavity. The device must produce sound and include a manual volume control with a high/low range of volume. The device must also have a range of pitch/tone settings with an internal and/or external pitch/tone setting adjustment(s). The device must include at least two batteries. The device must include a commercial warranty that meet or exceeds one year. Digital Intra-Oral Artificial Larynx Device (B.5.4 CLIN 04) The artificial larynx shall meet the following minimum technical requirements and minimum functions: The device is used intra-orally to produce speech in the absence of a functioning larynx. The device functions by intra-oral tube placement in the oral cavity. Sound vibration is conducted through a thin tube placed directly into the oral cavity where it can be shaped by the articulators (tongue, lips) to produce speech. The digital device is a dedicated intra-oral device and cannot be used by manual placement against the neck or cheek surface. The device must be battery powered, hand-held, and have a manually depressed button that activates sound which is conducted from the device through the intra-oral tube directly into the oral cavity. The device must produce sound and include a manual volume control with a high/low range of volume. The device must also have a range of pitch/tone settings with an internal and/or external pitch/tone setting adjustment(s). The device must include at least two batteries. The device must include a commercial warranty that meets or exceeds one year. The device is digital. Eligible vendors shall be FDA Class 1 Device Registered. Request for Proposals shall be issued on or about July 12, 2019. Please contact Star M. Yeo, Contract Specialist in writing for additional details at contact@example.gov

More opportunities from Department Of Veterans Affairs → Commodities & Services Acquisition Service (36C791)

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NAICS: 334510
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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 single-award, 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 (SWD) devices, and portable neuromodulation systems for headache disorders, along with associated consumables such as electrodes and lead wires. 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 methodologies vary by item: CLINs X001 through X004 are awarded based on Lowest Price Technically Acceptable (LPTA) procedures, while CLIN X005 is evaluated using a Best-Value Tradeoff method, weighting technical factors at 60 percent, price at 25 percent, and past performance at 15 percent. Responsive proposals must include a signed SF 1449, a Technical Capability Statement, FDA 510(k) clearance letters, and three past performance documents. Non-manufacturers must provide OEM-issued Authorized Distributor Letters. Mandatory certifications include the Price Matrix (Attachment 0001), Limitations on Subcontracting (Attachment 0003), and either the Buy American Certificate (Attachment 0004) for small businesses or the Trade Agreements Certificate (Attachment 0005) for large businesses. Product samples for every offered CLIN/SLIN must be shipped to the Denver Logistics Service facility. Following several amendments, the final deadline for the receipt of all proposal documentation and product samples is November 2, 2026, at 12:00 PM CDT.
Electromedical and Electrotherapeutic Apparatus Manufacturing

POSTED

4 days ago

DEADLINE

in 4 days
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