6515--SENZIME NEUROMUSCULAR BLOCKADE MONITORS "BRAND NAME OR EQUAL TO SENZIME IAW SOW". OEM LETTER FROM MANUFACTURER IS REQUIRED. IF NO OEM LETTER VENDOR WILL BE CONSIDERED NON-RESPONSIVE.
ID: 36C24525Q0509Type: Sources Sought
Overview

Buyer

VETERANS AFFAIRS, DEPARTMENT OFVETERANS AFFAIRS, DEPARTMENT OF245-NETWORK CONTRACT OFFICE 5 (36C245)LINTHICUM, MD, 21090, USA

NAICS

Surgical and Medical Instrument Manufacturing (339112)

PSC

MEDICAL AND SURGICAL INSTRUMENTS, EQUIPMENT, AND SUPPLIES (6515)
Timeline
    Description

    The Department of Veterans Affairs is seeking qualified vendors to provide fourteen Senzime TetraGraph Neuromuscular Blockade Monitors for the Washington DC VA Medical Center's Anesthesia department. This procurement aims to enhance patient safety during surgeries by enabling quantitative monitoring of neuromuscular blockade, in alignment with the latest guidelines from the American Society of Anesthesiologists. The contract requires delivery of the monitors within 60 days of award, along with necessary installation, training, and support services, ensuring compliance with government procurement standards. Interested vendors must submit their capability statements and pricing by May 14, 2025, to Contract Specialist Mohsin Abbas at Mohsin.Abbas2@va.gov, and must include an OEM authorization letter to avoid disqualification.

    Point(s) of Contact
    Mohsin AbbasContract Specialist
    Mohsin.Abbas2@va.gov
    Files
    Title
    Posted
    The Sources Sought Notice issued by the U.S. Department of Veterans Affairs identifies a need for purchasing fourteen Senzime TetraGraph Neuromuscular Blockade Monitors for its Anesthesia department. This acquisition aligns with the 2023 guidelines from the American Society of Anesthesiologists to enhance patient safety by enabling quantitative monitoring of neuromuscular blockage during surgeries. Vendors are encouraged to submit capability statements, pricing, and other relevant market information, emphasizing the need for an OEM authorization letter; failure to provide this will render submissions non-responsive. The contract requires delivery within 60 days of award and includes specifications for equipment features, installation, and training for clinical staff. The overall goal is to ensure an effective, safe monitoring process while adhering to government procurement standards. Responses are due by May 14, 2025, and will inform the potential development of a formal solicitation for this equipment purchase.
    The government document appears to consist of raw data and encrypted or corrupted information, making it difficult to extract specific content regarding RFPs (Requests for Proposals), federal grants, or state and local RFPs. Without coherent text, the document fails to present any identifiable main topics or key ideas. The structure seems unorganized, possibly due to data corruption, which hampers the ability to analyze or summarize the intended content related to government procurement processes. Consequently, any attempt to ascertain the document's purpose or central themes regarding federal funding opportunities cannot be successfully accomplished, as the necessary details are missing or illegible. Given this context, the significance and implications of the document remain unclear, highlighting a need for a properly formatted and readable version for effective analysis.
    The document outlines a government Request for Proposals (RFP) involving the procurement of medical supplies related to surgical instruments. It lists two primary items: the TetraGraph Next Gens (14 units) and the TetraSens Adult EZClick Sensor (1 box containing 20 sensors). Both items are specified under firm-fixed price contract terms and are identified as "brand name or equal" to SENZIME in accordance with the Statement of Work (SOW). The principal North American Industry Classification System (NAICS) code associated with the procurement is 339112, which pertains to surgical and medical instrument manufacturing, while the Product/Service Code is 6515, indicating medical and surgical instruments and supplies. Overall, this RFP seeks bids to acquire these specific medical devices, ensuring that suppliers can meet the established quality and compliance standards while facilitating the government's commitment to enhance its medical service provisions.
    The Washington DC VA Medical Center is seeking to procure fourteen Senzime TetraGraph Neuromuscular Monitors for its Anesthesia department to enhance patient safety during surgeries through quantitative monitoring of neuromuscular blockade. This technology meets the 2023 guidelines from the American Society of Anesthesiologists, addressing current limitations in monitoring methods, thereby reducing risks of adverse events post-surgery. The procurement includes necessary equipment, software, training, and installation services, all sourced from authorized distributors with manufacturer warranties. The contract specifies detailed equipment specifications, delivery logistics, COVID-19 safety protocols, on-site procedures, and requirements for training clinical staff. The contractor is responsible for installation, ongoing support, and documentation post-completion. The contract type is Firm-Fixed Price, with evaluation based on brand compliance, distribution legitimacy, delivery timelines, and pricing. This initiative reflects a commitment to improving healthcare quality and patient outcomes within the VA system.
    The VAAR 852.212-71 clause establishes strict requirements for procuring supplies and equipment within government contracts. It mandates that only new Original Equipment Manufacturer (OEM) items are acceptable, explicitly prohibiting the provision of used, refurbished, or gray market items. Gray market items are defined as OEM products sold outside authorized channels or by unauthorized dealers. Additionally, the clause forbids counterfeit items, which include any unauthorized reproductions or misleading representations of OEM goods. Vendors must be verified as OEMs, authorized dealers, or distributors, providing documentation to confirm their status. Compliance with OEM terms and conditions is required for all associated software licensing, warranties, and service agreements. This clause is essential for ensuring the integrity and authenticity of the supplies procured through Federal RFPs, thereby safeguarding both quality and compliance in government contracting.
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