Pressure Myograph System - Combined Notice of Intent and Sources Sought Notice
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The National Heart, Lung, and Blood Institute intends to negotiate a sole-source purchase order with DMT-USA Inc. for a complete pressure myograph system. This specialized equipment is designed for the ex vivo physiological assessment of small arteries and blood vessels from mouse models, enabling studies on vascular compliance, stiffness, diameter, and functional response. The required system must feature a pressure myograph chamber for vessels ranging from 60 micrometers to 1.2 millimeters, interchangeable cannulas, a longitudinal force transducer, integrated pressure transducers, and a microscope with an integrated camera and infrared illumination. Additionally, the acquisition includes real-time analysis software, all necessary pressure regulation and calibration components, and full delivery, installation, and user training. The government has identified DMT-USA Inc. as the only source capable of providing an integrated system that combines longitudinal force measurement with the necessary vessel-size flexibility and real-time acquisition software. The project will be performed at an NIH facility in Bethesda, Maryland, under NAICS code 339112. While this notice serves as an intent to negotiate a sole-source contract, the government is allowing other responsible sources to submit quotations and technical documentation by the specified deadline to demonstrate their ability to meet all essential requirements. The final decision regarding competition remains at the sole discretion of the government.
General Info
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NAICS
Place of Performance
Bethesda, MD, 20892, USASet-Aside
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Full Description
The National Heart, Lung, and Blood Institute intends to negotiate and award a purchase order on a sole-source basis to DMT-USA Inc., UEI DUDLHUXCKYJ7, under FAR 13.106-1(b)(1). The proposed acquisition is for one complete pressure myograph system for ex vivo physiological assessment of small arteries and other blood vessels obtained from mouse models.
The system will support studies of vascular compliance, stiffness, diameter, axial force, pressure, and functional response under near-physiological conditions. The required system must include, at minimum:
- A pressure myograph chamber capable of mounting vessels ranging from approximately 60 micrometers to at least 1.2 millimeters in diameter.
- Interchangeable cannulas suitable for the required vessel-size range.
- A longitudinal force transducer capable of measuring axial vessel force.
- Integrated inlet and outlet pressure transducers.
- A microscope with an integrated camera, infrared illumination, and appropriate objectives.
- Acquisition and analysis software providing real-time vessel-diameter tracking and display of experimental parameters.
- Necessary pressure regulation, flow measurement, vacuum, calibration, interface, tubing, cabling, computer, and installation components.
- Delivery, installation, operational verification, and basic user training.
The Government’s market research and technical assessment identified DMT-USA Inc. as the only source capable of providing an integrated pressure myograph with the required longitudinal force-measurement capability. This capability is essential for applying consistent vessel stretch and producing accurate, reliable, and reproducible vascular-function data. Other systems reviewed did not provide the complete combination of vessel-size flexibility, longitudinal force measurement, integrated pressure transducers, microscopy, and compatible real-time acquisition software required by NHLBI.
Delivery, installation, and training will be performed at an NIH facility in Bethesda, Maryland. The anticipated classification is PSC 6515, Medical and Surgical Instruments, Equipment, and Supplies, and NAICS 339112, Surgical and Medical Instrument Manufacturing.
This notice is not a request for competitive quotations. However, all responsible sources may submit a quotation and technical capability documentation demonstrating their ability to satisfy every essential requirement. Responses received by [response deadline] will be considered by the Government. A determination not to compete the proposed acquisition based on responses to this notice is solely within the Government’s discretion.
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