Intensive Care Ventilators

Added: Jun 27, 2018 6:45 pm The Naval Medical Logistics Command (NMLC) has a requirement for six (6) ventilators, intensive care [17-429] for Naval Hospital Jacksonville. Three (3) intensive care ventilators shall allow for ventilation of all patient populations, from neonate to adult. The remaining three (3) intensive care ventilators shall allow for ventilation of patient populations from pediatric to adult.

• The ventilators shall be capable of delivering tidal volumes of 5-2000 mL.
• The ventilators shall feature compressors.
• The ventilators shall feature automatic tube compensation.
• The ventilators shall also feature a trigger mechanism for both flow and pressure.
• The ventilators shall provide leak compensation.
• The ventilators shall provide the following ventilation modes: assist/control (A/C) ventilation, spontaneous/continuous positive airway pressure (CPAP), synchronized intermittent mandatory ventilation (SIMV), proportional assist ventilation (PAV), and bilevel/airway pressure release ventilation (APRV).
• The ventilator shall be capable of monitoring and displaying the following parameters: peak inspiratory pressure, mean airway pressure, positive end-expiratory pressure (PEEP), tidal volume, minute volume, spontaneous minute volume, fraction of inspired oxygen (FiO2), respiratory rate, expiratory rate, and inspiratory-to-expiratory (IE) ratio.
• Each ventilator shall include a rolling cart capable of supporting a humidifier.
• Each ventilator shall include two (2) rechargeable batteries to allow for transporting of patients without a disruption in ventilation.
• The ventilators shall run on an operating system (OS) that complies with Navy cybersecurity requirements.
• The vendor should include the option for clinician operator training.
• The power requirement is 120 VAC, 60 Hz.

Vendor shall be an Original Equipment Manufacturer (OEM) authorized dealer, authorized distributor, or authorized reseller for the proposed equipment/system, such that OEM warranty and service are provided and maintained by the OEM. All software licensing, warranty, and service associated with the equipment/system shall be in accordance with the OEM terms and conditions.

The system, including claims made for the product, shall be compliant with Food and Drug Administration (FDA) regulations, with respect to marketing and delivering medical products for use in the United States of America. These requirements shall apply even if delivery is requested outside of the United States of America. The system shall be installed in compliance with OSHA requirements.

Upon delivery, the vendor shall be responsible for uncrating the unit/system, transporting it through the facility to the location of intended use for installation, and removing all trash created in this process. If interim storage is required, the vendor shall make arrangements for the storage.