Multi - Therapy Infusion Pump

2026-11-03

1 . 0 Product Overview : This document outlines the requirements for a small , lightweight , and durable multi - therapy infusion pump designed for use in pre - hospital , aeromedical , and military environments . The Office of the Command Surgeon is seeking a portable device that offers a wide range of therapeutic applications in a compact and rugged form factor , capable of reliable function in demanding field conditions . The intended use for this device is for intravascular , subcutaneous , intra - arterial , epidural , and perineural infusions administered by licensed military healthcare professionals in clinical , ambulatory , and medical transport settings ( both air and ground ). 2 . 0 Core Capabilities and Specifications : The primary requirements for the infusion pump are focused on size , weight , and cube ( SWaP ) toensure it can be seamlessly integrated into already existing medical pack - outs and ruck sacks . Feature Required SpecificationDimensions Objective : Less than 6 ” x 4 ” x 2 ” Weight Less than 15 oz ( excluding battery ) Delivery Modes Must support : Continuous , Patient - Controlled Analgesia ( PCA ), Intermittent , Multi - Step , Total Parenteral ( TPN ), and Epidural infusions . Flow Rate 0 . 1 mL / h to 999 mL / hFlow Rate Accuracy ± 2 . 5 % under normal conditionsVolume to be Infused 0 . 1 mL to 9 , 999 mLDrug Library Must support up to 40 clinical care areas and at least 1 , 000 drugs per area . Power Source AC : 100 - 240V , 50 - 60 Hz DC : Rechargeable Li - Ion batteryBattery Life Minimum of 24 hours of continuous operation at a rate of 125 mL / h . Environmental Device must feature a touch screen that is fully operable when wet . The casing must be designed to withstand drops and fluid splashes . Operating Temperature + 5 ° C to + 40 ° C ( 41 ° F to 104 ° F ) The device must meet the following minimum standards for military and aeromedical use : Electromagnetic Compatibility : Must meet MIL - STD - 461G for Electromagnetic Interference ( EMI ) and Compatibility ( EMC ). Aeromedical Certification : Must be certified as " Safe - to - Fly " for use in military and commercial air transport . FDA Clearance : The device must have current FDA clearance for the indicated uses . Technical Considerations : The device must be capable of wired data connectivity . While a non - standard serial port is acceptable , it must be supplied with an appropriate adapter to ensure connectivity with modern computer systems ( e . g ., USB ). Consumables : Please specify if the infusion pump system requires proprietary consumables ( e . g ., administration sets ). Performance Testing : The device will be subject to a series of performance checks measuring the Volume to be Infused ( VTBI ) to validate accuracy and reliability . Submission : In response to this request for information , vendors shall submit a capability statement or white paper demonstrating that the proposed items meet all outlined specifications . Submissions must be received by the date specified in the SAM . gov announcement and submitted to the point of contact identified therein .

Florida

2026-05-09