Salient Characteristics.pdf
PDF 121 KB Posted
- Solicitation number
- PANHCA26P0000026643
- Issued by
-
Department of the Army Medical Command
About this file
This document outlines salient requirements for a federal contract opportunity requiring the provision of fifteen (15) CADD-Solis Ambulatory Infusion Pumps with accompanying lock boxes. The infusion pumps must be Patient Controlled Analgesics capable of administering medication via epidural and intravenous delivery modes, featuring a linear peristaltic pump mechanism. The devices must operate within a flow range of 0-100 ml/hr continuous or 0-500 ml/hr bolus, adjustable by at least 0.05 ml/hr increments, with a weight between 2-3 pounds for portability and ease of use.
The infusion pump system must be FDA-approved with no unresolved recalls and include critical safety features such as stream occlusion, air-in-line, system malfunction, empty reservoir, and low battery alarms or indicators. Devices must remain within their useful life expectancy, with units identified for discontinuation deemed non-acceptable. Additional requirements include event log capability, security key and/or security code functionality, compatibility with central lines, and proprietary cassette or IV bag reservoir systems. The seller must be an authorized dealer, distributor, or reseller and must provide fifteen lock boxes for secure storage and theft prevention, two copies of operator/user manuals, reprocessing instructions, and a warranty in accordance with Original Equipment Manufacturer guidance.
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Text version
The proposed offeror must be able to provide fifteen (15) CADD-Solis Ambulatory Infusion Pumps with lock boxes, extended description follows:
Salient Requirements:
• Seller must provide 15 each infusion Pumps as per characteristics listed below.
• Seller must provide 15 each Lock boxes which can store infusion pump and medication bag and provide protection against unauthorized access and theft.
• Seller must provide system that has been approved by the Food and Drug Administration
(FDA) and must not have any unresolved FDA recalls.
• Seller shall provide Infusion Pumps, Patient Controlled Analgesics capable of allowing patients the ability to administering medication.
• Seller shall provide device with delivery mode of epidural and intravenous.
• Seller shall provide device with pump mechanism of linear peristaltic.
• Seller shall provide device within its life expectancy. Device identified for discontinuation within the device’s life expectancy will be deemed non-acceptable.
• Seller shall provide device with indicators, alarms and dose error reduction.
• Seller shall provide device with stream occlusion, air in line, system malfunction, empty reservoir, low battery alarm/ indicator.
• Seller shall provide device with weight within the range of at least 2-3 pounds for ease of use and transport.
• Seller shall provide device with a flow range of at least 0-100 Continuous/0-500 Bolus and be able to be adjusted by at least 0.05ml/hr. and have a reservoir that is a proprietary cassette/ IV bag.
• Seller shall provide a device capable of providing event log.
• Seller shall provide Pump with capabilities key and/or security code.
• Seller shall provide pump must be compatible with central lines.
• Seller shall provide two copies of operator/user manual.
• Seller shall provide reprocessing instructions.
• Seller must be an authorized dealer, distributor, or reseller for the proposed system.
• Seller must provide a warranty for the system in accordance with Original Equipment
Manufacturer (OEM) guidance.
File details come from the government source that posted it. Updated .