Infusion documentation

A wide range of documents are available to answer your questions on your CareFusion infusion products. Click on the appropriate section below to access the information you need:

 

Click on a CareFusion Infusion product below for a list of available white papers on that topic:

Alaris® SE single and dual channel pumps

Alaris® System

Alaris® System - ROI

Gemini infusion system

MedSystem III® infusion pump

IV sets and accessories

SmartSite® needle-free valve

SmartSite® Vial Adapters

Texium® IV accessories

Click on a CareFusion Infusion product below for a list of available directions for use (DFU) on that topic:


Alaris® SE single and dual channel pumps

Alaris® System (includes DFU for each module)

Alaris® System quick reference guides / hang tags

MedSystem III® infusion System

Click on the links below for a list of frequently asked questions on that topic:


Administration

Alaris® System

Alaris® Pump module

Alaris PCA Module

MedSystem III infusion pump

Alaris Etc02

Alaris® Syringe module

Alaris® SE single and dual channel pumps

Gemini infusion system

IV sets and accessories

SmartSite® IV sets and accessories

HIPAA Documents

Manufacturer Disclosure Statement for Medical Device Security (MDS2)

The intent of the MDS2 is to supply healthcare providers with important information that can assist them in assessing the vulnerability and risks associated with electronic Protected Health Information (ePHI) transmitted or maintained by a product. Security risk assessment is a broad, organization-wide effort, therefore this document focuses on only those elements of the risk assessment process associated with products and systems that maintain or transmit ePHI. The MDS2 was created by the HIMSS Medical Device Security Workgroup and is in compliance with the HIPAA Security Rule.