6
Medfusion® Model 3500 pump V6
Operator’s Manual
Introduction
CAUTION: ALWAYS
verify that the software
version of the pump (displayed on screen during
power-up) and
Operator’s Manual
are the same. Refer
to this manual’s front page.
The Medfusion
®
Model 3500 pump V6 is a small,
lightweight and portable syringe infusion pump.
The pump offers a variety of delivery modes
programmable to meet specific patient care needs.
The actual modes available on a given pump, and
their location on a given screen, depend on the
custom setup. Fluids can be delivered from a variety
of syringe sizes (1-60 mL) and syringe manufacturers
in various delivery modes.
The Medfusion
®
Model 3500 pump V6 is equipped
with PharmGuard
®
Medication Safety Software, an
intuitive system designed to enhance safety while
maintaining simplicity, which can allow streamlined
implementation and improved work flow.
A pump
Configuration
is created on a PC
using the PharmGuard
®
Toolbox 2, Version 3
software (PharmGuard
®
Toolbox 2), and then the
Configuration is sent to the pump. The Configuration
may contain global settings, Profile definitions, library
definitions, Drug Programs and syringe definitions
(see page 14 for discussion about libraries).
The Medfusion
®
Model 3500 pump V6 imports and
exports data to assist in history data management.
The pump communicates via the IR port on the rear
of the pump. Pump Configurations and firmware can
be updated, and infusion settings and events history
downloaded in combination with the PharmGuard
®
Toolbox 2 software application.
The pump also has the FlowSentry™ pressure
monitor (rapid occlusion detection) feature, which
is a comprehensive array of pressure-related safety
features, including rapid alarm response and
reduced false alarms. Pressure trending is shown
in the pump display, allowing earlier opportunities
for intervention, as well as a post-occlusion bolus
reduction feature.
Indications for use
The Medfusion
®
Model 3500 pump V6 is indicated
for the following uses:
• In the administration of fluids requiring precisely
controlled infusion rates including blood or
blood products, lipids, drugs, antibiotics, enteral
solutions and other therapeutic fluids.
• By the following delivery routes: arterial, epidural,
intravenous, intrathecal, subcutaneous and
enteral.
• By the following delivery modes: continuous,
volume/time, mass, body surface area, body
weight, intermittent and bolus.
• In critical care, anesthesia, neonatal and pediatric
applications or other healthcare settings where
the use of the syringe infusion pump can be
monitored or supervised by a clinician.
• Inside the MRI room mounted outside the 150
Gauss line and with shielded magnets of field
strength of 1.5 Tesla.
WARNINGS:
• This equipment/system is intended for use by
healthcare professionals only.
• Before using any Medfusion
®
Model 3500 pump
V6, users must be thoroughly familiar with the
contents of the operator’s manual, including all
warnings, cautions, and instructions for use.
• The user should ensure that the performance
offered by the pump is fit for the intended use and
that the pump is not used in any way or for any
purpose other than its intended purpose.
• This pump is not to be used in any intra-articular
space infusion.
• If the pump is used to deliver life-sustaining
medications, an additional pump must be
available for situations where an interruption in
infusion could be dangerous.
• The pump must be positioned in an MR
environment such that it is
secured to a non-
moveable object
and the magnetic fringe field
does
not exceed 150 gauss
. Exposing the Medfusion
®
Model 3500 pump to magnetic fields that exceed
150 gauss presents a risk of becoming a projectile
hazard and can lead to possible patient injury or
death. Irreversible damage to the pump can also
occur, rendering it inoperable.
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