Rigel MULTI-FLO Manual de usuario
Multi-Flo
Innovating Together.
Infusion Device Analyser
Copyright © 2012 SEAWARD GROUP
Last Update: 5th July 2012
Instruction Manual
385A550 Revision 1.0
i
Rigel Medical 24 Month Warranty Statement
Rigel Medical provides a standard 12-month manufacturer’s warranty against breakdown
during normal use. This warranty can be upgraded to a 24-month warranty (terms and
conditions apply*). Problems caused through misuse, damage, fair wear & tear,
consumables and accessories are excluded from standard warranty. Such components
found to be being used in excess of their manufacturer’s operating recommendations are
also excluded. Shipping to an authorised service center is the responsibility of the
sender.
*Terms and Conditions of 24 Month Warranty
The Rigel product must be registered with Rigel Medical within 30 days of purchase to
be eligible for the extended 24-month warranty. Instruments must be returned to an
authorised service center complete with proof of purchase within 13 months of purchase
for calibration at the current rate. Any items returned for calibration outside of the 13
month period stated above may not be eligible for the second 12 month section of
warranty. The second 12 month section of the warranty begins at the expiry of the initial
12 month period, not when the unit is calibrated.
Details correct at time of going to print. The manufacturer retains the right to make
amendments to the above terms and conditions without prior notice.
Calibration Statement
The Rigel Multi-Flo Infusion Device Analyser is fully calibrated and found to be within the
specified performance and accuracy at the time of production. The Seaward Group
provides its products through a variety of channels; therefore it may be possible that the
calibration date on the provided certificate may not represent the actual date of first use.
Experience has indicated that the calibration of this instrument in not effected by storage
prior to receipt by the user. We therefore recommend that the recalibration period be
based on a 12 month interval from the first date the unit is placed in to service.
Date received into service; / / .
ii
© Copyright 2012
All rights reserved. Nothing from this edition may be multiplied, or made public in any
form or manner, either electronically, mechanically, by photocopying, recording, or in any
manner, without prior written consent from the SEAWARD GROUP. This also applies to
accompanying drawings and diagrams.
Due to a policy of continuous development the SEAWARD GROUP reserves the right to
alter the equipment specification and description outlined in this publication without prior
notice and no part of this publication shall be deemed to be part of any contract for the
equipment unless specifically referred to as an inclusion within such contract.
iii
Disposal of old product
The Rigel Multi-Flo has been designed and manufactured with high quality materials and
components, which can be recycled and reused.
When this symbol is attached to a product it means the product is covered by the
European Directive 2002/96/EC.
Please familiarise yourself with the appropriate local separate collection system for
electrical and electronic products or contact your local supplier for further information.
Please dispose of this product according to local regulations. Do not dispose of this
product along with normal waste material. By offering your old products for recycling,
you will help prevent potential negative consequences for the environment and human
health.
iv
Certificate of Conformity
Manufactured by:
Seaward Electronic Ltd, Bracken Hill, South West Industrial Estate
Peterlee, County Durham, SR8 2SW, England
As the manufacturer of the apparatus listed, declare under our sole responsibility that
the product:
Rigel Multi-Flo Infusion Device Analyser
To which the declaration relates are in conformity with the relevant clauses of the
following standard:
BS EN 61010-1:2010 Safety requirements for electrical equipment for measurement,
control, and laboratory use - Part 1: General requirements.
BS EN 61326:2006 Electrical equipment for measurement, control, and laboratory use -
EMC requirements.
Performance: The instrument operates within specification when used under the
conditions in the above standards EMC and Safety Standards.
The product identified above conforms to the requirements of Council Directive
2004/108/EC and 2006/95/EC.
This Conformity is indicated by the symbol , i.e. “Conformité Européenne”
Seaward Electronic Ltd. is registered under BS EN ISO9001:2000 Certificate No.:
Q05356.
1 | Page Rigel Medical Multi-Flo user Manual V1.0
Introduction............................................................................................................ 2
Design Philosophy ......................................................................................................... 2
Unpacking the Multi-Flo ................................................................................................. 3
Warnings and Cautions ......................................................................................... 4
User Notes ..................................................................................................................... 4
Safety Notes .................................................................................................................. 4
Multi-Flo Overview................................................................................................. 6
1 Getting Started................................................................................................ 7
1.1 Before you Switch On! ........................................................................................ 7
1.2 Turning the Multi-Flo On and Off ........................................................................ 7
1.3 Accessing the Multi-Flo Tests............................................................................. 7
1.4 Setting the Time/Date ......................................................................................... 8
1.5 Displaying the Multi-Flo Information ................................................................... 9
2 Analysing an Infusion Device........................................................................ 10
2.1 Connecting an Infusion Device to the Multi-Flo ................................................ 10
2.2 Priming the Channels ....................................................................................... 10
2.3 Patient Controlled Analgesia (PCA) test........................................................... 11
2.4 Occlusion test ................................................................................................... 12
2.5 Flow Rate/Volume test...................................................................................... 14
2.6 Draining the Channels ...................................................................................... 15
3 Maintaining the Rigel Multi-Flo ..................................................................... 17
3.1 Cleaning............................................................................................................ 17
3.2 User Maintenance............................................................................................. 17
3.3 Return Instructions............................................................................................ 18
4 Accessories .................................................................................................. 19
4.1 Optional Accessories ........................................................................................ 19
4.2 Replacement Spare Parts................................................................................. 19
5 Specifications................................................................................................ 20
5.1 Technical Specifications ................................................................................... 20
5.2 General Specifications...................................................................................... 21
5.3 Environmental Conditions................................................................................. 21
6 Support ......................................................................................................... 22
6.1 Contact Us ........................................................................................................ 22
2 | Page Rigel Medical Multi-Flo user Manual V1.0
Introduction
Design Philosophy
The Rigel Multi-Flo Infusion Device Analyser provides accurate and fast analysis of the
performance of all common infusion devices. The Multi-Flo’s instant flow measurement
allows for high resolution flow and pressure analyses and provides a highly accurate
calibration method for proving the correct function of all infusion devices.
Infusion devices can be tested under positive and negative pressure settings whilst
bolus and PCA tests are conducted with the highest possible resolution.
Measuring flow rates, volume and pressure, the Multi-Flo is available in 1, 2 and 4
channel configuration which can be upgraded in the future to include additional channels
up to a maximum of 4 channels. The Multi-Flo will ensure it meets your current and
future requirements.
Note; This version of the manual (V1.0) describes the manual function of the Multi-Flo
only. Software upgrades available by the end of 2012 will activate the automatic testing
sequences, remote PC control, data storage and download. Register your product asap
to receive notification of the free firmware upgrade. To register your product, please visit:
www.rigelmedical.com/register-product
3 | Page Rigel Medical Multi-Flo user Manual V1.0
Unpacking the Multi-Flo
Carefully unpack all items from the box and ensure the following items are included:
Rigel Multi-Flo Infusion Device Analyser
Mains Power Lead
Multi-Flo Quick Start Guide
Utilities Disc
USB Bluetooth Adaptor
4 | Page Rigel Medical Multi-Flo user Manual V1.0
Warnings and Cautions
User Notes
Ensure that the Multi-Flo is operated with the distilled or de-ionised water only.
The following symbols are used throughout this Instruction Manual;
Warning of electrical danger! Indicates instructions must be followed to avoid
danger to persons.
Important, follow the documentation! This symbol indicates that the operating
instructions must be adhered to in order to avoid danger.
Safety Notes
Users - The Rigel Multi-Flo Infusion Device Analyser is designed for use by
adequately trained technical personnel only.
Operation - The Rigel Multi-Flo Infusion Device Analyser is designed for use
within the published specifications. Any application outside of these
specifications or any unauthorised user modifications may result in hazardous
conditions or improper operation.
Operation - Refer to the Device Under Test (DUT) manufacturer operating
instructions to ensure safe operation whilst analysing the DUT.
Safety - Ensure that only accessories supplied by the manufacturer or
accessories that meet the manufacturer’s specification are used.
Safety - Where safe operation of the Multi-Flo is no longer possible it should be
immediately shut down and secured to prevent accidental operation.
5 | Page Rigel Medical Multi-Flo user Manual V1.0
It must be assumed that safe operation is no longer possible:
if the instrument or leads show any sign of damage or
the instrument does not function or
after long periods of storage under adverse environmental conditions.
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