Coltene SciCan BRAVO G4 Manuel D'utilisation page 5

1. FOREWORD
The instructions inform the user on how to properly operate the device. It is extremely important to read this manual
carefully and thoroughly before using the device.
This publication must not be reproduced, copied or transferred in any manner (electronically, mechanically, via
photocopies, translations or other means) without the prior written consent of the manufacturer.
The manufacturer has a company policy of continual development. Therefore, some of the instructions, specifications
and figures given in this manual may slightly differ from the purchased product. The manufacturer reserves the right to
make changes to this manual without giving prior notice.
The original text is in Italian; this is a translation from the original in Italian.
1.1 SYMBOLS USED
Type in Gray Box
Type in Gray Box
1.2 SYMBOLS ON THE DEVICE
I / O
2xT15A 250V
1.3 RELEVANT STANDARDS
The product described in this manual is manufactured in accordance with safety standards and doesn't represent any
danger for the operator if used according to the following instructions.
The product is complying with the following standards as applicable:
IEC 61010-1:2010 + A1:2016,
IEC 61010-2-040:2015,
IEC 61326-1:2012,
IEC 62304:2006 + A1:2015,
ANSI/AAMI ST55:2016,
ASME Boiler and Pressure Vessel Code Section VIII, Division 1
Pay particular attention to the paragraphs marked in a gray box.
Potential danger for people, environment and property.
Follow the procedures indicated in the manual to prevent potential damage to
materials, devices and/or property.
Potential danger due to high temperature.
Switch ON / OFF.
Fuses 2xT15A 250V.
Safety requirements for electrical equipment for measurement, control, and laboratory use,
Part 1: General requirements.
Safety requirements for electrical equipment for measurement, control, and laboratory use,
Part 2-040 Particular. requirements for sterilizers and washer-disinfectors used to treat medical
materials.
Electrical equipment for measurement, control and laboratory use – EMC requirements, Part 1:
General requirements.
Medical device software - Software life-cycle processes.
Table top steam sterilizers.
1
Disposal in accordance with state/local
regulation.
Refer to the User Manual.