CEFLA VENUS PLUS - General Warnings; Symbols

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OPERATOR’S MANUAL
EN
1. GENERAL WARNINGS
• These instructions explain how to correctly use the following operating lights:
VENUS PLUS (code 96601020, 96601072)
VENUS PLUS L version (code 96601060, 96601071)
VENUS PLUS MCT version (code 96601069, 96601070)
VENUS PLUS E version (code 96601090)
VENUS PLUS CL version (code 96601024)
VENUS PLUS CL -L version (code 96601063)
VENUS PLUS CL MCT version (code 96601080)
Read this manual thoroughly before using the device.
• The devices described in this manual are manufactured by CEFLA s.c. - via Selice Provinciale 23/A - 40026
Imola (BO) Italy, a manufacturer complying with the European Directive on medical devices.
• All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted
in any form or by any means, electronic, mechanical, photocopying, recording, translation, or otherwise,
without the prior written permission of the manufacturer.
• Themanufacturerhasacompanypolicyofcontinualdevelopment.Althougheverye󰀨ortismadetokeep
technicaldocumentationup-to-dateatalltimessomeoftheinstructions,specicationsandguresgivenin
thismanualmayslightlydi󰀨erfromthepurchasedproduct.Themanufacturerreservestherighttomake
changes without prior notice.
• The original text is in Italian; translation from the original in Italian.
• For operators in Europe: it is necessary to report any serious incident that occurred in relation to the equipment
toCeas.c.andtothecompetentauthorityoftheMemberStatewheretheuserand/orpatientislocated.
1.1. SYMBOLS
Note the meaning of the following symbols and
expressions:
1) Degree of protection against direct and indirect
contact with the applied part: Type B.
2) Type of protection against direct and indirect
contact: CLASS II.
3) WARNING!
It indicates a condition in which the failure to
observe the instructions may result in equipment
damage or injury to the user and/or patient.
4) NOTE:
Identiesinformationthatisespeciallyimportant
for the user and/or the assistant.
5) Alternating current.
6) Part that can be sterilized in an autoclave up to
135°C.
7)
8)
ON / OFF control.
Equipment compliant with Regulation (EU)
2017/745 on Medical Devices.
9) Disposal symbol in accordance with Directive
2012/19/EU.
10) Manufacturer.
11) Equipment date of manufacture.
12) Product/equipmentidenticationcode.
13) "Refer to the instruction manual"
Means that for reasons of safety you need to
consult the instruction manual before using the
equipment.
14) Medical device.
15) The operator’s manual is provided in electronic
format.