User Manual: LLS-1
ODB-118-0070ENG
Page 7 of 36
14-01-2022
WARNING:
Do not modify any part of Oldelft Benelux supplied hardware, software or
software configuration. Any modification, installation or running an
application that has not explicitly been approved by Oldelft Benelux may
compromise patient safety and will result in termination of all warranty and
service contracts.
a. If this equipment is modified, repaired or maintained, appropriate
inspection and testing must be conducted to ensure continued safe
use of the equipment.
b. Do not leave problems unattended that may affect the safety of the
product. In case you have doubts concerning the LLS-1 save
operation, call the service number of your vender for further
instructions.
c. The LLS-1 stand should be cleaned regular to prevent the
accumulation of dust. The contact surface should be cleaned after
each patient for hygienic reasons.
WARNING:
The Oldelft Benelux products are designed for use and maintenance using
only parts available from Oldelft Benelux. No liability for failure can be
accepted by Oldelft Benelux through the use of parts obtained from other
suppliers unless written permission is obtained from Oldelft Benelux.
Copyright
All rights reserved. No part of this manual may be reproduced or transmitted in
any form whatsoever, including photocopying and recording without written
permission of the copyright holder: Oldelft Benelux B.V., Wiltonstraat 41, 3961 KW
VEENENDAAL, The Netherlands.
Concerning this Publication
Information contained in this publication is subject to change without notice.
Whenever the equipment is delivered with a documentation medium such as a CD
or DVD, the user shall always check the medium for latest information. This
information is part of Release Notes and Document Upgrade files.
Neither Oldelft Benelux B.V. and its subsidiaries nor anyone else who has been
involved with the development, production or delivery of the documentation be
liable for any special, incidental or consequential damages, whether based upon
breach of warranty, breach of contract, negligence, strict liability in tort or any
other legal theory.
This manual was originally drafted in the English language.
Note:
Any serious incident with the user and/or patient that has occurred in
relation to the device should be reported to the manufacturer and the
competent authority of the Member State in which the user and/or patient is
established.
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