Xstrahl RADiant, Руководство оператора

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About Xstrahl RADiant Operator Manual
PHET_OP_GB Version 7 ©2017 Xstrahl Ltd. All rights reserved 12/02/18 | i
About Us Xstrahl Limited produces specialist clinical solutions for medical
practitioners and their cancer and dermatology patients by offering a
range of superficial and orthovoltage X-Ray Therapy Systems, as
well as a comprehensive superficial therapy educational (STEP)
program for training and support.
Contact Information
Web www.xstrahl.com
Email support@xstrahl.com
Phone +44 (0) 1276 462696
Technical Support
Web www.xstrahl.com
Email support@xstrahl.com
Phone +44 (0) 1276 462696
Trademark Xstrahl
®
is a registered trademark of Xstrahl Limited.
Notice of Copyright
RADiant Operator Manual ©2018 Xstrahl Limited. All Rights
Reserved.
Disclaimer Unless specifically agreed to in writing, Xstrahl assumes no liability
for use of this document if unauthorised changes to the content or
format are made. Every care has been taken to ensure the information
in this document is accurate. However, Xstrahl assumes no
responsibility or liability for errors, inaccuracies or omissions which
may occur in this document.
To improve reliability, function or design, Xstrahl reserves the right
to change the product and/or this manual without notice.
Compliance The design of Xstrahl Systems is in compliance with internationally
recognised standards for safety. Xstrahl’s range of X
-Ray therapy
systems are classified as Class IIb Medical Devices in accordance
with the Medical Devices Directive.
RADiant has clearance by FDA for sale in the U.S.A and is
manufactured in accordance with ISO13485:2003 certified quality
management system.
Classification of
Equipment (ME)
Xstrahl’s X
-Ray Therapy Systems are classified as Class I Medical
Electrical (ME) equipment and are classified for continuous
operation with intermittent loading. With continuous operation of the
system in standby. After 20min continuous treatment exposure allow
4min cooling time (80% Duty Cycle).