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Dear Customer,
We are delighted that you have opted for this
.
This device will help you prevent venous diseases as well as reducing the risk of
spider veins and varicose veins. If you have a medical indication, please consult
your doctor before use.
The
is a medical product certi
fi
ed according to
DIN EN ISO 13485:2012 and meets the necessary safety and performance re-
quirements according to MDR:2017: (Appendix I)
–
DIN EN 60601-1:2013-12; VDE 0750-1:2013-12 - Part 1: IEC 60601-1:2005 + Cor. :2006
+Cor. :2007 + A1:2012; German version EN 60601-1:2006 +Cor. :2010 + A1:2013
–
DIN EN 60601-1-1:2002-08; VDE 0750-1-1:2002-08 - Part 1-1: IEC 60601-1-1:2000
German version EN 60601-1-1:2001
–
DIN EN 60601-1-2:2016-05; VDE 0750-1-2:2016-05- Part 1-2: IEC 60601-1-2:2014
German version EN 60601-1-2:2015
–
DIN EN 60601-1-6:2016-02; VDE 0750-1-6:2016-02- Part 1-6: IEC 60601-1-6:2010 +
A1:2013; German version EN 60601-1-6:2010 + A1:2015
–
DIN EN 60601-1-11:2016-04; VDE 0750-1-11:2016-04 Part 1-11: IEC 60601-1-11:2015;
German version EN 60601-1-11:2015;
–
REACH EG 1907/2006; EU 2011/65/EU (RoHS II);
–
EN ISO 10993-1
If you have any questions about the device or about spare parts / accessories,
please contact the customer service department via our website:
www.venenwalker.com
or by phone on +49 (0) 38851 314337*
(Mon – Fri, 8 am – 12 midday)
*
All the very best with the
Yours sincerely,
GlobalMIND!
The illustrations in these instructions may differ slightly from the actual
device.
*
Cost will be incurred for German landline calls. The rates vary according to the provider.
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