VenenWalker Pro 2 Manual De Instrucciones página 30

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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
DIN EN ISO 13485:2016 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 60601-1-2:2016-05; 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
The illustrations in these instructions may differ slightly from the actual
device.
*
Calls to German landlines are subject to your provider's charges.
is a medical product certified according to
*
.
!