2
GB
Always read the instructions for use before using the device for the first
time, and follow all directions.
B
ody
F
loating type application part. The device is guaranteed to provi-
de protection against electric shock with an approved leakage current.
This device carries the recycling icon in accordance with EU Directive
2002/96/EC. It must not be disposed of in domestic waste. Contact the
dealer or manufacturer for disposal.
0000
Declaration of conformity with reference to Council Directive 93/42/EEC of
14 June 1993 concerning medical devices, including amended Directive
2007/47/EC of 21 September 2007. If a Notified Body (4-digit numerical
code) is specified, this is a Class IIa medical device.
Manufacturer
Year of manufacture
Serial number of the device
Batch code
Use by
Medical device
Indicates a potentially hazardous situation. If it is not
avoided, it may result in material damage.
Indicates a potentially hazardous situation. If it is not
avoided, it may result in injury.
User information: contains important information,
e.g. about the configuration.
Icons
Summary of Contents for SaneoVITAL TENS/EMS
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