35
Skin in the treatment area turns red. How to proceed:
Immediately stop treatment and wait until your skin has returned to its
normal condition. If the redness is under the electrode and disappears
quickly, there is no risk – this is caused by the locally stimulated,
increased blood flow.
However, consult your doctor before you continue treatment if the
skin irritation persists and this is accompanied by an itchy sensation
or inflammation. This may be caused by an allergic reaction to the
adhesive surface.
13. Replacement parts and wearing parts
You can obtain the following replacement parts directly from
Customer Services:
Designation
Item number and/or order
number
8 x adhesive electrodes
(45 x 45 mm)
Item 661.02
4 x adhesive electrodes
(50 x 100 mm)
Item 661.01
14. Technical specifications
Name and model
EM 49
Type
EM 49
Output waveform
Biphasic rectangular pulse
Pulse length
50 – 450 µs
Pulse frequency
1 – 150 Hz
Output voltage
max. 100 Vpp (500 ohm)
Output current
max. 200 mApp (500 ohm)
Voltage supply
3 x AAA batteries
Treatment time
Adjustable from 5 to 100 minutes
Intensity
Adjustable from 0 to 50
Operating conditions
10°C – 40°C (50°F – 104°F) at a relative
humidity of 30 – 85%
Storage conditions
-10 °C – 50 °C (14 °F – 122 °F) at a relative
humidity of 10 – 95%
Dimensions
132 x 63 x 29.5 mm (including belt clip)
Weight
83 g (including belt clip, without batteries),
117 g (including belt clip and batteries)
Note: If the device is not used according to the instructions
specified, perfect functionality cannot be guaranteed!
We reserve the right to make technical changes to improve and
develop the product.
This device complies with European standards EN60601-1 and
EN60601-1-2 and is subject to special precautionary measures with
regard to electromagnetic compatibility. Please note that portable
and mobile HF communication systems may interfere with this unit.
More details can be requested from the stated Customer Services
address or found at the end of the instructions for use.
This device meets the requirements of European Directive
93/42/EEC for medical products, as well as those of the
Medizinproduktegesetz (German Medical Devices Act).
Subject t
o err
ors and changes
