Beurer EM80 - Инструкция по эксплуатации - Страница 32

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(3) Check that the electrodes are positioned properly and make sure that the 

adhesive electrodes are not overlapping.

(4) Increase pulse intensity in stages.

(5) The batteries are almost empty. Replace these.

You are aware that the electrodes feel uncomfortable. What should I do?

(1) The electrodes are badly positioned. Check positioning and if necessary 

reposition the electrodes.

(2) The electrodes are worn. Due to the fact that current distribution can no 

longer be guaranteed evenly over the entire surface, these may lead to 

skin irritation. You must therefore replace these.

The skin in the treatment area becomes red. What should I do?

Stop treatment immediately and wait until the skin has returned to normal. If 

any redness beneath the electrode soon disappears, this is not dangerous 

and is due to the increased circulation which has been stimulated locally.

If, however, the skin irritation remains and there is possibly itching or inflam-

mation, please consult your doctor before further use. It may possibly be 

caused by an allergy to the adhesive surface.

11. Technical details

Name and model:  

EM80

Initial curve shape:  

biphase square-wave pulse

Pulse duration:  

40-250 μs

Pulse frequency:  

1-120 Hz

Output voltage:  

max. 90 Vpp (at 500 Ohm)

Output current:  

max. 180 mApp (at 500 Ohm)

Power supply:  

3x AA batteries

Treatment time:  

adjustable from 5 to 90 minutes

Intensity:  

adjustable from 0 to 15

Operating conditions:   10°C-40°C (50°F-104°F) with a relative humidity

of 30-85%

Storage conditions:  

-10°C-50°C (14°F-122°F) with a relative humidity

of 10-95%

Dimensions:  

170 x 125 x 48 mm

Weight:  

235 g (without batteries) , 310 g (incl. batteries)

Explanation of symbols: Application part type BF 

Caution! Read the instructions for Use. 

 The device can emit effective output values 

above 10 mA, averaged over every five second 

interval.

The serial number is located on the device or in the battery compartment.
Note: If the device is not used according to these specifications, perfect 

functioning is not guaranteed.

We reserve the right to make any technical alterations that are necessary in 

order to improve and develop the product further.
This unit is in line with European Standards EN60601-1, EN60601-1-2 and 

EN60601-2-10 (In accordance with IEC 61000-4-2, IEC 61000-4-3, IEC 

61000-4-4, IEC 61000-4-5, IEC 61000-4-6, IEC 610004-8 and IEC 610004-

11) and is subject to particular precautions with regard to electromagnetic 

compatibility (EMC). Please note that portable and mobile HF communication 

systems may interfere with this unit. For more details, please contact custo-

mer service at the address indicated.
The device meets the requirements of the European Medical Products 

Directive 93/42/EC and the German Medical Products Act. For this device, 

a functional test and instruction in accordance with Section 5 of the Medical 

Devices Operator Ordinance (MPBetreibV) is not required. It is also not neces-

sary to carry out safety checks in accordance with Section 6 of the Medical 

Devices Operator Ordinance (MPBetreibV).

12. Notes on electromagnetic compatibility

WARNING! 

•  The device is suitable for use in all environments listed in these instructions 

for use, including domestic environments.

•  The use of the device may be limited in the presence of electromagnetic dis-

turbances. This could result in issues such as error messages or the failure 

of the display/device.

•  Avoid using this device directly next to other devices or stacked on top of other 

devices, as this could lead to faulty operation. If, however, it is necessary to 

use the device in the manner stated, this device as well as the other devices 

must be monitored to ensure they are working properly.