Technical Details - Sanitas SEM 43 Instructions For Use Manual

Digital ems/tens unit
Hide thumbs Also See for SEM 43:
Table of Contents

Advertisement

Available languages

Available languages

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 inflamma-
tion, 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:
SEM 43
Initial curve shape:
biphase square-wave pulse
Pulse duration:
50 – 450 μs
Pulse frequency:
1–150 Hz
Output voltage:
max. 100 Vpp (at 500 Ohm)
Output current:
max. 200 mApp (at 500 Ohm)
Power supply:
3x 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) 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:
135 x 66 x 29 mm (incl. belt clip)
Weight:
107 g, (incl. belt clip, without batteries)
133 g, (incl. belt clip and batteries)
Explanation of symbols: Application part type BF
Caution! Read the instructions for Use.
Note: If the machine is not used according to these specifications, perfect func-
tioning is not guaranteed.
We reserve the right to make any technical alterations that are necessary in or-
der to improve and develop the product further.
This unit is in line with European Standards EN60601-1, EN60601-1-2 and
EN60601-2-10 and is subject to particular precautions with regard to electroma-
gnetic compatibility (EMC). Please note that portable and mobile HF communi-
cation systems may interfere with this unit. For more details, please contact cus-
tomer service at the address indicated.
The machine meets the requirements of the European Medical Products
Directive 93/42/EC and the German Medical Products Act.
27

Hide quick links:

Advertisement

Chapters

Table of Contents
loading

Table of Contents