SPORT-ELEC ULTRANOMADE Modo De Empleo página 17

Tabla de contenido

Publicidad

Idiomas disponibles
  • ES

Idiomas disponibles

  • ESPAÑOL, página 27
U nit
3  
Class IIa medical device in accordance with Directive 93/42/CEE.
Software version . . . . ....... ....... ..... ....... ....... ....... ........ ....... .. 1
Type of current . . . . . ... ....... ....... ..... ....... ....... ....... ....... ........ Symmetrical biphasic rectangular
Number of programs .. ....... ....... ........ ....... ....... ....... ....... ... 4 programs
Number of adjustable independent channels ...... ........ ....... ... 1
Current . . . . . . . . . . . . . . . ..... ....... ............ ....... ....... ....... ....... ......
Frequency range/Pulse width range . ....... ....... ....... ....... ....... From 50 to 70 Hz / 234 μs
Power . . . . . . . . . . . . . . . . . ... ........ ........... ....... ........ ....... ....... ....... 3 batteries AAA - LR3 1.5 V
Unit dimensions and weight ... ..... ....... ....... ....... ........ ....... .. 92 x 81 x 22 mm - 90 g
Automatic stop at the end of each program .... ....... ....... ....... . Yes - after approx. 5 min of inactivity
Activation safety . . . ...... ....... ....... ....... ....... ....... ........ ....... .. 100 %
Detection absence of contact . ..... ....... ....... ....... ........ ....... .. Yes
Indicator of power . ..... ....... ............ ....... ....... ....... ....... ...... LCD display: 1 bar graph
Indicator of low and/or defective battery ... ........ ....... ....... ...... Yes - LCD display
Indicator of programs ... ........ ....... ....... ....... ....... ....... ........ . LCD display: icons 1-2-3-4
Temperature/Relative humidity for storage ..... ....... ........ ....... 0 °C to + 40 °C / 10 % to 90 %
Temperature/Relative humidity for use ...... ....... ....... ........ .... + 5 °C to + 40 °C / 20 % to 65 %
Connection of the electrode ........... ....... ....... ....... ....... ....... 2 snap fasteners
Warning . . . . . . . . . . . . . . . ...... ....... ........ ....... ....... ....... ....... ....... .
Conformity . . . . . . . . . . .... ....... ............ ....... ....... ........ ....... ...... EN60601-1 / EN60601-2-10
Guarantee/Life cycle . ....... ........ .... ....... ........ ....... ....... ....... . 2 years
S tandardized symbols / pictograms
4  
Approved medical devices.
CE marking concerning medical appliances.
 
Device in contact with the patient,
excluding the heart area.
 
These units are free of materials likely to
have a negative impact on the
environment.
 
Caution :
Read the instructions for use.
 
Maximum intensity per channel up to
1 kΩ : 60 mA.
 
Relative humidity for storage :
from 10 to 90%.
X. RECYCLING
Please respect national regulations when you dispose of your product when it reaches the end of its life.
Please take it to a suitable place in order to ensure that it is disposed of in a safe and environmentally-friendly
manner.
- USER MANUAL
from 0 to 60 mA - from 0 to 60 Vcc - from 0 to 1000 Ω
Read the instructions carefully.
 
Temperature for storage :
from 0 to 40° C.
 
Name of the manufacturer bringing the device
to the market.
 
Please contribute to protect the environment
by observing the disposal instructions.
 
The manufacturer respects the environmental
law and contributes to the cost of recovery
and recycling.
Follow the user manual instructions..
 
Do not use if you carry a pacemaker.
 
Do not use if you are pregnant.
 
This device is intended for domestic use.
17

Publicidad

Tabla de contenido
loading

Tabla de contenido