PART 1 - General information
11
SYMBOLS
The product complies with the
Medical Device Regulation (EU) 2017/745
MD
This product is a medical device
Legal manufacturer
Date of manufacture
Serial number
Item no. / Catalogue number: 7 digits
Consulting the manual is mandatory
Warning triangle indicates when special attention is nec-
essary
For indoor use
This product is a class ll equipment (IEC 61140)
The product is a type B equipment according to EN 60601-1
Max. user weight
Electronic scrap. When disposing of the products,
sub-components should be recycled
IPX6w
This product is washable
U In:100-
240VAC,
50/60Hz
The mains voltage must be 100-240 V AC.
200 W
Max power consumption is 200 W
(SMPS: Switch mode power supply).
I In:
max.3,9A
The current used is max 3,9 A
Int.:10% -
2/18min on/off
The system should only be used 10% of the time. After 2
min of continuous use it requires 18 min rest.
Max 200W/80
sec./
100W/40sec
@25˚C
In continuous use at 25˚C 200 W can be supplied for 80
sec - then the power consumption will be reduced to 100
W for 40 sec.
0
+50
This product must be stored between 0 and 50
°
C
5
40°C
This product must be used between 5 and 40˚C
20
90%
This product must be stored between 20 and 90% humidity
at
30
°
C
Keep dry (when stored)
Rev.
Revision no. of the label
Hand control symbols
Power / stop button
Tighten the sheet on the red or blue bar
Slacken the sheet on the red or blue bar
Symbols only on sub components
The hand control and the control unit complies with the EMC
Directive 2014/30/EU and the Low Voltage Directive 2014/35/
EU
The component complies with the EMC regulation of Australia
and New Zealand.
The component complies with China RoHS.
Type + item Product no/catalogue no
Date
Date of production
W/O
Work order
The product / system label is placed on the corner posts at the foot end.
Содержание 6200000
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