21
Technical Details
Operating time
The device is designed for extend-
ed usage.
Declaration of conformity
We declare under our sole respon-
sibility, that the products podiatry
unit 0967, 0968 and 0969 to which
this declaration relates, are conform
to the following standards or norma-
tive documents:
93/42/EEC medical devices directive
hadewe GmbH
–
Grambartstraße 10
–
30165 Hannover
Accessories
Art. No.
5115
paper filter
5179
micro filter
3752
filter
0970
foot switch
The clamping system is designed
for rotating instruments, which have
a shaft of 2,35mm in accordance
with ISO EN ISO 179-1.
Disposal
The device and filter may
contain infectious material
such as residual sanding
dust or skin particles. Therefore
please bear in mind the following
disposal instructions.
Disposing of the device
Old devices bought in Germany that
correspond to the electronic device
law should be sent directly to the
manufacturer (hadewe). We will
dispose of the device free of
charge. The devices should not be
taken to public disposal plants
(WEEE Reg.Nr DE20392713, b2b
device). For disposal of this unit out
of Germany, please contact the site
where you bought this hadewe
product.
Note for the disposal of the device/
treatment system:
Wear protecting gloves of the class
2 in accordance with DIN 374-2
during the disassembling of the
device. Also, wear a protective
mask for your face according EN
14683 version IIR or EN 149 FFP2.
Disposal of dust filter and coarse
dust filter
The filter bag and the coarse dust
filter are considered low contami-
nated waste. Dispose those in in
transparent, liquid- tight, resistant
plastics sacks and to not dispose
them compressed in the regular
household garbage.
Compulsory registration
Operators, distributors and retailers
who were informed about the occur-
rences regarding §29 of the Medical
Devices law must report this. The
method of reporting is detailed in
the Medical Devices Safety Plan
Ordinance. Outside of Germany the
corresponding local conditions ap-
ply
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