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Idiomas disponibles
Aesculap
High-frequency surgical device GN300
3.5
Presetting the correct voltage
The mains voltage must correspond to the voltage indicated on the type
plate at the back of the unit.
The correct voltage for the HF generator is indicated in the window
located at the back of the device. The standard voltage for the unit in
Europe is: 230 V.
Risk of death by electric shock!
►
Unplug the device before replacing the fuse sets.
DANGER
►
If the indicated voltage does not correspond to the actual mains volt-
age, change the setting at the rear panel of the power unit:
– Release clip B using a suitable screwdriver A and remove the fuse
holder 82.
– Pull out the voltage selection element 82 under the fuse holder.
– Reinsert the voltage selection element so that the desired voltage C
is legible.
– Reinsert the fuse holder 82.
Imprint C
110
230
80
A
B
82
Fig. 16 Device connection with fuse holder and voltage selection ele-
ment
12
®
Voltage range
100 V to 120 V (± 10 %)
220 V to 240 V (± 10 %)
81
C
Legend
80 Device connector
81 Voltage selection element
82 Fuse holder
A Screwdriver
B Clip
C Voltage selection element imprint
4.
Working with the high-frequency sur-
gical device GN300
4.1
System set-up
Connecting the accessories
Risk of injury due to unapproved configuration
using additional components!
►
DANGER
For all applied components, ensure that their
classification matches that of the application
component (e.g. Type BF or Type CF) of the
respective device.
Combinations of accessories that are not mentioned in the present
instructions for use may only be employed if they are specifically intended
for the respective application, and if they do not compromise the perfor-
mance and safety characteristics of the products.
All configurations must comply with basic standard IEC/DIN EN 60601-1.
Any individual connecting devices with one another is responsible for such
configuration and must ensure compliance with basic standard IEC/DIN
EN 60601-1 or applicable national standards.
Danger to life for patients and users due to inad-
vertent current supply to an instrument!
►
DANGER
Make certain that only one patient cable is con-
nected to any output socket.
The insulation of the accessories (e.g. HF cables, instruments) must be
adequately rated for the maximum peak output voltage (see IEC/DIN
EN 60601-2-2).
►
Please address your B. Braun/Aesculap partner or Aesculap Technical
Service with any inquiries in this respect; for a contact address, see
Technical Service.
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