Working With The Hf Surgical Device Gn060; System Set-Up; Function Checks - Braun Aesculap GN060 Instrucciones De Manejo

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4.
Working with the HF surgical device
GN060
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.
Risk to life for patients and users due to inadver-
tent current supply to an instrument!
DANGER
Make certain that not more than one patient
cable is connected 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 contact your B. Braun/Aesculap partner or Aesculap Technical
Service (address: see Technical Service) with any inquiries in this
respect.
Connecting the power supply
Risk of death by electric shock!
Only ever connect the product to power mains
with equipment grounding conductor.
DANGER
Set up the device in such a way that disconnect-
ing the power cord is straightforwardly possible.
Note
Before operating the device, make certain that the supply voltage marked
on the plug of the device matches that of the supply voltage being used. To
change the setting, see Presetting the correct voltage.
The HF device GN060 must only be operated with an alternating current
from 50 Hz to 60 Hz. The mains voltage must be between 100 V and 120 V
or between 220 V and 240 V. The voltage is preselected on the mains volt-
age connector on the rear side of the device. Insert the power cord only in
a properly mounted schuko power socket (for this see VDE 0107).
To prepare the device for operation, proceed as follows:
Connect the HF device to the mains voltage using a power cord (LED 1
illuminates).
Connect the bipolar cable to the socket 14 or 15.
Connect foot switch to the socket 16.
Activate button 3 (LED 1 and LED 2 illuminate).
The HF device is ready for operation.
Note
The isolation of the power cable from the device must also be treated as
secure isolation from the mains in the sense of the IEC norm. When aligning
the device, ensure that an isolation of the mains plug is possible without
any problems.
4.2

Function checks

Connect the HF device to the mains voltage.
Green LED 1 must illuminate.
Activate "Device on/off" button 3.
LED 2 must illuminate. All LEDs and segments of the display illuminate
briefly.
For HF devices with the "automatic starting" option: In the display, the
"AU" display appears briefly.
The HF device is operable based on the basic settings approximately 1 s
after activation of the button.
The LEDs 5 and 18 illuminate in the display field.
In the display, "0.1" must be displayed as a dosage level.
Press "+" key 10.
The dosage level must be able to be increased to 9.9.
Press "-" key 7.
The dosage level must be able to be reduced to 0.1.
Press key 4.
For signaling the "Macro" mode, LED 6 in the display field must illumi-
nate. "01" must be displayed as a dosage level.
The dosage level can be set between the limit levels "01" and "50" with
the "+" button 10 and the "-" button 7.
If the "automatic starting" option is built in: Press key 19.
The activation type must change. The activation type is displayed with
LED 17 or LED 18.
Check memory function see Store device settings and see Retrieve
stored device settings.
Connect foot switch to the socket 16 and activate.
The acoustic and visual operating display 9 must correspond.
9

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