Working With The Camera Heads; General Notes On Use; System Set-Up - Aesculap PV481 Instrucciones De Manejo

Aesculap
2D camera heads PV481, PV482, PV485
5.

Working with the camera heads

5.1

General notes on use

The camera cable is fragile when bent, kinked, twisted, pulled, or pressed.
Observe the maximum bend radius of 7 cm and handle the cable with care.
Do not make any changes to the cable and do not load with sharp-edged
objects.
5.2

System set-up

Risk of infection due to unsterile parts!
►
Ensure that unsterile components do not enter
the sterile area.
WARNING
►
Process products and accessories that are deliv-
ered unsterile before use and only use them with
sterile accessories.
Risk of infection due to unsterile, soiled or contam-
inated products!
►
Only use the camera head in the sterile area if
WARNING
it is in sterile condition. To do so, use the camera
head with the correctly applied sterile cover or
after sterilization process.
Risk to patient due to addition of leakage currents!
►
If the product is used with medical electrical
equipment and/or power-driven endoscope
WARNING
accessories, the leakage currents can multiply.
Risk to patient and user from burns, sparks or
explosion!
►
WARNING When using a high frequency surgical device
during an endoscopic procedure, observe the
safety instructions of the corresponding
instructions for use.
Risk of injury due to improper use!
►
Observe the intended use of the product.
WARNING
►
Do not use the endoscope as a lever.
Interference of electromagnetic emissions with the
image quality (e.g. minor banding, minor color
changes on the monitor image)!
CAUTION
►
Check the image quality if used in combination
with additional peripheral devices (e.g. monitor,
video equipment).
8
®
Note
In combination with the camera control unit, PV480 or PV630, the endo-
scope is classed as a type CF defibrillation-proof applied part.
Note
Before application of endoscopic high frequency surgery (HF surgery) pre-
pare the patient accordingly.
Note
Take measures to remove or avoid formation of combustible gases (e.g.
gastro-intestinal tract/colonoscopy, urinary bladder/transuretheral resec-
tion).
Connecting the accessories
Risk of injury due to unapproved configuration
using additional components!
►
DANGER For all components used, ensure that their clas-
sification matches that of the applied part (e.g.
type CF defibrillation-proof) 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.
Any equipment connected at the interfaces must also demonstrably meet
the respective IEC standards (e.g. IEC 60950 for data processing equip-
ment, and IEC/DIN EN 60601-1 medical electrical equipment).
All configurations must meet the basic standard IEC/DIN EN 60601-1. The
person connecting the devices is responsible for the configuration and
must ensure that the basic standard IEC/DIN EN 60601-1 or the corre-
sponding national standards are met.
►
Please contact your B. Braun/Aesculap partner or Aesculap Technical
Service, (address: see Technical Service) with any inquiries in this
respect.