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Risk to patient if the device power fails!
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Use the device only with an uninterruptable power supply.
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To guarantee a continuous power supply a medical emergency supply
(USP) is suggested.
Risk to patient if the live image fails!
The shock of a defibrillator can cause the live image to drop out. It can take
up to 3 seconds until the live image is correctly displayed again.
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After defibrillation, verify correct rendering of the live image.
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Restart camera control unit if necessary by switching off and on.
Risk to patient due to incorrect application!
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Use the product only after instruction by the manufacturer or by an
authorized person.
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The instructions for use enclosed with the individual camera compo-
nents and all products used (e.g., high frequency surgery) must be
observed.
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Endoscopic procedures may only be carried out by specialists who have
the necessary medical training, knowledge and experience.
Risk to patient and user due to premature wear!
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Handle and maintain the product properly.
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Use the product only in accordance with the intended purpose.
Risk to the patient if the product is not used gently/a damaged product is
used!
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Handle the product with appropriate care.
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Do not use the product if it has been subjected to strong mechanical
stress or if it has been dropped, and send the product to the manufac-
turer or an authorized repair center for inspection.
Device failure due to incorrect storage and usage conditions!
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Store and operate the product only within the specified environmental
conditions.
Erroneous method of operation through reduced electromagnetic stability
or increased electromagnetic emitted interference!
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Use the product only with the recommended components and accesso-
ries.
Possible restricted function if third party devices are used!
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Use the product with the recommended components and accessories.
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The full functionality of the product can only be guaranteed if the rec-
ommended accessory components are used.
Note
Additional equipment and/or peripheral devices which are connected to the
interfaces of the product must show their relevant specifications (such as
IEC/EN/DIN 60601-1).
Note
No modification of this medical electric device is allowed.
Note
To guarantee optimal function of the product, use in controlled environ-
mental conditions is recommended (e.g., air-conditioned operating room).
Note
Always handle the medical device very carefully as it contains sensitive
optic, mechanic and electronic components.
8
Note
Ensure that all devices operated in the vicinity meet their relevant EMC
requirements.
Note
The Full HD CMOS camera control unit provides visualization of the interior
of the body during minimally invasive procedures. The camera control unit
may not be used for diagnosis.
Note
Images and videos recorded are for documentation purposes only. Do not
use for diagnosis or findings, as the image quality is reduced in the event of
data compression.
Note
Only operate the camera control unit when it is closed. Only operate the
device in a horizontal position.
Note
Before putting into operation, check the compatibility of all components
and accessories using the accessories list.
Note
All accessories and spare parts must only be procured from the manufac-
turer.
Note
Spare parts and fuses must only be replaced by authorized personnel.
Note
The connection of electrical devices to a multiple socket creates a system
and can lead to a reduced level of safety.
Note
To disconnect the device completely from power, pull out the power cord on
the rear of the device.
Note
Only operate the device with the original cables (included in scope of deliv-
ery) or with specified cables/components.
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See "Information on electromagnetic compatibility (EMC) for 2D cam-
era platform PV480" TA022467, see B. Braun eIFU at eifu.bbraun.com
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Only combine Aesculap products with each other.
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Always adhere to applicable standards.
Ambient conditions
The following environmental conditions apply to the use of the product:
Temperature
10 °C to 37 °C
Relative humidity
30 % to 90 %
Atmospheric pressure
700 hPa to 1 060 hPa
2.3.3
Sterility
The product is supplied non-sterile and must be used under non-sterile
conditions.
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Inspect the new product after removing its transport packaging and
prior to first use to ensure it is in good working order.
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