Installation
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Connecting the device with other devices
WARNING - HAZARD DUE TO ELECTROMAGNETIC INTERFERENCE
RADIATION
When connecting external devices to the interfaces of the device, the
responsible organization must ensure that the requirements defined in
IEC 60601-1-2 are met.
WARNING - RISK OF ELECTRIC SHOCK
Additional equipment connected to medical electrical equipment must
comply with the current IEC or ISO standards (e.g. IEC 62368-1 for data
processing equipment). Furthermore all configurations must comply with
the requirements for medical electrical systems in accordance with
IEC 60601-1.
When connecting further equipment to medical device, you are
configuring a medical system and are thus responsible for ensuring
compliance with the requirements for medical electrical systems.
Please observe that local laws take priority over the above-mentioned
requirements. If in doubt, consult your local representative or ZEISS
Service.
WARNING - RISK OF ELECTRIC SHOCK
Equipment which is connected to the autorefractor/keratometer system
and placed inside the patient environment must be powered from a
medically-isolated power source or must be a medically-isolated device.
Equipment powered from a non-isolated source can result in chassis
leakage currents exceeding safe levels. Chassis leakage current generated
by an accessory or device connected to a non-isolated outlet may add to
the chassis leakage current of the autorefractor/keratometer system.
Summary of Contents for VISUREF 150
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