Nidek Medical AFC-330, Руководство оператора

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VII
:
CAUTION
• Each time before connecting a USB flash drive to the device, be sure to check it for
viruses.
If the device is infected with a virus and any problem occurs, NIDEK does not assume
responsibility or compensate for damages.
• Users are responsible for managing captured image data.
NIDEK will not assume any responsibility for loss of data.
• Equipment connected to the analog or digital interfaces must be certified according
to the representative appropriate national standards (such as EN 60601-1 and IEC
60601-1). Further more, all configurations shall comply with the system standard IEC
60601-1. Anyone who connects additional equipment to the signal input part or signal
output part configures a medical system, and is therefore responsible that the system
complies with the requirements of the system standard IEC 60601-1. If in doubt,
consult the technical service department of your local representative.
• This device is classified as Group 1 according to “4.4 Optical radiation hazard with
fundus cameras” in ISO 10940: 2009 Ophthalmic instruments—Fundus cameras, and
conforms to the standard.