2 Introduction
2.6 Type and version
The type, serial number and version of the device is written in the device type label and on the tubehead.
The device is Class I, Type B and with IP 20 protection.
The focal length is specified in the cone label in addition to type and version.
The software version is momentarily shown on remote control display after powering on the device.
2.7 Labels on the device
Labels on the picture are for reference purposes only. Actual texts and images may not be accurate.
2.8 Configurations
WARNING!
USE LIMITATION:
The device or its parts must not be changed or modified in any way
without approval and instructions from the manufacturer. The use of accessories, transducers, and
cables other than those specified may result in degraded ELECTROMAGNETIC COMPATIBILITY of
the device.
WARNING!
If you suspect any electro-magnetic interference affecting or caused by the device,
call service. Portable and mobile RF communications equipment can interfere with operation of the
medical electrical equipment.
NOTICE!
To maintain safe and correct operation of the device, only the approved accessories
should be used. All the standard and optional items and approved accessories are suitable for use
within the patient environment.
FOCUS
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