Barco Eonis MDRC-2324, User Manual

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R5910550 /00 Eonis 29
Indications for use
This display can also be used in the patient area.
Contra-Indications
This display is not intended to be used for direct diagnosis and therapeutic interventional radiology.
Manufacturing country
The manufacturing country of the product is indicated on the product label ( “ Made in …” ).
Importers contact information
To find your local importer, contact one of Barco ’ s regional offices via the contact information provided on our
website ( www.barco.com ).
FCC class B
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1)
this device may not cause harmful interference, and (2) this device must accept any interference received,
including interference that may cause undesired operation.
This device has been tested and found to comply with the limits for a Class B digital device, pursuant to Part
15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference
in a residential installation. This device generates, uses and can radiate radio frequency energy and, if not
installed and used in accordance with the instructions, may cause harmful interference to radio
communications. However, there is no guarantee that interference will not occur in a particular installation. If
this device does cause harmful interference to radio or television reception, which can be determined by
turning the device off and on, the user is encouraged to try to correct the interference by one or more of the
following measures:
• Reorient or relocate the receiving antenna.
• Increase the separation between the device and receiver.
• Connect the device into an outlet on a circuit different from that to which the receiver is connected.
• Consult the dealer or an experienced radio/TV technician for help.
Changes or modifications not expressly approved by the party responsible for compliance could void the
user's authority to operate the equipment.
FCC responsible : Barco Inc., 3059 Premiere Parkway Suite 400, 30097 Duluth GA, United States, Tel: +1
678 475 8000
Canadian notice
CAN ICES-3 (B)/NMB-3(B)
5.5 EMC notice
General information
This device is for use in professional healthcare facility environments only.
With the installation of the device, use only the delivered external cables and power supply or a spare part
provided by the legal manufacturer. Using another can result in a decrease of the immunity level of the device.
WARNING: Use of this equipment adjacent to or stacked with other equipment should be avoided
because it could result in improper operation. If such use is necessary, this equipment and the other
equipment should be observed to verify that they are operating normally.
WARNING: Use of accessories, transducers and cables other than those specified or provided by
the manufacturer of this equipment could result in increased electromagnetic emissions or
decreased electromagnetic immunity of this equipment and result in improper operation.
Important information