Sony UP-D75MD, Руководство пользователя

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Owner's Record
The model and serial numbers are located at the rear.
Record these numbers in the space provided below.
Refer to these numbers whenever you call upon your
Sony dealer regarding this product.
Model No. ____________________
Serial No. ____________________
To reduce the risk of fire or electric shock, do
not expose this apparatus to rain or moisture.
To avoid electrical shock, do not open the
cabinet. Refer servicing to qualified personnel
only.
THIS APPARATUS MUST BE EARTHED.
To disconnect the main power, unplug the AC
IN connector.
For the customers in the U.S.A.
This equipment has been tested and found to comply
with the limits for a Class A digital device, pursuant to
Part 15 of the FCC Rules. These limits are designed to
provide reasonable protection against harmful
interference when the equipment is operated in a
commercial environment. This equipment generates,
uses, and can radiate radio frequency energy and, if not
installed and used in accordance with the instruction
manual, may cause harmful interference to radio
communications. Operation of this equipment in a
residential area is likely to cause harmful interference in
which case the user will be required to correct the
interference at his own expense.
You are cautioned that any changes or modifications not
expressly approved in this manual could void your
authority to operate this equipment.
All interface cables used to connect peripherals must be
shielded in order to comply with the limits for a digital
device pursuant to Subpart B of Part 15 of FCC Rules.
For the customers in Canada
This unit has been certified according to Standard CSA
C22.2 No.601.1.
For the customers in the U.S.A. and
Canada
Model UP-D75MD is Non-Patient Equipment.
This unit can not be used in the vicinity of patients.
* Patient Vicinity
When you use this product connected to 240 V single
phase, be sure to connect this product to a center tapped
circuit.
Important safeguards/notices for use in
the medical environments
1. All the equipments connected to this unit shall be
certified according to Standard IEC60601-1,
IEC60950-1, IEC60065 or other IEC/ISO Standards
applicable to the equipments.
2. Furthermore all configurations shall comply with the
system standard IEC 60601-1-1. Everybody 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 IEC60601-1-1.
If in doubt, consult the qualified service personnel.
This unit can not be used in the patient environment.
* Patient Environment
WARNING
This symbol indicates the equipotential
terminal which brings the various parts of a
system to the same potential.
R1.83m
(6 feet)
R1.5m