Sony UPA-P100MD Guia De Inicio Rapido página 2

WARNING
To prevent fire or shock hazard, do not expose the unit to
rain or moisture.
To avoid electrical shock, do not open the cabinet. Refer
servicing to qualified personnel only.
THIS APPARATUS MUST BE EARTHED.
For UPA-P100MD
Symbol on the products
This symbol indicates the equipotential
terminal which brings the various parts of a
system to the same potential.
This symbol is intended to alert the user to the
presence of important operating and
maintenance (servicing) instructions in the
literature accompanying the appliance.
When using a LAN cable: For safety, do not connect to the
connector for peripheral device wiring that might have
excessive voltage.
For the customers in the U.S.A.
(for UPA-P100MD)
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.
This device requires shielded interface cables to comply with
FCC emission limits.
Model UPA-P100MD is Non-Patient Equipment.
This unit can not be used in the vicinity of patients.
* Patient Vicinity
For the customers in Canada
(for UPA-P100MD)
This unit has been certified according to Standard CSA
C22.2 NO.601.1.
2
For UPA-P100MD
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, IEC60065
or other IEC/ISO Standards applicable to the equipments.
2 When this unit is used together with other equipment in
the patient area*, the equipment shall be either powered
by an isolation transformer or connected via an additional
protective earth terminal to system ground unless it is
certified according to Standard IEC60601-1.
* Patient Area
3 The leakage current could increase when connected to
other equipment.
4 This equipment generates, uses, and can radiate
frequency energy. If it is not installed and used in
accordance with the instruction manual, it may cause
interference to other equipment. If this unit causes
interference (which can be determined by unplugging the
power cord from the unit), try these measures: Relocate
the unit with respect to the susceptible equipment. Plug
this unit and the susceptible equipment into different
branch circuit. Consult your dealer. (According to
Standard EN60601-1-2 and CISPR11, Class B, Group 1)
Caution
When you dispose of the unit or accessories, you must obey
the law in the relative area or country and the regulation in
the relative hospital.
Warning on power connection for medical use
Use a proper power cord for your local power supply.
United States Canada
Plug Type HOSPITAL
GRADE*
Female end E62405
Cord type E159216
Min.Type SJT Min.Type SJT
Min.18AWG
Minimum cord 10A/125V
set rating
Safety UL Listed
approval
*Note: Grounding reliability can only be achieved when the
equipment is connected to an equivalent receptacle
marked 'Hospital Only' or 'Hospital Grade'.
Continental
Europe
HOSPITAL LP-34A
GRADE*
LR53182 LS-60
LL112007-1 H05VV-F
Min.18AWG
10A/125V 10A/250V
CSA VDE