Sony UP-21MD User Manual

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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 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 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 again 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.
For the customers in Canada
This unit has been certified according to Standard CSA 
C22.2 NO.601.1.
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
Use a proper power cord for your local power supply.
Warning on power connection for medical use
Please use the following power supply cord.
With connectors (plug or female) and cord types other 
than those indicated in this table, use the power supply 
cord that is approved for use in your area.
*Note: Grounding reliability can only be achieved when the equip-
ment is connected to an equivalent receptacle marked ‘Hospital Only’ 
or ‘Hospital Grade’.
WARNING
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.
United States
Canada
Plug Type
HOSPITAL GRADE*
HOSPITAL GRADE*
Female end
E62405, E35708
LR53182, LL022442, 
LL088408
Cord type
E159216, E35496
Min.Type SJT
Min.18 AWG
LL112007-1, LL20262, 
LL32121, LL84494
Min.Type SJT
Min.18AWG
Minimum cord set 
rating
10A/125V
10A/125V
Safety approval
UL Listed
CSA
R1.5m