Sony LMD-1950MD - Manual (Page 2)

2
Owner’s Record
The model and serial numbers are located at the rear.
Record these numbers in the spaces provided below.
Refer to these numbers whenever you call upon your
Sony dealer regarding this product.
Model No. ____________________
Serial No. ____________________
WARNING
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 plug.
WARNING
When installing the unit, incorporate a readily
accessible disconnect device in the fixed wiring, or
connect the power cord to socket-outlet which must be
provided near the unit and easily accessible.
If a fault should occur during operation of the unit,
operate the disconnect device to switch the power
supply off, or disconnect the power cord.
In the event of a malfunction or when maintenance is
necessary, consult an authorized Sony dealer.
This unit contains substances which can pollute the
environment if disposed carelessly. Please contact our
nearest representative office or your local environmental
office in case of disposal of this unit.
For the customers in Canada
This unit has been certified according to Standard CSA
C22.2 NO.601.1.
FOR THE CUSTOMERS IN THE USA
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.
This product contains mercury. Disposal of this product
may be regulated if sold in the United States. For
disposal or recycling information, please contact your
local authorities or the Electronics Industries Alliance
(http://www.eiae.org).
For the customers in the U.S.A. and Canada
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 IEC60601-1-1.
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.
3. The leakage current could increase when connected
to other equipment.
4. This equipment generates, uses, and can radiate radio
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.
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