Sony LMD-DM20 Instructions For Use Manual page 3

User manual (lmd-dm20, dm30, dm50 user manual)
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For the customers in Europe
The manufacturer of this product is Sony Corporation,
1-7-1 Konan, Minato-ku, Tokyo, 108-0075 Japan.
The Authorized Representative for EMC and product
safety is Sony Deutschland GmbH, Hedelfinger Strasse
61, 70327 Stuttgart, Germany. For any service or
guarantee matters please refer to the addresses given in
separate service or guarantee documents.
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. For this particular equipment, all accessory
equipment connected as noted above, must be
connected to mains via an additional isolation
transformer conforming with the construction
requirements of IEC60601-1 and providing at least
Basic Insulation.
5. 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 laws in the relative area or country and the
regulations in the relative hospital.
For the customers in the USA
Lamp in this product contains mercury. Disposal of
these materials may be regulated due to environmental
considerations. For disposal or recycling information,
please contact your local authorities or the
Telecommunications Industry Association
(www.eiae.org).
WARNING on power connection
Use a proper power cord for your local power supply.
1. Use the approved Power Cord (3-core mains lead) /
Appliance Connector / Plug with earthing-contacts
that conforms to the safety regulations of each
country if applicable.
2. Use the Power Cord (3-core mains lead) / Appliance
Connector / Plug conforming to the proper ratings
(Voltage, Ampere).
If you have questions on the use of the above Power
Cord / Appliance Connector / Plug, please consult a
qualified service personnel.
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.
United States and Canada
Plug Type
HOSPITAL GRADE*
Cord Type
Min. Type SJT
Min. 18 AWG
Minimum Rating
10A/125V
for Plug and
Appliance
Couplers
Safety Approval
UL Listed and CSA
*Note: Grounding reliability can only be achieved when the
equipment is connected to an equivalent receptacle marked 'Hospital
Only' or 'Hospital Grade'.
Symbols on the unit
This symbol indicates the manufacturer, and
appears next to the manufacturer's name and
address.
Refer to the operating instructions
Follow the directions in the operating
instructions for parts of the unit on which this
mark appears.
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