Sony DXC-C33P Instructions For Use Manual page 3

For the customers in Europe
The manufacturer of this product is Sony
Corporation, 1-7-1 Konan, Minato-ku,
Tokyo, Japan.
The Authorized Representative for EMC,
medical devices, and product safety is Sony
Deutschland GmbH, Hedelfinger Strasse 61,
70327 Stuttgart, Germany; TEL: (0)711
5858 0; FAX: (0)711 5858 235.
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.
This unit can not be used in the patient
environment.
* Patient Environment.
3. Do not touch the patient simultaneously
while you are contacting with this
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. The leakage current could increase when
connected to other equipment.
6. 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.
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