For the customers in Europe (for
DXC-C33P)
Important safeguards/notice 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.
GB
3
GB