- 3 -
●
Obstructions or dirt on the probe’s red light or detector may cause a probe failure. Make
sure there are no obstructions and the probe is clean.
●
The AC adapter and accessories used with the device should be complied with the
requirement of IEC60601-1.
●
For routine equipment maintenance, please refer to the service procedures at the
associated section as indicated in the manual.
●
As to the other concerns for attention, please carefully look through the speci
fi
c chapter in
this instruction.
●
Federal law restricts this device to sale by or on the order of a physician.
This pulse oximeter is designed and tested in compliance with the EMC standard, complying
with the international standard for the EMC of the electronic medical device - IEC 60601-1-2.
However, because of the proliferation of radio frequency transmitting equipment and
other sources of electrical noise in the health-care and home environments (e.g. cellular
phones, mobile two-way radios, electrical appliances), it is possible that high levels of
such interference due to close proximity or strength of a source, may result in disruption of
performance of this device.
This apparatus complies with the IEC 60601-1-2 international standard. The requirements of
this international standard are: CISPR11, GROP1, and CLASS B.
1.3 Electromagnetism Interference
INSTRUCTION MANUAL
