Biocompatibility tests have been performed on all the applied parts, some
exceptional allergic patients may still have anaphylaxis. Do not apply to those
who have anaphylaxis.
For the individual patients, there should be a more prudent inspecting in the
placing process. The sensor can not be placed on the edema and tender tis-
sue.
The local law should be followed when disposing of the expired device or its
accessories.
DO NOT operate in the environment where strong electro-magnetic interferen-
ce exists, such as radiogram, television, radiophone, etc.
Please pay attention to the SpO
patient.
Attentions
Keep the oximeter away from dust, vibration, corrosive substances, explosive
materials, high temperature and moisture.
If the Oximeter gets wet, please stop operating it and do not resume operation
until it is dry and checked for correct operation. When it is carried from a cold
environment to a warm and humid environment, please do not use it immedia-
tely. Allow at least 15 minutes for the Oximeter to reach ambient temperature.
DO NOT operate the button on the front panel with sharp materials or sharp
point.
DO NOT use high temperature or high pressure steam disinfection on the oxi-
meter and probes. Refer to related chapter for instructions regarding cleaning
and disinfection.
The intended use of this device is not for therapy purpose.
The equipment is IP22 with protection against harmful solid foreign objects
and ingress of liquid. So that means the equipment is protected against solid
foreign objects of 12.5mm and greater, and protected against vertically falling
water drops when enclosure tilted up to 15°.
Please pay attention to the effects of lint, dust, light (including sunlight), etc
Declaration of Conformity
The manufacturer hereby declares that this device complies with the following
standards: IEC 60601-1:2005+A1: 2012, IEC60601-1-2:2014, IEC60601-1-
11:2010, ISO 80601-2-61:2011 and follows the provisions of the council directive
MDD93/42/EEC.
ENGLISH
probe cable while using to avoid strangulating
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