Gima SP-20 Mode D'emploi page 38

tional 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 tissue.
 The local law should be followed when disposing of the expired device or its acces-
sories.
 DO NOT operate in the environment where strong electro-magnetic interference
exists, such as radiogram, television, radiophone, etc.
 Please pay attention to the SpO
patient.
Notes
 Keep the oximeter away from dust, vibration, corrosive substances, explosive ma-
terials, 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 environ-
ment to a warm and humid environment, please do not use it immediately. 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 oximeter
and probes. Refer to related chapter for instructions regarding cleaning and disin-
fection.
 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 stand-
ards:
IEC 60601-1: 2020 Medical electrical equipment-Part 1: General requirements for ba-
sic safety and essential performance;
ISO 80601-2-61: 2017 - Medical electrical equipment -- Part 2-61: Particular require-
ments for basic safety and essential performance of pulse Oximeter equipment.
And it also follows the provisions of the council directive MDD 93/42/EEC.
ENGLISH
probe cable while using to avoid strangulating
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