Caution; Maintenance - Riester ri-pen Instrucciones Para El Uso

cording to the instructions of use of the respective manufacturer of disinfectant.
Only disinfectants with proven effectiveness according to national guidelines
should be used. After disinfecting, wipe the diagnostic penlight with a damp
cloth to remove potential residue.
Please make sure that the cloth is moistened but not wet, so no moisture pene-
trates the openings of the examination lamp.
Make sure that glass and lenses are only cleaned with a dry and clean cloth.

Caution!

The diagnostic instruments are not sterile devices; they cannot be sterilized.
Caution!
Never place the examination lamps in liquids! Make sure that no liquids penet-
rate the housing interior! The article is not approved for machine reprocessing
and sterilisation.
This can lead to irreparable damage!
If a reusable device shows signs of material deterioration, it should no longer
be used and should be disposed of according to the procedures described in the
Disposal/Warranty section.

2.9. Maintenance

The instruments and their accessories require no special maintenance.
If an instrument needs to be tested for any reason, please contact the Riester
office directly, or contact an authorized Riester dealer in your area, the details
of which we will provide you upon request.
CAUTION!
There may be a risk of ignition if the device is operated in the presence of flam-
mable mixtures of pharmaceuticals and air, oxygen, nitrous oxide or anaes-
thetic gases! Safety information according to international standard IEC 60601-
1 „Medical electrical equipment - Part 1: General requirements for basic safety
and essential performance": It is not permitted to open the battery handle in
the vicinity of the patient or to touch batteries and the patient simultaneously.
3. Electromagnetic compatibility
according to IEC 60601-1-2, 2014, Ed. 4.0
Caution:
Medical electrical equipment is subject to special precautions regarding elec-
tromagnetic compatibility
(EMC).
Portable and mobile radio frequency communication devices can affect medical
electrical equipment. The ME device is intended for operation in a home health
care electromagnetic environment and for professional facilities such as indus-
trial areas and hospitals.
The user of the device should ensure that it is operated within such an en-
vironment.
Warning:
The ME device may not be stacked, arranged or used directly next to or with
other devices. When use close to or stacked with other devices is required, the
ME device and the other ME devices must be monitored to ensure intended
operation within this configuration. This ME device is intended for use by me-
dical professionals only. This device may cause radio frequency interference or
interfere with the operation of nearby devices. It may become necessary to take
appropriate corrective measures, e.g. re-positioning, re-configuring or shiel-
ding the ME device.
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