Warnings/Caution - Riester e-scope Mode D'emploi

1.8. Warnings/caution

Warning
The general warning symbol indicates a potentially dangerous situation that can lead
to serious injuries.
Do not use in a magnetic resonance environment!
There is a risk of ignition of gases if the device is operated in the presence of flam-
mable mixtures or mixtures of medicinal products and air or oxygen or nitrous oxide!
The device must not be operated in rooms in which flammable mixtures or mixtu-
res of pharmaceuticals and air or oxygen or nitrous oxide are present, e.g. operating
theatres.
Electric shock!
The housing of the ri-scope L may only be opened by authorised persons.
Damage to the device due to a fall or strong ESD influence!
If the device is not functioning, it must be returned to the manufacturer for repair.
The device must be used in a controlled environment.
The device must not be exposed to harsh environmental conditions.
Caution!:
The caution symbol indicates a potentially dangerous situation that can lead to minor
or moderate injuries. It can also be used to warn of unsafe practices.
The faultless and safe functioning of the ri-scope L instruments can only be guaran-
teed if Riester original parts and accessories are used.
Old electronic devices must be disposed of in accordance with the institutional guide-
lines for the disposal of expired devices.
Cleaning frequency and sequence must comply with the cleaning regulations of
non-sterile products in the respective facility. Cleaning/disinfection instructions in the
instructions for use must be observed.
We recommend removing the (rechargeable) batteries from the battery handle before
cleaning or disinfecting.
Clean and disinfect the Instruments carefully so that no liquid penetrates the interior.
Never place the Instrument in liquids!
The instruments with battery handles are supplied in a non-sterile condition. Do not
use ethylene, oxide gas, heat, autoclaves, or other methods that place undue stress
on the material to sterilize the device. The devices have not been approved for mecha-
nical reprocessing or sterilisation. This leads to irreparable damage!
The patient is not the intended operator.
The product may only be used by qualified personnel.
Qualified personnel are doctors or nurses in hospitals, medical facilities, clinics and
medical practices.
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