Instructions for use arco-matic 200 M / 300 M - Version 2018-05-08 GBR ID no. 2038823A
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Important safety information
Use of the product
This product is state-of-the-art and was built
according to recognised safety rules. Nevertheless,
risks to the life and limb of users or third parties
may occur, or this product and other assets may be
adversely aff ected by the use of this product. This
product must only be used in sound condition and
for its intended use.
Suitability for use in oxygenated atmosphere
The examination chair must not be operated in an
oxygenated atmosphere.
Technical changes
It is not permitted to modify the examination and
treatment chair without the consent of the manufac-
turer.
Attaching accessories
When mounting accessories , always check the
condition of the accessory, and make sure that it is
attached securely.
Replacement parts
Replacement parts have to meet the requirements
established by SCHMITZ u. Söhne. Using original
replacement parts guarantees at all times that the
parts comply with requirements.
Non-slip setup
Before and during use of the product, it must be
ensured that the product has suffi
cient fl oor adhe-
sion and that there is good slip resistance for both
product and user.
Mandatory training
This product may only be operated by persons
instructed in its proper use.
Patient positioning
The user must be familiar with and must comply with
the applicable organisational and national rules and
regulations for the proper positioning of patients.
The nursing staff are responsible for ensuring that
the patients are positioned in such a way that no
threats are posed to respiration, the nervous system
or the circulatory system. This applies in particular to
anaesthetised or unconscious patients.
HF devices
Combination with HF or defi brillator devices is
possible. Please note that the patient must be insu-
lated from the examination and treatment chair. Use
electrically insulated underlays between the patient
and the examination and treatment chair. To this end,
the instructions for use issued by the device manu-
facturer must be complied with.
Checklist
Perform a visual and functional check regularly
according to the device-specifi c checklist provided
in these instructions for use.