Clements SUC84602, Руководство пользователя

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supply tolerated, which is indicated on the adapters and
extensions.
4. For repairs, exclusively contact technical service and request the
use of original spare parts. Failure to comply with the above can
jeopardise the safety of the device.
5. Use only for the purpose intended. Don’t use for anything other
than the use defined by the manufacturer.
The manufacturer will not be responsible for damage due to
improper use or connection to an electrical system not complying
with current regulation.
6. Instrument and accessory disposal must be done according to
current regulations in the country of use.
7. WARNING: Do not change this equipment without the permission
of the manufacturer. None of electric or mechanical parts have
been designed to be repaired by customers or end-users. Don’t
open the device, do not mishandle the electric / mechanical parts.
Always contact technical assistance
8. Using the device in environmental conditions different than those
indicated in this manual may harm seriously the safety and the
technical characteristics of the same.
9. The medical device is in contact with the patient by means of a
disposable probe (not supplied with the device). If this device must
be used with a specific suction probe, the end user is responsible
for making sure it complies with the ISO 10993-1 rule.
10. The product and its parts are biocompatible in accordance with
the requirements of regulation EN 60601-1.
11. Operation of the device is very simple and therefore no further
explanations are required other than those indicated in the
following user manual.
12. The medical device requires special precautions regarding
electromagnetic compatibility and must be installed and used
in accordance with the information provided with the
accompanying documents. The HiFlo2 Max device must be
installed and used away from mobile and portable RF
communication devices (mobile phones, transceivers, etc.) that
may interference with the said device.