Connected Devices; Safe Connection With Other Electrical Equipment; Patient Safety; Patient Monitoring - Dräger Oxylog 3000 plus Instructions For Use Manual

Connected devices

WARNING
Risk of electric shock and of device malfunc-
tion
Any connected devices or device combination
not complying with the requirements set out in
these instructions for use may compromise
the correct functioning of the medical device
and lead to an electric shock. Before operat-
ing the medical device, strictly comply with
the instructions for use of all connected
devices or device combinations.
Safe connection with other electrical
equipment
WARNING
Risk of patient injury
Electrical connections to equipment not listed
in these instructions for use or these
assembly instructions must only be made
when approved by each respective manufac-
turer.

Patient safety

The design of the medical device, the
accompanying literature, and the labeling on the
medical device are based on the assumption that
the use of the equipment is restricted to trained
professionals, and that certain inherent
characteristics of the medical device are known to
the trained operator. Instructions, warnings, and
caution statements are therefore largely limited to
the specifics of the Dräger medical device.
This publication excludes references to various
hazards which are obvious to a medical
professional and operator of this medical device, to
the consequences of medical device misuse, and to
potentially adverse effects in patients with abnormal
conditions.
Instructions for use Oxylog 3000 plus SW 1.n
For your safety and that of your patients
Medical device modification or misuse can be
dangerous.
WARNING
Risk of patient injury
Do not make therapeutic decisions based
solely on individual measured values and
monitoring parameters.

Patient monitoring

The operators of the medical device are
responsible for choosing appropriate safety
monitoring that provides adequate information on
medical device performance and patient condition.
Patient safety may be achieved through a wide
variety of means, ranging from electronic
surveillance of medical device performance and
patient condition, to simple, direct observation of
clinical signs.
The responsibility for the selection of the best level
of patient monitoring lies solely with the medical
device operator.
Information on electromagnetic
compatibility
General information on electromagnetic
compatibility (EMC) pursuant to the international
EMC standard IEC 60601-1-2:
Electromedical devices are subject to special
precautionary measures concerning
electromagnetic compatibility (EMC) and must be
installed and put into operation in accordance with
the EMC information. Refer to section
"EMC declaration" on page 151.
WARNING
Do not use portable and mobile RF telecom-
munication devices (such as cellular phones)
in the immediate vicinity of the medical
device.
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