Safety precautions • 7
17-10-01-266-002a/07-2018B
2.2 Basic safety precautions
Using the software ► Please take note of the information in these instructions for use.
► Keep the instructions for use and the declaration of conformity they
include in a safe place. The current version of the instructions for use can
be found at www.seca.com. The instructions for use are a component of
the software and must be available at all times.
CAUTION!
Patient hazard, malfunction
► Only install the secaconnect 103 software on PCs equipped with an
antivirus program. Always keep your antivirus program up to date to
protect your computer system from current and future malware. The
secaconnect 103 software is protected from manipulation and was
checked for malware at the time the software was created.
► Use the
secaconnect 103 PC software only for the specified intend-
ed use.
► Keep other electrical medical devices, e.g. high-frequency surgical
devices, a minimum distance of approx. 1 meter away to prevent in-
correct measurements or wireless transmission interference.
► Keep HF devices such as cell phones and televisions, for example,
a minimum distance of approx. 1 meter away to prevent incorrect
measurements or wireless transmission interference.
► The actual transmission output of HF equipment may require mini-
mum distances of more than 1 meter. Details can be found at
www.seca.com.
Handling the device ► Please take note of the information in these instructions for use.
► Keep the instructions for use in a safe place. The instructions for use are a
component of the device and must be available at all times.
DANGER!
Risk of explosion
Do not use the device in an environment in which one of the following
gases has accumulated:
–oxygen
– flammable anesthetics
– other flammable substances/air mixtures
CAUTION!
Patient hazard, damage to device
► Additional devices which are connected to electrical medical devic-
es must provide evidence of compliance with the relevant IEC or ISO
standards (e.g. IEC 60950 for data-processing devices). Further-
more, all configurations must comply with the requirements of stan-
dards for medical systems (see IEC 60601-1-1 or Section 16 of the
3rd edition of IEC 60601-1 respectively). Anyone connecting addi-
tional devices to electrical medical devices is considered a system
configurer and is therefore responsible for ensuring that the system
complies with the requirements of standards for systems. Your at-
➔ Using the software
➔ Handling the device
➔ Preventing electric shock
➔ Prevent damage to device
➔ Handling measured results
➔ Handling packaging material
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