Operation Manual

EN
22
INTRODUCTION
the START/STOP key to prevent
further inflation.
• The device is not approved for
AP or APG categories.
• Avoid interference signals
emitted by strong electromag-
netic fields or rapid transient
disturbances to prevent measur-
ing errors.
• The device is not suited for
continuous blood pressure
monitoring in medical emer-
gencies. Blood circulation may
be disrupted.
• The cuff material has been test-
ed and is proven to correspond
to the requirements of ISO
10993-5:2009 and ISO 10993-
10:2010. It does not cause skin
irritation or other reactions.
• Please use only the ACCES-
SORIES and removable parts
prescribed by the manufacturer.
Otherwise, danger may arise for
the user and the device.
• Please inform Soehnle customer
service of unexpected operating
status or events.
• The optional adapter is a
component of the MEDICAL
ELECTRICAL DEVICE.
• The plugs/pins of the adapter
plug isolate the device against
the mains power supply.
• Please do not place the device
in a location in which it is
difficult to disconnect from the
power supply.
• Keep the device outside of
the reach of small children/
pets to prevent the inhalation
or swallowing of small parts.
The cable/cord poses a risk of
strangulation.
• When stored at the minimum
storage temperature between
uses, electrical medical devices
must be warmed up for at least
30 minutes before they are
operational. When stored at the
maximum permissible storage
temperature between uses,
electrical medical devices must
cool off for at least 30 minutes
before they are operational.
• Please carefully monitor a
possible interruption of blood
circulation and a possible injury
of the patient.
• Do not place the cuff over a
wound as this may cause further
injuries.
• Do not place the cuff on the
same arm on which other
electrical medical devices are
placed.