General Information - Lowenstein Medical prisma CHECK Gebrauchsanweisung

2.2 General information

• Use of third-party products may lead to functional failures and
restricted fitness of purpose. Biocompatibility may also be
compromised. Please note that in these cases, any claim under
warranty and liability will be void if neither the accessories nor
original replacement parts recommended in the instructions for
use are used.
• Repairs, servicing and maintenance should only be carried out
by the manufacturer, or by a technician expressly authorized by
the manufacturer.
• The device is subject to special precautions with regard to EMC
(electromagnetic compatibility). Maintain the recommended
safety distances
between the device and devices which emit high-frequency
radiation (e.g. cellphones) to prevent malfunctions.
• Only connect up the approved SpO
SpO connection cable.
2
• Please note that no SpO
combination with WM 100 TD therapy devices.
• A functional test facility cannot be used to assess the accuracy
of the SpO
• When used with non-approved electrical medical devices or
systems, increased electromagnetic emissions or reduced radio
interference immunity may occur.
• The operator is responsible for ensuring the compatibility of the
therapy device and all the connected components and
accessories prior to the application with the patient.
Only have modifications to the unit carried out by the
manufacturer, or by a technician expressly authorized by the
manufacturer.
• Please observe the chapter on hygienic preparation in order to
avoid infection or bacterial contamination (see chapter
"Hygienic preparation").
• Also observe the respective instructions for use for the therapy
device, the components, and the accessories.
(see "10.2 Safety distances", page 44)
or pulse rate alarms occur in
2
values.
2
sensors and the approved
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prisma CHECK EN 29