Guidelines; Warranty/Service - Beurer FT 90 Mode D'emploi

16. Guidelines

The device complies with the EU Medical Devices Directive 93/42/EEC, the German Medical Devices Act (Mediz-
inproduktgesetz), the ASTM E 1965 - 98 and the European standard EN 60601-1-2 (in accordance with CISPR11,
IEC61000-4-2, IEC61000-4-3, IEC61000-4-8) and is subject to particular precautions with regard to electromag-
netic compatibility.
Notes on electromagnetic compatibility
• The device is suitable for use in all environments listed in these instructions for use, including domestic envi-
ronments.
• The use of the device may be limited in the presence of electromagnetic disturbances. This could result in issues
such as error messages or the failure of the display/device.
• Avoid using this device directly next to other devices or stacked on top of other devices, as this could lead to
faulty operation. If, however, it is necessary to use the device in the manner stated, this device as well as the
other devices must be monitored to ensure they are working properly.
• The use of accessories other than those specified or provided by the manufacturer of this device can lead to
an increase in electromagnetic emissions or a decrease in the device's electromagnetic immunity; this can
result in faulty operation.
• Failure to comply with the above can impair the performance of the device.

17. Warranty/service

In case of a claim under the warranty please contact your local dealer or the local representation which is men-
tioned in the list "service international".
In case of returning the unit please add a copy of your receipt and a short report of the defect.
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