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22
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This device complies with the EU Directive 93/42/EEC concerning medical products, the Medizinproduktege-
setz (German Medical Devices Act), the ASTM (American Society for Testing and Materials) E 1965 - 98 and the
European Standard EN 12470-5: Clinical thermometers – Part 5: Requirements for infrared ear thermometers
(with maximum device) ISO 80601-2-56 and the European Standard EN60601-1-2 (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. Please note that portable and mobile HF communication systems may interfere with this unit.
For more details, please contact our Customer Services at the address indicated.
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If you should have any questions about using our devices, please contact either your retailer or customer
services.
Notes on electromagnetic compatibility
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The device is suitable for use in all environments listed in these instructions for use, including domestic
environments.
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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.
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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.
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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.
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Failure to comply with the above can impair the performance of the device.
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