Beurer TL 85 Mode D'emploi page 23

Brightness: 10,000 lux (this point about the light intensity is merely for information purposes. With regard
to the standard IEC 60601-2-83, this light source is classified as an Exempt Group).
Notes on electromagnetic compatibility
The device complies with Regulation (EU) 2017/745 of the European Parliament and of the Council on
medical devices and the respective national regulations and the European standard EN 60601-1-2 (in ac-
cordance with CISPR 11, IEC61000-3-2, IEC61000-3-3, IEC 61000-4-2, IEC 61000-4-3, IEC 61000-4- 4,
IEC 61000-4- 5, IEC 61000-4- 6, IEC 61000-4- 11, IEC 61000-4-8) and is subject to particular precauti-
ons with regard to electromagnetic compatibility.
• The device is suitable for use in all environments listed in these instructions for use, including domestic
environments.
• 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 immu-
nity; this can result in faulty operation.
• Failure to comply with the above can impair the performance of the device.
Mains adapter
Model no.
Input
Output
Protection
Classification
13. WARRANTY
Further information on the warranty and warranty conditions can be found in the warranty leaflet supplied.
Notification of incidents
For users/patients in the European Union and identical regulation systems (EU Medical Device Regulation
(MDR) 2017/745), the following applies: If during or through use of the product a major incident occurs,
notify the manufacturer and/or their representative of this as well as the respective national authority of
the member state in which the user/patient is located.
LXCP62 (II)-240
100–240 V ~ 50/60 Hz, 1.5 A max.
24 V DC, 2.5 A
The device is double-protected.
Polarity of the DC voltage connection
IP24, protection class II
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