
24
Subject t
o err
ors and changes
• 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.
LXCP62 (II)-240
Input
100–240 V ~ 50/60 Hz, 1.5 A max
Output
24 V DC, 2.5 A
Protection
The device is double-protected.
Polarity of the DC voltage connection
Classification
IP24, protection class II
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.
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