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Protection class
Interval usage
Safety requirements according to EN 60601-1
Child use and care articles– Drinking equipment according to EN 14350
Device for expressing breast milk
Device with fine vacuum and low flow
Applied part, type BF
Device for use in the absence of explosive or poisonous gas mixtures or nitrogen oxides (nitrous oxide)
Technical specifications are subject to change without notification to allow for updates
Notes on electromagnetic compatibility
The device complies with the Regulation (EU) 2017/745 of the European Parliament and of the Council on medical devices as well as the re-
spective national provisions, as well as the European standard EN 60601-1-2 (in accordance with CISPR 11, IEC 61000-3-2, IEC 61000-3-3,
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
precautions with regard to electromagnetic compatibility.
• The device is suitable for use in all environments listed in these instructions for use, including domestic environments.
• The device may not be fully usable 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 outlined above, 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 resistance to electromagnetic interference; this can result in faulty operation.
• Failure to comply with the above could impair the performance of the device.
12. MAINS ADAPTER
Model no.
Input
Output
Housing and protective
covers
13. GUARANTEE / SERVICE
Further information on the guarantee and guarantee conditions can be found in the guarantee 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.
LXCP12-006100BEH
100 – 240 V, 50 – 60 Hz 0.5 A max.
6 V DC, 1 A
Polarity of the DC voltage connection
Insulated/protection class 2
The housing of the mains adapter protects users from touching live parts or parts that could be live (for
example with fingers, needles, or testing hooks). The user must not touch the patient and the output
connector of the AC mains adapter at the same time.
The device is double protected and corresponds to protection class 2
30 minutes ON / 30 minutes OFF
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