Appendix
Page 70
heyer_LUVAR_UserManual_EN-3_CRev-1
Item
Item number
Image
Patient instruction for use
320003
Electromagnetic compatibility
The device meets the requirements of standard IEC 60601-1-2:2014/AMD1:2020
and is intended for use in the electromagnetic environment described below.
Environmental conditions deviating from this could impair the performance of the
device or lead to failure of the device.
WARNING: Risk of injury due to electromagnetic interference!
• Replacing the components listed below may result in increased electromag-
netic interference emissions or reduced electromagnetic interference immuni-
ty for the respiratory therapy device and lead to faulty operation:
Ö Power supply unit, DA-80A24
Electromagnetic interference emission
Guidelines and manufacturer’s declaration – electromagnetic interference emission
The LUVAR respiratory therapy device with or without the H100 respiratory hu-
midifier is intended for use in domestic settings as well as in appropriate clinical
settings. Device users must ensure that it is used in such a setting. When used in a
residential setting (for which Class B is typically required by CISPR 11), this device
may not provide adequate protection from radio communication services. The user
may need to take remedial action such as relocating or repositioning the device.
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