KaVo KaVoLUX 540 LED U, Technician'S Instructions

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Technician's instructions KaVoLUX 540 LED U / T
2 Safety | 2.2 Purpose – Proper use
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The product complies with the requirements of DIN EN ISO 9680.
The KaVoLUX 540 LED U can be mounted to the following treatment units:
▪ ESTETICA E80 / E80 Vision
▪ ESTETICA E70 / E70 Vision
▪ ESTETICA E50 / E50 Life
The KaVoLUX 540 LED T can be mounted in the following positions/to the following
treatment centres:
▪ on the ceiling
▪ Primus 1058 / 1058 Life
▪ Status 1080
▪ Globus 1078
▪ ESTETICA Sensus 1066
▪ ESTETICA Comfort 1065
▪ ESTETICA Standard 1063
▪ ESTETICA E30
▪ DSEclinical
▪ CENTRO support system
Intended use also comprises the observation of all indications in the instructions for
used as well as adherence to prescribed inspections and maintenance.
Application of and compliance with the general guidelines and/or national laws, na-
tional regulations, and the rules of technology applicable to this product for start-up
and use of the KaVo product for the intended purpose are to be applied and complied
with.
The user must ensure that the device works safely and is in a satisfactory condition
before each use.
Note
The treatment light may no longer be operated if the functional safety and the fault-
less condition of the device cannot be guaranteed.
2.2.1 Information on electromagnetic compatibility
Note
Based on IEC 60601-1-2 (DIN EN 60601-1-2) concerning the electromagnetic com-
patibility of electrical medical devices, we must draw your attention to the following
points:
• Electrical medical devices are subject to special precautionary measures regard-
ing electromagnetic compatibility and must be operated in accordance with the
KaVo installation instructions.
• High-frequency communications devices can affect the operation of electrical
medical devices.
Further details of the technical EMC description are available on request.