Electromagnetic compatibility (en 60650-1), Fcc statement (usa), Emc-compliance for canada – Kontron Medi Client IIA 104 (EOL) User Manual
Page 12: Electromagnetic compatibility for eu, Electromagnetic compatibility (en60601-1-2)

5. General Safety Instructions
Medi Client IIA - Instructions for use (Version 1.03)
5.3. Electromagnetic Compatibility (EN 60650-1)
5.3.1. FCC Statement (USA)
This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of the
FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential
installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in
accordance with the instructions, may cause harmful interference to radio communications. However, there is no
guarantee that interference will not occur in a particular installation.
If this equipment does cause harmful interference to radio or television reception, which can be determined by turning
the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following
measures:
Reorient or relocate the receiving antenna.
Increase the separation between the equipment and receiver.
Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
Consult the dealer or an experienced radio/TV technician for help.
5.3.2. EMC-Compliance for Canada
(English): This Class B digital apparatus complies with the Canadian ICES-003.
(French) : Cet appareil numérique de la class B est conforme à la norme NMB-003 du Canada.
5.3.3. Electromagnetic Compatibility for EU
This product has been designed for low level of radiated emission for residential, commercial and light-industrial
environments and high immunity level for industrial environmental. This product complies with the European Council
Directive on the approximation of the laws of the member states relating to electromagnetic compatibility
(2004/108/EC).
If the user modifies and/or adds to the equipment (e.g. installation of add-on cards) the prerequisites for the CE
conformity declaration (safety requirements) may no longer apply.
5.4. Electromagnetic Compatibility (EN60601-1-2)
The separation distances are written with regard to the Medi Client IIA system. The numbers provided will not guarantee
faultless operation but should provide reasonable assurance of such. This information may not be applicable to other
medical electrical equipment, and older equipment may be particularly susceptible to interference.
General Information
Medical electrical equipment needs special precautions regarding electromagnetic compatibility (EMC) and needs to be
installed and put into service according to the EMC information provided in this “Instruction for Use”.
Portable and mobile RF communications equipment can affect medical electrical equipment.
Cables and accessories not specified within the “Instructions for Use” are not authorized. Using other cables and/or
accessories may adversely impact safety, performance and electromagnetic compatibility (increased emission and
decreased immunity).
Caution:
The Medi Client IIA should not be used adjacent to or stacked with other equipment; if adjacent or stacked use is
inevitable, the equipment should be observed to verify normal operation in the configuration in which it will be used.
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