Emc Declaration - Berrcom JXB-195 Instruction Manual

XIII. EMC DECLARATION
The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare and clinic environments.
Warning: Do not use it near active HF surgical equipment and the RF shielded room of an ME system
for magnetic resonance imaging, where the intensity of EM disturbances is high.
Warning: Use of this equipment adjacent to or stacked with other equipment should be avoided
because it could result in improper operation. If such use is necessary, this equipment and the other
equipment should be observed to verify that they are operating normally.
Warning: Use of accessories, transducers, and cables other than those specified or provided by the
manufacturer of this equipment could result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in improper operation."
Warning: Portable RF communications equipment (including peripherals such as antenna cables and
external antennas) should be used no closer than 30 cm (12 inches) to any part of the equipment
JXB-195, including cables specified by the manufacturer. Otherwise, degradation of the performance
of this equipment could result.
1， All necessary instructions for maintaining BASIC SAFETY and ESSENTIAL PERFORMANCE with
regard to electromagnetic disturbances for the excepted service life.
Portable and mobile RF communication equipment may affect the performance of the JXB-195,
avoiding strong electromagnetic interference when used, such as near mobile phones, microwave
ovens, etc.
2， Guidance and manufacturer's declaration -electromagnetic emissions and immunity
DISPOSAL: Do not dispose of this product as unsorted municipal
waste. Collection of such waste separately for special treatment is
necessary.
Manufacturer
Serial number
Date of manufacture
Model number
Made in China
Medical device
Symbol of European Authorized Representative, expressly indicate
the name and address of European Authorized Representative
after the symbol
The CE labelling certifies that the product complies with the
essential requirements of Directive 93/42/EEC on medical device.
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