The monitor N10/N10A/N10C/N12/N12A/N12C/N15/N15A/N15C complies with the applicable EMC
requirements in IEC 60601-1-2:2014, IEC 60601-2-25:2011, IEC 60601-2-27:2011, IEC 80601-2-30:2018,
IEC 60601-2-34:2011, ISO 80601-2-55:2018, ISO 80601-2-56:2017+A1:2018, ISO 80601-2-61:2017.
Please follow the EMC instructions in the User’s Manual to install and use the Monitor.
Portable and mobile RF communication equipment may affect the performance of the monitor
N10/N10A/N10C/N12/N12A/N12C/N15/N15A/N15C. To protect the Monitor against strong
electromagnetic interference, please keep it away from mobile phones, microwave ovens, etc.
Refer to the attached guidance and manufacturer’s statement.
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 the normal operation.
Class-A equipment are intended to work in industrial environments. Considering this product’s
conduction disturbance and radiation disturbance, it may be difficult to ensure its EMC in non-
industrial environments.
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.
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 N series patient monitor,
including cables specified by the manufacturer. Otherwise, degradation of the performance of this
equipment could result.
Inaccurate results may occur, if the monitor N10/N10A/N10C/N12/N12A/N12C/N15/N15A/N15C
operates at the PR, RR and HR below the allowed extreme low limit specified on this User’s Manual.
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