Biolight Meditech E30 - Appendix F Guidance and Manufacturers; Appendix F Guidance and Manufacturers Declaration of EMC

E30 Digital Electrocardiograph User’s Manual
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Appendix F Guidance and Manufacturer’s
Declaration of EMC
Guidance and manufacturer’s declaration – electromagnetic emissions-
for all EQUIPMENT and SYSTEMS
Row
Guidance and manufacture’s declaration – electromagnetic emission
The E30 Digital Electrocardiograph is intended for use in the electromagnetic environment specified below. The
customer or the user of E30 Digital Electrocardiograph should assure that it is used in such an environment.
Emission test Compliance Electromagnetic environment – guidance
RF emissions
CISPR 11
Group 1
The E30 Digital Electrocardiograph uses RF energy
only for its internal function. Therefore, its RF
emissions are very low and are not likely to cause any
interference in nearby electronic equipment.
RF emission
CISPR 11
Class A
The E30 Digital Electrocardiograph is suitable for use
in all establishments other than domestic, and may be
used in domestic establishments and those directly
connected to the public low-voltage power supply
network that supplies building used for domestic
purposes, provided the following warning is heeded.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/ flicker
emissions
IEC 61000-3-3
Complies